Miniats O P, Mitchell L, Barnum D A
Can J Comp Med. 1970 Jul;34(3):269-76.
In a study of the response of gnotobiotic pigs to coliform infections, 45 one-week-old germfree pigs were divided into five groups and each group was inoculated orally with a different strain of Escherichia coli. Three of these were enteropathogenic swine strains, P307[08:K87(B), K88 a,b (L):H19]; P570 [0138:K81]; P568[0141:K85a,b(B), K88a,b(L):H4], one was a virulent human strain, H224, [026:K60(B6)], and one was a non-enteropathogenic swine strain, P581[OX13:K68]. It was attempted to protect a portion of the pigs with orally administered specific antisera and sera from non-immunized specific pathogenfree (SPF) pigs. Observations were made on the clinical response, bacterial counts of feces and intestinal contents, gross pathological changes, distribution of the organisms in organs and serum hemagglutinin titers. Infection with E. coli P307 resulted in diarrhea, dehydration and death, unless the pig was protected with specific antiserum. The pigs infected with E. coli P570 had a transient diarrhea but retained their appetites and recovered. Those infected with the other three strains remained healthy throughout. No circulating hemagglutinating antibody against the test strains of E. coli could be detected in any of the pigs seven days or earlier post-inoculation. Relationship could not be established between the numbers of viable E. coli in the feces and the presence of clinical colibacillosis. Orally administered specific antiserum afforded protection against strain P307, but did not reduce the number of E. coli in the gut or alter their distribution in the internal organs. This suggested that the protective effect of specific antibody in the intestine was due to its action on a metabolite (enterotoxin) produced by E. coli P307 rather than the organism itself.
在一项关于无菌猪对大肠埃希菌感染反应的研究中,45头1周龄的无菌猪被分成5组,每组经口接种不同菌株的大肠埃希菌。其中3株是猪肠道致病性菌株,P307[08:K87(B),K88 a,b (L):H19];P570 [0138:K81];P568[0141:K85a,b(B),K88a,b(L):H4],1株是强毒力的人源菌株,H224,[026:K60(B6)],1株是猪非肠道致病性菌株,P581[OX13:K68]。研究尝试用经口给予的特异性抗血清以及来自未免疫的无特定病原体(SPF)猪的血清保护部分猪。对临床反应、粪便和肠道内容物的细菌计数、大体病理变化、细菌在器官中的分布以及血清血凝素滴度进行了观察。感染大肠埃希菌P307会导致腹泻、脱水和死亡,除非猪用特异性抗血清进行保护。感染大肠埃希菌P570的猪出现短暂腹泻,但仍有食欲并康复。感染其他3株菌株的猪在整个实验过程中保持健康。在接种后7天或更早时间,任何猪体内均未检测到针对测试大肠埃希菌菌株的循环血凝抗体。粪便中大肠埃希菌活菌数量与临床大肠杆菌病的存在之间未建立联系。经口给予的特异性抗血清对P307菌株有保护作用,但未减少肠道内大肠埃希菌数量,也未改变其在体内器官中的分布。这表明肠道中特异性抗体的保护作用是由于其对大肠埃希菌P307产生的一种代谢产物(肠毒素)起作用,而非对细菌本身起作用。