Comparative analyses of phenotypic methods and 16S rRNA, khe, rpoB genes sequencing for identification of clinical isolates of Klebsiella pneumoniae

被引:24
|
作者
He, Yanxia [1 ,2 ]
Guo, Xianguang [4 ]
Xiang, Shifei [5 ]
Li, Jiao [1 ]
Li, Xiaoqin [6 ]
Xiang, Hui [5 ]
He, Jinlei [1 ]
Chen, Dali [1 ]
Chen, Jianping [1 ,3 ]
机构
[1] Sichuan Univ, West China Sch Preclin & Forens Med, Dept Parasitol, Chengdu 610041, Peoples R China
[2] Hubei Univ Nationalities, Dept Pathogen Biol & Immunol, Coll Med, Enshi 445000, Peoples R China
[3] Sichuan Univ, Anim Dis Prevent & Food Safety Key Lab Sichuan Pr, Chengdu 610041, Peoples R China
[4] Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China
[5] Hubei Univ Nationalities, Affiliated Minda Hosp, Enshi 445000, Peoples R China
[6] Cent Hosp Enshi Autonomous Prefecture, Enshi 445000, Peoples R China
来源
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY | 2016年 / 109卷 / 07期
基金
中国国家自然科学基金;
关键词
16S rRNA; khe; rpoB; Bayesian phylogenetic analysis; Species identification; Klebsiella pneumoniae; ANTIMICROBIAL SUSCEPTIBILITY; PHYLOGENETIC GROUPS; COMB; NOV; PCR; INTERFACE; OUTBREAK; DNA; ENTEROBACTERIACEAE; GENEALOGIES; BACTEREMIA;
D O I
10.1007/s10482-016-0702-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The present work aimed to evaluate 16S rRNA, khe and rpoB gene sequencing for the identification of Klebsiella pneumoniae in comparison with phenotypic methods. Fifteen clinical isolates were examined, which were initially identified as K. pneumoniae subsp. pneumoniae using the automated VITEK 32 system in two hospitals in Enshi City, China. Their identity was further supported by conventional phenotypic methods on the basis of morphological and biochemical characteristics. Using Bayesian phylogenetic analyses and haplotypes network reconstruction, 13 isolates were identified as K. pneumoniae, whereas the other two isolates (K19, K24) were classified as Shigella sp. and Enterobacter sp., respectively. Of the three genes, 16S rRNA and khe gene could discriminate the clinical isolates at the genus level, whereas rpoB could discriminate Klebsiella at the species and even subspecies level. Overall, the gene tree based on rpoB is more compatible with the currently accepted classification of Klebsiella than those based on 16S rRNA and khe genes, showing that rpoB can be a powerful tool for identification of K. pneumoniae isolates. Above all, our study challenges the utility of khe as a species-specific marker for identification of K. pneumoniae.
引用
收藏
页码:1029 / 1040
页数:12
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