Cargando…

Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants

This study characterized high-quality whole-genome sequences of a sentinel, surveillance-based collection of 1710 Neisseria gonorrhoeae (GC) isolates from 2019 collected in the USA as part of the Gonococcal Isolate Surveillance Project (GISP). It aims to provide a detailed report of strain diversity...

Descripción completa

Detalles Bibliográficos
Autores principales: Reimche, Jennifer L., Clemons, Arvon A., Chivukula, Vasanta L., Joseph, Sandeep J., Schmerer, Matthew W., Pham, Cau D., Schlanger, Karen, St Cyr, Sancta B., Kersh, Ellen N., Gernert, Kim M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272886/
https://www.ncbi.nlm.nih.gov/pubmed/37171855
http://dx.doi.org/10.1099/mgen.0.001006
_version_ 1785059598820966400
author Reimche, Jennifer L.
Clemons, Arvon A.
Chivukula, Vasanta L.
Joseph, Sandeep J.
Schmerer, Matthew W.
Pham, Cau D.
Schlanger, Karen
St Cyr, Sancta B.
Kersh, Ellen N.
Gernert, Kim M.
author_facet Reimche, Jennifer L.
Clemons, Arvon A.
Chivukula, Vasanta L.
Joseph, Sandeep J.
Schmerer, Matthew W.
Pham, Cau D.
Schlanger, Karen
St Cyr, Sancta B.
Kersh, Ellen N.
Gernert, Kim M.
author_sort Reimche, Jennifer L.
collection PubMed
description This study characterized high-quality whole-genome sequences of a sentinel, surveillance-based collection of 1710 Neisseria gonorrhoeae (GC) isolates from 2019 collected in the USA as part of the Gonococcal Isolate Surveillance Project (GISP). It aims to provide a detailed report of strain diversity, phylogenetic relationships and resistance determinant profiles associated with reduced susceptibilities to antibiotics of concern. The 1710 isolates represented 164 multilocus sequence types and 21 predominant phylogenetic clades. Common genomic determinants defined most strains’ phenotypic, reduced susceptibility to current and historic antibiotics (e.g. bla (TEM) plasmid for penicillin, tetM plasmid for tetracycline, gyrA for ciprofloxacin, 23S rRNA and/or mosaic mtr operon for azithromycin, and mosaic penA for cefixime and ceftriaxone). The most predominant phylogenetic clade accounted for 21 % of the isolates, included a majority of the isolates with low-level elevated MICs to azithromycin (2.0 µg ml(−1)), carried a mosaic mtr operon and variants in PorB, and showed expansion with respect to data previously reported from 2018. The second largest clade predominantly carried the GyrA S91F variant, was largely ciprofloxacin resistant (MIC ≥1.0 µg ml(−1)), and showed significant expansion with respect to 2018. Overall, a low proportion of isolates had medium- to high-level elevated MIC to azithromycin ((≥4.0 µg ml(−1)), based on C2611T or A2059G 23S rRNA variants). One isolate carried the penA 60.001 allele resulting in elevated MICs to cefixime and ceftriaxone of 1.0 µg ml(−1). This high-resolution snapshot of genetic profiles of 1710 GC sequences, through a comparison with 2018 data (1479 GC sequences) within the sentinel system, highlights change in proportions and expansion of select GC strains and the associated genetic mechanisms of resistance. The knowledge gained through molecular surveillance may support rapid identification of outbreaks of concern. Continued monitoring may inform public health responses to limit the development and spread of antibiotic-resistant gonorrhoea.
format Online
Article
Text
id pubmed-10272886
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-102728862023-06-17 Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants Reimche, Jennifer L. Clemons, Arvon A. Chivukula, Vasanta L. Joseph, Sandeep J. Schmerer, Matthew W. Pham, Cau D. Schlanger, Karen St Cyr, Sancta B. Kersh, Ellen N. Gernert, Kim M. Microb Genom Research Articles This study characterized high-quality whole-genome sequences of a sentinel, surveillance-based collection of 1710 Neisseria gonorrhoeae (GC) isolates from 2019 collected in the USA as part of the Gonococcal Isolate Surveillance Project (GISP). It aims to provide a detailed report of strain diversity, phylogenetic relationships and resistance determinant profiles associated with reduced susceptibilities to antibiotics of concern. The 1710 isolates represented 164 multilocus sequence types and 21 predominant phylogenetic clades. Common genomic determinants defined most strains’ phenotypic, reduced susceptibility to current and historic antibiotics (e.g. bla (TEM) plasmid for penicillin, tetM plasmid for tetracycline, gyrA for ciprofloxacin, 23S rRNA and/or mosaic mtr operon for azithromycin, and mosaic penA for cefixime and ceftriaxone). The most predominant phylogenetic clade accounted for 21 % of the isolates, included a majority of the isolates with low-level elevated MICs to azithromycin (2.0 µg ml(−1)), carried a mosaic mtr operon and variants in PorB, and showed expansion with respect to data previously reported from 2018. The second largest clade predominantly carried the GyrA S91F variant, was largely ciprofloxacin resistant (MIC ≥1.0 µg ml(−1)), and showed significant expansion with respect to 2018. Overall, a low proportion of isolates had medium- to high-level elevated MIC to azithromycin ((≥4.0 µg ml(−1)), based on C2611T or A2059G 23S rRNA variants). One isolate carried the penA 60.001 allele resulting in elevated MICs to cefixime and ceftriaxone of 1.0 µg ml(−1). This high-resolution snapshot of genetic profiles of 1710 GC sequences, through a comparison with 2018 data (1479 GC sequences) within the sentinel system, highlights change in proportions and expansion of select GC strains and the associated genetic mechanisms of resistance. The knowledge gained through molecular surveillance may support rapid identification of outbreaks of concern. Continued monitoring may inform public health responses to limit the development and spread of antibiotic-resistant gonorrhoea. Microbiology Society 2023-05-12 /pmc/articles/PMC10272886/ /pubmed/37171855 http://dx.doi.org/10.1099/mgen.0.001006 Text en © 2023 Crown Copyright https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License.
spellingShingle Research Articles
Reimche, Jennifer L.
Clemons, Arvon A.
Chivukula, Vasanta L.
Joseph, Sandeep J.
Schmerer, Matthew W.
Pham, Cau D.
Schlanger, Karen
St Cyr, Sancta B.
Kersh, Ellen N.
Gernert, Kim M.
Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants
title Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants
title_full Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants
title_fullStr Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants
title_full_unstemmed Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants
title_short Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants
title_sort genomic analysis of 1710 surveillance-based neisseria gonorrhoeae isolates from the usa in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272886/
https://www.ncbi.nlm.nih.gov/pubmed/37171855
http://dx.doi.org/10.1099/mgen.0.001006
work_keys_str_mv AT reimchejenniferl genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT clemonsarvona genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT chivukulavasantal genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT josephsandeepj genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT schmerermattheww genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT phamcaud genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT schlangerkaren genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT stcyrsanctab genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT kershellenn genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT gernertkimm genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants
AT genomicanalysisof1710surveillancebasedneisseriagonorrhoeaeisolatesfromtheusain2019identifiespredominantstraintypesandchromosomalantimicrobialresistancedeterminants