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ERIC-PCR Genotyping of Acinetobacter baumannii Isolated from Different Clinical Specimens

BACKGROUND: Acinetobacter baumannii is a major cause of hospital care-acquired infections, and this bacterium poses a significant challenge to health care worldwide. At King Fahd Hospital of the University (KFHU), Al Khobar, Saudi Arabia, there had been a significant increase in the number of cases...

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Autores principales: Aljindan, Reem, Alsamman, Khaldoon, Elhadi, Nasreldin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196677/
https://www.ncbi.nlm.nih.gov/pubmed/30787810
http://dx.doi.org/10.4103/sjmms.sjmms_138_16
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author Aljindan, Reem
Alsamman, Khaldoon
Elhadi, Nasreldin
author_facet Aljindan, Reem
Alsamman, Khaldoon
Elhadi, Nasreldin
author_sort Aljindan, Reem
collection PubMed
description BACKGROUND: Acinetobacter baumannii is a major cause of hospital care-acquired infections, and this bacterium poses a significant challenge to health care worldwide. At King Fahd Hospital of the University (KFHU), Al Khobar, Saudi Arabia, there had been a significant increase in the number of cases of A. baumannii infections. OBJECTIVE: The objective of this study was to determine the clonal relationship between A. baumannii collected from different specimens of patients admitted to KFHU using the enterobacterial repetitive intergenic consensus–polymerase chain reaction (ERIC-PCR) fingerprinting method. MATERIALS AND METHODS: A. baumannii strains were isolated from a total of 59 specimens from inpatients admitted to KFHU between January and September 2014. These specimens were mainly collected from wound, rectal and throat swabs and transtracheal aspiration. ERIC-PCR fingerprinting was used to determine the clonal relationship between the different isolated strains. RESULTS: Using ERIC-PCR fingerprinting genotype analysis, 51 strains of A. baumannii were clustered into seven groups, while the remaining 8 were single strains. The genetic relatedness of A. baumannii isolated from admitted patients was high, indicating cross-transmission within the hospitalized patients. CONCLUSION: This study found that the increase in the incidence of A. baumannii in patients at KFHU was likely due to the spread of seven epidemic clones, thereby highlighting the need for intensifying the infection control measures to prevent nosocomial transmission of A. baumannii. These results also demonstrate that ERIC-PCR is a reliable and rapid method for studying the clonal similarity between A. baumannii isolated from different clinical specimens.
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spelling pubmed-61966772019-02-20 ERIC-PCR Genotyping of Acinetobacter baumannii Isolated from Different Clinical Specimens Aljindan, Reem Alsamman, Khaldoon Elhadi, Nasreldin Saudi J Med Med Sci Original Article BACKGROUND: Acinetobacter baumannii is a major cause of hospital care-acquired infections, and this bacterium poses a significant challenge to health care worldwide. At King Fahd Hospital of the University (KFHU), Al Khobar, Saudi Arabia, there had been a significant increase in the number of cases of A. baumannii infections. OBJECTIVE: The objective of this study was to determine the clonal relationship between A. baumannii collected from different specimens of patients admitted to KFHU using the enterobacterial repetitive intergenic consensus–polymerase chain reaction (ERIC-PCR) fingerprinting method. MATERIALS AND METHODS: A. baumannii strains were isolated from a total of 59 specimens from inpatients admitted to KFHU between January and September 2014. These specimens were mainly collected from wound, rectal and throat swabs and transtracheal aspiration. ERIC-PCR fingerprinting was used to determine the clonal relationship between the different isolated strains. RESULTS: Using ERIC-PCR fingerprinting genotype analysis, 51 strains of A. baumannii were clustered into seven groups, while the remaining 8 were single strains. The genetic relatedness of A. baumannii isolated from admitted patients was high, indicating cross-transmission within the hospitalized patients. CONCLUSION: This study found that the increase in the incidence of A. baumannii in patients at KFHU was likely due to the spread of seven epidemic clones, thereby highlighting the need for intensifying the infection control measures to prevent nosocomial transmission of A. baumannii. These results also demonstrate that ERIC-PCR is a reliable and rapid method for studying the clonal similarity between A. baumannii isolated from different clinical specimens. Medknow Publications & Media Pvt Ltd 2018 2017-12-14 /pmc/articles/PMC6196677/ /pubmed/30787810 http://dx.doi.org/10.4103/sjmms.sjmms_138_16 Text en Copyright: © 2017 Saudi Journal of Medicine & Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Aljindan, Reem
Alsamman, Khaldoon
Elhadi, Nasreldin
ERIC-PCR Genotyping of Acinetobacter baumannii Isolated from Different Clinical Specimens
title ERIC-PCR Genotyping of Acinetobacter baumannii Isolated from Different Clinical Specimens
title_full ERIC-PCR Genotyping of Acinetobacter baumannii Isolated from Different Clinical Specimens
title_fullStr ERIC-PCR Genotyping of Acinetobacter baumannii Isolated from Different Clinical Specimens
title_full_unstemmed ERIC-PCR Genotyping of Acinetobacter baumannii Isolated from Different Clinical Specimens
title_short ERIC-PCR Genotyping of Acinetobacter baumannii Isolated from Different Clinical Specimens
title_sort eric-pcr genotyping of acinetobacter baumannii isolated from different clinical specimens
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196677/
https://www.ncbi.nlm.nih.gov/pubmed/30787810
http://dx.doi.org/10.4103/sjmms.sjmms_138_16
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