Loop-mediated isothermal amplification assay targeting the blaCTX-M9 gene for detection of extended spectrum β-lactamase-producing Escherichia coli and Klebsiella pneumoniae

被引:15
作者
Thirapanmethee, Krit [1 ]
Pothisamutyothin, Kanokporn [1 ]
Nathisuwan, Surakit [2 ]
Chomnawang, Mullika T. [1 ]
Wiwat, Chanpen [1 ]
机构
[1] Mahidol Univ, Dept Microbiol, Fac Pharm, Bangkok 10400, Thailand
[2] Mahidol Univ, Dept Pharm, Fac Pharm, Bangkok 10400, Thailand
关键词
extended-spectrum; -lactamase; Escherichia coli; Klebsiella pneumoniae; loop-mediated isothermal amplification; REVERSE TRANSCRIPTION; SENSITIVE DETECTION; ENTEROBACTERIACEAE; LAMP; SAMPLES; VIRUS; EPIDEMIOLOGY; PREVALENCE; INFECTION; THAILAND;
D O I
10.1111/1348-0421.12205
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Extended-spectrum -lactamases (ESBLs) produced by Enterobacteriaceae are one of the resistance mechanisms to most -lactam antibiotics. ESBLs are currently a major problem in both hospitals and community settings worldwide. Rapid and reliable means of detecting ESBL-producing bacteria is necessary for identification, prevention and treatment. Loop-mediated isothermal amplification (LAMP) is a technique that rapidly amplifies DNA with high specificity and sensitivity under isothermal conditions. This study was aimed to develop a convenient, accurate and inexpensive method for detecting ESBL-producing bacteria by a LAMP technique. ESBLs-producing Escherichia coli and Klebsiella pneumoniae were isolated from a tertiary hospital in Bangkok, Thailand and reconfirmed by double-disk synergy test. A set of four specific oligonucleotide primers of LAMP for detection of bla(CTX-M9) gene was designed based on bla(CTX-M9) from E. coli (GenBank Accession No. AJ416345). The LAMP reaction was amplified under isothermal temperature at 63 degrees C for 60min. Ladder-like patterns of band sizes from 226 bp of the bla(CTX-M9) DNA target was observed. The LAMP product was further analyzed by restriction digestion with MboI and TaqI endonucleases. The fragments generated were approximately 168, 177 and 250 bp in size for MboI digestion and 165, 193, 229, 281 and 314 bp for TaqI digestion, which is in agreement with the predicted sizes. The sensitivity of the LAMP technique to bla(CTX-M9) was greater than that of the PCR method by at least 10,000-fold. These results showed that the LAMP primers specifically amplified only the bla(CTX-M9) gene. Moreover, the presence of LAMP amplicon was simply determined by adding SYBR Green I in the reaction. In conclusion, this technique for detection of ESBLs is convenient, reliable and easy to perform routinely in hospitals or laboratory units in developing countries.
引用
收藏
页码:655 / 665
页数:11
相关论文
共 35 条
[1]   Isolation and Detection of Extended Spectrum β-Lactamase (ESBL)-Producing Enterobacteriaceae from Meat using Chromogenic Agars and Isothermal Loop-Mediated Amplification (LAMP) Assays [J].
Anjum, M. F. ;
Lemma, F. ;
Cork, D. J. ;
Meunier, D. ;
Murphy, N. ;
North, S. E. ;
Woodford, N. ;
Haines, J. ;
Randall, L. P. .
JOURNAL OF FOOD SCIENCE, 2013, 78 (12) :M1892-M1898
[2]   Sensitive and specific detection of Cryptosporidium species in PCR-negative samples by loop-mediated isothermal DNA amplification and confirmation of generated LAMP products by sequencing [J].
Bakheit, Mohammed A. ;
Torra, Dena ;
Palomino, Lily A. ;
Thekisoe, Oriel M. M. ;
Mbati, Peter A. ;
Ongerth, Jerry ;
Karanis, Panagiotis .
VETERINARY PARASITOLOGY, 2008, 158 (1-2) :11-22
[3]   Growing group of extended-spectrum β-lactamases:: The CTX-M enzymes [J].
Bonnet, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (01) :1-14
[4]  
Chanawong Aroonwadee, 2007, Southeast Asian Journal of Tropical Medicine and Public Health, V38, P493
[5]   SHV-1 β-lactamase is mainly a chromosomally encoded species-specific enzyme in Klebsiella pneumoniae [J].
Chaves, J ;
Ladona, MG ;
Segura, C ;
Coira, A ;
Reig, R ;
Ampurdanés, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (10) :2856-2861
[6]   Sequence-Specific Detection Method for Reverse Transcription, Loop-Mediated Isothermal Amplification of HIV-1 [J].
Curtis, Kelly A. ;
Rudolph, Donna L. ;
Owen, Michele .
JOURNAL OF MEDICAL VIROLOGY, 2009, 81 (06) :966-972
[7]   Rapid and sensitive detection of infectious spleen and kidney necrosis virus by loop-mediated isothermal amplification combined with a lateral flow dipstick [J].
Ding, W. C. ;
Chen, Jiong ;
Shi, Y. H. ;
Lu, X. J. ;
Li, M. Y. .
ARCHIVES OF VIROLOGY, 2010, 155 (03) :385-389
[8]   Phenotypic detection of extended-spectrum β-lactamase production in Enterobacteriaceae:: review and bench guide [J].
Drieux, L. ;
Brossier, F. ;
Sougakoff, W. ;
Jarlier, V. .
CLINICAL MICROBIOLOGY AND INFECTION, 2008, 14 :90-103
[9]   Extended-spectrum ß-lactamase-producing and AmpC-producing Escherichia coli from livestock and companion animals, and their putative impact on public health: a global perspective [J].
Ewers, C. ;
Bethe, A. ;
Semmler, T. ;
Guenther, S. ;
Wieler, L. H. .
CLINICAL MICROBIOLOGY AND INFECTION, 2012, 18 (07) :646-655
[10]   Comparison of Nine Phenotypic Methods for Detection of Extended-Spectrum β-Lactamase Production by Enterobacteriaceae [J].
Garrec, Helene ;
Drieux-Rouzet, Laurence ;
Golmard, Jean-Louis ;
Jarlier, Vincent ;
Robert, Jerome .
JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (03) :1048-1057