<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Fan J</submitter><pubmed_abstract>&lt;i>Salmonella enterica&lt;/i> is a zoonotic food-borne pathogen threatening public health around the world. As is the case with many other pathogens, the spread of mobilized colistin resistance (&lt;i>mcr&lt;/i>) alleles is of grave concern. In this study, totally 689 clinical &lt;i>Salmonella&lt;/i> isolates were collected from a local hospital in Hangzhou, Zhejiang Province, China between 2009 and 2018. Resistance genes were screen by PCR. Two &lt;i>mcr-9-&lt;/i>positive &lt;i>Salmonella&lt;/i> strains S15 and S639 were identified which belong to serotype Typhimurium and Thompson, respectively. We observed that both &lt;i>mcr-9&lt;/i> genes were located on conjugative IncHI2 plasmids which encoded numerous resistance genes, likely facilitating the dissemination of &lt;i>mcr-9&lt;/i> by co-resistance mechanisms. The &lt;i>mcr-9&lt;/i> cassettes encoded on the two plasmids were not identical: downstream of the &lt;i>mcr-9&lt;/i> genes, we found IS&lt;i>1&lt;/i> on one plasmid (pS15), while the other had a &lt;i>WbuC&lt;/i>-IS&lt;i>26&lt;/i> (pS639). Despite the presence of &lt;i>mcr-9&lt;/i> cassettes, the strains were not rendered colistin resistant. Yet, it is of epidemiological importance to implement surveillance to be able to observe and possibly control the spread of &lt;i>mcr-9&lt;/i> due to its potential to mediate resistance to the last-resort antibiotic colistin.</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>852434</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8969412</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Molecular Genetic Characteristics of Plasmid-Borne &lt;i>mcr-9&lt;/i> in &lt;i>Salmonella enterica&lt;/i> Serotype Typhimurium and Thompson in Zhejiang, China.</pubmed_title><pmcid>PMC8969412</pmcid><pubmed_authors>Fang Y</pubmed_authors><pubmed_authors>Hua X</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Fan J</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Xu Q</pubmed_authors><pubmed_authors>Leptihn S</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Zhao D</pubmed_authors><pubmed_authors>Cai H</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular Genetic Characteristics of Plasmid-Borne &lt;i>mcr-9&lt;/i> in &lt;i>Salmonella enterica&lt;/i> Serotype Typhimurium and Thompson in Zhejiang, China.</name><description>&lt;i>Salmonella enterica&lt;/i> is a zoonotic food-borne pathogen threatening public health around the world. As is the case with many other pathogens, the spread of mobilized colistin resistance (&lt;i>mcr&lt;/i>) alleles is of grave concern. In this study, totally 689 clinical &lt;i>Salmonella&lt;/i> isolates were collected from a local hospital in Hangzhou, Zhejiang Province, China between 2009 and 2018. Resistance genes were screen by PCR. Two &lt;i>mcr-9-&lt;/i>positive &lt;i>Salmonella&lt;/i> strains S15 and S639 were identified which belong to serotype Typhimurium and Thompson, respectively. We observed that both &lt;i>mcr-9&lt;/i> genes were located on conjugative IncHI2 plasmids which encoded numerous resistance genes, likely facilitating the dissemination of &lt;i>mcr-9&lt;/i> by co-resistance mechanisms. The &lt;i>mcr-9&lt;/i> cassettes encoded on the two plasmids were not identical: downstream of the &lt;i>mcr-9&lt;/i> genes, we found IS&lt;i>1&lt;/i> on one plasmid (pS15), while the other had a &lt;i>WbuC&lt;/i>-IS&lt;i>26&lt;/i> (pS639). Despite the presence of &lt;i>mcr-9&lt;/i> cassettes, the strains were not rendered colistin resistant. Yet, it is of epidemiological importance to implement surveillance to be able to observe and possibly control the spread of &lt;i>mcr-9&lt;/i> due to its potential to mediate resistance to the last-resort antibiotic colistin.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2024-11-12T10:49:47.327Z</modification><creation>2024-11-12T10:49:47.327Z</creation></dates><accession>S-EPMC8969412</accession><cross_references><pubmed>35369459</pubmed><doi>10.3389/fmicb.2022.852434</doi></cross_references></HashMap>