Ecology and evolutionary trajectories of morbilliviruses in Neotropical bats

IF 20.5 1区 生物学 Q1 MICROBIOLOGY
Wendy K. Jo, Andres Moreira-Soto, Angélica Cristine Almeida Campos, Luiz Gustavo Bentim Góes, Maria Angélica Mares-Guia, Andrea Rasche, Ana Maria Bispo de Filippis, Gabriela Hernández-Mora, Sham Nambulli, Daniel G. Streicker, W. Paul Duprex, Jan Felix Drexler
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Abstract

Bats are important reservoirs of paramyxoviruses, yet their role in the evolutionary origins of viruses pertaining to the paramyxoviral genus Morbillivirus, such as measles virus, remains unclear. Here, combining field surveys and data mining, we identified six divergent morbilliviruses by investigating wild bats (38/1,629 RT–PCR-positive) and non-human primates (NHP, 13/1,370 RT–PCR-positive) in Brazil and Costa Rica over 14 years. High morbillivirus concentrations of up to 109 RNA copies per g and RNA staining in different organs suggested systemic infection. Of 117 vampire bats, 35.9% had neutralizing antibodies against a primary vampire bat morbillivirus isolate, suggesting frequent non-fatal infections. In vitro assays using bat CD150 for cell entry and partial cross-neutralization of bat-associated morbillivirus by heterologous sera suggested conserved entry and antigenicity. NHP-associated, but not bat-associated morbilliviruses, used human CD150 and nectin-4 cellular receptors, suggesting differential zoonotic potential. Macroevolutionary reconstructions revealed predominance of Neotropical bat hosts during morbilliviral diversification, including bat-associated host shifts into Mexican pigs and Brazilian NHPs. These data argue for increased surveillance, experimental risk assessments and intervention strategies to mitigate risks of reservoir-bound morbilliviruses shifting hosts.

Abstract Image

新热带蝙蝠中麻疹病毒的生态学和进化轨迹
蝙蝠是副粘病毒的重要宿主,但它们在麻疹病毒等副粘病毒属麻疹病毒的进化起源中所起的作用尚不清楚。通过对巴西和哥斯达黎加的野生蝙蝠(38/ 1629 rt - pcr阳性)和非人灵长类动物(NHP, 13/ 1370 rt - pcr阳性)进行14年的调查,我们结合实地调查和数据挖掘,鉴定出6种不同的麻疹病毒。高麻疹病毒浓度高达每克109个RNA拷贝和不同器官的RNA染色提示全身性感染。在117只吸血蝙蝠中,35.9%的人对一种主要的吸血蝙蝠麻疹病毒分离物有中和抗体,这表明频繁的非致命性感染。利用蝙蝠CD150进入细胞和异源血清部分交叉中和蝙蝠相关麻疹病毒的体外实验表明,进入细胞和抗原性是保守的。nhp相关的,而不是蝙蝠相关的麻疹病毒,使用人类CD150和连接素-4细胞受体,提示不同的人畜共患潜力。宏观进化重建揭示了在麻疹病毒多样化过程中新热带蝙蝠宿主的优势,包括蝙蝠相关宿主向墨西哥猪和巴西NHPs的转移。这些数据支持加强监测、实验风险评估和干预策略,以减轻绑定库的麻疹病毒转移宿主的风险。
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来源期刊
Nature Microbiology
Nature Microbiology Immunology and Microbiology-Microbiology
CiteScore
44.40
自引率
1.10%
发文量
226
期刊介绍: Nature Microbiology aims to cover a comprehensive range of topics related to microorganisms. This includes: Evolution: The journal is interested in exploring the evolutionary aspects of microorganisms. This may include research on their genetic diversity, adaptation, and speciation over time. Physiology and cell biology: Nature Microbiology seeks to understand the functions and characteristics of microorganisms at the cellular and physiological levels. This may involve studying their metabolism, growth patterns, and cellular processes. Interactions: The journal focuses on the interactions microorganisms have with each other, as well as their interactions with hosts or the environment. This encompasses investigations into microbial communities, symbiotic relationships, and microbial responses to different environments. Societal significance: Nature Microbiology recognizes the societal impact of microorganisms and welcomes studies that explore their practical applications. This may include research on microbial diseases, biotechnology, or environmental remediation. In summary, Nature Microbiology is interested in research related to the evolution, physiology and cell biology of microorganisms, their interactions, and their societal relevance.
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