Department of Pathology and Microbiology, Faculté de Médecine Vétérinaire, Université de Montréal, 3200 rue Sicotte, Saint-Hyacinthe, Québec, J2S-2M2, Canada.
Braz J Microbiol. 2021 Dec;52(4):2499-2509. doi: 10.1007/s42770-021-00567-3. Epub 2021 Jul 10.
Enterotoxigenic Escherichia coli (ETEC) are responsible for diarrhea in humans as well as in farm animals. ETEC infections in newborn, suckling, and especially in post-weaning piglets are associated with reduced growth rate, morbidity, and mortality. ETEC express virulence factors as adhesin and enterotoxins that play a central role in the pathogenic process. Adhesins associated with pigs are of diverse type being either fimbrial or non-fimbrial. Enterotoxins belong to two groups: heat-labile (LT) and heat-stable (ST). Heterogeneity of ETEC strains encompass expression of various fimbriae (F4, F5, F6, F18, and F41) and enterotoxins (LT, STa, STb, and EAST1). In the late years, attempts to immunize animals against neonatal and post-weaning diarrhea were focused on the development of anti-adhesin strategies as this is the initial step of ETEC pathogenesis. Although those vaccines demonstrated some protection against ETEC infections, as enterotoxins are pivotal to the virulence of ETEC, a new generation of vaccinal molecules, which include adhesin and one or more enterotoxins, were recently tested. Some of these newly developed chimeric fusion proteins are intended to control as well human diarrhea as enterotoxins are more or less common with the ones found in pigs. As these could not be tested in the natural host (human), either a mouse or pig model was substituted to evaluate the protection efficacy. For the advancement of pig vaccine, mice were sometimes used for preliminary testing. This review summarizes advances in the anti-enterotoxin immunization strategies considered in the last 10 years.
肠产毒性大肠杆菌(ETEC)是导致人类和农场动物腹泻的原因。新生、哺乳期,特别是断奶后的仔猪 ETEC 感染与生长速度减慢、发病率和死亡率升高有关。ETEC 表达的毒力因子包括黏附素和肠毒素,在致病过程中起着核心作用。与猪相关的黏附素有多种类型,既有菌毛样的也有无菌毛样的。肠毒素分为两组:不耐热(LT)和耐热(ST)。ETEC 菌株的异质性包括多种菌毛(F4、F5、F6、F18 和 F41)和肠毒素(LT、STa、STb 和 EAST1)的表达。近年来,针对新生和断奶后腹泻的动物免疫尝试集中于开发抗黏附素策略,因为这是 ETEC 发病机制的初始步骤。尽管这些疫苗对 ETEC 感染表现出一定的保护作用,但由于肠毒素对 ETEC 的毒力至关重要,因此最近测试了新一代疫苗分子,其中包括黏附素和一种或多种肠毒素。这些新开发的嵌合融合蛋白中的一些旨在控制人类腹泻,因为肠毒素或多或少与猪中发现的肠毒素相同。由于这些不能在天然宿主(人类)中进行测试,因此替代了小鼠或猪模型来评估保护效力。为了推进猪疫苗的发展,有时会使用小鼠进行初步测试。本文综述了过去 10 年中考虑的抗肠毒素免疫接种策略的进展。