Maintained growth performance and reduced mortality of genetically resistant nursery pigs after an experimental virulent F18 enterotoxigenic Escherichia coli challenge.

IF 1.8 Q3 AGRICULTURE, DAIRY & ANIMAL SCIENCE Translational Animal Science Pub Date : 2025-01-17 eCollection Date: 2025-01-01 DOI:10.1093/tas/txaf004
Michael W Welch, Amanda J Cross, Iara D P Solar Diaz, Danielle C Johnson, Eric Parr, Tom A Rathje, Randy C Borg, Dustin D Boler
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Abstract

Enterotoxigenic Escherichia coli (ETEC) is a leading cause of postweaning diarrhea (PWD) and mortality of weaned pigs. The objective of this study was to evaluate genetic resistance of the polymorphism at nucleotide 307 (M307) in the FUT1 gene, to F18 E. coli infection considering different genotypes. A total of 179 pigs were used for this study. Pigs were genotyped for susceptibility to F18+ E. coli prior to the trial. Treatments included: genotype M307GA-heterozygous for E. coli susceptibility (A), genotype M307GG-homozygous E. coli susceptibility (B), or genotype M307AA-homozygous for E. coli resistance (C). Pigs were weighed, assigned to pens based on genotype, and allowed to acclimate for 3 d prior to the challenge. On days 4, 5, and 6, pigs were inoculated intraorally at the oropharynx with an F18+ E. coli isolate at a geometric mean concentration of 9.8 × 109. Growth rate (average daily gain [ADG]), feed intake (average daily feed intake), and gain-to-feed ratio (G:F) were calculated by pen. All pigs were humanely euthanized at the end of the trial. Two fixed sections of ileum and distal jejunum were collected from a subpopulation and tested by in situ hybridization (ISH) to evaluate F18+ E. coli adherence. Fresh ileum samples were used for enumeration of F18, total E. coli, and total bacteria by real-time polymerase chain reaction. Mortality rates during the trial were 26.7% for genotype A, 18.3% for genotype B, and 0.0% for genotype C (P < 0.01). Starting weights prior to inoculation were not different (P = 0.29) among genotypes. Overall, pigs from genotype C grew 223 g/d faster (P = 0.04) than genotype A. Pigs from genotype C tended to grow 185 g/d faster (P = 0.09) than genotype B. G:F for genotype C (0.74) was 23% greater (P < 0.01) than G:F for genotype A (0.60) and tended to be 12% greater (P = 0.07) than genotype B (0.66). There were no differences in ADG or G:F between genotypes A and B. F18-specifc Cq units were decreased by 7.74 and 6.47 in genotypes A and B compared with genotype C (P ≤ 0.03). Signal by ISH was increased by 14.0-fold in genotype A compared with genotype C (P = 0.02). Adherence was not different among genotypes (P = 0.40). Genotype A had greater mortality and poorer growth performance than genotype B or C. Genotype C had no mortalities during the trial, grew faster, was more feed efficient, and had less F18 E. coli in the ileal mucosa compared with genotype A. Resistant genotypes provide an opportunity to reduce PWD and mortality due to an F18+ E. coli infection.

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在实验性强毒F18产肠毒素大肠杆菌攻击后,保持了遗传抗性苗猪的生长性能并降低了死亡率。
产肠毒素大肠杆菌(ETEC)是断奶后腹泻(PWD)和断奶仔猪死亡的主要原因。本研究的目的是评估FUT1基因核苷酸307 (M307)多态性在不同基因型下对F18大肠杆菌感染的遗传抗性。本研究共使用179头猪。试验前对猪进行F18+大肠杆菌易感性基因分型。处理包括:基因型m307ga -大肠杆菌易感性(A),基因型m307gg -纯合子大肠杆菌易感性(B),或基因型m307aa -纯合子大肠杆菌耐药(C)。猪称重,根据基因型分配到猪圈中,并在攻毒前让其适应3天。在第4、5和6天,分别在猪口咽口内接种几何平均浓度为9.8 × 109的F18+大肠杆菌分离物。采用笔法计算生长率(平均日增重[ADG])、采食量(平均日采食量)和料重比(G:F)。在试验结束时,所有的猪都被人道地安乐死。从一个亚群中收集回肠和远空肠两段固定切片,采用原位杂交(ISH)检测F18+大肠杆菌粘附性。采用实时聚合酶链反应法对新鲜回肠标本进行F18、大肠杆菌总数和细菌总数的计数。试验期间,基因型A组死亡率为26.7%,基因型B组为18.3%,基因型C组为0.0% (P = 0.29)。总体而言,基因型C猪的生长速度比基因型a快223 g/d (P = 0.04)。基因型C猪的生长速度比基因型B快185 g/d (P = 0.09)。基因型C猪的g:F比基因型B猪的g:F(0.74)比基因型B猪的g:F(0.66)高23% (P = 0.07)。基因型A和基因型B的ADG和G:F无显著差异,基因型A和基因型B的f18特异性Cq单位比基因型C分别降低7.74和6.47 (P≤0.03)。基因型A与基因型C相比,ISH信号增加了14.0倍(P = 0.02)。不同基因型的依从性差异无统计学意义(P = 0.40)。与基因型B或C相比,基因型A的死亡率更高,生长性能更差。与基因型A相比,基因型C在试验期间没有死亡率,生长更快,饲料效率更高,回肠黏膜中的F18大肠杆菌较少。耐药基因型提供了减少因F18+大肠杆菌感染而导致的PWD和死亡率的机会。
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来源期刊
Translational Animal Science
Translational Animal Science Veterinary-Veterinary (all)
CiteScore
2.80
自引率
15.40%
发文量
149
审稿时长
8 weeks
期刊介绍: Translational Animal Science (TAS) is the first open access-open review animal science journal, encompassing a broad scope of research topics in animal science. TAS focuses on translating basic science to innovation, and validation of these innovations by various segments of the allied animal industry. Readers of TAS will typically represent education, industry, and government, including research, teaching, administration, extension, management, quality assurance, product development, and technical services. Those interested in TAS typically include animal breeders, economists, embryologists, engineers, food scientists, geneticists, microbiologists, nutritionists, veterinarians, physiologists, processors, public health professionals, and others with an interest in animal production and applied aspects of animal sciences.
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