Sarrazin E, Bertschinger H U
Institute of Veterinary Bacteriology, University of Zurich, Switzerland.
Vet Microbiol. 1997 Feb;54(2):133-44. doi: 10.1016/s0378-1135(96)01275-8.
Enterotoxigenic (ETEC) and enterotoxaemic (ETEEC) Escherichia (E.) coli that express F18 (F107) fimbriate colonize the small intestine and cause diarrhoea and/or oedema disease in weaned pigs. So far, two antigenic variants of F18 can be distinguished with a common antigenic factor designated 'a' and two specific factors called 'b' and 'c'. In this study the existence of crosswise anti-colonization immunity between E. coli strains that express F18ab or F18ac fimbrial variants, respectively, was demonstrated. Weaned pigs of susceptible genotype with respect to susceptibility to adhesion of E. coli with fimbriae F18 were inoculated with E. coli strains 3064STM (0157:K-:H-:F18ab; resistant to streptomycin) and 8199RIF (0141ab:K-:H4:F18ac; resistant to rifampicin). The faecal shedding was compared subsequent to immunization and homologous or heterologous challenge. An enzyme-linked immunosorbent assay (ELISA) was applied to measure IgA, IgM and IgG antibodies against the F18ab and F18ac antigens in saliva, faeces, serum and intestinal wash samples. About 8 log CFU/g of the inoculated strains were found in faeces of all pigs following immunization as well as in non-immunized controls after challenge. Bacterial counts of the inoculated strains after challenge were between 2 and 5 log lower, without any difference between homologous and heterologous challenge. Intestinal colonization with fimbriated E. coli resulted in production of significantly increased levels of anti-fimbrial antibodies, especially IgA, in serum and intestinal wash samples. There were higher levels of homologous than of heterologous anti-fimbrial antibodies. Production of antibodies against F18a or against another common fimbrial antigen is probably responsible for crosswise anti-colonization immunity between E. coli strains with F18ab and F18ac fimbrial variants. Serum F18-specific IgA may be a useful indicator of a mucosal immune response directed against F18 fimbriae.
表达F18(F107)菌毛的产肠毒素性(ETEC)和肠毒血症性(ETEEC)大肠杆菌可在断奶仔猪的小肠中定植,并引发腹泻和/或水肿病。到目前为止,F18的两种抗原变体可通过一种名为“a”的共同抗原因子以及两种名为“b”和“c”的特异性因子加以区分。在本研究中,分别表达F18ab或F18ac菌毛变体的大肠杆菌菌株之间交叉抗定植免疫的存在得到了证实。对易受F18菌毛大肠杆菌黏附影响的易感基因型断奶仔猪接种大肠杆菌菌株3064STM(0157:K-:H-:F18ab;对链霉素耐药)和8199RIF(0141ab:K-:H4:F18ac;对利福平耐药)。在免疫及同源或异源攻毒后比较粪便排菌情况。应用酶联免疫吸附测定(ELISA)来检测唾液、粪便、血清和肠道冲洗样本中针对F18ab和F18ac抗原的IgA、IgM和IgG抗体。免疫后所有猪的粪便以及攻毒后未免疫对照的粪便中均发现约8 log CFU/g的接种菌株。攻毒后接种菌株的细菌计数降低了2至5 log,同源攻毒和异源攻毒之间无任何差异。带有菌毛的大肠杆菌在肠道中的定植导致血清和肠道冲洗样本中抗菌毛抗体水平显著升高,尤其是IgA。同源抗菌毛抗体水平高于异源抗菌毛抗体水平。针对F18a或另一种共同菌毛抗原产生的抗体可能是具有F18ab和F18ac菌毛变体的大肠杆菌菌株之间交叉抗定植免疫的原因。血清F18特异性IgA可能是针对F18菌毛的黏膜免疫反应的有用指标。