Aboshady Hadeer M, Félicité Yoann, Hira Julien, Barbier Claude, Bambou Jean-Christophe
INRAE, ASSET, Petit-Bourg, France.
Department of Animal Production, Faculty of Agriculture, Cairo University, Cairo, Egypt.
Front Vet Sci. 2022 Jul 8;9:873467. doi: 10.3389/fvets.2022.873467. eCollection 2022.
In small ruminant production, gastrointestinal nematode (GIN) infection is one of the major causes of economic losses. The aim of this study was to compare the abomasal mucosa transcriptome of naïve and pre-infected goats at early time points after infection, in order to identify different pathways and upstream regulators involved in the host immune response. Naïve and pre-infected Creole kids were orally infected with 10,000 infective larvae (L3), and abomasal mucosa was sampled at 0, 4, and 6 days post-infection (dpi). At 6 dpi, all the animals were slaughtered to perform parasite burden counts. The mean number of L4 recovered in naïve kids was more than twice as high as that recovered in the pre-infected ones (5,860 and 2,474 respectively, < 0.001). RNA-seq analysis showed a number of differentially expressed genes (DEGs) very low for both naïve and pre-infected animals when comparing day 0 vs. day 4 post-infection. A total of 2,237 and 3,206 DEGs were identified comparing 0 vs. 6 dpi in naïve and pre-infected animals, respectively. Interestingly, only 18 DEGs were found for the comparison of pre-infected vs. naïve animals at 6 dpi. Ingenuity pathway analysis (IPA) showed that several immune responses were activated in pre-infected compared with naïve animals at 0 and 4 dpi such as Th2 and Th1 pathways, natural killer cell, B cell receptor, IL-2, and IL-15 signaling. On the other hand, both naïve and pre-infected animals showed activation for those pathways comparing 6 vs. 0 dpi, with no difference between them. A similar pattern was recorded for upstream regulator genes which were related to immunity like TNF, IL-1β, IL-2, IL-5, TGFβ1, IFNγ, TCR, IL-18, IL-6, and IL-4. Our results showed that at 0 and 4 dpi the immune response was activated toward Th1 and Th2 pathways in pre-infected kids compared to the naïve ones, however, the same immune response was developed in naïve kids as earlier as 6 dpi. We conclude that repeated infection in kid goats induced a concomitant early activation of a Th1 and Th2 immune response resulting in the regulation of worm establishment.
在小型反刍动物生产中,胃肠道线虫(GIN)感染是造成经济损失的主要原因之一。本研究的目的是比较初次感染和预先感染的山羊在感染后早期时间点的皱胃黏膜转录组,以确定参与宿主免疫反应的不同途径和上游调节因子。将初次感染和预先感染的克里奥尔山羊幼崽经口感染10,000条感染性幼虫(L3),并在感染后0、4和6天采集皱胃黏膜样本。在感染后6天,宰杀所有动物以进行寄生虫负荷计数。初次感染的幼崽中回收的L4平均数量比预先感染的幼崽高出两倍多(分别为5,860条和2,474条,<0.001)。RNA测序分析显示,在比较感染后第0天和第4天时,初次感染和预先感染的动物中差异表达基因(DEG)的数量都非常少。在初次感染和预先感染的动物中,分别比较0天和6天时,共鉴定出2,237个和3,206个DEG。有趣的是,在感染后6天比较预先感染和初次感染的动物时,仅发现18个DEG。 Ingenuity通路分析(IPA)显示,与初次感染的动物相比,预先感染的动物在感染后0天和4天时激活了几种免疫反应,如Th2和Th1途径、自然杀伤细胞、B细胞受体、IL-2和IL-15信号通路。另一方面,比较感染后6天和0天时,初次感染和预先感染的动物中这些途径均被激活,两者之间没有差异。与免疫相关的上游调节因子基因,如TNF、IL-1β、IL-2、IL-5、TGFβ1、IFNγ、TCR、IL-18、IL-6和IL-4,也记录到类似的模式。我们 的结果表明,在感染后0天和4天时,与初次感染的幼崽相比,预先感染的幼崽针对Th1和Th2途径激活了免疫反应,然而,初次感染的幼崽在感染后6天时也出现了相同的免疫反应。我们得出结论,幼龄山羊反复感染会诱导Th1和Th2免疫反应同时早期激活,从而调节蠕虫的定植。