www.fgks.org   »   [go: up one dir, main page]

You seem to have javascript disabled. Please note that many of the page functionalities won't work as expected without javascript enabled.
 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (2,946)

Search Parameters:
Keywords = Salmonella

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
83 pages, 571 KiB  
Article
Collider Bias Assessment in Colombian Indigenous Wiwa and Kogui Populations with Chronic Gastroenteric Disorder of Likely Infectious Etiology Suggests Complex Microbial Interactions Rather Than Clear Assignments of Etiological Relevance
by Hagen Frickmann, Joy Backhaus, Achim Hoerauf, Ralf Matthias Hagen and Simone Kann
Microorganisms 2024, 12(5), 970; https://doi.org/10.3390/microorganisms12050970 (registering DOI) - 11 May 2024
Viewed by 81
Abstract
Multiple microbial detections in stool samples of indigenous individuals suffering from chronic gastroenteric disorder of a likely infectious origin, characterized by recurring diarrhea of variable intensity, in the rural north-east of Colombia are common findings, making the assignment of etiological relevance to individual [...] Read more.
Multiple microbial detections in stool samples of indigenous individuals suffering from chronic gastroenteric disorder of a likely infectious origin, characterized by recurring diarrhea of variable intensity, in the rural north-east of Colombia are common findings, making the assignment of etiological relevance to individual pathogens challenging. In a population of 773 indigenous people from either the tribe Wiwa or Kogui, collider bias analysis was conducted comprising 32 assessed microorganisms including 10 bacteria (Aeromonas spp., Campylobacter spp., enteroaggregative Escherichia coli (EAEC), enteropathogenic Escherichia coli (EPEC), enterotoxigenic Escherichia coli (ETEC), Salmonella spp., Shiga toxin-producing Escherichia coli (STEC), Shigella spp./enteroinvasive Escherichia coli (EIEC), Tropheryma whipplei and Yersinia spp.), 11 protozoa (Blastocystis spp., Cryptosporidium spp., Cyclospora spp., Dientamoeba fragilis, Entamoeba coli, Entamoeba bangladeshi/dispar/histolytica/moshkovskii complex, Entamoeba histolytica, Endolimax nana, Giardia duodenalis, Iodamoeba buetschlii and Pentatrichomonas hominis), 8 helminths (Ascaris spp., Enterobius vermicularis, Hymenolepis spp., Necator americanus, Schistosoma spp., Strongyloides spp., Taenia spp. and Trichuris spp.), microsporidia (Encephalocytozoon spp.) and fungal elements (microscopically observed conidia and pseudoconidia). The main results indicated that negative associations potentially pointing towards collider bias were infrequent events (n = 14), while positive associations indicating increased likelihood of co-occurrence of microorganisms quantitatively dominated (n = 88). Microorganisms showing the most frequent negative associations were EPEC (n = 6) and Blastocystis spp. (n = 3), while positive associations were most common for Trichuris spp. (n = 16), Dientamoeba fragilis (n = 15), Shigella spp./EIEC (n = 12), Ascaris spp. (n = 11) and Blastocystis spp. (n = 10). Of note, positive associations quantitively dominated for Blastocystis spp. In conclusion, collider bias assessment did not allow clear-cut assignment of etiological relevance for detected enteric microorganisms within the assessed Colombian indigenous population. Instead, the results suggested complex microbial interactions with potential summative effects. Future studies applying alternative biostatistical approaches should be considered to further delineate respective interactions. Full article
(This article belongs to the Special Issue Novel Strategies in the Study of the Human Gut Microbiota 2.0)
11 pages, 1309 KiB  
Article
Genes of Salmonella enterica Serovar Enteritidis Involved in Biofilm Formation
by Seulgi Lee and Jinru Chen
Appl. Microbiol. 2024, 4(2), 771-781; https://doi.org/10.3390/applmicrobiol4020053 - 10 May 2024
Viewed by 297
Abstract
Although biofilms contribute to bacterial tolerance to desiccation and survival in low-moisture foods, the molecular mechanisms underlying biofilm formation have not been fully understood. This study created a mutant library from Salmonella Enteritidis using mini-Tn10 transposon mutagenesis. The biofilm-forming potential of acquired [...] Read more.
Although biofilms contribute to bacterial tolerance to desiccation and survival in low-moisture foods, the molecular mechanisms underlying biofilm formation have not been fully understood. This study created a mutant library from Salmonella Enteritidis using mini-Tn10 transposon mutagenesis. The biofilm-forming potential of acquired mutants was assessed before the genomic DNA of the mutants that formed significantly (p ≤ 0.05) less biofilm mass than their wildtype parent strain was extracted for deep DNA sequencing. The gene of each mutant interrupted by mini-Tn10 insertion was identified by aligning obtained sequencing data with the reference Genbank sequences using a BLAST search. Sixty-four mutant colonies were selected, and five mutants that formed the least amount of biofilm mass compared to the wildtype parent strain were selected for sequencing analysis. The results of the BLAST search revealed that the gene interrupted by mini-Tn10 in each mutant is responsible for the biosynthesis of aldehyde dehydrogenase (EutE), cysteine desulfurase (SufS or SufE), a transporter protein, porin OmpL, and a ribbon–helix–helix protein from the CopG family, respectively. Knock-off mutant construction is a possible approach to verify the potential of the identified genes to serve as targets of antimicrobial intervention to control Salmonella colonization on low-moisture foods and in their production environment. Full article
Show Figures

Figure 1

Figure 1
<p>Cultures of a selected <span class="html-italic">Salmonella</span> mutant on tryptic soy agar supplemented with 100 μg/mL ampicillin (<b>left</b>) and XLT-4 agar (<b>middle</b>), as well as the cultures of the <span class="html-italic">E. coli</span> donor BW20767 [pink] and the <span class="html-italic">Salmonella</span> mutant [colorless] (<b>right</b>) on MacConkey agar.</p>
Full article ">Figure 2
<p>Biofilm mass developed by wildtype and mutant <span class="html-italic">S. enteritidis</span>. The data represent the A<sub>550</sub> values of the solutions of crystal violet extracted from biofilm mass. The error bars represent the standard deviations of the means. Means followed by different letters are significantly different (<span class="html-italic">p</span> ≤ 0.05). SE-PC: positive control from the wildtype parent strain.</p>
Full article ">Figure 3
<p>Mini-Tn<span class="html-italic">10</span> insertion locations in the SE-L3, SE-L19, SE-L29, SE-S15, and SE-S26 mutants on a circular chromosome map of <span class="html-italic">S. enteritidis</span> (accession no. CP050716.1).</p>
Full article ">
17 pages, 417 KiB  
Article
Microbiological Assessment of Dairy Products Produced by Small-Scale Dairy Producers in Serbia
by Biljana Aleksic, Bozidar Udovicki, Jovana Kovacevic, Zorana Miloradovic, Ilija Djekic, Jelena Miocinovic, Nikola Tomic and Nada Smigic
Foods 2024, 13(10), 1456; https://doi.org/10.3390/foods13101456 - 8 May 2024
Viewed by 256
Abstract
The microbiological quality of dairy products from small-scale producers in Serbia was analysed. A total of 302 dairy products [raw (n = 111) and pasteurized milk cheeses (n = 79) and kajmak (n = 112)], were collected and tested for [...] Read more.
The microbiological quality of dairy products from small-scale producers in Serbia was analysed. A total of 302 dairy products [raw (n = 111) and pasteurized milk cheeses (n = 79) and kajmak (n = 112)], were collected and tested for the presence of pathogens, Listeria monocytogenes and Salmonella spp., and enumerated for Coagulase-positive staphylococci (CPS), Escherichia coli, and yeasts and moulds. None of the samples tested positive for Salmonella spp., while L. monocytogenes was recovered from one raw milk cheese and five kajmak samples. Raw milk cheese and kajmak also had higher levels of indicator microorganisms, namely E. coli and yeast and moulds. Molecular serotyping grouped L. monocytogenes isolates into serogroups 1 (1/2a and 3a) and 3 (1/2b, 3b, and 7). When exposed to eight antibiotics, L. monocytogenes isolates were mostly sensitive, with the exception of oxacillin and reduced susceptibility to clindamycin, penicillin G, and trimethoprim/sulfamethoxazole, emphasizing the importance of continuous surveillance for antimicrobial resistance. Samples that tested positive for Listeria spp. also had higher loads of indicator microorganisms, namely E. coli and yeast and moulds, suggesting lapses in hygiene practices during production. Collectively, these data emphasize the need for improved food safety and hygiene practices among small-scale dairy producers. This is crucial to reduce the microbial contamination and improve both the quality and safety of dairy products in the Serbian market. Full article
(This article belongs to the Special Issue Dairy Product: Microbiology, Sensory and Physico-Chemical Analysis)
18 pages, 2585 KiB  
Article
Unveiling the Novel Benefits of Co-Administering Butyrate and Active Vitamin D3 in Mice Subjected to Chemotherapy-Induced Gut-Derived Pseudomonas aeruginosa Sepsis
by Fu-Chen Huang and Shun-Chen Huang
Biomedicines 2024, 12(5), 1026; https://doi.org/10.3390/biomedicines12051026 (registering DOI) - 7 May 2024
Viewed by 248
Abstract
Cancer patients face increased susceptibility to invasive infections, primarily due to ulcerative lesions on mucosal surfaces and immune suppression resulting from chemotherapy. Pseudomonas aeruginosa (P. aeruginosa) bacteremia is notorious for its rapid progression into fatal sepsis, posing a significant threat to [...] Read more.
Cancer patients face increased susceptibility to invasive infections, primarily due to ulcerative lesions on mucosal surfaces and immune suppression resulting from chemotherapy. Pseudomonas aeruginosa (P. aeruginosa) bacteremia is notorious for its rapid progression into fatal sepsis, posing a significant threat to cancer patients, particularly those experiencing chemotherapy-induced neutropenia. This bacterial infection contributes significantly to morbidity and mortality rates among such individuals. Our latest report showed the mutually beneficial effects of postbiotic butyrate on 1,25-dihydroxyvitamin D3 (1,25D3)-controlled innate immunity during Salmonella colitis. Hence, we investigated the impact of butyrate and 1,25D3 on chemotherapy-induced gut-derived P. aeruginosa sepsis in mice. The chemotherapy-induced gut-derived P. aeruginosa sepsis model was established through oral administration of 1 × 107 CFU of the P. aeruginosa wild-type strain PAO1 in C57BL/6 mice undergoing chemotherapy. Throughout the infection process, mice were orally administered butyrate and/or 1,25D3. Our observations revealed that the combined action of butyrate and 1,25D3 led to a reduction in the severity of colitis and the invasion of P. aeruginosa into the liver and spleen of the mice. This reduction was attributed to an enhancement in the expression of defensive cytokines and antimicrobial peptides within the cecum, coupled with decreased levels of zonulin and claudin-2 proteins in the mucosal lining. These effects were notably more pronounced when compared to treatments administered individually. This study unveils a promising alternative therapy that involves combining postbiotics and 1,25D3 for treating chemotherapy-induced gut-derived P. aeruginosa sepsis. Full article
(This article belongs to the Special Issue Aryl Hydrocarbon Receptor in Human Diseases)
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>The combined administration of butyrate and 1,25D3 effectively mitigates colitis in mice that have undergone chemotherapy and subsequently developed gut-derived <span class="html-italic">P. aeruginosa</span> sepsis. Female C57BL/6 mice aged 6–8 weeks sourced from Charles River, USA, were bred and maintained under specific-pathogen-free conditions at the Center for Cellular and Biomolecular Research in Kaohsiung, Taiwan. These mice were infected with <span class="html-italic">P. aeruginosa</span> PAO1-LAC at a concentration of 10<sup>7</sup> CFU (suspended in 100 μL PBS). An open control group was administered 100 μL of sterile 1xPBS buffer. Prior to and following infection, the mice were orally administered either a vehicle control (5% dimethyl sulfoxide), 1,25D3 at a dosage of 0.2 μg/25g mice/day (VD group), butyrate (BU group), or a combination of 1,25D3 and butyrate (VD + BU group) on a daily basis, as described in the Materials and Methods section. Diarrhea situation scores (<b>a</b>) of mice were recorded daily. The cecum specimens were surgically removed, fixed in formaldehyde, and subsequently processed for staining with hematoxylin and eosin (H&amp;E). (<b>b</b>) Representative histological images of the cecum from various experimental groups were captured at magnifications of 2×, 20× and 50×. (<b>c</b>) Pathological scoring for colitis was conducted based on the assessment of cecum sections obtained from mice in different experimental groups. The data shown are means ± SEM (<span class="html-italic">n</span> = 6 mice/group). *, <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 2
<p>The immunoregulatory effects of combined administration of 1,25D3 and butyrate on cecal cytokines and antimicrobial peptides in mice that had undergone chemotherapy and subsequently developed gut-derived <span class="html-italic">P. aeruginosa</span> sepsis. Female C57BL/6 mice, aged 6 to 8 weeks and obtained from Charles River, USA, were bred and housed under specific-pathogen-free conditions at the animal facility within the Center for Cellular and Biomolecular Research in Kaohsiung, Taiwan. Mice were either infected with <span class="html-italic">P. aeruginosa</span> PAO1-LAC at a concentration of 10<sup>7</sup> CFU suspended in 100 μL PBS or given 100 μL of sterile 1xPBS buffer as an open control. Before and after infection, mice received daily oral gavage of vehicle control (5% dimethyl sulfoxide), vitamin D3 at a dose of 0.2 μg/25 g mice/day (VD group), or butyrate (BU group), or a combination of both 1,25D3 and butyrate (VD + BU group), as described in <a href="#sec2-biomedicines-12-01026" class="html-sec">Section 2</a>. Total RNA was isolated from the cecal tissues of the mice. Subsequently, the gene expressions of various markers including IL-6 (<b>a</b>), IL-1β (<b>b</b>), TNF-α (<b>c</b>), IL-17A (<b>d</b>), IL-22 (<b>e</b>), and CRAMP (a homolog of human cathelicidin LL-37) (<b>f</b>), as well as ATG16L1 (<b>g</b>) and AhR (<b>h</b>) mRNA, were assessed using real-time quantitative PCR. The values obtained were determined as fold increases relative to the levels observed in mice solely infected with <span class="html-italic">Salmonella</span> for comparison purposes. The presented data are displayed as means ± the standard error of the mean (SEM) with a sample size of 7 mice per group (<span class="html-italic">n</span> = 6 mice/group). An asterisk (*) denotes significant differences observed among the groups, as determined by one-way analysis of variance (ANOVA). *, <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 2 Cont.
<p>The immunoregulatory effects of combined administration of 1,25D3 and butyrate on cecal cytokines and antimicrobial peptides in mice that had undergone chemotherapy and subsequently developed gut-derived <span class="html-italic">P. aeruginosa</span> sepsis. Female C57BL/6 mice, aged 6 to 8 weeks and obtained from Charles River, USA, were bred and housed under specific-pathogen-free conditions at the animal facility within the Center for Cellular and Biomolecular Research in Kaohsiung, Taiwan. Mice were either infected with <span class="html-italic">P. aeruginosa</span> PAO1-LAC at a concentration of 10<sup>7</sup> CFU suspended in 100 μL PBS or given 100 μL of sterile 1xPBS buffer as an open control. Before and after infection, mice received daily oral gavage of vehicle control (5% dimethyl sulfoxide), vitamin D3 at a dose of 0.2 μg/25 g mice/day (VD group), or butyrate (BU group), or a combination of both 1,25D3 and butyrate (VD + BU group), as described in <a href="#sec2-biomedicines-12-01026" class="html-sec">Section 2</a>. Total RNA was isolated from the cecal tissues of the mice. Subsequently, the gene expressions of various markers including IL-6 (<b>a</b>), IL-1β (<b>b</b>), TNF-α (<b>c</b>), IL-17A (<b>d</b>), IL-22 (<b>e</b>), and CRAMP (a homolog of human cathelicidin LL-37) (<b>f</b>), as well as ATG16L1 (<b>g</b>) and AhR (<b>h</b>) mRNA, were assessed using real-time quantitative PCR. The values obtained were determined as fold increases relative to the levels observed in mice solely infected with <span class="html-italic">Salmonella</span> for comparison purposes. The presented data are displayed as means ± the standard error of the mean (SEM) with a sample size of 7 mice per group (<span class="html-italic">n</span> = 6 mice/group). An asterisk (*) denotes significant differences observed among the groups, as determined by one-way analysis of variance (ANOVA). *, <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 3
<p>Combination of postbiotic butyrate and active 1,25D3 attenuates systemic translocation of gut-derived <span class="html-italic">P. aeruginosa</span> in mice. Female C57BL/6 mice, aged 6 to 8 weeks and obtained from Charles River, USA, were bred and housed under specific-pathogen-free conditions at the animal facility within the Center for Cellular and Biomolecular Research in Kaohsiung, Taiwan. Mice were either infected with <span class="html-italic">P. aeruginosa</span> PAO1-LAC at a concentration of 10<sup>7</sup> CFU suspended in 100 μL PBS or given 100 μL of sterile 1xPBS buffer as an open control. Before and after infection, mice received daily oral gavage of vehicle control (5% dimethyl sulfoxide), vitamin D3 at a dose of 0.2 μg/25 g mice/day (VD group), or butyrate (BU group), or a combination of both 1,25D3 and butyrate (VD + BU group). The quantities of bacteria retrieved from liver (<b>a</b>) and spleen (<b>b</b>) homogenates of infected and treated mice were measured. The presented data are displayed as means ± SEM (<span class="html-italic">n</span> = 6 mice/group). An asterisk (*) denotes significant differences observed among the groups, as determined by one-way analysis of variance (ANOVA). *, <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 4
<p>The combined use of butyrate and active 1,25D3 reduced the expression of zonulin and claudin-2 proteins in the cecal tissue of mice that had undergone chemotherapy and subsequently developed gut-derived <span class="html-italic">P. aeruginosa</span> sepsis. Female C57BL/6 mice, aged 6 to 8 weeks and obtained from Charles River, USA, were bred and housed under specific-pathogen-free conditions at the animal facility within the Center for Cellular and Biomolecular Research in Kaohsiung, Taiwan. Mice were either infected with <span class="html-italic">P. aeruginosa</span> PAO1-LAC at a concentration of 10<sup>7</sup> CFU suspended in 100 μL PBS or given 100 μL of sterile 1xPBS buffer as an open control. Prior to and after infection, the mice were orally administered either a vehicle control (5% dimethyl sulfoxide), treated with 0.2 μg of 1,25D3 per 25 g of mice per day (VD group), given butyrate (BU group), or received both 1,25D3 and butyrate (VD + BU group) on a daily basis, as described in the Material and Methods section. The detection of zonulin (<b>a</b>), claudin-2 (<b>b</b>) and AhR (<b>c</b>) expression in these groups was performed through immunohistochemistry (IHC) staining (original magnification, 400×; scale bar, 25 µm; <span class="html-italic">n</span> = 3). Zonulin (<b>d</b>), claudin-2 (<b>e</b>) and AhR (<b>f</b>) protein expressions in the IHC images were analyzed using ImageJ software (Java 1.8.0_345). ** <span class="html-italic">p</span>&lt; 0.01, *** <span class="html-italic">p</span>&lt; 0.001.</p>
Full article ">Figure 4 Cont.
<p>The combined use of butyrate and active 1,25D3 reduced the expression of zonulin and claudin-2 proteins in the cecal tissue of mice that had undergone chemotherapy and subsequently developed gut-derived <span class="html-italic">P. aeruginosa</span> sepsis. Female C57BL/6 mice, aged 6 to 8 weeks and obtained from Charles River, USA, were bred and housed under specific-pathogen-free conditions at the animal facility within the Center for Cellular and Biomolecular Research in Kaohsiung, Taiwan. Mice were either infected with <span class="html-italic">P. aeruginosa</span> PAO1-LAC at a concentration of 10<sup>7</sup> CFU suspended in 100 μL PBS or given 100 μL of sterile 1xPBS buffer as an open control. Prior to and after infection, the mice were orally administered either a vehicle control (5% dimethyl sulfoxide), treated with 0.2 μg of 1,25D3 per 25 g of mice per day (VD group), given butyrate (BU group), or received both 1,25D3 and butyrate (VD + BU group) on a daily basis, as described in the Material and Methods section. The detection of zonulin (<b>a</b>), claudin-2 (<b>b</b>) and AhR (<b>c</b>) expression in these groups was performed through immunohistochemistry (IHC) staining (original magnification, 400×; scale bar, 25 µm; <span class="html-italic">n</span> = 3). Zonulin (<b>d</b>), claudin-2 (<b>e</b>) and AhR (<b>f</b>) protein expressions in the IHC images were analyzed using ImageJ software (Java 1.8.0_345). ** <span class="html-italic">p</span>&lt; 0.01, *** <span class="html-italic">p</span>&lt; 0.001.</p>
Full article ">
14 pages, 2576 KiB  
Article
Antibacterial, Trichomonacidal, and Cytotoxic Activities of Pleopeltis crassinervata Extracts
by Jhony Anacleto-Santos, Elisa Vega-Ávila, Leticia Pacheco, Manuel Lacueva-Arnedo, Alicia Gómez-Barrio, Alexandra Ibáñez-Escribano, Teresa de Jesús López-Pérez, Brenda Casarrubias-Tabarez, Fernando Calzada, Perla Yolanda López-Camacho and Norma Rivera-Fernández
Pharmaceutics 2024, 16(5), 624; https://doi.org/10.3390/pharmaceutics16050624 - 7 May 2024
Viewed by 259
Abstract
Pleopeltis crassinervata is a fern documented in ethnobotanical records for its use in Mexican traditional medicine to treat gastric disorders and mouth ulcers. Consequently, conducting biological and pharmacological assays is crucial to validate the therapeutic efficacy of this plant within the context of [...] Read more.
Pleopeltis crassinervata is a fern documented in ethnobotanical records for its use in Mexican traditional medicine to treat gastric disorders and mouth ulcers. Consequently, conducting biological and pharmacological assays is crucial to validate the therapeutic efficacy of this plant within the context of traditional medicine. In the present study, we investigated the biological activity of extracts and fractions obtained from P. crassinervata organs against bacteria (Salmonella typhimurium, Salmonella typhi, Staphylococcus aureus, Proteus mirabilis, Shigella flexneri, Bacillus subtilis, Escherichia coli) and Trichomonas vaginalis using in vitro models. The precipitate fraction obtained from the frond methanolic extract showed significant antibacterial activity (minimal inhibitory concentration [MIC] 120 µg/mL) against the Staphylococcus aureus strain and was effective against both Gram-positive and Gram-negative bacteria. The hexane fraction also obtained from frond methanolic extract, showed a trichomonacidal effect with an IC50 of 82.8 μg/mL and a low cytotoxic effect. Hsf6 exhibited the highest activity against T. vaginalis, and the GC-MS analysis revealed that the predominant compound was 16-pregnenolone. The remaining identified compounds were primarily terpene-type compounds. Full article
Show Figures

Figure 1

Figure 1
<p><span class="html-italic">T. vaginalis</span> trophozoites after 24 h exposure to <span class="html-italic">P. crassinervata</span> subfractions. Negative control: DMSO at a maximum concentration of 0.1%.</p>
Full article ">Figure 2
<p>Toxicity percentage in Vero cell cultures exposed to Hsf5 and Hsf6 for 24 h at a concentration range of 25–800 µg/mL for growth control. A control with 0.1% DMSO was included, showing 0% toxicity.</p>
Full article ">Figure 3
<p>In vitro trichomonacidal activity percentage in the axenic cultures of <span class="html-italic">T. vaginalis</span> exposed to mixtures of Hsf5 and Hsf6 for 24 h while maintaining the IC<sub>50</sub> of one Hsf constant in each assessment. Growth control (no-treatment) and 0.1% DMSO control were included, exhibiting 0% activity.</p>
Full article ">Figure 4
<p>Chromatogram of Hsf6 obtained after gas–mass chromatography (GC-MS) analysis for 1 h. Each peak corresponds to the spectrum of each compound; 15 peaks were detected.</p>
Full article ">Figure 5
<p>Chemical structures of eight compounds from the hexane subfraction 6 (Hsf6) with biological activity reported. (<b>A</b>) α-Cadinol; (<b>B</b>) 2-pentadecanone-6,10,14-trimethyl-; (<b>C</b>) dibutylphthalate; (<b>D</b>) β-sitosterol acetate; (<b>E</b>) 7-dehydrodiosgenin; (<b>F</b>) 3-(1,5-dimethyl-hexyl)-3a,10,10,12b-tetramethyl-1,2,3,3a,4,6,8,9,10,10a,11,12,12a,12b-tetradecahydro-benzo[4,5]cyclohepta[1,2-E]indene; (<b>G</b>) stigmasta-3,5-dien-7-one; (<b>H</b>) pregn-16-en-20-one, 3-hydroxy-, [3β,5β]. Structures of alkanes and alkenes without reported biological activity were excluded.</p>
Full article ">
13 pages, 1648 KiB  
Article
The Tomato Variety Affects the Survival of Shigella flexneri 2a in Fruit Pericarp
by Tania Henriquez, Simona Guerra, Marta Nerini, Diane Purchase and Massimiliano Marvasi
Pathogens 2024, 13(5), 379; https://doi.org/10.3390/pathogens13050379 - 1 May 2024
Viewed by 423
Abstract
The presence of enteric pathogens in produce can serve as a significant means of transmitting infections to consumers. Notably, tomatoes, as a type of produce, have been implicated in outbreaks caused by various human pathogens, such as Salmonella enterica and pathogenic Escherichia coli. [...] Read more.
The presence of enteric pathogens in produce can serve as a significant means of transmitting infections to consumers. Notably, tomatoes, as a type of produce, have been implicated in outbreaks caused by various human pathogens, such as Salmonella enterica and pathogenic Escherichia coli. However, the survival characteristics of Shigella spp. in tomatoes have not been thoroughly investigated. In this study, we assess the survival of S. flexneri 2a in two distinct varieties of post-harvested tomatoes. S. flexneri 2a was used to inoculate both regular-sized Vine tomatoes and cherry-type Mini Plum tomatoes. Our findings reveal no significant difference in Shigella survival in the pericarp of both varieties on day 2 post-inoculation. However, a significant disparity emerges on day 6, where all recovered Shigella colonies exclusively belong to the Mini Plum variety, with none associated with the Vine type. When Shigella was inoculated into the locular cavity (deep inoculation), no significant difference between varieties was observed. Additionally, we investigate the potential role of the SRL pathogenicity island (SRL PAI) in the survival and fitness of S. flexneri 2a in post-harvested tomatoes. Our results indicate that while the SRL PAI is not linked to the survival of the strains in tomato, it does impact their fitness. These findings underscore the variability in Shigella strains’ survival capabilities depending on the tomato variety, highlighting the importance of understanding Shigella ecology beyond the human host and identifying molecular determinants influencing bacterial survival to mitigate the risk of future outbreaks. The significance of this data on Shigella persistence in fresh vegetables should not be underestimated, as even a small number of Shigella cells can pose a threat to the health of individuals. Full article
(This article belongs to the Section Bacterial Pathogens)
Show Figures

Figure 1

Figure 1
<p>A schematic illustration of the procedure for the analysis of the persistence of <span class="html-italic">Shigella</span> strains in post-harvested tomato fruits. Mini Plum and Vine tomato varieties were used to inoculate <span class="html-italic">S. flexneri</span> 2a strains using pericarp or locular cavity inoculation. After 2 or 6 days of incubation at 25 °C (in this figure) but also 4 °C and 37° were tested. The tomatoes were macerated in a bag using a stomacher, and a serial dilution of the resulting suspension was plated in a media selective for <span class="html-italic">Shigella</span> isolation (Hektoen or XLD). Created with BioRender.com.</p>
Full article ">Figure 2
<p><span class="html-italic">Shigella</span> proliferation in tomato varieties Vine and Plum at different days and different temperatures. Circles represent biological replicas. Horizontal line is average of increase in proliferation. Error bars are standard error. (** <span class="html-italic">p</span> &lt; 0.0021). ns: not significant.</p>
Full article ">Figure 3
<p>Temperature-dependent <span class="html-italic">Shigella</span> proliferation in tomato varieties Vine and Plum. Circles represent biological replicas. Horizontal line is average of increase in proliferation. Error bars are standard error. (* <span class="html-italic">p</span> = 0.0332); (*** <span class="html-italic">p</span> = 0.0002); (**** <span class="html-italic">p</span> &lt; 0.0001). ns: not significant.</p>
Full article ">Figure 4
<p>Overall <span class="html-italic">Shigella</span> proliferation in tomato varieties Vine and Plum. Circles represent biological replicas. Horizontal line is average of increase in proliferation. Error bars are standard error.</p>
Full article ">Figure 5
<p>The role of the SRL PAI in the fitness of <span class="html-italic">S. flexneri</span> 2a strains in tomato fruits. The fitness test <span class="html-italic">S. flexneri</span> 2a YSH6000 (marked with the tetracycline-resistance cassette) was co-infected in a 1:1 ratio with <span class="html-italic">S. flexneri</span> 2a 1363 into the pericarp. The ratios of the wild type/mutant in the inoculum and in the recovered tomatoes were estimated by patching on selective media after 48 h of incubation. Values above 0 indicate that <span class="html-italic">S. flexneri</span> YSH6000 is outcompeting the mutant strain (or surviving longer). On the other hand, values below 0 indicate that <span class="html-italic">S. flexneri</span> 2a 1363 is outcompeting the wild type (or surviving longer). When the value is close to 0, no advantage in terms of fitness is measured. Dashed lines estimate a cut-off beyond which changes in competitive fitness are biologically significant. The box-plots encompass the lower and upper quartiles, thick lines within the box are the median values and the whiskers indicate the degree of dispersion of the data. (* <span class="html-italic">p</span> &lt; 0.05). Outliers are shown as dots.</p>
Full article ">
19 pages, 349 KiB  
Review
Natural Antimicrobials in Dairy Products: Benefits, Challenges, and Future Trends
by Maria Eduarda Marques Soutelino, Adriana Cristina de Oliveira Silva and Ramon da Silva Rocha
Antibiotics 2024, 13(5), 415; https://doi.org/10.3390/antibiotics13050415 - 1 May 2024
Viewed by 729
Abstract
This review delves into using natural antimicrobials in the dairy industry and examines various sources of these compounds, including microbial, plant, and animal sources. It discusses the mechanisms by which they inhibit microbial growth, for example, by binding to the cell wall’s precursor [...] Read more.
This review delves into using natural antimicrobials in the dairy industry and examines various sources of these compounds, including microbial, plant, and animal sources. It discusses the mechanisms by which they inhibit microbial growth, for example, by binding to the cell wall’s precursor molecule of the target microorganism, consequently inhibiting its biosynthesis, and interfering in the molecule transport mechanism, leading to cell death. In general, they prove to be effective against the main pathogens and spoilage found in food, such as Escherichia coli, Staphylococcus aureus, Bacillus spp., Salmonella spp., mold, and yeast. Moreover, this review explores encapsulation technology as a promising approach for increasing the viability of natural antimicrobials against unfavorable conditions such as pH, temperature, and oxygen exposure. Finally, this review examines the benefits and challenges of using natural antimicrobials in dairy products. While natural antimicrobials offer several advantages, including improved safety, quality, and sensory properties of dairy products, it is crucial to be aware of the challenges associated with their use, such as potential allergenicity, regulatory requirements, and consumer perception. This review concludes by emphasizing the need for further research to identify and develop effective and safe natural antimicrobials for the dairy industry to ensure the quality and safety of dairy products for consumers. Full article
Show Figures

Graphical abstract

Graphical abstract
Full article ">
16 pages, 3192 KiB  
Article
Bacitracin Methylene Disalicylate (BMD) Treatment Affects Spleen Proteome in Broiler Chicks Infected with Salmonella enteritidis
by Adedeji Adetunji, Theresa Casey, Uma K. Aryal, Tunde Ogundare, Jackeline Franco and Yewande Fasina
Antibiotics 2024, 13(5), 414; https://doi.org/10.3390/antibiotics13050414 - 1 May 2024
Viewed by 520
Abstract
Bacitracin Methylene Disalicylate (BMD), as a feed additive to poultry diets, enhances digestion, prevents Salmonella enteritidis (SE) colonization, and treats current infections. The objective of this study was to utilize a quantitative proteomic approach to determine the effect of BMD feed additive on [...] Read more.
Bacitracin Methylene Disalicylate (BMD), as a feed additive to poultry diets, enhances digestion, prevents Salmonella enteritidis (SE) colonization, and treats current infections. The objective of this study was to utilize a quantitative proteomic approach to determine the effect of BMD feed additive on broiler chickens challenged with SE in the spleen proteome. At 1 d of age, chicks were randomly allocated into four groups: control with and without SE challenge (CON, n = 60; CON-SE, n = 60), BMD with and without SE challenge (BMD, n = 60; BMD-SE, n = 60). Birds in the CON-SE and BMD-SE treatment were administered SE inoculum by oral gavage. On day three and day seven post-gavage, the spleen was collected aseptically from birds in each treatment group (CON, n = 4/day; CON-SE, n = 4/day; BMD, n = 4/day; BMD-SE, n = 4/day). Proteomic analysis by liquid chromatography-tandem mass spectrometry (LC-MS/MS) showed an increased abundance of 115 proteins and decreased of 77 due to the BMD. Proteins that decreased in abundance were enriched for fibrinogen complex and extracellular space, whereas proteins that increased in abundance were enriched for proteasome-mediated ubiquitin-dependent protein catabolic process and mitochondrion. Analysis of the interaction between BMD and the Salmonella challenge found 230 differentially abundant proteins including proteins associated with RNA binding, spliceosome, protein transport, and cell adhesion among the upregulated proteins, and those associated with protein folding, carbon metabolism, biosynthesis of nucleotide sugars, response to oxidative stress, positive regulation of NIK/NF-kappaB signaling, and inflammatory response among the downregulated proteins. The impact of BMD treatment on spleen proteome indicates an anti-apoptotic effect. BMD also modified the response of the spleen to the SE challenge with a marked decrease in proteins that prompt cytokine synthesis and an increase in proteins involved in the selective removal of unfolded proteins. Full article
Show Figures

Figure 1

Figure 1
<p>PLSDA (<b>A</b>) and the heat map with dendrogram resulting from hierarchical cluster analysis (<b>B</b>) of proteins extracted from spleen samples obtained from BMD, BMD-SE, CON, and CON-SE group broiler chickens (n = 4). The PLSDA score plot demonstrates distinct sample clusters based on BMD, BMD-SE, CON, and CON-SE groups, while the heat maps visualize the 100 most distinguishing proteins, with greater abundance indicated in red and lesser abundance in blue, relative to BMD (red), BMD-SE (green), CON (blue), and CON-SE (light blue) groups.</p>
Full article ">Figure 2
<p>The top scoring IPA protein networks DNA replication, recombination, and repair, cancer, gastrointestinal disease (<b>A</b>), infectious diseases, organismal injury and abnormalities, and cancer (<b>B</b>) are depicted for overall BMD treatment. In the figure, red denotes upregulation while green indicates downregulation, with color intensity reflecting the relative magnitude of change in protein expression. Solid lines represent direct interactions, whereas dashed lines signify indirect interactions. The protein interaction networks were constructed using QIAGEN Ingenuity Pathway Analysis, <a href="https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis/" target="_blank">https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis/</a> (accessed on 17 October 2022).</p>
Full article ">Figure 3
<p>The top scoring IPA protein networks cancer, dermatological diseases and conditions, RNA post-transcriptional modification (<b>A</b>), cellular assembly and organization, molecular transport, and RNA trafficking (<b>B</b>) are depicted for BMD treatment X <span class="html-italic">Salmonella</span> challenge. In the figure, red denotes upregulation while green indicates downregulation, with color intensity reflecting the relative magnitude of change in protein expression. Solid lines represent direct interactions, whereas dashed lines signify indirect interactions. The protein interaction networks were constructed using QIAGEN Ingenuity Pathway Analysis, <a href="https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis/" target="_blank">https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis/</a> accessed on 17 October 2022.</p>
Full article ">Figure 4
<p>The molecular and cellular function ontologies of proteins affected by BMD–SE treatment in the spleen established through IPA analysis. The <span class="html-italic">Y</span>-axis represents the negative logarithm of the <span class="html-italic">p</span>-value. The functional analyses were generated through the use of QIAGEN Ingenuity Pathway Analysis, <a href="https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis/" target="_blank">https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis/</a> accessed on 17 October 2022.</p>
Full article ">Figure 5
<p>IPA summary graph of the effect of BMD on spleen proteome. Blue color indicates a prediction that the following molecules: IL6 (interleukin-6), IL4 (interleukin-4), AGT (angiotensinogen), NCOA2 (nuclear receptor co-activator 2), and acute phase response signaling are inhibited. The protein interaction networks were constructed using QIAGEN Ingenuity Pathway Analysis <a href="https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis/" target="_blank">https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis/</a> accessed on 17 October 2022). Dashed lines represent an indirect relationship between molecules.</p>
Full article ">Figure 6
<p>Summary of results of the effects of BMD treatments on the spleen proteome in chicks. The summary image was generated using BioRender (Toronto, ON, Canada) <a href="http://www.biorender.com" target="_blank">www.biorender.com</a>, accessed on 2 April 2024.</p>
Full article ">
58 pages, 5337 KiB  
Review
Opportunistic Pathogens in Drinking Water Distribution Systems—A Review
by Mark W. LeChevallier, Toby Prosser and Melita Stevens
Microorganisms 2024, 12(5), 916; https://doi.org/10.3390/microorganisms12050916 - 30 Apr 2024
Viewed by 1161
Abstract
In contrast to “frank” pathogens, like Salmonella entrocolitica, Shigella dysenteriae, and Vibrio cholerae, that always have a probability of disease, “opportunistic” pathogens are organisms that cause an infectious disease in a host with a weakened immune system and rarely in [...] Read more.
In contrast to “frank” pathogens, like Salmonella entrocolitica, Shigella dysenteriae, and Vibrio cholerae, that always have a probability of disease, “opportunistic” pathogens are organisms that cause an infectious disease in a host with a weakened immune system and rarely in a healthy host. Historically, drinking water treatment has focused on control of frank pathogens, particularly those from human or animal sources (like Giardia lamblia, Cryptosporidium parvum, or Hepatitis A virus), but in recent years outbreaks from drinking water have increasingly been due to opportunistic pathogens. Characteristics of opportunistic pathogens that make them problematic for water treatment include: (1) they are normally present in aquatic environments, (2) they grow in biofilms that protect the bacteria from disinfectants, and (3) under appropriate conditions in drinking water systems (e.g., warm water, stagnation, low disinfectant levels, etc.), these bacteria can amplify to levels that can pose a public health risk. The three most common opportunistic pathogens in drinking water systems are Legionella pneumophila, Mycobacterium avium, and Pseudomonas aeruginosa. This report focuses on these organisms to provide information on their public health risk, occurrence in drinking water systems, susceptibility to various disinfectants, and other operational practices (like flushing and cleaning of pipes and storage tanks). In addition, information is provided on a group of nine other opportunistic pathogens that are less commonly found in drinking water systems, including Aeromonas hydrophila, Klebsiella pneumoniae, Serratia marcescens, Burkholderia pseudomallei, Acinetobacter baumannii, Stenotrophomonas maltophilia, Arcobacter butzleri, and several free-living amoebae including Naegleria fowleri and species of Acanthamoeba. The public health risk for these microbes in drinking water is still unclear, but in most cases, efforts to manage Legionella, mycobacteria, and Pseudomonas risks will also be effective for these other opportunistic pathogens. The approach to managing opportunistic pathogens in drinking water supplies focuses on controlling the growth of these organisms. Many of these microbes are normal inhabitants in biofilms in water, so the attention is less on eliminating these organisms from entering the system and more on managing their occurrence and concentrations in the pipe network. With anticipated warming trends associated with climate change, the factors that drive the growth of opportunistic pathogens in drinking water systems will likely increase. It is important, therefore, to evaluate treatment barriers and management activities for control of opportunistic pathogen risks. Controls for primary treatment, particularly for turbidity management and disinfection, should be reviewed to ensure adequacy for opportunistic pathogen control. However, the major focus for the utility’s opportunistic pathogen risk reduction plan is the management of biological activity and biofilms in the distribution system. Factors that influence the growth of microbes (primarily in biofilms) in the distribution system include, temperature, disinfectant type and concentration, nutrient levels (measured as AOC or BDOC), stagnation, flushing of pipes and cleaning of storage tank sediments, and corrosion control. Pressure management and distribution system integrity are also important to the microbial quality of water but are related more to the intrusion of contaminants into the distribution system rather than directly related to microbial growth. Summarizing the identified risk from drinking water, the availability and quality of disinfection data for treatment, and guidelines or standards for control showed that adequate information is best available for management of L. pneumophila. For L. pneumophila, the risk for this organism has been clearly established from drinking water, cases have increased worldwide, and it is one of the most identified causes of drinking water outbreaks. Water management best practices (e.g., maintenance of a disinfectant residual throughout the distribution system, flushing and cleaning of sediments in pipelines and storage tanks, among others) have been shown to be effective for control of L. pneumophila in water supplies. In addition, there are well documented management guidelines available for the control of the organism in drinking water distribution systems. By comparison, management of risks for Mycobacteria from water are less clear than for L. pneumophila. Treatment of M. avium is difficult due to its resistance to disinfection, the tendency to form clumps, and attachment to surfaces in biofilms. Additionally, there are no guidelines for management of M. avium in drinking water, and one risk assessment study suggested a low risk of infection. The role of tap water in the transmission of the other opportunistic pathogens is less clear and, in many cases, actions to manage L. pneumophila (e.g., maintenance of a disinfectant residual, flushing, cleaning of storage tanks, etc.) will also be beneficial in helping to manage these organisms as well. Full article
Show Figures

Figure 1

Figure 1
<p>Etiology of drinking water associated outbreaks (<span class="html-italic">n</span> = 928) by year, US, 1971–2014. Source: Benedict et al. [<a href="#B9-microorganisms-12-00916" class="html-bibr">9</a>].</p>
Full article ">Figure 2
<p>Examples of biofilms in water systems. From: LeChevallier [<a href="#B33-microorganisms-12-00916" class="html-bibr">33</a>].</p>
Full article ">Figure 3
<p>Average and standard deviation of water temperatures in treated water storages within a distribution system in Australia. Data from 2013–2022.</p>
Full article ">Figure 4
<p>Percentage of chlorine residuals greater than 0.2 mg/L in three regions of an Australian water system.</p>
Full article ">Figure 5
<p>AOC levels in 94 North American water systems. From Volk and LeChevallier [<a href="#B29-microorganisms-12-00916" class="html-bibr">29</a>].</p>
Full article ">Figure 6
<p>BDOC levels in 30 North American water systems. From Volk and LeChevallier [<a href="#B29-microorganisms-12-00916" class="html-bibr">29</a>].</p>
Full article ">Figure 7
<p>Decision tree for coliform occurrences in drinking water. Abbreviations: T °C, temperature in degrees Celsius, AOC, assimilable organic carbon. From Volk and LeChevallier [<a href="#B29-microorganisms-12-00916" class="html-bibr">29</a>].</p>
Full article ">Figure 8
<p>Legionella cases in Victoria, 2012 to 2020.</p>
Full article ">Figure 9
<p>Comparison of Legionnaires’ Disease (LD) and Pontiac Fever (PF) Cases 2006–2017. Adapted from Hamilton et al. [<a href="#B120-microorganisms-12-00916" class="html-bibr">120</a>].</p>
Full article ">Figure 10
<p>Concentration of culturable Legionella during outbreaks (red-orange) and routine monitoring (green). The black line is the 5 × 10<sup>4</sup> cfu/L action level as a break between sporadic cases and outbreaks. From NASEM [<a href="#B111-microorganisms-12-00916" class="html-bibr">111</a>].</p>
Full article ">Figure 11
<p>Relationship between <span class="html-italic">L. pneumophila</span> concentration and free chlorine residual. From LeChevallier [<a href="#B34-microorganisms-12-00916" class="html-bibr">34</a>].</p>
Full article ">Figure 12
<p>Relationship between temperature and concentration of <span class="html-italic">L. pneumophila</span>. From LeChevallier [<a href="#B34-microorganisms-12-00916" class="html-bibr">34</a>].</p>
Full article ">Figure 13
<p>Impact of distribution system flushing at site 824 to control the occurrence of culturable <span class="html-italic">L. pneumophila</span>. Symbols: d, downstream f site 824; u, upstream of site 824. From LeChevallier [<a href="#B34-microorganisms-12-00916" class="html-bibr">34</a>].</p>
Full article ">Figure 14
<p>Projected NTM cases in Queensland, Australia from 2020 to 2040. From Ratnatunga et al. [<a href="#B194-microorganisms-12-00916" class="html-bibr">194</a>].</p>
Full article ">Figure 15
<p>Occurrence of <span class="html-italic">M. avium</span> and <span class="html-italic">M. intracellulare</span> in distribution system biofilm samples (N = 55). Site # - site number. From Falkinham et al. [<a href="#B50-microorganisms-12-00916" class="html-bibr">50</a>].</p>
Full article ">Figure 16
<p>Disinfection of mycobacteria by free chlorine. Experimental conditions: pH 7.0, 25 °C, initial free chlorine concentration 0.5 mg/L.Adapted from Le Dantec et al. [<a href="#B216-microorganisms-12-00916" class="html-bibr">216</a>].</p>
Full article ">Figure 17
<p>Impact of pipe composition on biofilm growth of <span class="html-italic">M. avium</span>. Adapted from LeChevallier et al. [<a href="#B231-microorganisms-12-00916" class="html-bibr">231</a>].</p>
Full article ">Figure 18
<p>Seasonal occurrence of P. aeruginosa in Croatia. Adapted from Vukić Lušić et al. [<a href="#B246-microorganisms-12-00916" class="html-bibr">246</a>].</p>
Full article ">
14 pages, 850 KiB  
Article
Effects of Long-Term Coated Sodium Butyrate Supplementation on the Intestinal Health and Colonization of Cecal Salmonella of Laying Hens Infected with Salmonella enteritidis
by Siyu Xiong, Qi Zhang, Keying Zhang, Jianping Wang, Shiping Bai, Qiufeng Zeng, Huanwei Peng, Yue Xuan, Yadong Mu and Xuemei Ding
Animals 2024, 14(9), 1356; https://doi.org/10.3390/ani14091356 - 30 Apr 2024
Viewed by 339
Abstract
Salmonella enterica ser. Enteritidis (S. Enteritidis) is widely found in chickens and eggs, and it can potentially induce human illness. The investigation in this study centers on the impacts of long-term dietary supplementation with coated sodium butyrate (CSB) on intestinal well-being [...] Read more.
Salmonella enterica ser. Enteritidis (S. Enteritidis) is widely found in chickens and eggs, and it can potentially induce human illness. The investigation in this study centers on the impacts of long-term dietary supplementation with coated sodium butyrate (CSB) on intestinal well-being and the colonization of cecum Salmonella in laying hens infected with S. Enteritidis. We segregated a total of 120 Lohmann laying hens aged 51 weeks into four treatment categories: 0 (CON), 300 (CSB1), 500 (CSB2), and 800 (CSB3) mg/kg of CSB, supplemented with CSB from the first day of the experiment. A 24-week observation process was carried out for each laying hen. The S. Enteritidis was orally administered to all chickens on the morning of the first and third days of week 22 of the trial. After the S. Enteritidis challenge, egg production decreased the most in the CON group. Compared to the CON group, the three doses of CSB significantly improved egg production after the S. Enteritidis challenge (PANOVA < 0.05). S. Enteritidis challenge increased plasma DAO activity, but CSB supplementation reduced plasma DAO activity (Plinear < 0.05). The S. Enteritidis challenge disrupted intestinal villi morphology; compared to the CON group, the three dosages of CSB resulted in an increase in villus height (VH) and the ratio of villus height to crypt depth (V/C) in the duodenum, jejunum, and ileum of infected laying hens (Plinear < 0.05), with a significant increase in jejunal villus height (PANOVA < 0.05). A decrease in ileal crypt depth was also observed (Plinear < 0.05). CSB2 and CSB3 markedly increased the content of butyric acid in the cecum (PANOVA < 0.05). Additionally, in contrast to those in the CON group, the propionic acid content in the CSB supplementation group increased (Plinear < 0.05). Compared with those in the CON group, mRNA relative expression of the IL-6 and IL-1β in jejunum (Plinear < 0.05) and mRNA relative expression of the IL-1β in ileum (PANOVA < 0.05) were significantly lower, and mRNA relative expression of the IL-10 in ileum (Plinear < 0.05) were significantly higher in the CSB group. In addition, in contrast to the CON group, the CSB supplementation group significantly upregulated mRNA relative expression of the ZO-1 and CLDN1 (PANOVA < 0.05). Additionally, CSB supplementation reduced the number of Salmonella and increased the number of Lactobacilli in the cecum (Plinear < 0.05) and tended to increase the total bacteria count (Plinear = 0.069) and reduce the E. coli count (Plinear = 0.081). In conclusion, long-term dietary supplementation with coated sodium butyrate can alleviate intestinal injury and the colonization of cecum Salmonella in laying hens infected with S. Enteritidis. Full article
(This article belongs to the Section Poultry)
Show Figures

Figure 1

Figure 1
<p>The effects of coated sodium butyrate on intestinal permeability of laying hens challenged with <span class="html-italic">Salmonella.</span> (<b>A</b>) The serum D-La content of laying hens was measured using the ELISA Kit. (<b>B</b>) The serum DAO content of laying hens was measured using the ELISA Kit. Data are means ± SEM.</p>
Full article ">Figure 2
<p>The effects of coated sodium butyrate on the cecal microbes of laying hens challenged with <span class="html-italic">Salmonella</span> (log (copies/g)). (<b>A</b>) Total bacteria in the cecum. (<b>B</b>) The count of <span class="html-italic">Salmonella</span> in the cecum. (<b>C</b>) The count of <span class="html-italic">E. coli</span> in the cecum. (<b>D</b>)The count of <span class="html-italic">Lactobacillus</span> in the cecum. Data are means ± SEM.</p>
Full article ">
8 pages, 608 KiB  
Article
A Sublethal Concentration of Chlorine Induces Antibiotic Resistance in Salmonella via Production of Reactive Oxygen Species
by Mohammed Aljuwayd, Israa Abdullah Malli, Steven C. Ricke and Young Min Kwon
Appl. Microbiol. 2024, 4(2), 745-752; https://doi.org/10.3390/applmicrobiol4020051 - 30 Apr 2024
Viewed by 298
Abstract
Studies have shown that the production of reactive oxygen species (ROS) is triggered by bactericidal antibiotics, which contributes significantly to the killing of bacterial cells and increasing mutations in surviving cells. In this study, we hypothesized that exposure of Salmonella to sublethal concentrations [...] Read more.
Studies have shown that the production of reactive oxygen species (ROS) is triggered by bactericidal antibiotics, which contributes significantly to the killing of bacterial cells and increasing mutations in surviving cells. In this study, we hypothesized that exposure of Salmonella to sublethal concentrations of hypochlorite (NaOCl), a commonly used sanitizer in household and food industries increases mutation rates, leading to the development of antibiotic resistance. We found that a sublethal concentration (20 ppm) of NaOCl increased the mutation rates of S. typhimurium 14028s significantly (p < 0.05), which was prevented by the ROS scavenger thiourea, supporting that the increased mutation was due to NaOCl-triggered ROS production. We further found that the exposure of S. typhimurium 14028s to the same sublethal concentration of NaOCl increases resistance to kanamycin among the 3 antibiotics evaluated. The results of this study suggest that when NaOCl applied as a sanitizer fails to kill Salmonella due to diluted local concentrations or presence of organic materials, it can cause an adverse outcome of developing antibiotic resistance of the pathogen. Full article
Show Figures

Figure 1

Figure 1
<p>The mutation rates of <span class="html-italic">S. typhimurium</span> 14028s after exposure to a sublethal concentration of NaOCl. <span class="html-italic">S. typhimurium</span> 14028s was exposed to NaOCl (20 ppm) or NaOCl (20 ppm) plus thiourea (150 mM) before determination of the mutation rate using rifampicin. The same procedure was repeated with no exposure (no treatment; negative control) or exposure to H<sub>2</sub>O<sub>2</sub> (1 mM; positive control). Different letters denote statistical differences (<span class="html-italic">p</span> &lt; 0.0006).</p>
Full article ">Figure 2
<p>Development of antibiotic resistance after exposure to a sublethal concentration of NaOCl. <span class="html-italic">S. typhimurium</span> 14028s was exposed to NaOCl (20 ppm) or none (negative control) before determination of the resistance to different antibiotics (Amp, Cm or Km) as the % of the surviving cells.</p>
Full article ">
9 pages, 268 KiB  
Communication
Potentiation of the Antimicrobial Effect of Oxytetracycline Combined with Cinnamon, Clove, Oregano, and Red Thyme Essential Oils against MDR Salmonella enterica Strains
by Belén Huerta Lorenzo, Ángela Galán-Relaño, Emilio Barba-Sánchez, Antonio Romero-Salmoral, Ana L. Solarte Portilla, Lidia Gómez-Gascón and Rafael J. Astorga Márquez
Animals 2024, 14(9), 1347; https://doi.org/10.3390/ani14091347 - 30 Apr 2024
Viewed by 424
Abstract
Tetracyclines have a high resistance percentage in Salmonella spp. of both human and animal origin. Essential oils, such as cinnamon (Cinnamomum zeylanicum), clove (Eugenia caryophyllata), oregano (Origanum vulgare), and red thyme (Thymus zygis), have shown [...] Read more.
Tetracyclines have a high resistance percentage in Salmonella spp. of both human and animal origin. Essential oils, such as cinnamon (Cinnamomum zeylanicum), clove (Eugenia caryophyllata), oregano (Origanum vulgare), and red thyme (Thymus zygis), have shown bactericidal activity against this bacterium. However, in many cases, the minimum inhibitory concentration (MIC) exceeds the cytotoxicity limits. The objective of this study was to assess the in vitro efficacy of combining oxytetracycline with essential these oils against field multidrug-resistant (MDR) Salmonella enterica strains. The MIC of each product was determined using the broth microdilution method. The interaction was evaluated using the checkerboard method, by means of the fractional inhibitory concentration index (FICindex) determination. The results showed a positive interaction (synergy and additivity) between oxytetracycline and the four oils tested, resulting in a reduction in both products’ MICs by 2 to 4 times their initial value, in the case of oils, and by 2 to 1024 times in the case of the antibiotic. The combination of oxytetracycline and cinnamon achieved the best results (FICindex 0.5), with a decrease in the antibiotic effective concentration to below the sensitivity threshold (MIC of the combined oxytetracycline 0.5 µg/mL). There was no antagonistic effect in any case, although differences in response were observed depending on the bacterial strain. The results of this study suggest that combining oxytetracycline with cinnamon oil could be an effective alternative for controlling tetracycline-resistant strains of Salmonella. However, its individual use should be further evaluated through in vitro susceptibility tests. Full article
14 pages, 2964 KiB  
Article
Establishment of a Simple, Sensitive, and Specific Salmonella Detection Method Based on Recombinase-Aided Amplification Combined with dsDNA-Specific Nucleases
by Changyu Zhou, Yu Zhao, Boyan Guo, Ming Yang, Qiang Xu, Changwei Lei and Hongning Wang
Foods 2024, 13(9), 1380; https://doi.org/10.3390/foods13091380 - 29 Apr 2024
Viewed by 520
Abstract
Salmonella is a common foodborne pathogen that can cause food poisoning, posing a serious threat to human health. Therefore, quickly, sensitively, and accurately detecting Salmonella is crucial to ensuring food safety. For the Salmonella hilA gene, we designed Recombinase-aided amplification (RAA) primers and dsDNA-specific [...] Read more.
Salmonella is a common foodborne pathogen that can cause food poisoning, posing a serious threat to human health. Therefore, quickly, sensitively, and accurately detecting Salmonella is crucial to ensuring food safety. For the Salmonella hilA gene, we designed Recombinase-aided amplification (RAA) primers and dsDNA-specific nuclease (DNase) probes. The ideal primer and probe combination was found when conditions were optimized. Under UV light, a visual Salmonella detection technique (RAA-dsDNase) was developed. Additionally, the RAA-dsDNase was modified to further reduce pollution hazards and simplify operations. One-pot RAA-dsDNase-UV or one-pot RAA-dsDNase-LFD was developed as a Salmonella detection method, using UV or a lateral flow dipstick (LFD) for result observation. Among them, one-pot RAA-dsDNase and one-pot RAA-dsDNase-LFD had detection times of 50 min and 60 min, respectively, for detecting Salmonella genomic DNA. One-pot RAA-dsDNase-UV had a detection limit of 101 copies/μL and 101 CFU/mL, while one-pot RAA-dsDNase-LFD had a sensitivity of 102 copies/μL and 102 CFU/mL. One-pot RAA-dsDNase-UV and one-pot RAA-dsDNase-LFD assays may identify 17 specific Salmonella serovars witho ut causing a cross-reaction with the remaining 8 bacteria, which include E. coli. Furthermore, Salmonella in tissue and milk samples has been reliably detected using both approaches. Overall, the detection method developed in this study can quickly, sensitively, and accurately detect Salmonella, and it is expected to become an important detection tool for the prevention and control of Salmonella in the future. Full article
(This article belongs to the Section Food Microbiology)
Show Figures

Figure 1

Figure 1
<p>Schematic diagram and feasibility analysis of RAA-dsDNase detection for <span class="html-italic">Salmonella</span>. (<b>A</b>) The principle of RAA-dsDNase detection for <span class="html-italic">Salmonella</span> mainly includes three parts. (<b>I</b>) dsDNase has no degrading activity on ssDNA fluorescent probe. (<b>II</b>) When dsDNase was absent from the reaction system, the ssDNA fluorescent probe remains intact. (<b>III</b>) When the template DNA was amplified by RAA, then dsDNase was added to the system, and the ssDNA fluorescent probe was degraded and released a fluorescent signal. (<b>B</b>,<b>C</b>) Feasibility analysis of RAA-dsDNase detection for <span class="html-italic">Salmonella</span>.</p>
Full article ">Figure 2
<p>Sensitivity and specificity analysis of RAA-dsDNase. (<b>A</b>,<b>B</b>) The detection limit of RAA-dsDNase was 101 copies/μL (plasmid) and 101 CFU/mL (bacteria). (<b>C</b>) When the genomic DNA of <span class="html-italic">Salmonella</span> exists, RAA-dsDNase releases a strong fluorescent signal, while in the presence of genomic DNA of other species, including <span class="html-italic">Escherichia coli</span>, no fluorescent signal was produced. Strain numbers correspond to the details in <a href="#app1-foods-13-01380" class="html-app">Table S1</a>.</p>
Full article ">Figure 3
<p>Schematic diagram and feasibility analysis of one-pot RAA-dsDNase-UV and one-pot RAA-dsDNase-LFD detection for <span class="html-italic">Salmonella</span>. (<b>A</b>) Simultaneously adding the components of the RAA and dsDNase reactions into an EP tube, with RAA at the bottom of the tube and dsDNase and the fluorescent probe at the tube cap. After the RAA reaction was completed, it was briefly centrifuged, inverted to mix, and finally the results were observed using UV and LFD. (<b>B</b>,<b>C</b>) The feasibility analysis results showed that fluorescence or detection bands appeared only when the genomic DNA of <span class="html-italic">Salmonella</span> existed.</p>
Full article ">Figure 4
<p>Sensitivity analysis of one-pot RAA-dsDNase-UV and one-pot RAA-dsDNase-LFD. (<b>A</b>,<b>C</b>) The detection limit of one-pot RAA-dsDNase-UV was 101 copies/μL (plasmid) and 101 CFUs (bacteria). (<b>B</b>,<b>D</b>) The detection limit of one-pot RAA-dsDNase-LFD was 102 copies/μL (plasmid) and 102 CFU/mL (bacteria).</p>
Full article ">Figure 5
<p>Specificity analysis of one-pot RAA-dsDNase-UV and one-pot RAA-dsDNase-LFD. Specificity analysis results showed that one-pot RAA-dsDNase-UV and one-pot RAA-dsDNase-LFD could specifically detect <span class="html-italic">Salmonella</span>, without cross-reactivity to other strains of bacteria. Strain numbers correspond to the details in <a href="#app1-foods-13-01380" class="html-app">Table S1</a>.</p>
Full article ">Figure 6
<p>Detection of <span class="html-italic">Salmonella</span> in real samples. (<b>A</b>) Observation of liver tissue samples from sick and healthy chickens in clinical practice with the naked eye. The red arrow indicates the location of the nodule. (<b>B</b>) Traditional culture method was used to analyze <span class="html-italic">Salmonella</span> in the tissues of sick chickens, and the results showed typical morphology of <span class="html-italic">Salmonella</span> pullorum. (<b>C</b>) One-pot RAA-dsDNase-UV, one-pot RAA-dsDNase-LFD, and PCR analysis showed that significant fluorescent signals or detection bands were produced in the tissues of the hearts, livers, spleens, lungs, kidneys, and intestines of sick chicks, while no corresponding phenomenon was observed in healthy chicken tissues. (<b>D</b>) And similar results were obtained from PCR analysis. (<b>E</b>) Detection of <span class="html-italic">Salmonella</span> in milk using one-pot RAA-dsDNase-UV and one-pot RAA-dsDNase-LFD showed that both methods produced clear fluorescent signals or detection bands.</p>
Full article ">
13 pages, 1858 KiB  
Article
Fermented Rapeseed and Soybean Alone and in Combination with Macro Algae Inhibit Human and Pig Pathogenic Bacteria In Vitro
by Frederik Beck, Ninfa Rangel Pedersen and Dennis Sandris Nielsen
Microorganisms 2024, 12(5), 891; https://doi.org/10.3390/microorganisms12050891 - 29 Apr 2024
Viewed by 819
Abstract
Higher plants produce secondary metabolites expressing antimicrobial effects as a defense mechanism against opportunistic microorganisms living in close proximity with the plant. Fermentation leads to bioconversion of plant substrates to these bioactive compounds and their subsequent release via breakdown of plant cell walls. [...] Read more.
Higher plants produce secondary metabolites expressing antimicrobial effects as a defense mechanism against opportunistic microorganisms living in close proximity with the plant. Fermentation leads to bioconversion of plant substrates to these bioactive compounds and their subsequent release via breakdown of plant cell walls. Fermented feed products have recently started to become implemented in the pig industry to reduce overall disease pressure and have been found to reduce events such as post-weaning diarrhea. In this study, we investigate the antimicrobial potential of fermented soybean- and rapeseed-based pig feed supplements with and without added seaweed. The antimicrobial effect was tested in a plate well diffusion assay against a range of known human and livestock pathogenic bacteria. Further, we investigate the metabolite profiles based on liquid-chromatography mass-spectrometry (LC-MS) analysis of the fermented products in comparison to their unfermented constituents. We observed a pronounced release of potential antimicrobial secondary metabolites such as benzoic acids when the plant material was fermented, and a significantly increased antimicrobial effect compared to the unfermented controls against several pathogenic bacteria, especially Salmonella enterica Typhimurium, Listeria monocytogenes, Yersinia enterocolitica, and a strain of atopic dermatitis causing Staphylococcus aureus CC1. In conclusion, fermentation significantly enhances the antimicrobial properties of rapeseed, soybean, and seaweed, offering a promising alternative to zinc oxide for controlling pathogens in piglet feed. This effect is attributed to the release of bioactive metabolites effective against pig production-relevant bacteria. Full article
(This article belongs to the Section Food Microbiology)
Show Figures

Figure 1

Figure 1
<p>Variance of metabolite abundances across samples—Heat maps defining the relative abundance of major groups of metabolites analyzed in the LC-MS assay. In all groupings (benzoic acids (<b>A</b>), fatty acids (<b>B</b>), carbohydrates (<b>C</b>), indolyl carboxylic acids (<b>D</b>), and amino acids (<b>E</b>)), the different fermented products (FRSM = fermented rapeseed meal, FSBM = fermented soybean meal, +s = addition of seaweed) was compared with each other and the unfermented controls (RSM = unfermented rapeseed meal, SBM = unfermented soybean meal, A.N. = unfermented <span class="html-italic">A. nodosum</span>, S.L. = unfermented <span class="html-italic">S. latissima</span>.</p>
Full article ">Figure 2
<p>Side-by-side comparison dot plot of clearing zones observed in the agar well diffusion assays, in which extracts from fermented pig feed additives containing rapeseed and soybean meal, with and without seaweed and unfermented control products. The extracts are tested against the pathogenic bacteria <span class="html-italic">Listeria monocytogenes</span> (<b>A</b>–<b>C</b>), <span class="html-italic">Salmonella enterica Typhimurium</span> (<b>D</b>–<b>F</b>), <span class="html-italic">Yersinia enterocolitica</span> (<b>G</b>–<b>I</b>), and <span class="html-italic">Staphylococcus aureus</span> (<b>J</b>,<b>K</b>). Clearing zones were measured in mm from the edge of the well to the edge of the visible zone of complete bacterial growth inhibition. Error bars represent the standard deviation of the measured clearing zones in each product. Statistical differences were determined by non-parametric Wilcoxon signed rank tests.</p>
Full article ">Figure 3
<p>Heat inactivation of potential antimicrobial compounds—extracts of fermented products containing rapeseed (FRSM) and soybean meal (FSBM), alone and in combination with seaweed (FSBMS/FRSMS). Each of the extracts was heated at 40, 60, 80, and 100 °C and tested for its antimicrobial effects in a plate well diffusion assay against <span class="html-italic">Listeria monocytogenes</span> and <span class="html-italic">Salmonella</span> Typhimurium. Results of the heat treatment were compared to an untreated control (UT) and the extraction solvent ethyl acetate (C). Error bars visualize the calculated standard deviation.</p>
Full article ">
11 pages, 592 KiB  
Communication
Microbiological Risks of Traditional Raw Cow’s Milk Cheese (Koryciński Cheeses)
by Aleksandra Antoszewska, Elżbieta Maćkiw, Joanna Kowalska, Małgorzata Patoleta, Maja Ławrynowicz-Paciorek and Jacek Postupolski
Foods 2024, 13(9), 1364; https://doi.org/10.3390/foods13091364 - 28 Apr 2024
Viewed by 578
Abstract
Traditional and regional foods have been increasing in popularity among consumers in Poland for many years. The observed trend of searching for natural and authentic taste encourages many producers to craft products from raw milk, including Koryciński cheeses. The aim of this study [...] Read more.
Traditional and regional foods have been increasing in popularity among consumers in Poland for many years. The observed trend of searching for natural and authentic taste encourages many producers to craft products from raw milk, including Koryciński cheeses. The aim of this study was to assess the microbiological hazards resulting from the presence of pathogenic bacteria in Koryciński cheeses available in retail trade. The tests were carried out using accredited methods, including the detection of the presence of Salmonella spp., the enumeration of Listeria monocytogenes, the enumeration of coagulase-positive staphylococci, and the detection of staphylococcal enterotoxins in food when the number of coagulase-positive staphylococci in the sample exceeded the limit of 105 cfu/g. The research material consisted of 45 Koryciński cheeses. The tests conducted revealed that Salmonella spp. was not detected in any of the examined cheeses. However, coagulase-positive staphylococci were present in 68.9% of the samples. In as many as 15 tested cheeses, the level of S. aureus contamination was above 105 cfu/g; therefore, these samples were tested for the presence of staphylococcal enterotoxins. The presence of staphylococcal enterotoxins was found in one Koryciński cheese. In four cheeses, the number of L. monocytogenes exceeded the level of 102 cfu/g, the limit specified in Regulation 2073/2005 on microbiological criteria for foodstuffs. The obtained research results confirm the validity of monitoring the microbiological quality of Koryciński cheeses and the need to increase awareness of ensuring proper hygienic conditions of production, including the increased risk associated with unpasteurized milk products. Full article
(This article belongs to the Section Dairy)
Show Figures

Figure 1

Figure 1
<p>Results of compliance with the requirements of the microbiological criteria of Regulation. 2073/2005 for natural, cream, and smoked cheeses. * Food safety criteria. ** Process hygiene criteria.</p>
Full article ">Figure 2
<p>Results of compliance with the requirements of the microbiological criteria of Regulation. 2073/2005 for cheeses with additives. * Food safety criteria. ** Process hygiene criteria.</p>
Full article ">
Back to TopTop