Exploring multidrug-resistant Klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysis
Abstract Background Antibiotic-resistant Klebsiella pneumoniae has emerged as a critical public health threat worldwide. Understanding the antimicrobial resistance mechanisms of multidrug-resistant K. pneumoniae (MDR-Kp) and its prevalence in time and space would provide clinical significance for ma...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2023-09-01
|
Series: | BMC Microbiology |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12866-023-02974-y |
_version_ | 1797453704164540416 |
---|---|
author | Jing Yang Kai Zhang Chen Ding Song Wang Weiwei Wu Xiangqun Liu |
author_facet | Jing Yang Kai Zhang Chen Ding Song Wang Weiwei Wu Xiangqun Liu |
author_sort | Jing Yang |
collection | DOAJ |
description | Abstract Background Antibiotic-resistant Klebsiella pneumoniae has emerged as a critical public health threat worldwide. Understanding the antimicrobial resistance mechanisms of multidrug-resistant K. pneumoniae (MDR-Kp) and its prevalence in time and space would provide clinical significance for managing pathogen infection. Methods Eighteen clinical MDR-Kp strains were analyzed by whole genome sequencing (WGS), and the antimicrobial resistance genes and associated resistance mechanisms were compared with results obtained from the conventional microbiological test (CMT). The sequence homology across strains in our study and those previously collected over time from a wide geographical region was assessed by phylogenetic analysis. Results MDR-Kp strains were collected from eighteen patients who had received empirical treatment before strain collection, with sputum (83.3%, 15/18) being the primary source of clinical samples. The commonly received treatments include β-lactamase inhibitors (55.6%, 10/18) and carbapenems (50%, 9/18). Using CMT, we found that all 18 strains were resistant to aztreonam and ciprofloxacin, while 14 (77.8%) showed resistance to carbapenem. Polymyxin B and tigecycline were the only antibiotics to which MDR-Kp strains were sensitive. A total of 42 antimicrobial resistance mechanisms were identified by WGS, surpassing the 40 detected by the conventional method, with 25 mechanisms shared between the two techniques. Despite a 100% accuracy rate of WGS in detecting penicillin-resistant strains, the accuracy in detecting cephalosporin-resistant strains was only at 60%. Among all resistance genes identified by WGS, Klebsiella pneumoniae carbapenemase-2 (KPC-2) was present in all 14 carbapenem-resistant strains. Phenotypic analysis indicated that sequence type (ST) 11 isolates were the primary cause of these MDR-Kp infections. Additionally, phylogenic clustering analysis, encompassing both the clinical and MDR-Kp strains previously reported in China, revealed four distinct subgroups. No significant difference was observed in the sequence homology between K. pneumoniae strains in our study and those previously collected in East China over time. Conclusion The application of WGS in identifying potential antimicrobial-resistant genes of MDR-Kp has demonstrated promising clinical significance. Comprehensive genomic information revealed by WGS holds the promise of guiding treatment decisions, enabling surveillance, and serving as a crucial asset in understanding antibiotic resistance. |
first_indexed | 2024-03-09T15:26:35Z |
format | Article |
id | doaj.art-b0c12d75c1804fd98d58a21da1322617 |
institution | Directory Open Access Journal |
issn | 1471-2180 |
language | English |
last_indexed | 2024-03-09T15:26:35Z |
publishDate | 2023-09-01 |
publisher | BMC |
record_format | Article |
series | BMC Microbiology |
spelling | doaj.art-b0c12d75c1804fd98d58a21da13226172023-11-26T12:30:30ZengBMCBMC Microbiology1471-21802023-09-012311910.1186/s12866-023-02974-yExploring multidrug-resistant Klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysisJing Yang0Kai Zhang1Chen Ding2Song Wang3Weiwei Wu4Xiangqun Liu5Xuzhou Medical UniversityClinical Laboratory, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical UniversityXuzhou Central HospitalDinfectome IncDinfectome IncDepartment of Respiratory and Critical Care Medicine, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical UniversityAbstract Background Antibiotic-resistant Klebsiella pneumoniae has emerged as a critical public health threat worldwide. Understanding the antimicrobial resistance mechanisms of multidrug-resistant K. pneumoniae (MDR-Kp) and its prevalence in time and space would provide clinical significance for managing pathogen infection. Methods Eighteen clinical MDR-Kp strains were analyzed by whole genome sequencing (WGS), and the antimicrobial resistance genes and associated resistance mechanisms were compared with results obtained from the conventional microbiological test (CMT). The sequence homology across strains in our study and those previously collected over time from a wide geographical region was assessed by phylogenetic analysis. Results MDR-Kp strains were collected from eighteen patients who had received empirical treatment before strain collection, with sputum (83.3%, 15/18) being the primary source of clinical samples. The commonly received treatments include β-lactamase inhibitors (55.6%, 10/18) and carbapenems (50%, 9/18). Using CMT, we found that all 18 strains were resistant to aztreonam and ciprofloxacin, while 14 (77.8%) showed resistance to carbapenem. Polymyxin B and tigecycline were the only antibiotics to which MDR-Kp strains were sensitive. A total of 42 antimicrobial resistance mechanisms were identified by WGS, surpassing the 40 detected by the conventional method, with 25 mechanisms shared between the two techniques. Despite a 100% accuracy rate of WGS in detecting penicillin-resistant strains, the accuracy in detecting cephalosporin-resistant strains was only at 60%. Among all resistance genes identified by WGS, Klebsiella pneumoniae carbapenemase-2 (KPC-2) was present in all 14 carbapenem-resistant strains. Phenotypic analysis indicated that sequence type (ST) 11 isolates were the primary cause of these MDR-Kp infections. Additionally, phylogenic clustering analysis, encompassing both the clinical and MDR-Kp strains previously reported in China, revealed four distinct subgroups. No significant difference was observed in the sequence homology between K. pneumoniae strains in our study and those previously collected in East China over time. Conclusion The application of WGS in identifying potential antimicrobial-resistant genes of MDR-Kp has demonstrated promising clinical significance. Comprehensive genomic information revealed by WGS holds the promise of guiding treatment decisions, enabling surveillance, and serving as a crucial asset in understanding antibiotic resistance.https://doi.org/10.1186/s12866-023-02974-yKlebsiella pneumoniaeAntimicrobial susceptibility testingNext-generation sequencingConventional microbiological testCarbapenem |
spellingShingle | Jing Yang Kai Zhang Chen Ding Song Wang Weiwei Wu Xiangqun Liu Exploring multidrug-resistant Klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysis BMC Microbiology Klebsiella pneumoniae Antimicrobial susceptibility testing Next-generation sequencing Conventional microbiological test Carbapenem |
title | Exploring multidrug-resistant Klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysis |
title_full | Exploring multidrug-resistant Klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysis |
title_fullStr | Exploring multidrug-resistant Klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysis |
title_full_unstemmed | Exploring multidrug-resistant Klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysis |
title_short | Exploring multidrug-resistant Klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysis |
title_sort | exploring multidrug resistant klebsiella pneumoniae antimicrobial resistance mechanisms through whole genome sequencing analysis |
topic | Klebsiella pneumoniae Antimicrobial susceptibility testing Next-generation sequencing Conventional microbiological test Carbapenem |
url | https://doi.org/10.1186/s12866-023-02974-y |
work_keys_str_mv | AT jingyang exploringmultidrugresistantklebsiellapneumoniaeantimicrobialresistancemechanismsthroughwholegenomesequencinganalysis AT kaizhang exploringmultidrugresistantklebsiellapneumoniaeantimicrobialresistancemechanismsthroughwholegenomesequencinganalysis AT chending exploringmultidrugresistantklebsiellapneumoniaeantimicrobialresistancemechanismsthroughwholegenomesequencinganalysis AT songwang exploringmultidrugresistantklebsiellapneumoniaeantimicrobialresistancemechanismsthroughwholegenomesequencinganalysis AT weiweiwu exploringmultidrugresistantklebsiellapneumoniaeantimicrobialresistancemechanismsthroughwholegenomesequencinganalysis AT xiangqunliu exploringmultidrugresistantklebsiellapneumoniaeantimicrobialresistancemechanismsthroughwholegenomesequencinganalysis |