首页> 外文期刊>Journal of Animal Science >Effects of an F18 enterotoxigenic Escherichia coli challenge on growth performance, immunological status, and gastrointestinal structure of weaned pigs and the potential protective effect of direct-fed microbial blends
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Effects of an F18 enterotoxigenic Escherichia coli challenge on growth performance, immunological status, and gastrointestinal structure of weaned pigs and the potential protective effect of direct-fed microbial blends

机译:F18肠肠肠道大肠杆菌对断奶猪生长性能,免疫状态和胃肠结构的影响及直接喂养微生物混合物的潜在保护作用

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摘要

The objective of this experiment was to investigate the impact of an F18 enterotoxigenic Escherichia coli (ETEC) challenge on growth performance, aspects of intestinal function, and selected immune responses of piglets, as well as to evaluate potential protective effects of direct-fed microbial (DFM) blends. Seventy-two weaned piglets (6.4 +/- 0.2 kg body weight [BW]; similar to 21 d of age) were assigned to one of four treatments: 1) NC: Nonchallenged (n = 10), 2) positive challenged control (PC): F18 ETEC-challenged (n = 10), 3) PC + DFM1 (n = 8; three strains of Bacillus amyloliquefaciens; 7.5 x 10(5) colony-forming units [cfu]/g), or 4) PC + DFM2 (n=8; 2 strains of B. amyloliquefaciens and one strain of Bacillus subtilis; 1.5 x 10(5) cfu/g). Feed intake and BW were recorded on day 0, 7, and 17. Pigs were sham-infected either with 6 mL phosphate-buffered saline or inoculated with 6 mL F18 ETEC (similar to 1.9 x 10(9) cfu/mL) on day 7 (0 d postinoculation [dpi]). All ETEC-challenged pigs were confirmed to be genetically susceptible to F18. Pigs had ad libitum access to feed and water throughout the 17-d trial. Fecal scores were visually ranked and rectal temperatures were recorded daily. To evaluate ETEC shedding, fecal swabs were collected on dpi 0, 1, 2, 3, 5, 7, and 10. Blood samples were collected on dpi 0, 1, 2, 4, 7, and 10. Ileal tissues were collected at necropsy on dpi 10. All challenged treatments had lower final BW, decreased average daily gain (ADG), and average daily feed intake (ADFI) during the 10-d postchallenge period (P < 0.01). The DFM2 treatment increased E. coli shedding on dpi 2 and decreased iton dpi 7 (P < 0.05) compared with the PC. Rectal temperature decreased across all challenged treatments (P < 0.01). Ileal mRNA abundance of occludin (OCLN) and zonula occludens-1 (ZO-1) decreased in PC and DFM1 compared with NC (P < 0.05). Pigs fed DFM2 had intermediate ileal mRNA abundance of OCLN and increased ZO-1 mRNA compared with pigs in PC (P < 0.05). Interleukin 8 (IL-8) increased in the plasma of PC and DFM2 on dpi 2 compared with NC (P < 0.05). Mucosal IL-8 increased in PC compared with NC (P < 0.05). All challenged treatments tended to have elevated tumor necrosis factor-alpha (TNF-alpha) mRNA abundance compared with NC (P < 0.10). Challenged pigs had reduced secretory immunoglobulin A and villus height compared with NC pigs (P < 0.05). The impact of an ETEC challenge on intestinal function and the immune system has been revealed, information critical to developing improved treatment regimes.
机译:该实验的目的是探讨F18肠肠毒性大肠杆菌(ETEC)对生长性能,肠功能各方面的影响,以及选择仔猪的免疫应答,以及评估直接喂养微生物的潜在保护作用( DFM)混合。七十二头断奶仔猪(6.4 +/- 0.2公斤体重[BW];类似于21天),分配到四种治疗中的一种:1)NC:非挑战(n = 10),2)阳性攻击控制( PC):F18挑战(n = 10),3)PC + DFM1(n = 8;三种芽孢杆菌淀粉淀粉淀粉菌; 7.5×10(5)个菌落形成单元[CFU] / g)或4)PC + DFM2(n = 8; 2淀粉淀粉淀粉淀粉淀粉芽孢杆菌和枯草芽孢杆菌菌株; 1.5×10(5)CFU / g)。在第0天,7天和17天记录进料进料和BW.猪用6mL磷酸盐缓冲盐水进行假烧,或用6ml F18 ETEC接种(类似于1.9×10(9)CFU / mL) 7(0 d Postinuction [DPI])。确认所有ETEC挑战性猪都被证实遗传易受F18的影响。猪在17-D试验中有广告利用进料和水。粪便评分在视觉上排名,每天记录直肠温度。为了评估ETEC脱落,在DPI 0,1,2,3,5,7和10上收集粪便拭子。收集在DPI 0,1,2,4,7和10上收集血液样品。收集髂骨组织DPI 10的尸检10.所有挑战性治疗的最终BW都有较低的最终BW,平均每日增益(ADG)和10-D后期期间的平均日常进料摄入(ADFI)(P <0.01)。所述DFM2治疗增加大肠杆菌脱落在DPI 2和下降ITON dpi,采用PC机相比,图7(P <0.05)。直肠温度越来越大,所有挑战治疗(P <0.01)。与NC相比,在PC和DFM1中,难率mRNA丰富的闭塞素(OCLN)和ZONULA obcludens-1(ZO-1)降低(P <0.05)。与PC中的猪相比,饲喂DFM2的DFM2具有中间髂骨MRNA丰度和增加的ZO-1 mRNA(P <0.05)。与NC相比,白细胞介素8(IL-8)在DPI 2上的PC和DFM2上的血浆增加(P <0.05)。与NC相比,PC中粘膜IL-8增加(P <0.05)。与NC相比,所有挑战性的治疗往往具有升高的肿瘤坏死因子-α(TNF-α)mRNA丰度(P <0.10)。与NC猪相比,挑战性猪的分泌免疫球蛋白A和绒毛高度(P <0.05)。 ETEC挑战对肠功能和免疫系统的影响,揭示了对改进治疗制度的关键。

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