Genomic characterization of carbapenem-non-susceptible Pseudomonas aeruginosa in Singapore

Pseudomonas aeruginosa is a clinically important pathogen implicated in many hospital-acquired infections. Its propensity to acquire broad-spectrum resistance has earned the organism its status as a severe public health threat requiring urgent control measures. While whole-genome sequencing-based ge...

Full description

Bibliographic Details
Main Authors: Jocelyn Qi-Min Teo, Cheng Yee Tang, Jie Chong Lim, Shannon Jing-Yi Lee, Si Hui Tan, Tse-Hsien Koh, James Heng-Chiak Sim, Thuan-Tong Tan, Andrea Lay-Hoon Kwa, Rick Twee-Hee Ong
Format: Article
Language:English
Published: Taylor & Francis Group 2021-01-01
Series:Emerging Microbes and Infections
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/22221751.2021.1968318
_version_ 1818987809015332864
author Jocelyn Qi-Min Teo
Cheng Yee Tang
Jie Chong Lim
Shannon Jing-Yi Lee
Si Hui Tan
Tse-Hsien Koh
James Heng-Chiak Sim
Thuan-Tong Tan
Andrea Lay-Hoon Kwa
Rick Twee-Hee Ong
author_facet Jocelyn Qi-Min Teo
Cheng Yee Tang
Jie Chong Lim
Shannon Jing-Yi Lee
Si Hui Tan
Tse-Hsien Koh
James Heng-Chiak Sim
Thuan-Tong Tan
Andrea Lay-Hoon Kwa
Rick Twee-Hee Ong
author_sort Jocelyn Qi-Min Teo
collection DOAJ
description Pseudomonas aeruginosa is a clinically important pathogen implicated in many hospital-acquired infections. Its propensity to acquire broad-spectrum resistance has earned the organism its status as a severe public health threat requiring urgent control measures. While whole-genome sequencing-based genomic surveillance provides a means to track antimicrobial resistance, its use in molecular epidemiological surveys of P. aeruginosa remains limited, especially in the Southeast Asian region. We sequenced the whole genomes of 222 carbapenem-non-susceptible P. aeruginosa (CNPA) isolates collected in 2006–2020 at the largest public acute care hospital in Singapore. Antimicrobial susceptibilities were determined using broth microdilution. Clonal relatedness, multi-locus sequence types, and antimicrobial resistance determinants (acquired and chromosomal) were determined. In this study, CNPA exhibited broad-spectrum resistance (87.8% multi-drug resistance), retaining susceptibility only to polymyxin B (95.0%) and amikacin (55.0%). Carbapenemases were detected in 51.4% of the isolates, where IMP and NDM metallo-β-lactamases were the most frequent. Carbapenem resistance was also likely associated with OprD alterations or efflux mechanisms (ArmZ/NalD mutations), which occurred in strains with or without carbapenemases. The population of CNPA in the hospital was diverse; the 222 isolates grouped into 68 sequence types (ST), which included various high-risk clones. We detected an emerging clone, the NDM-1-producing ST308, in addition to the global high-risk ST235 clone which was the predominant clone in our population. Our results thus provide a “snapshot” of the circulating lineages of CNPA locally and the prevailing genetic mechanisms contributing to carbapenem resistance. This database also serves as the baseline for future prospective surveillance studies.
first_indexed 2024-12-20T19:12:35Z
format Article
id doaj.art-28fa35a1fd9d4179b821550b7fdcca68
institution Directory Open Access Journal
issn 2222-1751
language English
last_indexed 2024-12-20T19:12:35Z
publishDate 2021-01-01
publisher Taylor & Francis Group
record_format Article
series Emerging Microbes and Infections
spelling doaj.art-28fa35a1fd9d4179b821550b7fdcca682022-12-21T19:29:10ZengTaylor & Francis GroupEmerging Microbes and Infections2222-17512021-01-011011706171610.1080/22221751.2021.1968318Genomic characterization of carbapenem-non-susceptible Pseudomonas aeruginosa in SingaporeJocelyn Qi-Min Teo0Cheng Yee Tang1Jie Chong Lim2Shannon Jing-Yi Lee3Si Hui Tan4Tse-Hsien Koh5James Heng-Chiak Sim6Thuan-Tong Tan7Andrea Lay-Hoon Kwa8Rick Twee-Hee Ong9Department of Pharmacy, Singapore General Hospital, Singapore, SingaporeSaw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, SingaporeDepartment of Pharmacy, National University of Singapore, Singapore, SingaporeDepartment of Pharmacy, Singapore General Hospital, Singapore, SingaporeDepartment of Pharmacy, Singapore General Hospital, Singapore, SingaporeDepartment of Microbiology, Singapore General Hospital, Singapore, SingaporeDepartment of Microbiology, Singapore General Hospital, Singapore, SingaporeDepartment of Infectious Diseases, Singapore General Hospital, Singapore, SingaporeDepartment of Pharmacy, Singapore General Hospital, Singapore, SingaporeSaw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, SingaporePseudomonas aeruginosa is a clinically important pathogen implicated in many hospital-acquired infections. Its propensity to acquire broad-spectrum resistance has earned the organism its status as a severe public health threat requiring urgent control measures. While whole-genome sequencing-based genomic surveillance provides a means to track antimicrobial resistance, its use in molecular epidemiological surveys of P. aeruginosa remains limited, especially in the Southeast Asian region. We sequenced the whole genomes of 222 carbapenem-non-susceptible P. aeruginosa (CNPA) isolates collected in 2006–2020 at the largest public acute care hospital in Singapore. Antimicrobial susceptibilities were determined using broth microdilution. Clonal relatedness, multi-locus sequence types, and antimicrobial resistance determinants (acquired and chromosomal) were determined. In this study, CNPA exhibited broad-spectrum resistance (87.8% multi-drug resistance), retaining susceptibility only to polymyxin B (95.0%) and amikacin (55.0%). Carbapenemases were detected in 51.4% of the isolates, where IMP and NDM metallo-β-lactamases were the most frequent. Carbapenem resistance was also likely associated with OprD alterations or efflux mechanisms (ArmZ/NalD mutations), which occurred in strains with or without carbapenemases. The population of CNPA in the hospital was diverse; the 222 isolates grouped into 68 sequence types (ST), which included various high-risk clones. We detected an emerging clone, the NDM-1-producing ST308, in addition to the global high-risk ST235 clone which was the predominant clone in our population. Our results thus provide a “snapshot” of the circulating lineages of CNPA locally and the prevailing genetic mechanisms contributing to carbapenem resistance. This database also serves as the baseline for future prospective surveillance studies.https://www.tandfonline.com/doi/10.1080/22221751.2021.1968318Pseudomonas aeruginosawhole-genome sequencingresistomeclonesmulti-drug resistantgenomic surveillance
spellingShingle Jocelyn Qi-Min Teo
Cheng Yee Tang
Jie Chong Lim
Shannon Jing-Yi Lee
Si Hui Tan
Tse-Hsien Koh
James Heng-Chiak Sim
Thuan-Tong Tan
Andrea Lay-Hoon Kwa
Rick Twee-Hee Ong
Genomic characterization of carbapenem-non-susceptible Pseudomonas aeruginosa in Singapore
Emerging Microbes and Infections
Pseudomonas aeruginosa
whole-genome sequencing
resistome
clones
multi-drug resistant
genomic surveillance
title Genomic characterization of carbapenem-non-susceptible Pseudomonas aeruginosa in Singapore
title_full Genomic characterization of carbapenem-non-susceptible Pseudomonas aeruginosa in Singapore
title_fullStr Genomic characterization of carbapenem-non-susceptible Pseudomonas aeruginosa in Singapore
title_full_unstemmed Genomic characterization of carbapenem-non-susceptible Pseudomonas aeruginosa in Singapore
title_short Genomic characterization of carbapenem-non-susceptible Pseudomonas aeruginosa in Singapore
title_sort genomic characterization of carbapenem non susceptible pseudomonas aeruginosa in singapore
topic Pseudomonas aeruginosa
whole-genome sequencing
resistome
clones
multi-drug resistant
genomic surveillance
url https://www.tandfonline.com/doi/10.1080/22221751.2021.1968318
work_keys_str_mv AT jocelynqiminteo genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT chengyeetang genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT jiechonglim genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT shannonjingyilee genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT sihuitan genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT tsehsienkoh genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT jameshengchiaksim genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT thuantongtan genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT andrealayhoonkwa genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore
AT ricktweeheeong genomiccharacterizationofcarbapenemnonsusceptiblepseudomonasaeruginosainsingapore