Department of Poultry Science, The University of Georgia, Athens, GA 30602.
Southern Poultry Research Group, Athens, GA 30677.
Poult Sci. 2019 Jul 1;98(7):2800-2812. doi: 10.3382/ps/pez084.
The objective of this study was to evaluate performance, diversity, composition, and predicted function of the intestinal microbiota of broilers raised under 3 different methods to induce necrotic enteritis (NE). The chicks in Experiments 1 and 2 were vaccinated against coccidiosis on day 1. Experiment 1: non-challenged and challenged birds were raised in floor pens with new litter and 58 birds/pen. The challenge consisted of Eimeria maxima inoculation on day 14 and Clostridium perfringens via water on days 18 to 19. Cecal microbiota was evaluated on days 18, 21, and 28. Experiment 2: non-challenged and challenged birds were raised in floor pens with recycled litter and 50 birds/pen. The challenge consisted of C. perfringens via feed from days 18 to 20. Ileal and cecal microbiota were evaluated on day 21. In Experiment 3, non-challenged and challenged birds were raised in battery cages with 8 birds/cage. Challenged birds were inoculated with E. maxima on day 14 and with C. perfringens on days 19 to 21. In the 3 experiments, ileal or cecal microbiota or both were analyzed through 16S rRNA sequencing. The performance of the birds was impaired in the 3 studies, regardless of the method used to induce NE. In Experiment 1, the microbiota did not significantly change across ages. In Experiment 2, α-diversity indices were lower in challenged vs. non-challenged birds in both ileal and cecal microbiota. The cecal microbiota composition and function was more affected than the ileal microbiota. In Experiment 3, Chao index (α-diversity) increased in challenged vs. non-challenged birds, and the composition of the ileal and cecal microbiota was not significantly affected. In conclusion, the overall feed conversion ratio was more affected in Experiment 3 (5.2, 11.1, and 30% for Experiments 1, 2, and 3, respectively), which also showed the highest degree of NE lesions. However, the largest variations of diversity and composition of the microbiota were observed in Experiment 2, when birds were raised in floor pens with reused litter, vaccinated against coccidiosis, and challenged with C. perfringens on days 19 to 21.
本研究旨在评估 3 种不同方法诱导坏死性肠炎(NE)条件下肉鸡的肠道微生物菌群的性能、多样性、组成和预测功能。试验 1 和 2 中的雏鸡在第 1 天接种抗球虫病疫苗。试验 1:无挑战和有挑战的鸡在有新垫料的地板笼中饲养,每笼 58 只鸡。第 14 天通过接种柔嫩艾美耳球虫进行挑战,第 18 至 19 天通过饮水接种产气荚膜梭菌。第 18、21 和 28 天评估盲肠微生物群。试验 2:无挑战和有挑战的鸡在有再利用垫料的地板笼中饲养,每笼 50 只鸡。第 18 至 20 天通过饲料接种产气荚膜梭菌进行挑战。第 21 天评估回肠和盲肠微生物群。试验 3,无挑战和有挑战的鸡在笼中饲养,每笼 8 只鸡。第 14 天接种柔嫩艾美耳球虫,第 19 至 21 天接种产气荚膜梭菌。在这 3 个试验中,通过 16S rRNA 测序分析回肠或盲肠微生物群或两者。无论使用哪种方法诱导 NE,3 个试验中的鸡的性能都受到了损害。在试验 1 中,微生物群在各年龄段之间没有显著变化。在试验 2 中,与无挑战组相比, challenged 组的回肠和盲肠微生物群的 α 多样性指数均较低。盲肠微生物群的组成和功能比回肠微生物群受到的影响更大。在试验 3 中,与非 challenged 组相比, challenged 组的 Chao 指数(α 多样性)增加,回肠和盲肠微生物群的组成没有受到显著影响。总之,在试验 3 中,总体饲料转化率受到的影响更大(分别为 5.2%、11.1%和 30%),这也表明坏死性肠炎病变的程度最高。然而,在试验 2 中,当鸡在地板笼中饲养,重复使用垫料,接种抗球虫病疫苗,并在第 19 至 21 天接种产气荚膜梭菌时,观察到微生物群的多样性和组成的最大变化。