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Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China

Klebsiella pneumoniae is a wide-spread nosocomial pathogen. A rapid and sensitive molecular method for the detection of K. pneumoniae in clinical samples is needed to guide therapeutic treatment. In this study, we first described a loop-mediated isothermal amplification (LAMP) method for the rapid d...

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Autores principales: Dong, Derong, Liu, Wei, Li, Huan, Wang, Yufei, Li, Xinran, Zou, Dayang, Yang, Zhan, Huang, Simo, Zhou, Dongsheng, Huang, Liuyu, Yuan, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440914/
https://www.ncbi.nlm.nih.gov/pubmed/26052327
http://dx.doi.org/10.3389/fmicb.2015.00519
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author Dong, Derong
Liu, Wei
Li, Huan
Wang, Yufei
Li, Xinran
Zou, Dayang
Yang, Zhan
Huang, Simo
Zhou, Dongsheng
Huang, Liuyu
Yuan, Jing
author_facet Dong, Derong
Liu, Wei
Li, Huan
Wang, Yufei
Li, Xinran
Zou, Dayang
Yang, Zhan
Huang, Simo
Zhou, Dongsheng
Huang, Liuyu
Yuan, Jing
author_sort Dong, Derong
collection PubMed
description Klebsiella pneumoniae is a wide-spread nosocomial pathogen. A rapid and sensitive molecular method for the detection of K. pneumoniae in clinical samples is needed to guide therapeutic treatment. In this study, we first described a loop-mediated isothermal amplification (LAMP) method for the rapid detection of capsular polysaccharide synthesis regulating gene rcsA from K. pneumoniaein clinical samples by using two methods including real-time turbidity monitoring and fluorescence detection to assess the reaction. Then dissemination of K. pneumoniae strains was investigated from ICU patients in three top hospitals in Beijing, China. The results showed that the detection limit of the LAMP method was 0.115 pg/μl DNA within 60 min under isothermal conditions (61°C), a 100-fold increase in sensitivity compared with conventional PCR. All 30 non- K. pneumoniae strains tested were negative for LAMP detection, indicating the high specificity of the LAMP reaction. To evaluate the application of the LAMP assay to clinical diagnosis, of 110 clinical sputum samples collected from ICU patients with clinically suspected multi-resistant infections in China, a total of 32 K. pneumoniae isolates were identified for LAMP-based surveillance of rcsA. All isolates belonged to nine different K. pneumoniae multilocus sequence typing (MLST) groups. Strikingly, of the 32 K. pneumoniae strains, 18 contained the Klebsiella pneumoniae Carbapenemase (KPC)-encoding gene bla(KPC-2) and had high resistance to β-lactam antibiotics. Moreover, K. pneumoniae WJ-64 was discovered to contain bla(KPC-2) and bla(NDM-1)genes simultaneously in the isolate. Our data showed the high prevalence of bla(KPC-2) among K. pneumoniae and co-occurrence of many resistant genes in the clinical strains signal a rapid and continuing evolution of K. pneumoniae. In conclusion, we have developed a rapid and sensitive visual K. pneumoniae detection LAMP assay, which could be a useful tool for clinical screening, on-site diagnosis and primary quarantine purposes.
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spelling pubmed-44409142015-06-05 Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China Dong, Derong Liu, Wei Li, Huan Wang, Yufei Li, Xinran Zou, Dayang Yang, Zhan Huang, Simo Zhou, Dongsheng Huang, Liuyu Yuan, Jing Front Microbiol Microbiology Klebsiella pneumoniae is a wide-spread nosocomial pathogen. A rapid and sensitive molecular method for the detection of K. pneumoniae in clinical samples is needed to guide therapeutic treatment. In this study, we first described a loop-mediated isothermal amplification (LAMP) method for the rapid detection of capsular polysaccharide synthesis regulating gene rcsA from K. pneumoniaein clinical samples by using two methods including real-time turbidity monitoring and fluorescence detection to assess the reaction. Then dissemination of K. pneumoniae strains was investigated from ICU patients in three top hospitals in Beijing, China. The results showed that the detection limit of the LAMP method was 0.115 pg/μl DNA within 60 min under isothermal conditions (61°C), a 100-fold increase in sensitivity compared with conventional PCR. All 30 non- K. pneumoniae strains tested were negative for LAMP detection, indicating the high specificity of the LAMP reaction. To evaluate the application of the LAMP assay to clinical diagnosis, of 110 clinical sputum samples collected from ICU patients with clinically suspected multi-resistant infections in China, a total of 32 K. pneumoniae isolates were identified for LAMP-based surveillance of rcsA. All isolates belonged to nine different K. pneumoniae multilocus sequence typing (MLST) groups. Strikingly, of the 32 K. pneumoniae strains, 18 contained the Klebsiella pneumoniae Carbapenemase (KPC)-encoding gene bla(KPC-2) and had high resistance to β-lactam antibiotics. Moreover, K. pneumoniae WJ-64 was discovered to contain bla(KPC-2) and bla(NDM-1)genes simultaneously in the isolate. Our data showed the high prevalence of bla(KPC-2) among K. pneumoniae and co-occurrence of many resistant genes in the clinical strains signal a rapid and continuing evolution of K. pneumoniae. In conclusion, we have developed a rapid and sensitive visual K. pneumoniae detection LAMP assay, which could be a useful tool for clinical screening, on-site diagnosis and primary quarantine purposes. Frontiers Media S.A. 2015-05-22 /pmc/articles/PMC4440914/ /pubmed/26052327 http://dx.doi.org/10.3389/fmicb.2015.00519 Text en Copyright © 2015 Dong, Liu, Li, Wang, Li, Zou, Yang, Huang, Zhou, Huang and Yuan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Dong, Derong
Liu, Wei
Li, Huan
Wang, Yufei
Li, Xinran
Zou, Dayang
Yang, Zhan
Huang, Simo
Zhou, Dongsheng
Huang, Liuyu
Yuan, Jing
Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China
title Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China
title_full Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China
title_fullStr Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China
title_full_unstemmed Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China
title_short Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China
title_sort survey and rapid detection of klebsiella pneumoniae in clinical samples targeting the rcsa gene in beijing, china
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440914/
https://www.ncbi.nlm.nih.gov/pubmed/26052327
http://dx.doi.org/10.3389/fmicb.2015.00519
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