Graham Danielle, Petrone-Garcia Victor M, Hernandez-Velasco Xochitl, Coles Makenly E, Juarez-Estrada Marco A, Latorre Juan D, Chai Jianmin, Shouse Stephanie, Zhao Jiangchao, Forga Aaron J, Senas-Cuesta Roberto, Laverty Lauren, Martin Kristen, Trujillo-Peralta Carolina, Loeza Ileana, Gray Latasha S, Hargis Billy M, Tellez-Isaias Guillermo
Division of Agriculture, Department of Poultry Science, University of Arkansas, Fayetteville, AR, United States.
College of Higher Studies Cuautitlan, National Autonomous University of Mexico (UNAM), Cuautitlan Izcalli, Mexico.
Front Vet Sci. 2023 Aug 17;10:1224647. doi: 10.3389/fvets.2023.1224647. eCollection 2023.
A mixed spp. challenge model was designed to assess the effects of challenge on broiler chicken performance, intestinal integrity, and the gut microbiome for future use to evaluate alternative strategies for controlling coccidiosis in broiler chickens. The experimental design involved broiler chickens divided into two groups: a control group (uninfected) and a positive control group, infected with (EA), (EM), and (ET). At day-of-hatch, 240 off-sex male broiler chicks were randomized and allocated to one of two treatment groups. The treatment groups included: (1) Non-challenged (NC, = 5 replicate pens); and (2) challenged control (PC, = 7 replicate pens) with 20 chickens/pen. Pen weights were recorded at d0, d16, d31, d42, and d52 to determine average body weight (BW) and (BWG). Feed intake was measured at d16, d31, d42, and d52 to calculate feed conversion ratio (FCR). Four diet phases included a starter d0-16, grower d16-31, finisher d31-42, and withdrawal d42-52 diet. At d18, chickens were orally challenged with 200 EA, 3,000 EM, and 500 ET sporulated oocysts/chicken. At d24 (6-day post-challenge) and d37 (19-day post-challenge), intestinal lesion scores were recorded. Additionally, at d24, FITC-d was used as a biomarker to evaluate intestinal permeability and ileal tissue sections were collected for histopathology and gene expression of tight junction proteins. Ileal and cecal contents were also collected to assess the impact of challenge on the microbiome. BWG and FCR from d16-31 was significantly ( < 0.05) reduced in PC compared to NC. At d24, intestinal lesion scores were markedly higher in the PC compared to the NC. Intestinal permeability was significantly increased in the PC group based on serum FITC-d levels. Cadherin 1 (CDH1), calprotectin (CALPR), and connexin 45 (Cx45) expression was also upregulated in the ileum of the PC group at d24 (6-day post-challenge) while villin 1 (VIL1) was downregulated in the ileum of the PC group. Additionally, (ASV1) was enriched in the cecal content of the PC group. This model could be used to assess the effect of alternative coccidiosis control methods during the post-challenge with EA, EM, and ET.
设计了一种混合物种攻毒模型,以评估攻毒对肉鸡生产性能、肠道完整性和肠道微生物群的影响,供未来用于评估控制肉鸡球虫病的替代策略。实验设计将肉鸡分为两组:对照组(未感染)和阳性对照组,感染艾美耳球虫(EA)、巨型艾美耳球虫(EM)和堆型艾美耳球虫(ET)。在孵化日,将240只非性别的雄性肉鸡雏鸡随机分配到两个处理组之一。处理组包括:(1)未攻毒组(NC,n = 5个重复栏);(2)攻毒对照组(PC,n = 7个重复栏),每栏20只鸡。在第0天、第16天、第31天、第42天和第52天记录栏重,以确定平均体重(BW)和体重增重(BWG)。在第16天、第31天、第42天和第52天测量采食量,以计算饲料转化率(FCR)。四个日粮阶段包括开食期(第0 - 16天)、生长期(第16 - 31天)、育肥期(第31 - 42天)和停饲期(第42 - 52天)日粮。在第18天,给鸡口服200个EA、3000个EM和500个ET孢子化卵囊/只鸡。在第24天(攻毒后6天)和第37天(攻毒后19天)记录肠道病变评分。此外,在第24天,使用异硫氰酸荧光素 - d(FITC - d)作为生物标志物评估肠道通透性,并收集回肠组织切片进行组织病理学检查和紧密连接蛋白的基因表达分析。还收集回肠和盲肠内容物,以评估攻毒对微生物群的影响。与NC组相比,PC组在第16 - 31天的BWG和FCR显著降低(P < 0.05)。在第24天,PC组的肠道病变评分明显高于NC组。基于血清FITC - d水平,PC组的肠道通透性显著增加。在第24天(攻毒后6天),PC组回肠中钙黏蛋白1(CDH1)、钙保护蛋白(CALPR)和连接蛋白45(Cx45)的表达也上调,而PC组回肠中绒毛蛋白1(VIL1)下调。此外,ASV1在PC组的盲肠内容物中富集。该模型可用于评估在EA、EM和ET攻毒后替代球虫病控制方法的效果。