Eastern Regional Station, VPH Lab, ICAR-Indian Veterinary Research Institute, Kolkata, India.
Division of Bacteriology, National Institute of Cholera & Enteric Diseases, Kolkata, India.
Indian J Med Res. 2017 Jul;146(Supplement):S30-S37. doi: 10.4103/ijmr.IJMR_1877_15.
BACKGROUND & OBJECTIVES: Shigatoxic Escherichia coli (STEC) recovered from dairy animals of Kolkata, India, harboured the putative virulence genes; however, the animals did not exhibit clinical symptoms. Similarly, human isolates in this locality also showed variations in degree of symptoms. Hence, this study was designed to know the presence of recognized gene(s) in the locus of enterocyte effacement (LEE) pathogenicity island in these STEC isolates and functional status of the cardinal gene (eae) related to pathogenicity.
Genes were characterized using polymerase chain reaction (PCR) assays, and functional status of cardinal gene (eae) was evaluated by fluorescent actin staining (FAS) assay. Variation in eae gene was determined by intimin PCR.
Cattle STEC isolates carried 22 genes in LEE pathogenicity island in different frequencies ranging from 5.63 to 47.88 per cent of the isolates. In human isolates, the genes namely ler, escRSTU, orf 2, esc C, esc V, orf 3 and tir that are associated with secretory function, were found to be absent and rest of the genes were present in lower frequency. Further, the cardinal gene (eae) responsible for initiation of pathogenesis was in a very low frequency in human (n=2; 10.5%) and cattle (n=11; 15.5%) isolates. None of theseeae+ STEC isolates from human and cattle revealed positivity in FAS assay.
INTERPRETATION & CONCLUSIONS: Majority of human STEC isolates lacked the cardinal virulence gene (eae), and genes for secretory function that are essential for facilitating pathogenesis. This may partially be attributed to low occurrence of STEC in human clinical diarrhoea in this area. Although a few isolates (11 of 71) from cattle had eae gene, they did not express phenotypically. This could be one of the reasons for not appearing of clinical symptoms in the hosts.
从印度加尔各答的奶牛中分离出的志贺毒素大肠杆菌(STEC)携带假定的毒力基因;然而,这些动物并未表现出临床症状。同样,该地区的人类分离株也表现出症状严重程度的变化。因此,本研究旨在了解这些 STEC 分离株中肠上皮细胞黏附(LEE)致病岛中公认基因的存在情况以及与致病性相关的主要基因(eae)的功能状态。
使用聚合酶链反应(PCR)检测方法对基因进行特征分析,并通过荧光肌动蛋白染色(FAS)检测评估主要基因(eae)的功能状态。通过 intimin PCR 检测 eae 基因的变异情况。
牛源 STEC 分离株在 LEE 致病性岛中携带 22 个基因,其频率范围为 5.63%至 47.88%。在人源分离株中,与分泌功能相关的 ler、escRSTU、orf2、escC、escV、orf3 和 tir 基因缺失,其余基因的存在频率较低。此外,与发病机制起始相关的主要基因(eae)在人源(n=2;10.5%)和牛源(n=11;15.5%)分离株中频率非常低。这些来自人类和牛源的 eae+ STEC 分离株在 FAS 检测中均未呈阳性。
大多数人源 STEC 分离株缺乏主要毒力基因(eae)和分泌功能基因,这些基因对于促进发病机制至关重要。这可能部分归因于该地区人类临床腹泻中 STEC 的发生率较低。尽管牛源的少数分离株(71 株中的 11 株)有 eae 基因,但它们没有表型表达。这可能是宿主没有出现临床症状的原因之一。