New Multidrug-Resistant Salmonella enterica Serovar Anatum Clone, Taiwan, 2015-2017.
Salmonella, a prevalent foodborne pathogen that causes zoonoses worldwide, comprises 2 species, Salmonella enterica and S. bongori, and [approximately equal to]2,600 serovars (1). In Taiwan, salmonellosis has been primarily caused by the S. enterica serovars Enteritidis, Typhimurium, Stanley, Newport, and Albany, which together caused 70% of salmonellosis infections during 2004-2012 (2). During this period, Salmonella Anatum was not prevalent, causing only 0.4% of the infections. However, since 2015, Salmonella Anatum infections have increased, and most isolates are multidrug resistant (MDR). We report the epidemiologic trend of Salmonella Anatum infection of humans, the clonal relationships among strains recovered during 2004-2017, and the resistance mechanism of the newly emerging MDR strains.The Study
To investigate the epidemiologic trend, we analyzed the data in the Salmonella fingerprint database constructed by the Taiwan Centers for Disease Control. The database comprises demographic and experimental data, including pulsed-field gel electrophoresis (PFGE) fingerprints obtained by using the PulseNet standardized PFGE protocol (3), serotypes obtained using PFGE pattern comparison and conventional methods (4), and antimicrobial drug susceptibility testing results for isolates collected from hospitals nationwide. We conducted whole-genome sequencing for 68 Salmonella Anatum isolates from humans and animals and 9 isolates from chicken carcasses and abbatoir environments by using the Illumina MiSeq platform (https://www.illumina.com) and identified resistance genes, incompatibility groups of plasmids, and sequence types by using the whole-genome sequencing data. To investigate clonal relationships and locations of resistance genes, we constructed a dendrogram for Salmonella Anatum strains with whole-genome singlenucleotide polymorphism profiles to assess genetic relatedness among strains and determined the complete genomic sequence of Salmonella Anatum strain R16.0676 with whole-genome sequencing data generated by using a MinlON nanopore sequencer (https://nanoporetech. com/products/minion) and an Illumina MiSeq sequencer. To investigate mobility of resistance plasmids, we conducted conjugation experiments to transfer the resistance genes-carrying (R) plasmid from Salmonella Anatum strain R16.0676 into recipient Escherichia coli C600 and transferred an R plasmid from an E. coli transconjugant back to a rifampin-resistant mutant of Salmonella Anatum strain R13.0957 (Appendix, https://wwwnc.cdc.gov/EID/ article/25/1/18-1103-App1.pdf).
The Salmonella fingerprint database of the Taiwan Centers for Disease Control contained PFGE fingerprints for 34,160 Salmonella isolates recovered during 2004-2017, of which antimicrobial drug sensitivity test results were available for 23,018. Salmonella Anatum was not a prevalent serovar among those collected during 2004-2014 (Figure 1). However, the number of Salmonella Anatum infections increased in 2015 and subsequently underwent another sharp increase in 2016 and 2017. In 2017, Salmonella Anatum accounted for 14.2% of Salmonella infections in Taiwan and ranked as the third most frequently identified serovar.
Whole-genome single-nucleotide polymorphism analysis of Salmonella Anatum recovered from humans during 2004-2017 revealed 3 distinct lineages (Figure 2). Strains of lineage (L) 1 were either pansusceptible or MDR; they mostly appeared during 2004-2009 (Appendix Table 2). L2 comprised only 2 isolates, which emerged in 2005 and were pansusceptible. L3 comprised 2 sublineages; sublineage (SL) 3_1, first detected in 2011, was mostly pansusceptible, whereas SL3_2, which first emerged in 2013, was mostly MDR. The MDR strains of SL3_2 first appeared in 2015 and were resistant or of reduced susceptibility to 10 of the 14 antimicrobial drugs tested. SMX.642 was the predominant MDR strain, but the first 2 isolates recovered in 2013 were pansusceptible. Of the 9 isolates from chicken carcasses and abattoir environments, 5 belonged to SL3_1 and 4 to SL3_2. The new clone (L3) accounted for 91.9% of the total Salmonella Anatum infections during 2004-2017 and 99.6% in 2017. MDR strains accounted for 90.3% of the new clone recovered during 2011-2017 and 94.1% in 2017. All Salmonella Anatum isolates sequenced belonged to sequence type 64.
The chromosomal sequence of strain R16.0676 was 4,674,190 bp (GenBank accession no. CP029800) and was not noted to carry any horizontally transferable resistance gene. R16.0676 harbored 2 plasmids, which were designated pR16.0676_90k (90,137 bp; IncC; accession no. CP029802) and pR16.0676_34k (34,063 bp; IncN3; accession no. CP029801). pR16.0676_90k harbored 11 resistance genes, aadA2, blaDHA1, dfrA23, floR, lnu(F), qnrB4, strA, strB, sull, sul2, and tet(A), which were distributed in 2 antimicrobial resistance islands, ARI1 and ARI2 (Appendix Figure, panel A). ARI1 carried 5 resistance genes, floR, strA, strB, sul2, and tet(A), and was found in many IncC plasmids in the National Center for Biotechnology Information database (5). ARI2 carried the other 6 resistance genes, aadA2, [bla.sub.DHA-1], dfrA23, lnu(F), qnrB4, and sull. The resistance genes could confer resistance to cefoxitin, cefotaxime, ceftazidime, ampicillin, chloramphenicol, streptomycin, sulfonamide, tetracycline, and trimethoprim and reduced susceptibility to ciprofloxacin as shown by antimicrobial susceptibility testing (Figure 2). pR16.0676_90k shared 79% sequence identity with a 272-kb plasmid, pECAZ155_KPC (GenBank accession no. CP019001.1), which harbored only the sequence of ARI1 but not ARI2. pR16.0676_34k did not carry any resistance gene (Appendix Figure, panel B), but it shared 98% sequence identity with a 34.8-kb plasmid, pN-Cit (GenBank accession no. JQ996149.1). All MDR SL3_2 isolates, including the 4 isolates recovered from the abattoirs, harbored an IncC plasmid and the same 11 resistance genes identified in strain R16.0676. Strain R17.0132 acquired an additional mcr-1 gene and was resistant to colistin (Figure 2). We did not obtain any transconjugants with pR16.0676_90k, but we did obtain a transconjugant with a composite plasmid, which had the same sequences as pR16.0676_90k and pR16.0676_34k (Appendix Figure, panel C). This 125-kb composite plasmid probably resulted from insertion of pR16.0676_90k into pR16.0676_34k through an insertion sequence 26-mediated transposition process. The resulting plasmid acquired an additional copy of insertion sequence 26 and an 8-bp tandem repeat in the insertion site. More than a dozen genes are typically required for conjugation (6). pR16.0676_90k harbored only 3 genes, and pR16.0676_34k contained at least 12 genes related to conjugation. Fusion of the 2 plasmids caused the composite plasmid to become self-transmissible. When the composite plasmid was transferred back into a rifampin-resistant mutant of Salmonella Anatum strain R13.0957, we obtained transconjugants harboring only a 58-kb or 83-kb R plasmid, which were derived from the 125-kb plasmid through deletions (Appendix Figure, panel C). Accordingly, the composite plasmid was unstable in Salmonella Anatum.
Conclusions
We identified a new Salmonella Anatum clone that emerged in Taiwan in 2011. During 2011-2014, strains of the new clone were not resistant and caused few infections. The dramatic increase in Salmonella Anatum infections that occurred during 2016-2017 was strongly associated with the emergence of MDR strains in 2015. The most crucial concern regarding emergence of the MDR Salmonella Anatum clone was that all MDR strains carry [bla.sub.DHA-1], which encodes AmpC [beta]-lactamase and confers resistance to [beta]-lactam drugs, including third-generation cephalosporins. This resistance cannot be overcome by using [beta]-lactam inhibitors. Because these MDR strains can cause numerous infections in humans and are prevalent in animals used for food, urgent control measures are needed.
Acknowledgments
We thank the Bureau of Animal and Plant Health Inspection and Quarantine, Council of Agriculture and Agricultural Technology Research Institute, for providing Salmonella Anatum isolates recovered from chicken carcasses and abattoir environments.
This study was funded by the Ministry of Health and Welfare, Taiwan (grant no. MOHW107-CDC-C-315-124503).
Dr. Chiou is a principal investigator at the Centers for Disease Control, Ministry of Health and Welfare, Taiwan. His research interests include genotyping, molecular epidemiology, and antimicrobial resistance of foodborne bacterial pathogens.
References
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Address for correspondence: Chien-Shun Chiou, Centers for Disease Control, Center for Diagnostics and Vaccine Development, 5F No. 20, Wen-Sin South Third Rd, Taichung 40855, Taiwan; email: [email protected]
Author affiliation: Centers for Disease Control, Taichung, Taiwan
DOI: https://doi.org/10.3201/eid2501.181103
Caption: Figure 1. Distribution of the 6 most frequently identified Salmonella enterica serovars in Taiwan, 2004-2017. Numbers indicate increasing frequency of Salmonella Anatum.
Figure 2.Dendrogram of 36 representative Salmonella enterica serovar Anatum strains from Taiwan, 2004.2017, constructed with whole.genome SNP profiles with 883 SNPs.The complete genomic sequence of Salmonella Anatum strain GT.38 (GenBank accession no.CP013226) was used as the reference for SNP calling.Red, resistant; yellow, intermediate; green, susceptible.Lanes: 1, cefoxitin; 2, cefotaxime; 3, ceftazidime; 4, ertapenem; 5, nalidixic acid; 6, ciprofloxacin; 7, gentamicin; 8, ampicillin; 9, chloramphenicol; 10, streptomycin; 11, sulfamethoxazole; 12, tetracycline; 13, sulfamethoxazole. trimethoprim; 14, colistin.L, lineage; PFGE, pulsed.field gel electrophoresis; SNP, single.nucleotide polymorphism.A color version of this figure is available online (http://wwwnc.cdc. gov/EID/article/25/1/18-1103-F2.htm). Strain Year PFGE Source EA04.039 2004 SMX.088 Human EA04.047 2004 SMX.087 Human CC04.028 2004 SMX.082 Human CH07.062 2007 SMX.097 Human NC04.178 2004 SMX.090 Human NG13.040 2013 SMX.652 Human SG06.139 2006 SMX.101 Human CA08.145 2008 SMX.087 Human CF09.078 2009 SMX.082 Human R15.1294 2015 SMX.082 Human SN08.005 2008 SMX.107 Human R16.3115 2016 SMX.087 Human NJ08.181 2008 SMX.092 Human NK04.008 2004 SMX.093 Human R15.1977 2015 SMX.871 Human SQ13.084 2013 SMX.703 Human SA11.164 2011 SMX.768 Human R14.1408 2014 SMX.754 Human R15.0695 2015 SMX.768 Human R18.1457 2015 SMX.768 Chicken R16.3927 2016 SMX.768 Human R15.0600 2015 SMX.642 Human R16.3355 2016 SMX.1196 Human R16.4304 2016 SMX.1127 Human R16.4880 2016 SMX.903 Human R15.2697 2015 SMX.903 Human R16.0696 2016 SMX.642 Human R17.4426 2017 SMX.1205 Human R18.1458 2018 SMX.642 Abattoir R16.1486 2016 SMX.642 Human R17.5171 2017 SMX.1197 Human R16.1070 2016 SMX.1052 Human R17.0132 2017 SMX.1175 Human R17.4643 2017 SMX.1213 Human R13.0957 2013 SMX.642 Human NL05.024 2005 SMX.098 Human
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| Title Annotation: | DISPATCHES |
|---|---|
| Author: | Chiou, Chien-Shun; Hong, Yu-Ping; Liao, Ying-Shu; Wang, You-Wun; Tu, Yueh-Hua; Chen, Bo-Han; Chen, Y |
| Publication: | Emerging Infectious Diseases |
| Geographic Code: | 9TAIW |
| Date: | Jan 1, 2019 |
| Words: | 1913 |
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