Cargando…

Genomic Evolution of ST11 Carbapenem-Resistant Klebsiella pneumoniae from 2011 to 2020 Based on Data from the Pathosystems Resource Integration Center

(1) Objective: ST11 carbapenem-resistant Klebsiella pneumoniae (CRKP) is widespread throughout the world, and the mechanisms for the transmission and evolution of major serotypes, ST11-KL47 and ST11-KL64, were analyzed to investigate the global distribution and evolutionary characteristics of ST11 C...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Na, Tang, Yue, Yang, Xiaojing, Jin, Meiling, Chen, Jiali, Qin, Shiyu, Liu, Fangni, Liu, Xiong, Guo, Jinpeng, Wang, Changjun, Chen, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498433/
https://www.ncbi.nlm.nih.gov/pubmed/36140792
http://dx.doi.org/10.3390/genes13091624
_version_ 1784794757590941696
author Zhang, Na
Tang, Yue
Yang, Xiaojing
Jin, Meiling
Chen, Jiali
Qin, Shiyu
Liu, Fangni
Liu, Xiong
Guo, Jinpeng
Wang, Changjun
Chen, Yong
author_facet Zhang, Na
Tang, Yue
Yang, Xiaojing
Jin, Meiling
Chen, Jiali
Qin, Shiyu
Liu, Fangni
Liu, Xiong
Guo, Jinpeng
Wang, Changjun
Chen, Yong
author_sort Zhang, Na
collection PubMed
description (1) Objective: ST11 carbapenem-resistant Klebsiella pneumoniae (CRKP) is widespread throughout the world, and the mechanisms for the transmission and evolution of major serotypes, ST11-KL47 and ST11-KL64, were analyzed to investigate the global distribution and evolutionary characteristics of ST11 CRKP; (2) Methods: The Pathosystems Resource Integration Center (PATRIC) database was downloaded and all K. pneumoniae from 2011 to 2020 were screened to obtain ST11 CRKP genome assemblies with basic information. The relationship of serotype evolution between KL47 and KL64 was then investigated using statistical and bioinformatic analysis; (3) Results: In total, 386 ST11 CRKP isolates were included for analysis. Blood (31.09%, 120/386), respiratory tract (23.06%, 89/386), and feces (20.21%, 78/386) were the major sources of samples. China was the leading country where ST11 CRKP was isolated. KL47 and KL64 were found to be the most prevalent serotypes. ST11-KL64 CRKP [median 78(P(25)~P(75): 72~79.25)] had remarkably more virulence genes than the KL47 [median 63(P(25)~P(75): 63~69)], and the distinction was statistically significant (p < 0.001). A differential comparison of virulence genes between KL47 and KL64 revealed 35 differential virulence genes, including rmpA/rmpA2, iucABCD, iutA, etc. The comparison of the recombination of serotype-determining regions between the two serotypes revealed that KL64 CRKP carried more nucleotide sequences in the CD1-VR2-CD2 region than KL47 CRKP. More nucleotide sequences added approximately 303 base pairs (bp) with higher GC content (58.14%), which might facilitate the evolution of the serotype toward KL64; (4) Conclusions: KL47 and KL64 have become the predominant serotypes of ST11 CRKP. KL64 CRKP carries more virulence genes than KL47 and has increased by approximately 303 bp through recombinant mutations, thus facilitating the evolution of KL47 to KL64. Stricter infection prevention and control measures should be developed to deal with the epidemic transmission of ST11-KL64 CRKP.
format Online
Article
Text
id pubmed-9498433
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-94984332022-09-23 Genomic Evolution of ST11 Carbapenem-Resistant Klebsiella pneumoniae from 2011 to 2020 Based on Data from the Pathosystems Resource Integration Center Zhang, Na Tang, Yue Yang, Xiaojing Jin, Meiling Chen, Jiali Qin, Shiyu Liu, Fangni Liu, Xiong Guo, Jinpeng Wang, Changjun Chen, Yong Genes (Basel) Article (1) Objective: ST11 carbapenem-resistant Klebsiella pneumoniae (CRKP) is widespread throughout the world, and the mechanisms for the transmission and evolution of major serotypes, ST11-KL47 and ST11-KL64, were analyzed to investigate the global distribution and evolutionary characteristics of ST11 CRKP; (2) Methods: The Pathosystems Resource Integration Center (PATRIC) database was downloaded and all K. pneumoniae from 2011 to 2020 were screened to obtain ST11 CRKP genome assemblies with basic information. The relationship of serotype evolution between KL47 and KL64 was then investigated using statistical and bioinformatic analysis; (3) Results: In total, 386 ST11 CRKP isolates were included for analysis. Blood (31.09%, 120/386), respiratory tract (23.06%, 89/386), and feces (20.21%, 78/386) were the major sources of samples. China was the leading country where ST11 CRKP was isolated. KL47 and KL64 were found to be the most prevalent serotypes. ST11-KL64 CRKP [median 78(P(25)~P(75): 72~79.25)] had remarkably more virulence genes than the KL47 [median 63(P(25)~P(75): 63~69)], and the distinction was statistically significant (p < 0.001). A differential comparison of virulence genes between KL47 and KL64 revealed 35 differential virulence genes, including rmpA/rmpA2, iucABCD, iutA, etc. The comparison of the recombination of serotype-determining regions between the two serotypes revealed that KL64 CRKP carried more nucleotide sequences in the CD1-VR2-CD2 region than KL47 CRKP. More nucleotide sequences added approximately 303 base pairs (bp) with higher GC content (58.14%), which might facilitate the evolution of the serotype toward KL64; (4) Conclusions: KL47 and KL64 have become the predominant serotypes of ST11 CRKP. KL64 CRKP carries more virulence genes than KL47 and has increased by approximately 303 bp through recombinant mutations, thus facilitating the evolution of KL47 to KL64. Stricter infection prevention and control measures should be developed to deal with the epidemic transmission of ST11-KL64 CRKP. MDPI 2022-09-10 /pmc/articles/PMC9498433/ /pubmed/36140792 http://dx.doi.org/10.3390/genes13091624 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Na
Tang, Yue
Yang, Xiaojing
Jin, Meiling
Chen, Jiali
Qin, Shiyu
Liu, Fangni
Liu, Xiong
Guo, Jinpeng
Wang, Changjun
Chen, Yong
Genomic Evolution of ST11 Carbapenem-Resistant Klebsiella pneumoniae from 2011 to 2020 Based on Data from the Pathosystems Resource Integration Center
title Genomic Evolution of ST11 Carbapenem-Resistant Klebsiella pneumoniae from 2011 to 2020 Based on Data from the Pathosystems Resource Integration Center
title_full Genomic Evolution of ST11 Carbapenem-Resistant Klebsiella pneumoniae from 2011 to 2020 Based on Data from the Pathosystems Resource Integration Center
title_fullStr Genomic Evolution of ST11 Carbapenem-Resistant Klebsiella pneumoniae from 2011 to 2020 Based on Data from the Pathosystems Resource Integration Center
title_full_unstemmed Genomic Evolution of ST11 Carbapenem-Resistant Klebsiella pneumoniae from 2011 to 2020 Based on Data from the Pathosystems Resource Integration Center
title_short Genomic Evolution of ST11 Carbapenem-Resistant Klebsiella pneumoniae from 2011 to 2020 Based on Data from the Pathosystems Resource Integration Center
title_sort genomic evolution of st11 carbapenem-resistant klebsiella pneumoniae from 2011 to 2020 based on data from the pathosystems resource integration center
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498433/
https://www.ncbi.nlm.nih.gov/pubmed/36140792
http://dx.doi.org/10.3390/genes13091624
work_keys_str_mv AT zhangna genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT tangyue genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT yangxiaojing genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT jinmeiling genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT chenjiali genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT qinshiyu genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT liufangni genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT liuxiong genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT guojinpeng genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT wangchangjun genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter
AT chenyong genomicevolutionofst11carbapenemresistantklebsiellapneumoniaefrom2011to2020basedondatafromthepathosystemsresourceintegrationcenter