Spinler Jennifer K, Sontakke Amrita, Hollister Emily B, Venable Susan F, Oh Phaik Lyn, Balderas Miriam A, Saulnier Delphine M A, Mistretta Toni-Ann, Devaraj Sridevi, Walter Jens, Versalovic James, Highlander Sarah K
Texas Children's Microbiome Center, Department of Pathology, Texas Children's Hospital, Houston, TXDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX
Texas Children's Microbiome Center, Department of Pathology, Texas Children's Hospital, Houston, TXDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX.
Genome Biol Evol. 2014 Jun 19;6(7):1772-89. doi: 10.1093/gbe/evu137.
The vertebrate gut symbiont Lactobacillus reuteri has diversified into separate clades reflecting host origin. Strains show evidence of host adaptation, but how host-microbe coevolution influences microbial-derived effects on hosts is poorly understood. Emphasizing human-derived strains of L. reuteri, we combined comparative genomic analyses with functional assays to examine variations in host interaction among genetically distinct ecotypes. Within clade II or VI, the genomes of human-derived L. reuteri strains are highly conserved in gene content and at the nucleotide level. Nevertheless, they share only 70-90% of total gene content, indicating differences in functional capacity. Human-associated lineages are distinguished by genes related to bacteriophages, vitamin biosynthesis, antimicrobial production, and immunomodulation. Differential production of reuterin, histamine, and folate by 23 clade II and VI strains was demonstrated. These strains also differed with respect to their ability to modulate human cytokine production (tumor necrosis factor, monocyte chemoattractant protein-1, interleukin [IL]-1β, IL-5, IL-7, IL-12, and IL-13) by myeloid cells. Microarray analysis of representative clade II and clade VI strains revealed global regulation of genes within the reuterin, vitamin B12, folate, and arginine catabolism gene clusters by the AraC family transcriptional regulator, PocR. Thus, human-derived L. reuteri clade II and VI strains are genetically distinct and their differences affect their functional repertoires and probiotic features. These findings highlight the biological impact of microbe:host coevolution and illustrate the functional significance of subspecies differences in the human microbiome. Consideration of host origin and functional differences at the subspecies level may have major impacts on probiotic strain selection and considerations of microbial ecology in mammalian species.
脊椎动物肠道共生菌罗伊氏乳杆菌已分化为不同的进化枝,反映了宿主来源。菌株显示出宿主适应性的证据,但宿主 - 微生物共同进化如何影响微生物对宿主的作用却知之甚少。我们以人类来源的罗伊氏乳杆菌菌株为重点,将比较基因组分析与功能测定相结合,以研究遗传上不同生态型之间宿主相互作用的差异。在进化枝II或VI内,人类来源的罗伊氏乳杆菌菌株的基因组在基因含量和核苷酸水平上高度保守。然而,它们仅共享70 - 90%的总基因含量,表明功能能力存在差异。与人类相关的谱系以与噬菌体、维生素生物合成、抗菌物质产生和免疫调节相关的基因来区分。证明了23株进化枝II和VI菌株在罗伊氏菌素、组胺和叶酸产生上存在差异。这些菌株在调节髓样细胞产生人类细胞因子(肿瘤坏死因子、单核细胞趋化蛋白 - 1、白细胞介素[IL] - 1β、IL - 5、IL - 7、IL - 12和IL - 13)的能力方面也有所不同。对代表性进化枝II和进化枝VI菌株的微阵列分析揭示了AraC家族转录调节因子PocR对罗伊氏菌素、维生素B12、叶酸和精氨酸分解代谢基因簇内基因的全局调控。因此,人类来源的罗伊氏乳杆菌进化枝II和VI菌株在遗传上是不同的,它们的差异影响其功能谱和益生菌特性。这些发现突出了微生物:宿主共同进化的生物学影响,并说明了人类微生物组中亚种差异的功能意义。在亚种水平上考虑宿主来源和功能差异可能对益生菌菌株的选择以及哺乳动物物种中微生物生态学的考量产生重大影响。