Genomic and transcriptomic insights into vertebrate host-specific Lactobacillus johnsonii adaptation in the gastrointestinal tract.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-06-25 Epub Date: 2025-05-13 DOI:10.1128/msphere.00052-25
Keerthikka Ravi, Nicole R Falkowski, Gary B Huffnagle
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引用次数: 0

Abstract

We conducted a comparative genomic analysis of Lactobacillus johnsonii strains isolated from the gastrointestinal tract of diverse vertebrate hosts to explore the genetic basis of host specificity. We then utilized transcriptomics analysis to investigate the expression profile of identified rodent-specific genes in mouse isolate MR1 during in vitro and in vivo growth conditions. There was significant heterogeneity among strains, in both genome sequence and content, with phylogenetic clustering of strains into distinct clades associated with rodent or avian sources. There were not sufficient genomes to identify whether porcine isolates formed their own genetic clade. However, human isolates did not form a distinct clade. Functional enrichment analysis revealed significant enrichment of several genes, including surface proteins and accessory secretory pathway-related genes, as well as tyrosine decarboxylase genes in rodent isolates compared to avian isolates, including in mouse isolate MR1. A total of 40 genes were identified as rodent-associated, and all were transcriptionally active in L. johnsonii MR1. The global transcriptomic analysis of L. johnsonii MR1 was done using cells grown anaerobically, at 37˚C, under both the late-exponential phase and stationary phase, as well as during in vivo growth in the cecum of mono-colonized germ-free mice. Several of these genes were uniquely regulated during late exponential vs stationary phase growth and in vivo colonization in mice, highlighting their potential role in nutrient adaptation and host-microbe interactions.IMPORTANCELactobacillus johnsonii is a well-known probiotic species with health-beneficial properties, including host immunomodulation and pathogen inhibition. Its growing relevance in the medical industry highlights the need to understand its biology, particularly how it adapts to different host environments. In bacteria, niche adaptation is often accompanied by the loss or gain of coding sequences along with changes in the genome size. In this study, we explored the genetic diversity of L. johnsonii strains from the gastrointestinal tracts of various vertebrates such as rodents, birds, swine, and humans. We found associations between genome content and host species of origin and could conceptually demonstrate that these genes are being differentially transcribed under varying conditions. Several functions were associated with specific host groups, suggesting that L. johnsonii strains have adapted to their hosts over time.

基因组学和转录组学研究脊椎动物宿主特异性约氏乳杆菌在胃肠道中的适应性。
我们对从不同脊椎动物宿主胃肠道分离的约氏乳杆菌菌株进行了比较基因组分析,以探索宿主特异性的遗传基础。然后,我们利用转录组学分析来研究小鼠分离MR1在体外和体内生长条件下鉴定的啮齿动物特异性基因的表达谱。菌株之间在基因组序列和内容上存在显著的异质性,菌株的系统发育聚类为与啮齿动物或鸟类来源相关的不同分支。没有足够的基因组来确定猪分离株是否形成了自己的遗传进化支。然而,人类分离株并没有形成一个独特的分支。功能富集分析显示,与禽类分离物(包括小鼠分离物MR1)相比,啮齿动物分离物中有几个基因显著富集,包括表面蛋白和附属分泌途径相关基因,以及酪氨酸脱羧酶基因。共鉴定出40个与啮齿动物相关的基因,这些基因在约氏乳杆菌MR1中均具有转录活性。johnsonii MR1的转录组学分析是在37℃厌氧条件下,在指数后期和固定期以及在单定植无菌小鼠的盲肠中生长的细胞中进行的。这些基因中有几个在小鼠的指数期晚期与稳定期生长和体内定植过程中受到独特的调控,突出了它们在营养适应和宿主-微生物相互作用中的潜在作用。重要性约氏乳杆菌是一种众所周知的益生菌,具有有益健康的特性,包括宿主免疫调节和病原体抑制。它在医疗行业日益增长的相关性突出了了解其生物学的必要性,特别是它如何适应不同的宿主环境。在细菌中,生态位适应通常伴随着编码序列的丢失或获得以及基因组大小的变化。在这项研究中,我们探索了来自啮齿动物、鸟类、猪和人类等多种脊椎动物胃肠道的约氏乳杆菌菌株的遗传多样性。我们发现基因组内容与宿主物种起源之间存在关联,并且可以从概念上证明这些基因在不同条件下被差异转录。一些功能与特定的宿主群体有关,这表明约氏乳杆菌菌株随着时间的推移已经适应了它们的宿主。
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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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