Goetstouwers Tiphanie, Van Poucke Mario, Coppieters Wouter, Nguyen Van Ut, Melkebeek Vesna, Coddens Annelies, Van Steendam Katleen, Deforce Dieter, Cox Eric, Peelman Luc J
Laboratory of Animal Genetics, Faculty of Veterinary Medicine, Ghent University, Belgium.
Unit of Animal Genomics, GIGA-R and Faculty of Veterinary Medicine, University of Liège (B34), Liège (Sart Tilman), Belgium.
PLoS One. 2014 Aug 19;9(8):e105013. doi: 10.1371/journal.pone.0105013. eCollection 2014.
F4 enterotoxigenic Escherichia coli (F4 ETEC) are an important cause of diarrhea in neonatal and newly-weaned pigs. Based on the predicted differential O-glycosylation patterns of the 2 MUC13 variants (MUC13A and MUC13B) in F4ac ETEC susceptible and F4ac ETEC resistant pigs, the MUC13 gene was recently proposed as the causal gene for F4ac ETEC susceptibility. Because the absence of MUC13 on Western blot from brush border membrane vesicles of F4ab/acR+ pigs and the absence of F4ac attachment to immunoprecipitated MUC13 could not support this hypothesis, a new GWAS study was performed using 52 non-adhesive and 68 strong adhesive pigs for F4ab/ac ETEC originating from 5 Belgian farms. A refined candidate region (chr13: 144,810,100-144,993,222) for F4ab/ac ETEC susceptibility was identified with MUC13 adjacent to the distal part of the region. This candidate region lacks annotated genes and contains a sequence gap based on the sequence of the porcine GenomeBuild 10.2. We hypothesize that a porcine orphan gene or trans-acting element present in the identified candidate region has an effect on the glycosylation of F4 binding proteins and therefore determines the F4ab/ac ETEC susceptibility in pigs.
F4产肠毒素大肠杆菌(F4 ETEC)是新生仔猪和刚断奶仔猪腹泻的重要病因。基于对F4ac ETEC易感猪和F4ac ETEC抗性猪中2种MUC13变体(MUC13A和MUC13B)预测的差异O-糖基化模式,MUC13基因最近被提出是F4ac ETEC易感性的致病基因。由于来自F4ab/acR +猪的刷状缘膜囊泡在蛋白质免疫印迹上未检测到MUC13,且F4ac无法附着于免疫沉淀的MUC13,因此无法支持这一假设,于是使用来自5个比利时农场的52头对F4ab/ac ETEC无粘附性和68头强粘附性的猪进行了一项新的全基因组关联研究(GWAS)。确定了一个F4ab/ac ETEC易感性的精细候选区域(13号染色体:144,810,100 - 144,993,222),MUC13位于该区域远端附近。根据猪基因组构建10.2的序列,该候选区域缺乏注释基因且包含一个序列间隙。我们假设在所确定的候选区域中存在的一个猪孤儿基因或反式作用元件对F4结合蛋白的糖基化有影响,因此决定了猪对F4ab/ac ETEC的易感性。