Python P, Jörg H, Neuenschwander S, Asai-Coakwell M, Hagger C, Bürgi E, Bertschinger H U, Stranzinger G, Vögeli P
Institute of Animal Sciences, Swiss Federal Institute of Technology, ETH-Zentrum, Zurich, Switzerland.
J Anim Breed Genet. 2005 Apr;122 Suppl 1:5-14. doi: 10.1111/j.1439-0388.2005.00490.x.
Susceptibility to enterotoxigenic Escherichia coli with fimbriae F4ac is dominantly inherited in the pig. A three-generation pedigree was created to refine the position of F4acR on chromosome 13 comprising 202 pigs: eight parents, 18 F1 and 176 F2 pigs. The 17-point analysis indicates that F4acR lies between Sw207 and S0283. Recombinant offspring specify that the most probable order is Sw207-S0075-F4acR-Sw225-S0283. We observed six phenotypes for the three fimbrial variants F4ab, F4ac and F4ad. The two missing phenotypes F4abR-/F4acR+/F4adR+ and F4abR-/F4acR+/F4adR- indicate that pigs susceptible to F4ac are always susceptible to F4ab. Furthermore, a weak and a strong adhesion of F4ab and F4ad bacteria was observed. The weak receptor F4abR (F4abRw) was present only in pigs devoid of the receptor F4acR (F4abR+/F4acR-). In contrast, in pigs with the phenotype F4abR+/F4acR+, F4ab bacteria adhered to the majority of enterocytes. F4abRw constitutes a frequently observed phenotype whose inheritance is still unclear. Strong adhesion of F4ab and F4ac bacteria is most likely influenced by the same receptor that we name F4bcR. The number of F4ad bacteria that adhered to enterocytes was very variable in the adhesion test. Moreover, expression of F4adR was independent of age. Our segregation analyses indicated a dominant inheritance of F4adR, although the number of susceptible pigs was smaller than expected. We examined four genes as candidates for the F4acR locus: the transferrin receptor gene (TFRC) and three genes members of the glucosyl/galactosyltransferase family (B3GnT5, B3GALT3 and B4GALT4). Comparison of sequences from resistant and homozygous susceptible F4ac pigs did not reveal any causative single nucleotide polymorphism in the four genes. Two silent mutations at the positions 295 (C/T) and 313 (T/C) in B3GALT3 were found. Using the somatic cell hybrid panel, B3GnT5 and B3GALT3 were assigned to the chromosomal region SSC13q23-q41. No mutations were found in the cDNA sequences of these genes associated with the F4acR genotypes.
猪对带有F4ac菌毛的产肠毒素大肠杆菌的易感性呈显性遗传。构建了一个三代家系来精确定位位于13号染色体上的F4acR的位置,该家系包含202头猪:8头亲本、18头F1代猪和176头F2代猪。17点分析表明F4acR位于Sw207和S0283之间。重组后代表明最可能的顺序是Sw207-S0075-F4acR-Sw225-S0283。我们观察到三种菌毛变体F4ab、F4ac和F4ad的六种表型。两种缺失的表型F4abR-/F4acR+/F4adR+和F4abR-/F4acR+/F4adR-表明对F4ac易感的猪总是对F4ab易感。此外,观察到F4ab和F4ad细菌的弱黏附和强黏附。弱受体F4abR(F4abRw)仅存在于缺乏受体F4acR(F4abR+/F4acR-)的猪中。相反,在具有F4abR+/F4acR+表型的猪中,F4ab细菌黏附于大多数肠上皮细胞。F4abRw是一种常见的表型,其遗传方式仍不清楚。F4ab和F4ac细菌的强黏附很可能受我们命名为F4bcR的同一受体影响。在黏附试验中,黏附于肠上皮细胞的F4ad细菌数量变化很大。此外,F4adR的表达与年龄无关。我们的分离分析表明F4adR呈显性遗传,尽管易感猪的数量比预期的少。我们研究了四个基因作为F4acR位点的候选基因:转铁蛋白受体基因(TFRC)和糖基/半乳糖基转移酶家族的三个基因成员(B3GnT5、B3GALT3和B4GALT4)。抗性和纯合易感F4ac猪的序列比较未在这四个基因中发现任何致病单核苷酸多态性。在B3GALT3的295位(C/T)和313位(T/C)发现了两个沉默突变。使用体细胞杂种板,将B3GnT5和B3GALT3定位到染色体区域SSC13q23-q41。在与F4acR基因型相关的这些基因的cDNA序列中未发现突变。