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Molecular characteristics of the ompA gene of serotype B Chlamydia trachomatis in Qinghai Tibetan primary school students

机译:青海藏族小学生血清型B型沙眼衣原体ompA基因的分子特征

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To study the molecular characteristics of Chlamydia trachomatis , the major outer membrane protein gene ( ompA ) of C. trachomatis from primary school students with trachoma residing in the Qinghai Tibetan area was sequenced and compared with the same serotype in GenBank. In Jianshetang Primary School and Galeng Central Primary School in the Galeng Tibetan Township of Qinghai Haidong Sala Autonomous County, scraped samples were collected from the upper tarsal conjunctiva and lower conjunctival sac of both eyes of 45 students with trachoma, stored at 4°C, and transported to Beijing Tongren Hospital by air within 24 h. The samples were screened for C. trachomatis by real-time PCR. The ompA gene from the C. trachomatis -positive samples was amplified by nested PCR. The serotype was confirmed by National Center for Biotechnology Information (NCBI) BLAST search and homology analysis. The entire ompA gene sequence was compared with the corresponding gene sequences of serotype B strains available in GenBank. Of the 45 students aged 6–13 years with trachoma, 26 C. trachomatis -positive students were identified by the initial real-time PCR screening (average age, (9.09±1.63) years; sex ratio, 1.0), accounting for 57.78% (26/45). The cycle threshold values for real-time PCR were 16.79–37.77. Half (13/26) of C. trachomatis -positive students had a bacterial copy number of >105. The compliance rate of the ompA gene sequences with the C. trachomatis serotype B strains in GenBank was up to 99%. Two novel genetic mutations were found when the ompA gene was compared with those of the 11 serotype B strains in GenBank. The two non-synonymous mutations were located at (i) position 271 in the second constant domain, an adenine (A) to guanine (G) substitution (ACT→GCT), changing the amino acid at position 91 from threonine to alanine (Thr→Ala) in all 26 strains; and (ii) position 887 in the fourth variable domain, a cytosine (C) to thymine (T) substitution (GCA→GTA), changing the amino acid at residue 296 from alanine to valine (Ala→Val) in four of the 26 strains. Six mutations were identified relative to ATCC VR-573. The strains could be divided into two gene clusters according to the mutation at nucleotide position 887: CQZ-1 (China Qinghai Tibetan-1) and CQZ-2 (China Qinghai Tibetan-2). We thus detected two novel serotype B mutant strains of C. trachomatis among study subjects with trachoma.
机译:为了研究沙眼衣原体的分子特征,对青海藏族地区小学生沙眼衣原体的主要外膜蛋白基因(ompA)进行了测序,并与GenBank中相同的血清型进行了比较。在青海海东萨拉族自治县嘎棱藏族乡的建设社小学和嘎棱中心小学,从45名沙眼学生的双眼的睑板结膜和结膜下囊中收集了刮取的样品,并在4℃下保存,并在24小时内空运到北京同仁医院。通过实时PCR筛选样品中的沙眼衣原体。通过巢式PCR扩增来自沙眼衣原体阳性样品的ompA基因。通过国家生物技术信息中心(NCBI)BLAST搜索和同源性分析确认了血清型。将整个ompA基因序列与GenBank中可用的血清型B菌株的相应基因序列进行比较。在45位6-13岁的沙眼学生中,通过实时荧光定量PCR筛选(平均年龄(9.09±1.63)岁;性别比1.0)确定了沙眼衣原体阳性学生26名,占57.78%。 (26/45)。实时PCR的循环阈值为16.79–37.77。沙眼衣原体阳性学生中有一半(13/26)的细菌拷贝数> 10 5 。 GenBank中沙眼衣原体B型血清菌株对ompA基因序列的依从率高达99%。将ompA基因与GenBank中的11种B型血清型菌株进行比较时,发现了两个新的基因突变。这两个非同义突变位于第二个恒定域的(i)位置271,腺嘌呤(A)取代鸟嘌呤(G)(ACT→GCT),将位置91的氨基酸从苏氨酸变为丙氨酸(Thr →Ala)在所有26个菌株中; (ii)在第四个可变域中的887位,由胞嘧啶(C)取代胸腺嘧啶(T)(GCA→GTA),从而在26个残基中的四个残基296处的氨基酸从丙氨酸变为缬氨酸(Ala→Val)株。相对于ATCC VR-573,鉴定出六个突变。根据887位核苷酸的突变,该菌株可分为两个基因簇:CQZ-1(中国青海藏族1)和CQZ-2(中国青海藏族2)。因此,我们在沙眼的研究对象中检测到沙眼衣原体的两种新型B型血清突变株。

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