白莉, 白雪梅, 赵爱兰, 叶长芸, 徐建国. tccP2基因在临床分离肠致病性大肠埃希菌中的特征分析[J]. 疾病监测, 2011, 26(2): 96-99. DOI: 10.3784/j.issn.1003-9961.2011.02.005
引用本文: 白莉, 白雪梅, 赵爱兰, 叶长芸, 徐建国. tccP2基因在临床分离肠致病性大肠埃希菌中的特征分析[J]. 疾病监测, 2011, 26(2): 96-99. DOI: 10.3784/j.issn.1003-9961.2011.02.005
BAI Li, BAI Xue-mei, ZHAO Ai-lan, YE Chang-yun, XU Jian-guo. Genetic characteristics of tccP2 gene of clinical isolates of enteropathogenic Escherichia coli[J]. Disease Surveillance, 2011, 26(2): 96-99. DOI: 10.3784/j.issn.1003-9961.2011.02.005
Citation: BAI Li, BAI Xue-mei, ZHAO Ai-lan, YE Chang-yun, XU Jian-guo. Genetic characteristics of tccP2 gene of clinical isolates of enteropathogenic Escherichia coli[J]. Disease Surveillance, 2011, 26(2): 96-99. DOI: 10.3784/j.issn.1003-9961.2011.02.005

tccP2基因在临床分离肠致病性大肠埃希菌中的特征分析

Genetic characteristics of tccP2 gene of clinical isolates of enteropathogenic Escherichia coli

  • 摘要: 目的 分析2001 - 2003年某省儿童医院分离的268株大肠埃希菌 tccP2 基因的携带情况及该基因的分子特征。 方法 PCR方法筛查临床分离的268株大肠埃希菌中EHEC、EPEC菌株;再筛查 tccP2 基因的携带情况,克隆阳性菌株 tccP2 基因,并进行核苷酸测序,同时与GenBank数据库进行比对。 结果 2001 - 2003年临床分离的菌株共检测到7株EPEC菌株,其中有2株菌 tccP2 基因阳性,长度分别为1458 bp,核苷酸和氨基酸的一致性为100%,与国际上公布的str.11128(O111 ∶ H-)菌株的 tccP2 基因比对发现核苷酸一致性为61.3%;氨基酸序列比对,发现其N-端与str.11128(O111 ∶ H-)菌株具有完全相同的特异的87个核苷酸序列,脯氨酸富集重复片段序列几乎一致,较str.11128(O111 ∶ H-)菌株多4个重复片段。 结论 在中国临床分离的菌株中也存在具有 tccP2 基因的EPEC菌株,应进一步加大临床标本中该类菌株的分离与监测。

     

    Abstract: Objective To study the carriage and genetic characteristic of tccP2 gene of 268 strains of Escherichia.coli isolated in a children's hospital in china during 2001 to 2003. Methods All the strains were subjects to test for virulence genes by PCR, then tccP2 gene detection was conducted. The tccP2 gene in positive strainwas cloned, sequenced and compared with the nucleotide acid sequences of str.11128(O111 ∶ H-) downloaded from Genbank. Results Among 7 EPEC strains identified from clinical strains during 2001 to 2003, two were tccP2 gene positive. The length of tccP2 gene were both 1458 bp. The tccP2 genes of the two strains showed 100% identity at the nucleic acid level. Compared with the tccP2 gene of str.11128(O111 ∶ H-), the sequence identity was 61.3%. Amino acid sequence alignment indicted that the first 87 amino acids identified as 100% as the str.11128(O111:H-) at N terminal, proline-rich repeats and the last truncated showed high level of identity other than 4 more repeats of the 2 strains. Conclusion It is necessary to strengthen the monitoring and isolation of EPEC strains with tccP2 gene in clinical isolates due to the fact of the detection of such strains in hospitals.

     

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