墨西哥无尾蝙蝠和北美同域蝙蝠中地理上广泛分布的新型嗜血支原体和巴尔通体。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY mSphere Pub Date : 2025-01-28 Epub Date: 2024-12-11 DOI:10.1128/msphere.00116-24
Daniel J Becker, Kristin E Dyer, Lauren R Lock, Beckett L Olbrys, Shawn A Pladas, Anushka A Sukhadia, Bret Demory, Juliana Maria Nunes Batista, Micaela Pineda, Nancy B Simmons, Amanda M Adams, Winifred F Frick, M Teague O'Mara, Dmitriy V Volokhov
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引用次数: 0

摘要

在蝙蝠中,特别是在北美,细菌病原体的特征仍然很差。我们描述了在三个墨西哥无尾蝙蝠(Tadarida brasiliensis)群体中发现的新型(在某些情况下是全裸的)血浆(阳性10.1%)和巴尔通体(阳性25.6%),这是一种可以季节性旅行数百公里的部分迁徙物种。分子分析在新热带软体动物蝙蝠中鉴定出三种与另一种新的念珠菌属最相似的念珠菌属。我们还在同域性洞穴肌炎(myotis velifer)和苍白蝙蝠(Antrozous pallidus)中检测到新的血浆,后者96.5%的序列与候选血人支原体相关。我们鉴定出9个巴尔通体基因群,其中洞穴肌炎的巴尔通体基因群与mayotimonensis候选巴尔通体的相似性为96.1%。我们还在迁徙的墨西哥无尾蝙蝠中检测到罗查利巴尔通体,这是该人类病原体在翼翅目中的首次报道。在迁徙的墨西哥无尾蝙蝠在北美居住期间,每月对其进行抽样调查,发现这两种细菌病原体的感染具有明显的季节性,在春季迁徙后流行率上升,在生育季节达到高峰,在秋季迁徙时下降。这里观察到的血浆和巴尔通体的大量多样性和季节性表明,有必要对蝙蝠进行额外的纵向、基因组和免疫学研究,以告知One Health方法。重要性:已经对蝙蝠进行了大量的病毒采样,但对细菌病原体的研究仍然不足。然而,细菌性病原体可以对人类健康和蝙蝠的发病率甚至死亡率产生重大影响。血浆和巴尔通体是蝙蝠中特别感兴趣的兼性细胞内细菌,因为它们的高流行率和大量的遗传多样性。调查还支持这些细菌从蝙蝠到人类的貌似人畜共患传播,包括血人支原体候选菌和马约提蒙巴尔通体候选菌。因此,有必要在全球蝙蝠多样性(超过1480种)中对这些细菌进行更深入的表征,以了解蝙蝠和人类的感染风险,尽管迄今为止对北美蝙蝠进行的监测很少。我们在这里描述了新的(在某些情况下是全身性的)血浆和巴尔通体跨越三个殖民地的墨西哥无尾蝙蝠和同域蝙蝠物种。我们发现这些病原体具有高度的遗传多样性和季节性,包括与人类病原体密切相关的谱系,如罗查利姆巴尔通体。
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Geographically widespread and novel hemotropic mycoplasmas and bartonellae in Mexican free-tailed bats and sympatric North American bat species.

Bacterial pathogens remain poorly characterized in bats, especially in North America. We describe novel (and in some cases panmictic) hemoplasmas (10.1% positivity) and bartonellae (25.6% positivity) across three colonies of Mexican free-tailed bats (Tadarida brasiliensis), a partially migratory species that can seasonally travel hundreds of kilometers. Molecular analyses identified three novel Candidatus hemoplasma species most similar to another novel Candidatus species in Neotropical molossid bats. We also detected novel hemoplasmas in sympatric cave myotis (Myotis velifer) and pallid bats (Antrozous pallidus), with sequences in the latter 96.5% related to Candidatus Mycoplasma haematohominis. We identified nine Bartonella genogroups, including those in cave myotis with 96.1% similarity to Candidatus Bartonella mayotimonensis. We also detected Bartonella rochalimae in migratory Mexican free-tailed bats, representing the first report of this human pathogen in the Chiroptera. Monthly sampling of migratory Mexican free-tailed bats during their North American occupancy period also revealed significant seasonality in infection for both bacterial pathogens, with prevalence increasing following spring migration, peaking in the maternity season, and declining into fall migration. The substantial diversity and seasonality of hemoplasmas and bartonellae observed here suggest that additional longitudinal, genomic, and immunological studies in bats are warranted to inform One Health approaches.

Importance: Bats have been intensively sampled for viruses but remain mostly understudied for bacterial pathogens. However, bacterial pathogens can have significant impacts on both human health and bat morbidity and even mortality. Hemoplasmas and bartonellae are facultative intracellular bacteria of special interest in bats, given their high prevalence and substantial genetic diversity. Surveys have also supported plausible zoonotic transmission of these bacteria from bats to humans, including Candidatus Mycoplasma haematohominis and Candidatus Bartonella mayotimonensis. Greater characterization of these bacteria across global bat diversity (over 1,480 species) is therefore warranted to inform infection risks for both bats and humans, although little surveillance has thus far been conducted in North American bats. We here describe novel (and in some cases panmictic) hemoplasmas and bartonellae across three colonies of Mexican free-tailed bats and sympatric bat species. We find high genetic diversity and seasonality of these pathogens, including lineages closely related to human pathogens, such as Bartonella rochalimae.

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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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