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10 pages, 660 KiB  
Article
The Prevalence of Encephalitozoon cuniculi in Domestic Rabbits (Oryctolagus cuniculus) in the North-Western Region of Romania Using Serological Diagnosis: A Preliminary Study
by Anca-Alexandra Doboși, Anamaria Ioana Paștiu, Lucia-Victoria Bel and Dana Liana Pusta
Microorganisms 2024, 12(7), 1440; https://doi.org/10.3390/microorganisms12071440 (registering DOI) - 16 Jul 2024
Abstract
Encephalitozoon cuniculi is a microsporidian, domestic rabbits being the main host. The disease can be acute or subclinical, but treatment options are limited and usually with unrewarding results; therefore, diagnosis and prevention of encephalitozoonosis in rabbits are of the utmost importance. This study [...] Read more.
Encephalitozoon cuniculi is a microsporidian, domestic rabbits being the main host. The disease can be acute or subclinical, but treatment options are limited and usually with unrewarding results; therefore, diagnosis and prevention of encephalitozoonosis in rabbits are of the utmost importance. This study aims to obtain the first preliminary information of the prevalence of E. cuniculi in the north-western region of Romania. A total of 176 rabbits were clinically examined and 2 mL of blood was sampled from each. An enzyme-linked immunosorbent assay (ELISA) kit by Medicago (Medicago, Uppsala, Sweden) on the resulted blood serum was utilized. Statistical analysis of the results was conducted using the EpiInfo 2000 software (CDC, Atlanta, GA, USA). A total prevalence of 39.2% (69/176) was identified, with statistically significant differences in relation to the rabbits’ clinical status, age, season of sampling, breeding system, body condition score and county of origin; the different family farms tested also had a statistically significant difference. This study gives the first preliminary information on this pathogen distribution on Romania’s territory, but further studies need to be performed on larger regions to declare the prevalence in the country. Full article
(This article belongs to the Special Issue State-of-the-Art Parasitic and Bacterial Infections in Romania 2.0)
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Figure 1

Figure 1
<p>The counties of origin and the number of rabbits tested for <span class="html-italic">Encephalitozoon cuniculi</span> in the north-western region of Romania. The shade of color is in accordance with the resulted prevalence.</p>
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17 pages, 1294 KiB  
Article
Molecular Characterization of Hepatitis B Virus in People Living with HIV in Rural and Peri-Urban Communities in Botswana
by Bonolo B. Phinius, Wonderful T. Choga, Motswedi Anderson, Margaret Mokomane, Irene Gobe, Tsholofelo Ratsoma, Basetsana Phakedi, Gorata Mpebe, Lynnette Bhebhe, Tendani Gaolathe, Mosepele Mosepele, Joseph Makhema, Roger Shapiro, Shahin Lockman, Rosemary Musonda, Sikhulile Moyo and Simani Gaseitsiwe
Biomedicines 2024, 12(7), 1561; https://doi.org/10.3390/biomedicines12071561 - 14 Jul 2024
Viewed by 288
Abstract
Abstract: (1) Background: Hepatitis B virus (HBV) sequencing data are important for monitoring HBV evolution. We aimed to molecularly characterize HBV sequences from participants with HBV surface antigen-positive (HBsAg+) serology and occult hepatitis B infection (OBI+). (2) Methods: We utilized archived plasma samples [...] Read more.
Abstract: (1) Background: Hepatitis B virus (HBV) sequencing data are important for monitoring HBV evolution. We aimed to molecularly characterize HBV sequences from participants with HBV surface antigen-positive (HBsAg+) serology and occult hepatitis B infection (OBI+). (2) Methods: We utilized archived plasma samples from people living with human immunodeficiency virus (PLWH) in Botswana. HBV DNA was sequenced, genotyped and analyzed for mutations. We compared mutations from study sequences to those from previously generated HBV sequences in Botswana. The impact of OBI-associated mutations on protein function was assessed using the Protein Variation Effect Analyzer. (3) Results: Sequencing success was higher in HBsAg+ than in OBI+ samples [86/128 (67.2%) vs. 21/71 (29.2%)]. Overall, 93.5% (100/107) of sequences were genotype A1, 2.8% (3/107) were D3 and 3.7% (4/107) were E. We identified 13 escape mutations in 18/90 (20%) sequences with HBsAg coverage, with K122R having the highest frequency. The mutational profile of current sequences differed from previous Botswana HBV sequences, suggesting possible mutational changes over time. Mutations deemed to have an impact on protein function were tpQ6H, surfaceV194A and preCW28L. (4) Conclusions: We characterized HBV sequences from PLWH in Botswana. Escape mutations were prevalent and were not associated with OBI. Longitudinal HBV studies are needed to investigate HBV natural evolution. Full article
8 pages, 278 KiB  
Article
Can Hematological Inflammatory Indices Be Used to Differentiate Modic Type 1 Changes from Brucella Spondylodiscitis?
by Volkan Şah and Ali İrfan Baran
Medicina 2024, 60(7), 1131; https://doi.org/10.3390/medicina60071131 - 14 Jul 2024
Viewed by 246
Abstract
Background and Objectives: Differentiation between brucella spondylodiscitis and Modic type I changes (MC1) includes difficulties. Hematological inflammatory indices (HII) such as neutrophil to lymphocyte ratio (NLR) and aggregate index of systemic inflammation (AISI) are suggested as indicators of inflammation and infection and [...] Read more.
Background and Objectives: Differentiation between brucella spondylodiscitis and Modic type I changes (MC1) includes difficulties. Hematological inflammatory indices (HII) such as neutrophil to lymphocyte ratio (NLR) and aggregate index of systemic inflammation (AISI) are suggested as indicators of inflammation and infection and have diagnostic, prognostic, and predictive roles in various diseases. This study aimed to evaluate differences between brucella spondylodiscitis and MC1 in terms of HII. Materials and Methods: Thirty-five patients with brucella spondylodiscitis and thirty-seven with MC1 were enrolled in the study. Brucella spondylodiscitis and MC1 were diagnosed by microbiological, serological, and radiological diagnostic tools. HII (NLR, MLR, PLR, NLPR, SII, SIRI, AISI) were derived from baseline complete blood count. Results: The two groups were similar for age (p = 0.579) and gender (p = 0.092), leukocyte (p = 0.127), neutrophil (p = 0.366), lymphocyte (p = 0.090), and monocyte (p = 0.756) scores. The Brucella spondylodiscitis group had significantly lower pain duration (p < 0.001), higher CRP and ESR levels (p < 0.001), and lower platelet count (p = 0.047) than the MC1 group. The two groups had similarity in terms of HII: NLR (p = 0.553), MLR (p = 0.294), PLR (p = 0.772), NLPR (p = 0.115), SII (p = 0.798), SIRI (p = 0.447), and AISI (p = 0.248). Conclusions: Increased HII can be used to differentiate infectious and non-infectious conditions, but this may be invalid in brucellosis. However, pain duration, CRP and ESR levels, and platelet count may be useful to distinguish brucella spondylodiscitis from MC1. Full article
16 pages, 6000 KiB  
Article
Comprehensive Study of the IBMP ELISA IgA/IgM/IgG COVID-19 Kit for SARS-CoV-2 Antibody Detection
by Sibelle Botogosque Mattar, Paola Alejandra Fiorani Celedon, Leonardo Maia Leony, Larissa de Carvalho Medrado Vasconcelos, Daniel Dias Sampaio, Fabricio Klerynton Marchini, Luis Gustavo Morello, Vanessa Hoysan Lin, Sandra Crestani, Aquiles Assunção Camelier, André Costa Meireles, André Luiz Freitas de Oliveira Junior, Antônio Carlos Bandeira, Yasmin Santos Freitas Macedo, Alan Oliveira Duarte, Tycha Bianca Sabaini Pavan, Isadora Cristina de Siqueira and Fred Luciano Neves Santos
Diagnostics 2024, 14(14), 1514; https://doi.org/10.3390/diagnostics14141514 - 13 Jul 2024
Viewed by 282
Abstract
COVID-19 laboratory diagnosis primarily relies on molecular tests, highly sensitive during early infection stages with high viral loads. As the disease progresses, sensitivity decreases, requiring antibody detection. Since the beginning of the pandemic, serological tests have been developed and made available in Brazil, [...] Read more.
COVID-19 laboratory diagnosis primarily relies on molecular tests, highly sensitive during early infection stages with high viral loads. As the disease progresses, sensitivity decreases, requiring antibody detection. Since the beginning of the pandemic, serological tests have been developed and made available in Brazil, but their diagnostic performance varies. This study evaluated the IBMP ELISA IgA/IgM/IgG COVID-19 kit performance in detecting SARS-CoV-2 antibodies. A total of 90 samples, including 64 from COVID-19 patients and 26 pre-pandemic donors, were assessed based on time post symptom onset (0–7, 8–14, and 15–21 days). The kit showed 61% sensitivity, 100% specificity, and 72% accuracy overall. Sensitivity varied with time, being 25%, 57%, and 96% for 0–7, 8–14, and 15–21 days, respectively. Similar variations were noted in other commercial tests. The Gold ELISA COVID-19 (IgG/IgM) had sensitivities of 31%, 71%, and 100%, while the Anti-SARS-CoV-2 NCP ELISA (IgG) and Anti-SARS-CoV-2 NCP ELISA (IgM) showed varying sensitivities. The IBMP ELISA kit displayed high diagnostic capability, especially as the disease progressed, complementing COVID-19 diagnosis. Reproducibility assessment revealed minimal systematic and analytical errors. In conclusion, the IBMP ELISA IgA/IgM/IgG COVID-19 kit is a robust tool for detecting anti-SARS-CoV-2 antibodies, increasing in efficacy over the disease course, and minimizing false negatives in RT-PCR COVID-19 diagnosis. Full article
(This article belongs to the Section Diagnostic Microbiology and Infectious Disease)
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<p>Flowchart illustrating study design in conformity with the Standards for Reporting of Diagnostic Accuracy Studies (STARD) guidelines. Source base layer and credit base layer: <a href="https://data.humdata.org/" target="_blank">https://data.humdata.org/</a> (accessed on 14 April 2024) under creative commons attribution for intergovernmental organizations: <a href="https://data.humdata.org/dataset/geoboundaries-admin-boundaries-for-brazil" target="_blank">https://data.humdata.org/dataset/geoboundaries-admin-boundaries-for-brazil</a> (accessed on 14 April 2024).</p>
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<p>Graphical analysis of reactivity index (<b>A</b>) and area under the ROC curve (AUC) (<b>B</b>) obtained with serum samples from SARS-CoV-2-positive and SARS-CoV-2-negative samples. The cut-off value is the reactivity index = 1.0 and the shaded area represents the gray zone (0.80 ≤ IR &lt; 1.10). Performance parameters (<b>C</b>) obtained for IBMP Spike IgA/IgM/IgG ELISA. SEN, sensitivity; SPE, specificity; ACC, accuracy; PLR, positive likelihood ratio; NLR, negative likelihood ratio; DOR, diagnostic odds ratio; Kappa, Cohen’s Kappa coefficient; GR, gray zone; RI, reactivity index; POS, positive; NEG, negative.</p>
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<p>Analysis of SARS-CoV-2-positive samples classified by symptom onset. Graphical analysis of reactivity index (<b>A</b>) and area under the ROC curve (AUC) (<b>B</b>) determined using serum samples from SARS-CoV-2 positive and SARS-CoV-2-negative samples. The cut-off value is the reactivity index = 1.0 and the shaded area represents the gray zone (0.80 ≤ IR &lt; 1.10). Performance parameters determined for the IBMP Spike IgA/IgM/IgG ELISA (<b>C</b>). SEN, sensitivity; SPE, specificity; ACC, accuracy; PLR, positive likelihood ratio; NLR, negative likelihood ratio; DOR, diagnostic odds ratio; Kappa, Cohen’s Kappa coefficient; GZ, gray zone; RI, reactivity index; POS, positive; NEG, negative.</p>
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<p>Deming regression fit (left) and Bland–Altman plots (right) comparing two replicates (Rep 1 and Rep 2) of the IBMP Spike IgA/IgM/IgG ELISA for the detection of anti-SARS-CoV-2 using SARS-CoV-2-positive (<span class="html-italic">n</span> = 64) and -negative (<span class="html-italic">n</span> = 26) samples.</p>
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<p>Interference of bilirubin, hemoglobin, and triglycerides on the IBMP Spike IgA/IgM/IgG ELISA signal. Red line (positive samples); Blue line (negatieg samples).</p>
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<p>Comparison of the reactivity index (RI) and sensitivity (SEN) of the IBMP Spike IgA/IgM/IgG ELISA with three available commercial kits. IB, IBMP Spike IgA/IgM/IgG ELISA; GD, GOLD ELISA COVID-19 IgG/IgM; EG, Anti-SARS-CoV-2 IgG ELISA; EM, Anti-SARS-CoV-2 NCP IgM ELISA.</p>
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<p>Seroconversion of COVID-19 by IBMP Spike IgA/IgM/IgG ELISA and three commercial assays in serum samples obtained at different time points post symptom onset.</p>
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15 pages, 718 KiB  
Article
Clinical Study and Serological Diagnosis of Vector-Borne Pathogens in Sardinian Dogs
by Valentina Chisu, Antonio Tanda, Sara Sechi, Maria Luisa Pinna Parpaglia, Gabriella Masu, Federica Loi and Giovanna Masala
Vet. Sci. 2024, 11(7), 313; https://doi.org/10.3390/vetsci11070313 - 12 Jul 2024
Viewed by 288
Abstract
Canine vector-borne diseases (CVBDs) comprise a group of infectious diseases caused by a wide range of pathogens transmitted by arthropod vectors. Clinical signs commonly involve symptoms such as fever, anorexia, weight loss, blood disorders, hepatosplenomegaly, and others that can lead to death in [...] Read more.
Canine vector-borne diseases (CVBDs) comprise a group of infectious diseases caused by a wide range of pathogens transmitted by arthropod vectors. Clinical signs commonly involve symptoms such as fever, anorexia, weight loss, blood disorders, hepatosplenomegaly, and others that can lead to death in dogs with comorbidities. Some pathogens responsible for CVBDs constitute a serious threat to human health due to their zoonotic transmission. This study aimed to determine the prevalence of zoonotic vector-borne diseases (Rickettsia rickettsii, Anaplasma phagocytophilum, Ehrlichia canis, Bartonella henselae, and Leishmania infantum) in domestic Sardinian dogs with and without clinical signs of these pathogens. Blood serum samples were collected from 142 dogs and examined through serological analysis. Clinical signs suggestive of these pathogens were also evaluated. The results obtained showed that 33 (33/140; 23.6%), 22 (22/134; 16.4%), 14 (14/142; 9.9%), 20 (20/66; 30.3%), and 26 (26/108; 24.1%) dogs were seropositive for Rickettsia sp., Anaplasma sp., Ehrlichia sp., Bartonella sp., and Leishmania sp. antibodies, respectively. Among these dogs, 12 dogs presented with at least one clinical sign (8.5%), while 18 (12.7%) showed more than two symptoms at the same time. Furthermore, among the asymptomatic dogs (93/142; 65.5%), 13% (n = 12) tested positive for A. phagocytophilum, 12% (n = 11) tested positive for B. henselae, 9% (n = 8) tested positive for E. canis, 12% (n = 11) tested positive for L. infantum, and 19% (n = 18) tested positive for R. rickettsii. This survey represents the first study assessing different canine vector-borne pathogens in dogs from North Sardinia. Since the pathogens detected here represent emerging zoonotic diseases, these results highlight the need to undertake further studies to increase the knowledge of these under-reported vector-borne pathogens in Sardinia. Full article
10 pages, 1106 KiB  
Article
The Effect of Sample Handling on Rabies-Neutralizing Antibody Stability
by Samantha J. Pralle, Stephanie K. Gatrell, Cassidy C. Keating and Susan M. Moore
Biologics 2024, 4(3), 232-241; https://doi.org/10.3390/biologics4030016 - 12 Jul 2024
Viewed by 264
Abstract
The measurement of rabies-neutralizing antibody is important for monitoring the response to rabies vaccination. For all the purposes of measurement, such as routine monitoring of vaccine response in humans and animals, serosurveys, and biologics qualification, accurate and precise results are necessary. The risks [...] Read more.
The measurement of rabies-neutralizing antibody is important for monitoring the response to rabies vaccination. For all the purposes of measurement, such as routine monitoring of vaccine response in humans and animals, serosurveys, and biologics qualification, accurate and precise results are necessary. The risks associated with sample handling variation, which may impact the test results, can be overlooked within a laboratory. To determine the robustness of rabies-neutralizing antibodies in human and animal serum, samples were treated to mimic various possible deviations in the sample handling protocols. Potential deviations were designed to investigate common client inquiries and possible sample conditions experienced during shipping, storage, and laboratory processes. The treatments included the duration that sera were kept at a temperature greater than that of a refrigerator (room temperature, zero hours to two weeks), the number and duration of heat inactivation treatments (i.e., heat inactivation directly from freezer storage, etc.), the number of freeze–thaw cycles (zero, four, or six cycles), and the storage duration of sample dilutions in chamber slides before the addition of virus (zero hours to overnight). The results provided evidence for the robustness of rabies antibodies and the antibodies’ neutralizing function in uncontaminated, clear human and animal serum. In addition, prolonged heat exposure was identified as exerting the greatest impact on the measurement of rabies antibodies. Full article
(This article belongs to the Section Diagnostics)
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Figure 1
<p>Influence of room temperature storage time on RFFIT IU/mL result: (<b>a</b>) The effect of room temperature storage by number of hours on the measured rabies-neutralizing antibody (IU/mL) is displayed. The dotted line represents the acceptable level for rabies vaccination seroconversion. (<b>b</b>) The comparison of room temperature-stored samples’ results (IU/mL) to the control sample results (stored at 2 to 8 °C until testing). The black line is the control data trendline line; the colored dotted trendlines correspond to the data sets per treatment by color in the legend.</p>
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<p>The influence of heat inactivation time on RFFIT IU/mL result: (<b>a</b>) The effect of different HI and storage schemes on the measured rabies-neutralizing antibody (IU/mL) is displayed. The dotted line represents the acceptable level for rabies vaccination seroconversion. (<b>b</b>) The comparison of the heat inactivation scheme sample results (IU/mL) to the control sample results. The black line is the control data trendline line; the colored dotted trendlines correspond to the data sets per treatment by color in the legend.</p>
Full article ">Figure 3
<p>The influence of 2 to 8 °C storage time of serum sample dilutions in chamber slides on RFFIT IU/mL result: (<b>a</b>) The effect of different storage times on the measured rabies-neutralizing antibody (IU/mL) is displayed. The dotted line represents the acceptable level for rabies vaccination seroconversion. (<b>b</b>) The comparison of the chamber slide storage time sample results (IU/mL) to the control sample results. The black line is the overall data trendline line; colored dotted trendlines correspond to the data sets per treatment by color in the legend.</p>
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<p>RFFIT IU/mL results of test panels after 4 and 6 freeze–thaw cycles compared to the control panel (no freeze–thaw cycle): (<b>a</b>) The effect of freeze–thaw cycles on the measured rabies-neutralizing antibody (IU/mL) is displayed. The dotted line represents the acceptable level for rabies vaccination seroconversion. (<b>b</b>) The comparison of the freeze–thaw test panel results (IU/mL) to the control samples. The black line is the overall data trendline line; colored dotted trendlines correspond to the data sets per treatment by color in the legend.</p>
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10 pages, 908 KiB  
Article
Lack of Serological Response by Delivery to Syphilis Treatment Does Not Impact Pregnancy Outcomes
by Konrad Kaminiów, Agnieszka Kotlarz, Martyna Kiołbasa and Maciej Pastuszczak
J. Clin. Med. 2024, 13(14), 4031; https://doi.org/10.3390/jcm13144031 - 10 Jul 2024
Viewed by 360
Abstract
Objectives: Maternal syphilis can lead to serious adverse pregnancy outcomes, including neonatal death. A 4-fold decline in blood non-treponemal titer at six months after the treatment of syphilis compared to the baseline is considered as an adequate serological response. However, the duration of [...] Read more.
Objectives: Maternal syphilis can lead to serious adverse pregnancy outcomes, including neonatal death. A 4-fold decline in blood non-treponemal titer at six months after the treatment of syphilis compared to the baseline is considered as an adequate serological response. However, the duration of normal human gestation does not allow the ascertainment of an adequate serological response. Aim: The aim of this study was to assess correlations between the lack of a 4-fold decrease in non-treponemal titer by delivery after syphilis treatment and fetal and newborns’ condition and serological outcomes. Methods: Fourteen pregnant patients (gestational age 16–22 weeks) diagnosed with early syphilis (secondary or latent) were treated with intramuscular benzathine penicillin and subsequently monitored clinically, serologically, and ultrasonographically at monthly intervals. Based on the non-treponemal test results at delivery, patients were stratified into two groups: those with a 4-fold decline in titers and those without such a decline. All newborns were clinically and serologically assessed for congenital syphilis at birth and then monitored until serological tests became negative. Results: Fifty percent of the included women did not achieve a 4-fold decline in non-treponemal titer by delivery. Patients from the group showing a 4-fold decline in RPR titer at delivery and those without such a decline did not differ in basic demographic and clinical characteristics or in ultrasound parameters used for fetal assessment. Based on the clinical and laboratory assessments of newborns on the day of delivery and during a 6-month follow-up, none were diagnosed with congenital syphilis or required treatment for syphilis. Conclusions: The lack of an adequate serological response to syphilis therapy by delivery among patients treated between 16 and 22 weeks of pregnancy does not appear to be associated with adverse fetal and neonatal outcomes. Full article
(This article belongs to the Section Dermatology)
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<p>Proportion of pregnant patients without a 4-fold decline in non-treponemal test titers at follow-up after treatment.</p>
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<p>Fetal ultrasound parameters among patients with and without a 4-fold decline in non-treponemal test titers by the time of delivery.</p>
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14 pages, 2808 KiB  
Article
Serological Screening and Risk Factors Associated with Leishmania infantum Positivity in Newly Diagnosed HIV Patients in Greece
by Chrysa Voyiatzaki, Apollon Dareios Zare Chormizi, Maria E. Tsoumani, Antonia Efstathiou, Konstantinos Konstantinidis, Georgios Chrysos, Aikaterini Argyraki, Vasileios Papastamopoulos, Effie G. Papageorgiou and Marika Kotsianopoulou
Microorganisms 2024, 12(7), 1397; https://doi.org/10.3390/microorganisms12071397 - 10 Jul 2024
Viewed by 361
Abstract
A serological screening was conducted to detect IgG antibodies against Leishmania infantum (L. infantum) in newly diagnosed human immunodeficiency virus (HIV) patients in Greece. The study also examined potential risk factors and the agreement of commercially available serological methods. IgG antibodies [...] Read more.
A serological screening was conducted to detect IgG antibodies against Leishmania infantum (L. infantum) in newly diagnosed human immunodeficiency virus (HIV) patients in Greece. The study also examined potential risk factors and the agreement of commercially available serological methods. IgG antibodies against L. infantum were detected using enzyme-linked immunosorbent assay (ELISA), indirect immunofluorescence antibody test (IFAT), and Western blot (WB). Out of 155 samples, 14 (9.0%) tested positive for IgG antibodies against L. infantum using at least two methods. Statistical analysis showed substantial agreement between WB and IFAT methods (Cohen’s kappa = 0.75) but moderate overall agreement among the three methods (Fleiss’ kappa = 0.42). Additionally, HIV+ intravenous drug users faced 3.55 times (p = 0.025) higher risk of testing positive for L. infantum IgG, positing that anthroponotic transmission between these patients is a plausible hypothesis based on existing literature. Non-invasive and cost-effective techniques are preferred to detect asymptomatic infections, and leishmaniasis screening should be conducted immediately after HIV diagnosis in endemic regions to enable prophylactic treatment for leishmaniasis in addition to antiretroviral therapy. To maximize sensitivity, performing at least two different serological methods for each patient is recommended. Full article
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Figure 1
<p>Symmetric three-set Venn diagram of the <span class="html-italic">Leishmania infantum</span> immunoglobulin G (IgG) detection results, output by the three examined assays, namely, Western blot (WB), enzyme-linked immunosorbent assay (ELISA), and indirect immunofluorescence antibody test (IFAT). All possible intersections and exclusive regions of each different set of positive [<span class="html-italic">L. infantum</span> IgG (+)] or negative [<span class="html-italic">L. infantum</span> IgG (−)] assay results have been drawn and colored accordingly. The displayed numbers between the parentheses represent the total number of positive or negative results of the respective assay designated by a line, while the numbers within the colorful regions correspond to the number of positive or negative assay results that are unique to a specific assay or union of assays.</p>
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<p>Heatmap figure illustrating the results of <span class="html-italic">L. infantum</span> IgG detection for each one of the 155 examined HIV+ patients (− = IgG negative, gray zone = ambiguous result, + = IgG positive) after the implementation of the three studied immunoassay methods, namely, Western blot (WB), enzyme-linked immunosorbent assay (ELISA), and immunofluorescence antibody test (IFAT). The appropriate color legend has been applied (<span class="html-italic">L. infantum</span> IgG negative samples in white, ambiguous <span class="html-italic">L. infantum</span> IgG detection in light grey, <span class="html-italic">L. infantum</span> IgG positive samples in black), highlighting the convergence/agreement of <span class="html-italic">L. infantum</span> IgG detection results per immunoassay method per HIV+ patient.</p>
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21 pages, 4258 KiB  
Article
Lonicera japonica Thunb. Ethanol Extract Exerts a Protective Effect on Normal Human Gastric Epithelial Cells by Modulating the Activity of Tumor-Necrosis-Factor-α-Induced Inflammatory Cyclooxygenase 2/Prostaglandin E2 and Matrix Metalloproteinase 9
by Hsi-Lung Hsieh, Ming-Chin Yu, Yu-Chia Chang, Yi-Hsuan Wu, Kuo-Hsiung Huang and Ming-Ming Tsai
Curr. Issues Mol. Biol. 2024, 46(7), 7303-7323; https://doi.org/10.3390/cimb46070433 - 9 Jul 2024
Viewed by 226
Abstract
Gastric inflammation-related disorders are commonly observed digestive system illnesses characterized by the activation of proinflammatory cytokines, particularly tumor necrosis factor-α (TNF-α). This results in the induction of cyclooxygenase-2 (COX-2)/prostaglandin E2 (PEG2) and matrix metallopeptidase-9 (MMP-9). These factors contribute to the [...] Read more.
Gastric inflammation-related disorders are commonly observed digestive system illnesses characterized by the activation of proinflammatory cytokines, particularly tumor necrosis factor-α (TNF-α). This results in the induction of cyclooxygenase-2 (COX-2)/prostaglandin E2 (PEG2) and matrix metallopeptidase-9 (MMP-9). These factors contribute to the pathogenesis of gastric inflammation disorders. We examined the preventive effects of Lonicera japonica Thunb. ethanol extract (Lj-EtOH) on gastric inflammation induced by TNF-α in normal human gastric mucosa epithelial cells (GES-1). The GES-1 cell line was used to establish a model that simulated the overexpression of COX-2/PGE2 and MMP-9 proteins induced by TNF-α to examine the anti-inflammatory properties of Lj extracts. The results indicated that Lj-EtOH exhibits significant inhibitory effects on COX-2/PEG2 and MMP-9 activity, attenuates cell migration, and provides protection against TNF-α-induced gastric inflammation. The protective effects of Lj-EtOH are associated with the modulation of COX-2/PEG2 and MMP-9 through the activation of TNFR–ERK 1/2 signaling pathways as well as the involvement of c-Fos and nuclear factor kappa B (NF-κB) signaling pathways. Based on our findings, Lj-EtOH exhibits a preventive effect on human gastric epithelial cells. Consequently, it may represent a novel treatment for the management of gastric inflammation. Full article
(This article belongs to the Special Issue Bioactive Natural and Synthetic Saccharides against Human Diseases)
15 pages, 8651 KiB  
Article
Molecular and Serological Surveillance for Mycobacterium leprae and Mycobacterium lepromatosis in Wild Red Squirrels (Sciurus vulgaris) from Scotland and Northern England
by Zijie Zhou, Anouk van Hooij, Gaby N. Wassenaar, Emma Seed, Els M. Verhard-Seymonsbergen, Paul L. A. M. Corstjens, Anna L. Meredith, Liam A. Wilson, Elspeth M. Milne, Katie M. Beckmann and Annemieke Geluk
Animals 2024, 14(13), 2005; https://doi.org/10.3390/ani14132005 - 7 Jul 2024
Viewed by 510
Abstract
Leprosy is a poverty-associated infectious disease in humans caused by Mycobacterium leprae or M. lepromatosis, often resulting in skin and peripheral nerve damage, which remains a significant public health concern in isolated areas of low- and middle-income countries. Previous studies reported leprosy [...] Read more.
Leprosy is a poverty-associated infectious disease in humans caused by Mycobacterium leprae or M. lepromatosis, often resulting in skin and peripheral nerve damage, which remains a significant public health concern in isolated areas of low- and middle-income countries. Previous studies reported leprosy in red squirrels in the British Isles, despite the fact that autochthonous human cases have been absent for centuries in this region. To investigate the extent of M. leprae and M. lepromatosis presence in wild red squirrels in the northern UK, we analyzed 220 blood/body cavity fluid samples from opportunistically sampled red squirrels (2004–2023) for specific antibodies against phenolic glycolipid-I, a cell wall component specific for these leprosy bacilli. Additionally, we assessed bacillus-derived DNA by real-time PCR (qPCR) in 250 pinnae from the same cohort. M. lepromatosis and M. leprae DNA were detected by qPCR in 20.4% and 0.8% of the squirrels, respectively. No cases of co-detection were observed. Detectable levels of anti-PGL-I antibodies by UCP-LFA were observed in 52.9% of animals with the presence of M. lepromatosis determined by qPCR, and overall in 15.5% of all animals. In total, 22.6% (n = 296) of this UK cohort had at least some exposure to leprosy bacilli. Our study shows that leprosy bacilli persist in red squirrels in the northern UK, emphasizing the necessity for ongoing molecular and serological monitoring to study leprosy ecology in red squirrels, gain insight into potential zoonotic transmission, and to determine whether the disease has a conservation impact on this endangered species. Full article
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<p>Presence of <span class="html-italic">M. lepromatosis</span> and <span class="html-italic">M. leprae</span> in red squirrels found between 2014 and 2023 by qPCR. The DNA samples (<span class="html-italic">n</span> = 250) derived from the pinna of red squirrels were assessed for the presence of 202 (left panel; <b>A</b>–<b>C</b>) and RLEP (right panel; <b>D</b>–<b>F</b>) sequences by qPCR. Ct values ≤ 30 were considered to indicate the presence of mycobacteria, Ct values ≥ 35 were considered negative, and 30 &lt; Ct values &lt; 35 were considered indeterminate for leprosy bacilli DNA. The Ct values for each animal (<b>A</b>,<b>D</b>) and frequency of outcomes (<b>B</b>,<b>E</b>) are represented on the <span class="html-italic">y</span>-axis, and the years of collection represented on the <span class="html-italic">x</span>-axis. The proportion for each of the three outcomes are provided in (<b>C</b>,<b>F</b>). ud, undetermined.</p>
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<p>Categorization of <span class="html-italic">M. lepromatosis</span> presence. The outcomes of 202 qPCR in red squirrels found between 2014 and 2023 are summarized by sex (<b>A panel</b>: 128 males and 118 females) and age (<b>B panel</b>: 15 juveniles, 33 subadults, and 200 adults). Further detailed information is shown in <a href="#animals-14-02005-f001" class="html-fig">Figure 1</a>.</p>
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<p>Summary of the RLEP and 202 qPCR results. The Ct values of 202 qPCR for each animal are represented on the <span class="html-italic">y</span>-axis, and the Ct values of RLEP qPCR for each animal are represented on the <span class="html-italic">x</span>-axis. Further detailed information is shown in <a href="#animals-14-02005-f001" class="html-fig">Figure 1</a>. Ct values ≤ 30 were considered positive, Ct values ≥ 35 were considered negative, and 30 &lt; Ct values &lt; 35 were considered indeterminate for leprosy bacilli DNA. ud, undetermined.</p>
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<p>Anti-PGL-I antibody levels in red squirrels. Anti-PGL-I antibody levels were measured by UCP-LFA in blood/body cavity fluid samples from red squirrels (n = 220). UCP-LFA results are displayed as the ratio value (R) between test (T) and flow control (FC) levels. The results were categorized and analyzed based on squirrel sex (<b>A</b>), age (<b>B</b>), and qPCR outcome (<b>C</b>). The correlation of anti-PGL-I antibody UCP-LFA and 202 qPCR is shown in (<b>D</b>) (<span class="html-italic">n</span> = 174); details of 202 qPCR shown in <a href="#animals-14-02005-f001" class="html-fig">Figure 1</a>. Fluid samples with ratio values (<span class="html-italic">n</span> = 34) in UCP-LFA, positive in RLEP qPCR (<span class="html-italic">n</span> = 2), Ct values &lt; 20 in 202 qPCR (n = 3), and negative in two qPCR assays (<span class="html-italic">n</span> = 5) were measured by ELISA using anti-human and anti-mouse antibodies (<span class="html-italic">n</span> = 44, <b>E</b>). The ELISA results of anti-PGL-I antibody are displayed as optical density at 450 nm corrected for background OD values (OD<sub>450-background</sub>). Differences between groups were determined by Kruskal–Wallis test with Dunn’s correction for multiple testing (<b>A</b>–<b>C</b>); <span class="html-italic">p</span>-values: *, <span class="html-italic">p</span> &lt; 0.05; ****, and <span class="html-italic">p</span> &lt; 0.0001 (<b>A</b>). The “r” value is the Spearman correlation coefficient (<b>D</b>,<b>E</b>).</p>
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<p>Venn diagram of results from molecular and serological analyses. Details shown in <a href="#animals-14-02005-t002" class="html-table">Table 2</a>.</p>
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<p>Geographical distribution of leprosy bacillus assay outcomes for red squirrels from the northern UK. Pie charts indicate the regions where squirrels were found and are color-coded for assay outcomes as indicated in the legend box. Numbers within circles indicate the number of animals tested. Squirrels submitted from unknown locations in Scotland are indicated on the upper left. Ab, antibody.</p>
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14 pages, 1173 KiB  
Article
Dementia Prevalence and Onchocerca volvulus Infection among Rural Elderly Persons in the Ntui Health District, Cameroon: A Population-Based Study
by Wepnyu Yembe Njamnshi, Joseph Nelson Siewe Fodjo, Kongnyu Gamnsi Njamnshi, Leonard Ngarka, Michel K. Mengnjo, Leonard N. Nfor, Martine A. F. Tsasse, Julius N. Taryunyu Njamnshi, Gladys Maestre, Jose E. Cavazos, Sudha Seshadri, Laurent S. Etoundi Ngoa, Marie-Thérèse Obama Abena Ondoa, Bernard Fongang, Anne-Cécile Zoung-Kanyi Bissek and Alfred K. Njamnshi
Pathogens 2024, 13(7), 568; https://doi.org/10.3390/pathogens13070568 - 6 Jul 2024
Viewed by 423
Abstract
Recent research suggests that infection with Onchocerca volvulus induces neurocognitive decline. This study sought to compare the cognitive outcomes of elderly persons based on onchocerciasis infection status and report the overall prevalence of dementia in the rural Ntui Health District in Cameroon. A [...] Read more.
Recent research suggests that infection with Onchocerca volvulus induces neurocognitive decline. This study sought to compare the cognitive outcomes of elderly persons based on onchocerciasis infection status and report the overall prevalence of dementia in the rural Ntui Health District in Cameroon. A community-based approach was used to recruit 103 participants aged ≥60 years. Dementia screening was done using the Community Screening Interview for Dementia (CSID) tool with a cut-off value of ≤29.5. O. volvulus infection was determined via microscopic examination of skin snips and serological testing of Ov16 antibodies using rapid diagnostic tests. Overall, the prevalence of dementia was 10.7%. Among the tested individuals, 17.9% (15/84) and 62.1% (41/66) were positive for O. volvulus and Ov16 antibodies, respectively. A multivariable linear regression model of CSID scores found a significant positive association with education level (8.654; 95% CI: 2.0870 to 15.222). However, having a positive skin snip for O. volvulus (−3.399; 95% CI: −6.805 to 0.007) and inhaling tobacco (−5.441; 95% CI: −9.137 to −1.744) tended to lower the CSID scores. Ongoing onchocerciasis transmission in the Ntui Health District may constitute a risk factor for dementia. Strengthening onchocerciasis elimination and adopting healthier lifestyles would contribute to dementia prevention among the elderly residing in endemic communities. Full article
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<p>Prevalence of dementia by age and by sex.</p>
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<p>Mean cognitive scores by onchocerciasis exposure and education level. CSID: Community Screening Interview for Dementia; OV: <span class="html-italic">Onchocerca volvulus</span>.</p>
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11 pages, 1428 KiB  
Article
Detection and Serological Evidence of European Bat Lyssavirus 1 in Belgian Bats between 2016 and 2018
by Inne Nauwelaers, Claudia Van den Eynde, Sanne Terryn, Bob Vandendriessche, Wout Willems, Daan Dekeukeleire and Steven Van Gucht
Trop. Med. Infect. Dis. 2024, 9(7), 151; https://doi.org/10.3390/tropicalmed9070151 - 5 Jul 2024
Viewed by 319
Abstract
Lyssaviruses are neurotropic viruses capable of inducing fatal encephalitis. While rabies virus has been successfully eradicated in Belgium, the prevalence of other lyssaviruses remains uncertain. In this study, we conducted a survey on live animals and passive surveillance to investigate the presence of [...] Read more.
Lyssaviruses are neurotropic viruses capable of inducing fatal encephalitis. While rabies virus has been successfully eradicated in Belgium, the prevalence of other lyssaviruses remains uncertain. In this study, we conducted a survey on live animals and passive surveillance to investigate the presence of lyssaviruses in Belgium. In 2018, a total of 113 saliva samples and 87 blood samples were collected from bats. Saliva was subjected to RT-qPCR to identify lyssavirus infections. Additionally, an adapted lyssavirus neutralisation assay was set up for the detection of antibodies neutralising EBLV-1 in blood samples. Furthermore, we examined 124 brain tissue samples obtained from deceased bats during passive surveillance between 2016 and 2018. All saliva samples tested negative for lyssaviruses. Analysis of the blood samples uncovered the presence of lyssavirus-neutralising antibodies in five bat species and 32% of samples with a wide range depending on bat species, suggesting past exposure to a lyssavirus. Notably, EBLV-1 was detected in brain tissue samples from two Eptesicus serotinus specimens collected in 2016 near Bertrix and 2017 near Étalle, confirming for the first time the presence of EBLV-1 in Belgium and raising awareness of the potential risks associated with this species of bats as reservoirs of the virus. Full article
(This article belongs to the Special Issue Treatment and Risk Assessment of Rabies)
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<p>Collection sites in Flanders where bats were captured for saliva and blood collection and sampling. Sampling sites indicated on the map from left to right are Diksmuide, Liezele, Duffel, Herentals and Arendonk. Map created in R using the mapview package (<a href="https://cran.r-project.org/web/packages/mapview/index.html" target="_blank">https://cran.r-project.org/web/packages/mapview/index.html</a>, accessed on 7 June 2024).</p>
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<p>Locations in Belgium where bats were found during passive surveillance. Map created in R using the mapview package (<a href="https://cran.r-project.org/web/packages/mapview/index.html" target="_blank">https://cran.r-project.org/web/packages/mapview/index.html</a>, accessed on 7 June 2024).</p>
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<p>Locations in Belgium where bats were found during passive surveillance. Two <span class="html-italic">E. serotinus</span> bats tested positive for EBLV-1, one in 2016 in Bertrix and one in 2017 in Étalle, which is 30 km southeast of Bertrix. Map created in R using the mapview package (<a href="https://cran.r-project.org/web/packages/mapview/index.html" target="_blank">https://cran.r-project.org/web/packages/mapview/index.html</a>, accessed on 7 June 2024).</p>
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27 pages, 11149 KiB  
Article
Precision Farming Multimodal Technologies Using Optical Sensors for the Detection of Citrus Tristeza Virus Endemics
by Athanasios V. Argyriou, Nikolaos Tektonidis, Evangelos Alevizos, Konstantinos P. Ferentinos, Nektarios N. Kourgialas and Matthaios M. Mathioudakis
Sustainability 2024, 16(13), 5748; https://doi.org/10.3390/su16135748 - 5 Jul 2024
Viewed by 384
Abstract
Citrus trees and their fruits have significant nutritional value and contain antioxidants that are important components of the Mediterranean diet. However, pathogenic diseases pose a threat to citriculture by reducing crop yield and quality. Therefore, there is a need for novel technologies to [...] Read more.
Citrus trees and their fruits have significant nutritional value and contain antioxidants that are important components of the Mediterranean diet. However, pathogenic diseases pose a threat to citriculture by reducing crop yield and quality. Therefore, there is a need for novel technologies to maintain healthy citrus crops and enable early and accurate detection of the related pathogens, such as the citrus tristeza virus (CTV). Remote sensing offers a non-destructive, cost effective and efficient method for assessing plant health dynamics. It can provide insights into chlorophyll content, water stress and disease presence. This study provides new insights by integrating a combination of remote sensing approaches (FCCs, NDVI, PCA), optical and proximal techniques with in situ field data collection as well as various serological/molecular technologies to detect CTV effectively and evaluate its temporal epidemiology pattern. In addition, the integration of the adopted techniques in case studies of known fields being infected by CTV provides the basis for remote sensing procedures, such as random forest machine learning algorithm, to become powerful in verifying and identifying new CTV-infected fields in a broader extent coverage area, reaching 89.7% accuracy assessment. Thus, it offers decision-makers a robust approach that contributes to CTV epidemiology monitoring and can aid in the development of effective and sustainable disease management strategies. Full article
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<p>The Area of Interest (AOI), Vatolakos region, in western area of Crete Island, Greece (Source: Google Earth, 2024). The AOI and the primary case study fields to be examined are characterized by flat surface terrain as derived by the Digital Elevation Model (DEM) of ALOS-Palsar (12.5 m spatial resolution).</p>
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<p>The four fields (CF1 to CF4) selected as case studies, in which infected trees with CTV were determined from previous field surveys and laboratory analysis during the years 2020 and 2021 (Source: UAV imagery, date acquisition: 13 July 2022).</p>
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<p>Flowchart of the methodological framework.</p>
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<p>Visualization of the NDVI mean values in a UAV image and the Sentinel-2 NDVI time-series flowcharts during the period 1 January 2017–14 June 2023 for the infected case study fields (<b>A</b>) CF1, (<b>B</b>) CF2, (<b>C</b>) CF3 and (<b>D</b>) CF4. In the figures (<b>left</b>) the reddish hues, with lower NDVI mean values, indicate the distribution of unhealthy vegetation within the field. In the graphs (<b>right</b>), a drop in the NDVI mean average values was observed in the latter years during summertime. CTV was detected during (<b>A</b>) 2021 in CF1, while the NDVI time series indicated a drop in NDVI values during the summer of 2019 onwards (red line), (<b>B</b>) 2021 in CF2, while the NDVI time series indicated a drop in NDVI values during the summer of 2021 onwards (red line), (<b>C</b>) 2020 in CF3, while the NDVI time series indicated a drop in NDVI values during the summer of 2019 onwards (red line) and (<b>D</b>) 2020 in CF4, while the NDVI time series indicated a drop in NDVI values during the summer of 2019 onwards (red line). The black line indicates the abrupt drop in NDVI values due to the eradication of the field ((<b>A</b>) after 2022, (<b>C</b>) during summer 2021). The green line indicates the healthy status of the field from 2017 to 2018 (<b>A</b>,<b>C</b>,<b>D</b>) or 2017 to 2020 (<b>B</b>).</p>
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<p>The False Color Composite (FCCs) of natural color (RGB 321) for the satellite imageries (<b>A</b>) GeoEye-1 (acquisition: 2 June 2017), (<b>B</b>) Pleiades (acquisition: 28 July 2018), (<b>C</b>) Worldview-2 (acquisition: 21 May 2021) and (<b>D</b>) the UAV image (acquisition: 13 July 2022) (<b>D</b>). Case study fields CF1 to CF4 are indicated in red boxes.</p>
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<p>FCCs of three different satellite images in Zoom, (<b>A</b>) GeoEye-1 (acquisition date: 2 June 2017), (<b>B</b>) Pleiades (acquisition date: 28 July 2018), (<b>C</b>) WorldView-2 (acquisition date: 21 May 2021) consisting of the RED-Principal Component 1-NDVI in an RGB composition highlighting specific trees infected by CTV virus from the case study field CF1 (in red box). In the yellow asterisk, the CTV-infected trees were detected as positive during 2020 and 2021. Healthy vegetation appears in bluish hues, while the infected trees are in darker brownish/yellowish hues.</p>
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<p>The initial four case study fields (CF1 to CF4) in conjunction with the <b>nine</b> candidate fields with CTV-infected trees (CdF1 to CdF9), as suggested by the satellite/UAV imageries techniques, overlaid in WorldView-2 (date: May 2021) RGB combination Red-PC1-NDVI.</p>
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<p>Suggested AOI with potential markers of infected CTV trees, as shown in (<b>A</b>) in RGB 321 (natural color), (<b>B</b>) in NDVI visualization (green hues show healthy vegetation) from UAV imagery (acquisition date July 2022). The variations of the detected markers might indicate the number of genotypes present on each infected tree, either existing as sole or more than one.</p>
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<p>The UAV image (acquisition date 13 July 2022) visualization with FCC (RGB 321) (left images) and the RF outcomes (right images) for the case study filed. (<b>A</b>) CF2, and candidate fields (<b>B</b>) CdF4, (<b>C</b>) CdF6, (<b>D</b>) CdF7, all infected with CTV. Reddish hues indicate the CTV-infected trees.</p>
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<p>The individual NDVI for the diverse satellite and UAV sensors for CF1 to CF4 CTV-infected fields. Greenish hues highlight healthy vegetation, while yellowish hues are unhealthy, such as the ones infected by CTV.</p>
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<p>The individual PCA analysis for the diverse satellite sensors for CF1 to CF4 CTV-infected fields, with most of the information being compressed within Principal Component 1 (PC1).</p>
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<p>In the proximity of the case study fields, there were trees, primarily found in nearby abandoned fields, with an observed strong reflectance in the near-infrared band which was associated with climbing plants growing on the citrus trees. For instance, (<b>a</b>) FCC 321, in the 2017 GeoEye-1 satellite image; (<b>b</b>) Near-infrared band (high values in black color) in the 2017 GeoEye-1 satellite image; (<b>c</b>) FCC 321, in the Pleiades satellite image; (<b>d</b>) Near-infrared band (high values in black color), in the Pleiades satellite image.</p>
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<p>In the proximity of the case study fields, there were trees, primarily found in nearby abandoned fields, with an observed strong reflectance in the near-infrared band which was associated with climbing plants growing on the citrus trees. For instance, (<b>a</b>) FCC 321, in the 2017 GeoEye-1 satellite image; (<b>b</b>) Near-infrared band (high values in black color) in the 2017 GeoEye-1 satellite image; (<b>c</b>) FCC 321, in the Pleiades satellite image; (<b>d</b>) Near-infrared band (high values in black color), in the Pleiades satellite image.</p>
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14 pages, 2870 KiB  
Article
Tailoring COVID-19 Vaccination Strategies in High-Seroprevalence Settings: Insights from Ethiopia
by Esayas Kebede Gudina, Kira Elsbernd, Daniel Yilma, Rebecca Kisch, Karina Wallrafen-Sam, Gemeda Abebe, Zeleke Mekonnen, Melkamu Berhane, Mulusew Gerbaba, Sultan Suleman, Yoseph Mamo, Raquel Rubio-Acero, Solomon Ali, Ahmed Zeynudin, Simon Merkt, Jan Hasenauer, Temesgen Kabeta Chala, Andreas Wieser and Arne Kroidl
Vaccines 2024, 12(7), 745; https://doi.org/10.3390/vaccines12070745 (registering DOI) - 5 Jul 2024
Viewed by 337
Abstract
This study aimed to retrospectively assess the cost-effectiveness of various COVID-19 vaccination strategies in Ethiopia. It involved healthcare workers (HCWs) and community participants; and was conducted through interviews and serological tests. Local SARS-CoV-2 variants and seroprevalence rates, as well as national COVID-19 reports [...] Read more.
This study aimed to retrospectively assess the cost-effectiveness of various COVID-19 vaccination strategies in Ethiopia. It involved healthcare workers (HCWs) and community participants; and was conducted through interviews and serological tests. Local SARS-CoV-2 variants and seroprevalence rates, as well as national COVID-19 reports and vaccination status were also analyzed. A cost-effectiveness analysis was performed to determine the most economical vaccination strategies in settings with limited vaccine access and high SARS-CoV-2 seroprevalence. Before the arrival of the vaccines, 65% of HCWs had antibodies against SARS-CoV-2, indicating prior exposure to the virus. Individuals with prior infection exhibited a greater antibody response to COVID-19 vaccines and experienced fewer new infections compared to those without prior infection, regardless of vaccination status (5% vs. 24%, p < 0.001 for vaccinated; 3% vs. 48%, p < 0.001 for unvaccinated). The cost-effectiveness analysis indicated that a single-dose vaccination strategy is optimal in settings with high underlying seroprevalence and limited vaccine availability. This study underscores the need for pragmatic vaccination strategies tailored to local contexts, particularly in high-seroprevalence regions, to maximize vaccine impact and minimize the spread of COVID-19. Implementing a targeted approach based on local seroprevalence information could have helped Ethiopia achieve higher vaccination rates and prevent subsequent outbreaks. Full article
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<p>Flow diagram of participant recruitment at baseline (pre) and follow-up (post) visits.</p>
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<p>National infection spread and local SARS-CoV-2 variant pattern during the study period. (<b>A</b>) National RT-PCR test positivity rate and critical cases of COVID-19 in Ethiopia. (<b>B</b>) Frequencies of SARS-CoV-2 variants sequenced in Jimma based on 419 RT-PCR positive samples collected from January to September 2021 [<a href="#B24-vaccines-12-00745" class="html-bibr">24</a>].</p>
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<p>(<b>A</b>,<b>B</b>) Pre-post antibody response by vaccination status and evidence of prior SARS-CoV-2 infection. Participants with either N- or S- specific antibody response above the cutoff for positivity at the pre visit were considered to have prior infection. Relationship between N- and S-specific antibody response. (<b>C</b>) Individual change and summary boxplots in S-specific antibody response. (<b>D</b>) Frequency of infection according to vaccination status and prior infection. Notes: (<b>C</b>) Dotted line: Anti-S antibodies under 0.2 were categorized at 0.2. Dashed line: positive cutoff considered as evidence for receptor-binding domain-specific (RBD) antibodies. * Number of participants with titer below 0.2 (<b>D</b>) Only significant <span class="html-italic">p</span>-values are shown.</p>
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<p>The cost in USD per unit increase in utility (i.e., per percentage point increase in the percentage of the adult population of Ethiopia with anti-spike levels above 275 BAU/mL compared to a no-vaccination scenario) for three different vaccination strategies and for AstraZeneca (<b>A</b>) vs. Pfizer (<b>B</b>). The strategy with the lowest cost per unit increase in utility for varying per-test costs and previous infection prevalence for AstraZeneca (<b>C</b>) vs. Pfizer (<b>D</b>).</p>
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<p>SARS-CoV-2 seroprevalence and proportion vaccinated. Seroprevalence was estimated among HCWs and general community members from a large seroepidemiological survey [<a href="#B24-vaccines-12-00745" class="html-bibr">24</a>]. Population proportion vaccinated was estimated based on Ethiopian national data (<a href="https://www.facebook.com/EthiopiaFMoH" target="_blank">https://www.facebook.com/EthiopiaFMoH</a>, accessed on 26 December 2023) and [<a href="#B11-vaccines-12-00745" class="html-bibr">11</a>]. Major vaccination campaigns in Ethiopia are indicated by shaded areas.</p>
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12 pages, 2614 KiB  
Article
Lymphocytic Choriomeningitis Virus Infections in Hungary between 2017–2023—Investigation of the First Congenital Infections
by Anita Koroknai, Anna Nagy, Orsolya Nagy, Nikolett Csonka, Eszter Mezei, Katalin Szomor and Mária Takács
Diagnostics 2024, 14(13), 1436; https://doi.org/10.3390/diagnostics14131436 - 5 Jul 2024
Viewed by 460
Abstract
Lymphocytic choriomeningitis virus (LCMV) is a neglected rodent-borne arenavirus, primarily spread by common house mouse species. Acquired human infections range from asymptomatic to mild flu-like symptoms and self-resolving neurological diseases. In contrast, intrauterine LCMV infection is associated with high mortality and morbidity. Infection [...] Read more.
Lymphocytic choriomeningitis virus (LCMV) is a neglected rodent-borne arenavirus, primarily spread by common house mouse species. Acquired human infections range from asymptomatic to mild flu-like symptoms and self-resolving neurological diseases. In contrast, intrauterine LCMV infection is associated with high mortality and morbidity. Infection of the fetus often leads to fetal death, and surviving fetuses may develop vision impairment and central nervous system developmental disorders. LCMV is mainly diagnosed by serological methods using in-house indirect immunofluorescence assays. LCMV nucleic acid is detected by the nested RT-PCR method and confirmed by Sanger sequencing. In Hungary, 23 acquired lymphocytic choriomeningitis cases were diagnosed between 2017 and 2023. Ten out of 23 confirmed patients proved to be positive by the PCR method. Two cases of intrauterine LCMV infections were detected in 2019 and 2021, respectively. The IgG antibody titers measured in the infant’s serum samples were much higher than the IgG titers of the maternal serum samples. Both IgM and IgA antibodies were detectable in the infants’ sera. As the microbiological diagnosis of LCMV is rather challenging and the symptoms are very similar to the clinical picture of other common teratogenic pathogens such as cytomegalovirus or Toxoplasma gondii, intrauterine LCMV infections might still be underdiagnosed. Full article
(This article belongs to the Special Issue Diagnosis and Management of Meningitis)
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<p>The annual number of laboratory-diagnosed LCMV cases in Hungary between 2017 and 2023.</p>
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<p>Age and gender distribution of acquired LCMV-infected patients in Hungary between 2017 and 2023.</p>
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<p>Maximum likelihood phylogenetic tree of LCMV sequences based on the 390 nucleotide-long region of the L segment RNA polymerase (RdRp) gene. The Lassa virus was used as an outgroup. Sequences obtained from CSF samples of three Hungarian patients are indicated by green circles (GenBank accession numbers: PP236383, PP236384, and PP236385). LCMV sequences were named as follows: GenBank accession number, strain name, host species, country of origin, and the year of the isolation/submission (if data were available). Roman numerals (I–III) represent the different LCMV lineages defined according to Albariño et al. [<a href="#B2-diagnostics-14-01436" class="html-bibr">2</a>].</p>
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<p>The annual number of laboratory-diagnosed LCMV cases and the number of clinical samples tested for LCMV in Hungary, between 1991 and 2023. (Based on the data of the National Center for Public Health and Pharmacy, Budapest, Hungary) The framed part represents the data of the period discussed in this study. Red arrows indicate the years when the two congenital cases were diagnosed.</p>
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