Genetic environment of β-lactamase genes of extended-spectrum β-lactamase-producing Klebsiella pneumoniae isolates from patients with lower respiratory tract infection in China

被引:7
|
作者
Liu Lin [1 ]
Wang Xiaorong [2 ]
An Shuchang [3 ]
Zhang Xiangyan [4 ]
Chen Lin [1 ]
Li Yuqian [1 ]
Xu Li [1 ]
Zhang Yijie [1 ]
Gao Zhancheng [1 ]
机构
[1] Peking Univ, Peoples Hosp, Dept Resp & Crit Care Med, Beijing 100044, Peoples R China
[2] Huazhong Univ Sci & Technol, Dept Resp Med, Affiliated Union Hosp, Wuhan 430022, Hubei, Peoples R China
[3] Tsinghua Univ, Affiliated Hosp 1, Dept Resp Med, Beijing 100016, Peoples R China
[4] Guizhou Prov Peoples Hosp, Dept Resp & Crit Care Med, Guiyang 550002, Guizhou, Peoples R China
关键词
Klebsiella pneumoniae; promoter; beta-lactamase; insertion sequence; ESCHERICHIA-COLI; BLA(CTX-M); RESISTANCE; ENTEROBACTERIACEAE; PREVALENCE; CTX-M-3; MOBILIZATION; EXPRESSION; PROMOTERS; PLASMIDS;
D O I
10.3760/cma.j.issn.0366-6999.20133307
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Extended-spectrum beta-lactamase (ESBL)-producing Klebsiella pneumoniae (K. pneumoniae) is one of the most popular pathogens that cause refractory respiratory tract infection. The genetic environment, including insertion sequences and the types of promoter, plays a key role in exploration of the mechanism of prevalence and dismission of the ESBL-producing K. pneumoniae isolates. The aim of the investigation was to target analysis the genetic environment and promoter sequences of bla(CTX-M), bla(SHV) and bla(TEM), the most popular beta-lactamase genes harbored by ESBL-producing K. pneumoniae isolates. Methods From February 2010 to July 2011, 158 of 416 K. pneumoniae isolates producing ESBL from patients with lower respiratory tract infection were collected from seven tertiary hospitals from Beijing, Anhui, Fujian, Liaoning, Hebei and Inner Mongolia Autonomous Region in China. The genetic environment including promoters of 10 types of bla(CTX-M), 18 types of bla(SHV) and 2 types of bla(TEM) were analyzed by amplification and direct sequencing with various sets of PCR primers. Results ISEcp1 was located upstream of the 5' end of the bla(CTX-M) gene in 130 (97.0%) out of 134 K. pneumoniae isolates harboring bla(CTX-M) and provided a conserved promoter to bla(CTX-M). A non-coding sequence preceded by kdpC and recF was identified in all of the bla(SHV) genes except bla(SHV-12) and bla(SHV-2a). IS26 was also found upstream of 1 bla(CTX-M-15), 10 bla(SHV-1), strains, 4 bla(TEM-1) and all of the bla(SHV-2), bla(SHV-2a), bla(SHV-5) and bla(SHV-12). Eighty-seven of 91 strains harboring bla(TEM-1) carried a copy of Tn2 and IS26-bla(TEM-1), fragments were also detected in 4 strains. With respect to K. pneumoniae, the genetic environment of bla(CTX-M-38), bla(SHV-142) and bla(TEM-135) were firstly elaborated, and four kinds of novel genetic environment of bla(CTX-M-3), bia(CTX-M-15) and bla(TEM-1) have been detected as well. Conclusions Perfective implementation of the genetic environment information of beta-lactamase gene needs to be further explored and supplemented. ISEcp1 and IS26 elements are widespread upstream of the bla(CTX-M), bla(SHV) and bla(TEM) genes and contribute to horizontal transmission and genetic expression.
引用
收藏
页码:2445 / 2450
页数:6
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