Oyofo B A, Subekti D S, Svennerholm A M, Machpud N N, Tjaniadi P, Komalarini T S, Setiawan B, Campbell J R, Corwin A L, Lesmana M
United States Naval Medical Research Unit No. 2, Jakarta, Indonesia.
Am J Trop Med Hyg. 2001 Aug;65(2):120-4. doi: 10.4269/ajtmh.2001.65.120.
Infection caused by enterotoxigenic Escherichia coli (ETEC) poses a serious health problem among children and adults in developing countries. Colonization of the small intestinal mucosa by ETEC strains is mediated by antigenically specific fimbriae, also known as colonization factor antigens (CFA). The significance of this study arises from reports that active and passive immunization with ETEC strains harboring CFAs has previously been shown to induce protective immunity against diarrhea in animal models. The aim of this study was to determine toxin-associated CFAs of ETEC isolated from a diarrheal disease case-control study in Jakarta, Indonesia. Thirteen hundred and twenty-three diarrheic and control patients with lactose-fermenting colonies were screened by ganglioside GM1-enzyme-linked immunosorbent assay (GM1-ELISA) for heat-labile (LT) and heat-stable (ST) toxins. Two hundred and forty-six (19%) ETEC isolates identified by GM1-ELISA for the LT/ST toxins were screened for CFAs by Dot blot assay using monoclonal antibodies against CFA/I, II, and IV and against the putative colonization antigens (PCF) PCFO159, PCFO166, CS7, and CS17. Of the 246 ETEC isolates, 177 (72%) elaborated ST, 56 (23%) produced LT, while 13 (5%) elicited both the ST and LT toxins. CFA testing of the 246 ETEC isolates showed that 21 (8%) expressed CFA/I, 3 (1%) exhibited CFA/II, 14 (6%) elaborated CFA/IV, while 7 (3%) expressed PCFO159 and PCFO159 plus CS5. No CFAs or PCFs could be associated with 201 (82%) of the ETEC strains. This report documents the types of CFAs associated with ETEC strains in Jakarta, Indonesia. These data may help current research efforts on the development of CFA-based vaccines for humans against ETEC and provide additional information for future ETEC vaccine trials in Southeast Asia.
产肠毒素大肠杆菌(ETEC)引起的感染在发展中国家的儿童和成人中构成严重的健康问题。ETEC菌株对小肠黏膜的定植是由抗原特异性菌毛介导的,也称为定植因子抗原(CFA)。本研究的意义源于此前有报道称,在动物模型中,用携带CFA的ETEC菌株进行主动和被动免疫已被证明可诱导针对腹泻的保护性免疫。本研究的目的是确定从印度尼西亚雅加达的一项腹泻病病例对照研究中分离出的ETEC的毒素相关CFA。通过神经节苷脂GM1-酶联免疫吸附测定(GM1-ELISA)对1323例腹泻患者和乳糖发酵菌落对照患者进行不耐热(LT)和耐热(ST)毒素筛查。通过斑点印迹法,使用针对CFA/I、II和IV以及推定定植抗原(PCF)PCFO159、PCFO166、CS7和CS17的单克隆抗体,对通过GM1-ELISA鉴定出LT/ST毒素的246株(19%)ETEC分离株进行CFA筛查。在246株ETEC分离株中,177株(72%)产生ST,56株(23%)产生LT,而13株(5%)同时产生ST和LT毒素。对246株ETEC分离株的CFA检测表明,21株(8%)表达CFA/I,3株(1%)表达CFA/II,14株(6%)产生CFA/IV,而7株(3%)表达PCFO159和PCFO159加CS5。201株(82%)ETEC菌株未发现CFA或PCF。本报告记录了印度尼西亚雅加达与ETEC菌株相关的CFA类型。这些数据可能有助于目前针对人类开发基于CFA的抗ETEC疫苗的研究工作,并为未来在东南亚进行的ETEC疫苗试验提供更多信息。