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猪13号染色体上产肠毒素大肠杆菌F4ac肠道受体位点的精细定位

Fine-mapping of the intestinal receptor locus for enterotoxigenic Escherichia coli F4ac on porcine chromosome 13.

作者信息

Python P, Jörg H, Neuenschwander S, Hagger C, Stricker C, Bürgi E, Bertschinger H U, Stranzinger G, Vögeli P

机构信息

Institute of Animal Sciences, Swiss Federal Institute of Technology, ETH-Zentrum, Zurich, Switzerland.

出版信息

Anim Genet. 2002 Dec;33(6):441-7. doi: 10.1046/j.1365-2052.2002.00915.x.

Abstract

The aim of this study was to refine the localization of the receptor locus for fimbriae F4ac. Small intestinal enterocyte preparations from 187 pigs were phenotyped by an in vitro adhesion test using two strains of Escherichia coli representing the variants F4ab and F4ac. The three-generation pedigree comprised eight founders, 18 F1 and 174 F2 animals, for a total of 200 pigs available for the linkage analysis. Results of the adhesion tests on 171 F2 pigs slaughtered at 8 weeks of age show that 23.5% of the pigs were adhesive for F4ab and non-adhesive for F4ac (phenotype F4abR+/F4acR-; R means receptor). Pigs of this phenotype were characterized by a weak adhesion receptor for F4ab. No pigs were found expressing only F4acR and lacking F4abR. Receptors for F4ab and F4ac (F4abR+/F4acR+) were expressed by 54.5% of the pigs. Animals of this phenotype strongly bound both F4ab and F4ac E. coli. In the segregation study, the serum transferrin (TF) gene and 10 microsatellites on chromosome 13 were linked with F4acR (recombination fractions (theta) between 0.00 and 0.11 and lod score values (Z) between 11.4 and 40.4). The 11-point analysis indicates the F4acR locus was located in the interval S0068-Sw1030 close to S0075 and Sw225, with recombination fractions (theta) of 0.05 between F4acR and S0068, 0.04 with Sw1030, and 0.00 with S0075 and Sw225. The lack of pigs displaying the F4abR-/F4acR+ phenotype and the presence of two phenotypes for F4abR (a strong receptor present in phenotype F4abR+/F4acR+ and a weak receptor in phenotype F4abR+/F4acR-) led us to conclude that the receptor for F4ac binds F4ab bacteria as well, and that it is controlled by one gene localized between S0068 and Sw1030 on chromosome 13.

摘要

本研究的目的是优化F4ac菌毛受体位点的定位。使用代表F4ab和F4ac变体的两株大肠杆菌,通过体外黏附试验对187头猪的小肠肠上皮细胞制剂进行表型分析。这个三代谱系包括8个奠基者、18头F1代和174头F2代动物,总共200头猪可用于连锁分析。对171头8周龄屠宰的F2代猪进行黏附试验的结果表明,23.5%的猪对F4ab有黏附性而对F4ac无黏附性(表型为F4abR+/F4acR-;R表示受体)。这种表型的猪的特征是对F4ab的黏附受体较弱。未发现仅表达F4acR而缺乏F4abR的猪。54.5%的猪表达F4ab和F4ac的受体(F4abR+/F4acR+)。这种表型的动物能强烈结合F4ab和F4ac大肠杆菌。在分离研究中,血清转铁蛋白(TF)基因和13号染色体上的10个微卫星与F4acR连锁(重组率(θ)在0.00至0.11之间,对数优势分数值(Z)在11.4至40.4之间)。11点分析表明,F4acR位点位于靠近S0075和Sw225的S0068-Sw1030区间内,F4acR与S0068之间的重组率(θ)为0.05,与Sw1030之间为0.04,与S0075和Sw225之间为0.00。缺乏表现出F4abR-/F4acR+表型的猪以及F4abR存在两种表型(F4abR+/F4acR+表型中存在强受体,F4abR+/F4acR-表型中存在弱受体),这使我们得出结论,F4ac的受体也能结合F4ab细菌,并且它由位于13号染色体上S0068和Sw1030之间的一个基因控制。

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