Cargando…
230. Nontyphoidal Salmonella from Clinical and Retail Meat Sources Reveal Antimicrobial Resistance Genes for Ceftriaxone and Ciprofloxacin
BACKGROUND: Pennsylvania participates in the National Antimicrobial Resistance Monitoring System (NARMS), which includes monitoring of Nontyphoidal Salmonella (NTS), a leading cause of bacterial foodborne illnesses in the United States. METHODS: Clinical NTS isolates submitted to the Pennsylvania De...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645062/ http://dx.doi.org/10.1093/ofid/ofab466.432 |
_version_ | 1784610231562534912 |
---|---|
author | M’ikanatha, Nkuchia M Yin, Xin Fu, Yezhi Sayeed, Sameera Carr, Christopher Dettinger, Lisa Hackman, Nicole Dudley, Edward Tate, Heather |
author_facet | M’ikanatha, Nkuchia M Yin, Xin Fu, Yezhi Sayeed, Sameera Carr, Christopher Dettinger, Lisa Hackman, Nicole Dudley, Edward Tate, Heather |
author_sort | M’ikanatha, Nkuchia M |
collection | PubMed |
description | BACKGROUND: Pennsylvania participates in the National Antimicrobial Resistance Monitoring System (NARMS), which includes monitoring of Nontyphoidal Salmonella (NTS), a leading cause of bacterial foodborne illnesses in the United States. METHODS: Clinical NTS isolates submitted to the Pennsylvania Department of Health (2015-18) were tested for susceptibility to 15 antimicrobial agents and analyzed by whole-genome sequencing (WGS). Concurrently, we conducted a prospective microbiological survey of NTS in retail meat products (chicken breasts, ground turkey, and pork chops) with susceptibility testing and WGS. RESULTS: Of a sample of 426 clinical Salmonella isolates from humans analyzed for antimicrobial susceptibility, 65 (15.3%) had decreased susceptibility to ciprofloxacin (DSC). Ampicillin resistance was observed in 39 (9.2%) and 15 (3.5%) were ceftriaxone-resistant. Ten ceftriaxone-resistant isolates had genetic elements that confer resistance to third generation extended-spectrum cephalosporins (ESC) [bla(CMY−2,) n=8 and bla(CTX-M-65,) n=2]. The bla(CTX-M-65-) positive isolates had a mutation in gyrA that confers fluoroquinolone resistance. Thirteen clinical isolates carried plasmid-mediated fluoroquinolone resistance genes (PMQR) [qnrB19, qnrS1, qnrA1]. We detected NTS in 131 (3.8%) of 3480 meat samples tested. 7 (5.3%) had DSC, while 38 (29%) and 21 (16%) were resistant to ampicillin and ceftriaxone, respectively. Four S. Infantis isolates had DSC and a bla(CTX-M-65) gene plus a mutation in gyrA. Thirteen meat isolates had the bla(CMY-2) gene. One additional bla(CTX-M-65-)positive S. Infantis without gyrA from ground turkey (SRR6351119) differed from four clinical isolates by ≤10 single-nucleotide polymorphisms. Percent of isolates from patients and meat sources that demonstrated resistance to amoxicillin-clavulanate (AMC), ceftriaxone, and decreased susceptibility to ciprofloxacin (DSC) to nine antimicrobial classes tested. [Image: see text] Among isolates from patients, resistance to ceftriaxone, a third-generation cephalosporin preferred for severe infections in children, increased from zero in 2015 to 5.8% in 2017. Overall, DSC increased in isolates from human sources while in strains from meat sources, DSC increased from zero in 2015 to over five percent in 2018. CONCLUSION: NTS isolated from human and meat sources were multi-drug resistant. Demonstration of similar resistance genes in meat and in ill humans may be consistent with spread of antibiotic-resistant pathogens from food sources. Dissemination of genes that confer resistance to third generation cephalosporins and fluoroquinolones, including some on mobile plasmids, may undermine recommended treatment for severe NTS infections. These results underscore the need for antimicrobial stewardship efforts in both agriculture and human medicine. DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-8645062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-86450622021-12-06 230. Nontyphoidal Salmonella from Clinical and Retail Meat Sources Reveal Antimicrobial Resistance Genes for Ceftriaxone and Ciprofloxacin M’ikanatha, Nkuchia M Yin, Xin Fu, Yezhi Sayeed, Sameera Carr, Christopher Dettinger, Lisa Hackman, Nicole Dudley, Edward Tate, Heather Open Forum Infect Dis Poster Abstracts BACKGROUND: Pennsylvania participates in the National Antimicrobial Resistance Monitoring System (NARMS), which includes monitoring of Nontyphoidal Salmonella (NTS), a leading cause of bacterial foodborne illnesses in the United States. METHODS: Clinical NTS isolates submitted to the Pennsylvania Department of Health (2015-18) were tested for susceptibility to 15 antimicrobial agents and analyzed by whole-genome sequencing (WGS). Concurrently, we conducted a prospective microbiological survey of NTS in retail meat products (chicken breasts, ground turkey, and pork chops) with susceptibility testing and WGS. RESULTS: Of a sample of 426 clinical Salmonella isolates from humans analyzed for antimicrobial susceptibility, 65 (15.3%) had decreased susceptibility to ciprofloxacin (DSC). Ampicillin resistance was observed in 39 (9.2%) and 15 (3.5%) were ceftriaxone-resistant. Ten ceftriaxone-resistant isolates had genetic elements that confer resistance to third generation extended-spectrum cephalosporins (ESC) [bla(CMY−2,) n=8 and bla(CTX-M-65,) n=2]. The bla(CTX-M-65-) positive isolates had a mutation in gyrA that confers fluoroquinolone resistance. Thirteen clinical isolates carried plasmid-mediated fluoroquinolone resistance genes (PMQR) [qnrB19, qnrS1, qnrA1]. We detected NTS in 131 (3.8%) of 3480 meat samples tested. 7 (5.3%) had DSC, while 38 (29%) and 21 (16%) were resistant to ampicillin and ceftriaxone, respectively. Four S. Infantis isolates had DSC and a bla(CTX-M-65) gene plus a mutation in gyrA. Thirteen meat isolates had the bla(CMY-2) gene. One additional bla(CTX-M-65-)positive S. Infantis without gyrA from ground turkey (SRR6351119) differed from four clinical isolates by ≤10 single-nucleotide polymorphisms. Percent of isolates from patients and meat sources that demonstrated resistance to amoxicillin-clavulanate (AMC), ceftriaxone, and decreased susceptibility to ciprofloxacin (DSC) to nine antimicrobial classes tested. [Image: see text] Among isolates from patients, resistance to ceftriaxone, a third-generation cephalosporin preferred for severe infections in children, increased from zero in 2015 to 5.8% in 2017. Overall, DSC increased in isolates from human sources while in strains from meat sources, DSC increased from zero in 2015 to over five percent in 2018. CONCLUSION: NTS isolated from human and meat sources were multi-drug resistant. Demonstration of similar resistance genes in meat and in ill humans may be consistent with spread of antibiotic-resistant pathogens from food sources. Dissemination of genes that confer resistance to third generation cephalosporins and fluoroquinolones, including some on mobile plasmids, may undermine recommended treatment for severe NTS infections. These results underscore the need for antimicrobial stewardship efforts in both agriculture and human medicine. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2021-12-04 /pmc/articles/PMC8645062/ http://dx.doi.org/10.1093/ofid/ofab466.432 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Poster Abstracts M’ikanatha, Nkuchia M Yin, Xin Fu, Yezhi Sayeed, Sameera Carr, Christopher Dettinger, Lisa Hackman, Nicole Dudley, Edward Tate, Heather 230. Nontyphoidal Salmonella from Clinical and Retail Meat Sources Reveal Antimicrobial Resistance Genes for Ceftriaxone and Ciprofloxacin |
title | 230. Nontyphoidal Salmonella from Clinical and Retail Meat Sources Reveal Antimicrobial Resistance Genes for Ceftriaxone and Ciprofloxacin |
title_full | 230. Nontyphoidal Salmonella from Clinical and Retail Meat Sources Reveal Antimicrobial Resistance Genes for Ceftriaxone and Ciprofloxacin |
title_fullStr | 230. Nontyphoidal Salmonella from Clinical and Retail Meat Sources Reveal Antimicrobial Resistance Genes for Ceftriaxone and Ciprofloxacin |
title_full_unstemmed | 230. Nontyphoidal Salmonella from Clinical and Retail Meat Sources Reveal Antimicrobial Resistance Genes for Ceftriaxone and Ciprofloxacin |
title_short | 230. Nontyphoidal Salmonella from Clinical and Retail Meat Sources Reveal Antimicrobial Resistance Genes for Ceftriaxone and Ciprofloxacin |
title_sort | 230. nontyphoidal salmonella from clinical and retail meat sources reveal antimicrobial resistance genes for ceftriaxone and ciprofloxacin |
topic | Poster Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645062/ http://dx.doi.org/10.1093/ofid/ofab466.432 |
work_keys_str_mv | AT mikanathankuchiam 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin AT yinxin 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin AT fuyezhi 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin AT sayeedsameera 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin AT carrchristopher 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin AT dettingerlisa 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin AT hackmannicole 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin AT dudleyedward 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin AT tateheather 230nontyphoidalsalmonellafromclinicalandretailmeatsourcesrevealantimicrobialresistancegenesforceftriaxoneandciprofloxacin |