Mitri Christian, Bischoff Emmanuel, Belda Cuesta Eugeni, Volant Stevenn, Ghozlane Amine, Eiglmeier Karin, Holm Inge, Dieme Constentin, Brito-Fravallo Emma, Guelbeogo Wamdaogo M, Sagnon N'Fale, Riehle Michelle M, Vernick Kenneth D
Unit of Insect Vector Genetics and Genomics, Department of Parasites and Insect Vectors, Institut Pasteur, Paris, France.
CNRS Unit of Evolutionary Genomics, Modeling, and Health (UMR2000), Institut Pasteur, Paris, France.
Front Microbiol. 2020 Feb 26;11:306. doi: 10.3389/fmicb.2020.00306. eCollection 2020.
The commensal gut microbiome is contained by the enteric epithelial barrier, but little is known about the degree of specificity of host immune barrier interactions for particular bacterial taxa. Here, we show that depletion of leucine-rich repeat immune factor APL1 in the Asian malaria mosquito is associated with higher midgut abundance of just the family , and not generalized dysbiosis of the microbiome. The effect is explained by the response of a narrow clade containing two main taxa related to and . Analysis of field samples indicate that these two taxa are recurrent members of the wild microbiome. Triangulation using sequence and functional data incriminated relatives of and NFIX57 as candidates for the component, and , , and LTGPAF-6F as candidates for the component. APL1 presence is associated with host ability to specifically constrain the abundance of a narrow microbiome clade of the , and the immune factor may promote homeostasis of this clade in the enteric microbiome for host benefit.
共生肠道微生物群被肠道上皮屏障所包裹,但对于宿主免疫屏障与特定细菌类群相互作用的特异性程度,我们了解甚少。在此,我们表明,亚洲疟蚊中富含亮氨酸重复序列的免疫因子APL1的缺失仅与一个科的中肠丰度增加有关,而不是微生物群的普遍失调。这种效应可以通过一个狭窄进化枝的反应来解释,该进化枝包含与 和 相关的两个主要类群。对野外样本的分析表明,这两个类群是野生 微生物群的常见成员。利用序列和功能数据进行三角测量,确定了 和NFIX57的亲属作为 成分的候选者,以及 、 、 和LTGPAF - 6F作为 成分的候选者。APL1的存在与宿主特异性限制 一个狭窄微生物进化枝丰度的能力有关,并且该免疫因子可能促进肠道微生物群中这个进化枝的稳态,以利于宿主。