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研究报告:球虫病的管理方案是肉鸡坏死性肠炎模型的主要决定因素。

Research Note: The administration schedule of coccidia is a major determinant in broiler necrotic enteritis models.

机构信息

Department of Pathology, Bacteriology and Avian diseases, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

Department of Pathology, Bacteriology and Avian diseases, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

出版信息

Poult Sci. 2021 Mar;100(3):100806. doi: 10.1016/j.psj.2020.10.060. Epub 2020 Nov 5.

Abstract

A reliable and reproducible in vivo experimental model is an essential tool to study the pathogenesis of broiler necrotic enteritis and to evaluate control methods. Most current in vivo models use Eimeria as predisposing factor. Nevertheless, most models only result in a limited number of animals with intestinal necrosis. This research describes the necrotic enteritis incidence and severity using 2 previously described experimental models varying in the time point and frequency of Eimeria administration: single late and early repeated Eimeria administration models. In an in vivo model in which Clostridium perfringens is administered at 3 consecutive days between day 18 and 20 of age, birds belonging to the single late Eimeria administration regimen received a single administration of a tenfold dose of a live attenuated Eimeria vaccine on the second day of C. perfringens challenge. Broilers belonging to the early repeated administration regimen were inoculated with the same Eimeria vaccine 4 and 2 d before the start of the C. perfringens challenge. Early repeated coccidial administration resulted in a significant increase in average necrotic lesion score (value 3.26) as compared with a single late Eimeria administration regimen (value 1.2). In addition, the number of necrotic enteritis-positive animals was significantly higher in the group that received the early repeated coccidial administration. Single Eimeria administration during C. perfringens challenge resulted in a skewed distribution of lesion scoring with hardly any birds in the high score categories. A more centered distribution was obtained with the early repeated Eimeria administration regimen, having observations in every lesion score category. These findings allow better standardization of a subclinical necrotic enteritis model and reduction of the required numbers of experimental animals.

摘要

一种可靠且可重现的体内实验模型是研究肉鸡坏死性肠炎发病机制和评估控制方法的重要工具。目前大多数体内模型使用艾美耳球虫作为诱发因素。然而,大多数模型仅导致有限数量的动物出现肠道坏死。本研究使用两种先前描述的实验模型描述了坏死性肠炎的发生率和严重程度,这两种模型在艾美耳球虫给药的时间点和频率上有所不同:单次晚期和早期重复艾美耳球虫给药模型。在一种在 18 日龄至 20 日龄连续 3 天给予产气荚膜梭菌的体内模型中,单次晚期艾美耳球虫给药方案组的鸡只在产气荚膜梭菌攻毒的第二天接受一次十倍剂量的活减毒艾美耳球虫疫苗的单次给药。早期重复给药方案组的鸡只在产气荚膜梭菌攻毒前 4 天和 2 天接种相同的艾美耳球虫疫苗。与单次晚期艾美耳球虫给药方案相比,早期重复球虫给药显著增加了平均坏死病变评分(值为 3.26)。此外,接受早期重复球虫给药的动物中坏死性肠炎阳性动物的数量显著增加。在产气荚膜梭菌攻毒期间单次给予艾美耳球虫导致病变评分呈偏态分布,几乎没有高评分类别的鸡只。早期重复艾美耳球虫给药方案获得了更居中的分布,每个病变评分类别都有观察结果。这些发现允许更好地标准化亚临床坏死性肠炎模型,并减少实验动物的数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4c3/7936161/b1047e46d23d/gr1.jpg

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