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Genomic Characterization of Clinical Extensively Drug-Resistant Acinetobacter pittii Isolates
Carbapenem-resistant Acinetobacter pittii (CRAP) is a causative agent of nosocomial infections. This study aimed to characterize clinical isolates of CRAP from a tertiary hospital in Northeast Thailand. Six isolates were confirmed as extensively drug-resistant Acinetobacter pittii (XDRAP). The bla(N...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912037/ https://www.ncbi.nlm.nih.gov/pubmed/33503968 http://dx.doi.org/10.3390/microorganisms9020242 |
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author | Chopjitt, Peechanika Putthanachote, Nuntiput Ungcharoen, Ratchadaporn Hatrongjit, Rujirat Boueroy, Parichart Akeda, Yukihiro Tomono, Kazunori Hamada, Shigeyuki Kerdsin, Anusak |
author_facet | Chopjitt, Peechanika Putthanachote, Nuntiput Ungcharoen, Ratchadaporn Hatrongjit, Rujirat Boueroy, Parichart Akeda, Yukihiro Tomono, Kazunori Hamada, Shigeyuki Kerdsin, Anusak |
author_sort | Chopjitt, Peechanika |
collection | PubMed |
description | Carbapenem-resistant Acinetobacter pittii (CRAP) is a causative agent of nosocomial infections. This study aimed to characterize clinical isolates of CRAP from a tertiary hospital in Northeast Thailand. Six isolates were confirmed as extensively drug-resistant Acinetobacter pittii (XDRAP). The bla(NDM-1) gene was detected in three isolates, whereas bla(IMP-14) and bla(IMP-1) were detected in the others. Multilocus sequence typing with the Pasteur scheme revealed ST220 in two isolates, ST744 in two isolates, and ST63 and ST396 for the remaining two isolates, respectively. Genomic characterization revealed that six XDRAP genes contained antimicrobial resistance genes: ST63 (A436) and ST396 (A1) contained 10 antimicrobial resistance genes, ST220 (A984 and A864) and ST744 (A56 and A273) contained 9 and 8 antimicrobial resistance genes, respectively. The single nucleotide polymorphism (SNP) phylogenetic tree revealed that the isolates A984 and A864 were closely related to A. pittii YB-45 (ST220) from China, while A436 was related to A. pittii WCHAP100020, also from China. A273 and A56 isolates (ST744) were clustered together; these isolates were closely related to strains 2014S07-126, AP43, and WCHAP005069, which were isolated from Taiwan and China. Strict implementation of infection control based upon the framework of epidemiological analyses is essential to prevent outbreaks and contain the spread of the pathogen. Continued surveillance and close monitoring with molecular epidemiological tools are needed. |
format | Online Article Text |
id | pubmed-7912037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79120372021-02-28 Genomic Characterization of Clinical Extensively Drug-Resistant Acinetobacter pittii Isolates Chopjitt, Peechanika Putthanachote, Nuntiput Ungcharoen, Ratchadaporn Hatrongjit, Rujirat Boueroy, Parichart Akeda, Yukihiro Tomono, Kazunori Hamada, Shigeyuki Kerdsin, Anusak Microorganisms Article Carbapenem-resistant Acinetobacter pittii (CRAP) is a causative agent of nosocomial infections. This study aimed to characterize clinical isolates of CRAP from a tertiary hospital in Northeast Thailand. Six isolates were confirmed as extensively drug-resistant Acinetobacter pittii (XDRAP). The bla(NDM-1) gene was detected in three isolates, whereas bla(IMP-14) and bla(IMP-1) were detected in the others. Multilocus sequence typing with the Pasteur scheme revealed ST220 in two isolates, ST744 in two isolates, and ST63 and ST396 for the remaining two isolates, respectively. Genomic characterization revealed that six XDRAP genes contained antimicrobial resistance genes: ST63 (A436) and ST396 (A1) contained 10 antimicrobial resistance genes, ST220 (A984 and A864) and ST744 (A56 and A273) contained 9 and 8 antimicrobial resistance genes, respectively. The single nucleotide polymorphism (SNP) phylogenetic tree revealed that the isolates A984 and A864 were closely related to A. pittii YB-45 (ST220) from China, while A436 was related to A. pittii WCHAP100020, also from China. A273 and A56 isolates (ST744) were clustered together; these isolates were closely related to strains 2014S07-126, AP43, and WCHAP005069, which were isolated from Taiwan and China. Strict implementation of infection control based upon the framework of epidemiological analyses is essential to prevent outbreaks and contain the spread of the pathogen. Continued surveillance and close monitoring with molecular epidemiological tools are needed. MDPI 2021-01-25 /pmc/articles/PMC7912037/ /pubmed/33503968 http://dx.doi.org/10.3390/microorganisms9020242 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chopjitt, Peechanika Putthanachote, Nuntiput Ungcharoen, Ratchadaporn Hatrongjit, Rujirat Boueroy, Parichart Akeda, Yukihiro Tomono, Kazunori Hamada, Shigeyuki Kerdsin, Anusak Genomic Characterization of Clinical Extensively Drug-Resistant Acinetobacter pittii Isolates |
title | Genomic Characterization of Clinical Extensively Drug-Resistant Acinetobacter pittii Isolates |
title_full | Genomic Characterization of Clinical Extensively Drug-Resistant Acinetobacter pittii Isolates |
title_fullStr | Genomic Characterization of Clinical Extensively Drug-Resistant Acinetobacter pittii Isolates |
title_full_unstemmed | Genomic Characterization of Clinical Extensively Drug-Resistant Acinetobacter pittii Isolates |
title_short | Genomic Characterization of Clinical Extensively Drug-Resistant Acinetobacter pittii Isolates |
title_sort | genomic characterization of clinical extensively drug-resistant acinetobacter pittii isolates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912037/ https://www.ncbi.nlm.nih.gov/pubmed/33503968 http://dx.doi.org/10.3390/microorganisms9020242 |
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