Université Paris-Saclay, INRAE, AgroParisTech, GABI, 78350, Jouy-en-Josas, France.
Mouse Genetics Laboratory, Department of Genomes and Genetics, Institut Pasteur, Paris, France.
Genet Sel Evol. 2022 Jan 29;54(1):7. doi: 10.1186/s12711-022-00699-6.
Salmonella Enteritidis (SE) is one of the major causes of human foodborne intoxication resulting from consumption of contaminated poultry products. Genetic selection of animals that are more resistant to Salmonella carriage and modulation of the gut microbiota are two promising ways to decrease individual Salmonella carriage. The aims of this study were to identify the main genetic and microbial factors that control the level of Salmonella carriage in chickens (Gallus gallus) under controlled experimental conditions. Two-hundred and forty animals from the White Leghorn inbred lines N and 6 were infected by SE at 7 days of age. After infection, animals were kept in isolators to reduce recontamination of birds by Salmonella. Caecal contents were sampled at 12 days post-infection and used for DNA extraction. Microbiota DNA was used to measure individual counts of SE by digital PCR and to determine the bacterial taxonomic composition, using a 16S rRNA gene high-throughput sequencing approach.
Our results confirmed that the N line is more resistant to Salmonella carriage than the 6 line, and that intra-line variability is higher for the 6 line. Furthermore, the 16S analysis showed strong significant differences in microbiota taxonomic composition between the two lines. Among the 617 operational taxonomic units (OTU) observed, more than 390 were differentially abundant between the two lines. Furthermore, within the 6 line, we found a difference in the microbiota taxonomic composition between the high and low Salmonella carriers, with 39 differentially abundant OTU. Using metagenome functional prediction based on 16S data, several metabolic pathways that are potentially associated to microbiota taxonomic differences (e.g. short chain fatty acids pathways) were identified between high and low carriers.
Overall, our findings demonstrate that the caecal microbiota composition differs between genetic lines of chickens. This could be one of the reasons why the investigated lines differed in Salmonella carriage levels under experimental infection conditions.
肠炎沙门氏菌(SE)是由食用受污染的家禽产品引起的人类食源性中毒的主要原因之一。选择对沙门氏菌携带更具抗性的动物和调节肠道微生物群是降低个体沙门氏菌携带量的两种有前途的方法。本研究的目的是在受控实验条件下确定控制鸡(Gallus gallus)中沙门氏菌携带水平的主要遗传和微生物因素。从白来航鸡的 N 系和 6 系两个近交系中选择 240 只鸡,在 7 日龄时感染 SE。感染后,将动物饲养在隔离器中,以减少沙门氏菌对鸟类的再次污染。在感染后 12 天采集盲肠内容物进行 DNA 提取。使用微生物 DNA 通过数字 PCR 测量 SE 的个体计数,并使用 16S rRNA 基因高通量测序方法确定细菌分类组成。
我们的结果证实,N 系比 6 系更能抵抗沙门氏菌的携带,而 6 系的系内变异性更高。此外,16S 分析显示,两条线之间的微生物群分类组成存在显著差异。在所观察到的 617 个操作分类单元(OTU)中,超过 390 个 OTU 在两条线之间差异丰富。此外,在 6 系中,我们发现高和低沙门氏菌携带者之间的微生物群分类组成存在差异,有 39 个差异丰富的 OTU。使用基于 16S 数据的宏基因组功能预测,确定了一些与微生物群分类差异潜在相关的代谢途径(例如短链脂肪酸途径)。
总的来说,我们的研究结果表明,鸡的盲肠微生物群组成在遗传系之间存在差异。这可能是研究的两个系在实验感染条件下沙门氏菌携带水平不同的原因之一。