Molecular ecology of novel amdoparvoviruses and old protoparvoviruses in Spanish wild carnivorans.

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES Infection Genetics and Evolution Pub Date : 2025-01-12 DOI:10.1016/j.meegid.2025.105714
Marta Canuti, Francesco Mira, Diego Villanúa, Ruth Rodríguez-Pastor, Annalisa Guercio, Fermín Urra, Javier Millán
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Abstract

Wild carnivorans are key hosts of parvoviruses of relevance for animal health and wildlife conservation. However, the distribution and diversity of parvoviruses among wild carnivorans are under-investigated, particularly in Southern Europe. We evaluated the presence, spread, and diversity of multi-host protoparvoviruses (canine parvovirus type 2 (CPV-2), feline panleukopenia virus (FPV)), and amdoparvoviruses in 12 carnivoran species from Northern Spain to explore viral ecology. Broad-range PCRs were used to screen spleens (N = 157) and intestines (N = 116) from 171 road-killed mustelids, viverrids, and felids; identified viruses were molecularly characterized. We detected an Asian-like CPV-2c strain in the spleen of one wildcat (Felis silvestris, 1/40, 2.5 %), a globally distributed FPV strain in the spleen of one Eurasian badger (Meles meles, 1/35, 2.9 %), a novel amdoparvovirus (European mustelid amdoparvovirus 1), in the intestine and spleen of one stone marten (Martes foina, 1/16, 6.3 %) and in the spleen of one Eurasian badger (1/35, 2.9 %), the red fox fecal amdovirus (RFFAV) in the intestine and spleen of three wildcats (3/40, 7.5 %), and a novel amdoparvovirus closely related to RFFAV (European felid amdoparvovirus 1) in one wildcat (1/40, 2.5 %). We observed a correlation between the phylogeny of carnivorans and the one of amdoparvoviruses, possibly indicating virus-host co-evolution. Species originating from North America and Eurasia formed different clades, indicating local segregation in the absence of man-linked transboundary movements. In contrast, CPV-2 and FPV strains were internationally dispersed. Different parvovirus species co-occur in sympatric host populations, and higher viral diversity and additional hosts will likely be identified in future studies.

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西班牙野生食肉动物新型虫帕病毒和古老原虫病毒的分子生态学研究。
野生食肉动物是与动物健康和野生动物保护相关的细小病毒的主要宿主。然而,细小病毒在野生食肉动物中的分布和多样性尚未得到充分调查,特别是在南欧。我们评估了多宿主原细小病毒(犬细小病毒2型(CPV-2),猫泛白细胞减少病毒(FPV))和amdoparvovirus)在西班牙北部12种食肉动物中的存在,传播和多样性,以探索病毒生态学。采用广谱pcr技术筛选171只公路死亡鼠、猪瘟和猫科动物的脾脏(N = 157)和肠道(N = 116);鉴定出的病毒具有分子特征。在1只野猫(Felis silvestris, 1/40, 2.5 %)的脾脏中检测到一种亚洲样CPV-2c毒株,在1只欧亚獾(Meles Meles, 1/35, 2.9 %)的脾脏中检测到一种全球分布的FPV毒株,在1只石貂(Martes foina, 1/16, 6.3 %)的肠道和脾脏中检测到一种新型amdoparvovirus(欧洲鼠系amdoparvovirus 1),在1只欧亚獾(1/35,2.9 %)的脾脏中检测到一种新型amdoparvovirus(欧洲鼠系amdoparvovirus 1),在3只野猫(3/40,7.5 %)的肠道和脾脏中检测到红狐粪amdovirus (RFFAV)。在一只野猫身上发现一种与RFFAV(欧洲野猫amdoparvovirus 1)密切相关的新型amdoparvovirus(1/40, 2.5 %)。我们观察到食肉动物的系统发育与amdoparvov的系统发育之间存在相关性,可能表明病毒与宿主的共同进化。来自北美和欧亚大陆的物种形成了不同的分支,表明在没有人类跨界运动的情况下存在局部分离。相比之下,CPV-2和FPV菌株在国际上分散。不同的细小病毒种类共存于同域宿主种群中,在未来的研究中可能会发现更高的病毒多样性和更多的宿主。
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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
期刊最新文献
Genetic variations underlying aminoglycoside resistance in antibiotic-induced Mycobacterium intracellulare mutants. Revealing a novel GI-19 lineage infectious bronchitis virus sub-genotype with multiple recombinations in South Korea using whole-genome sequencing. Considerable genetic diversity within Paragonimus heterotremus in Luang Prabang, northern Lao People's Democratic Republic. Molecular ecology of novel amdoparvoviruses and old protoparvoviruses in Spanish wild carnivorans. Genotypic and phenotypic diversity of Mycobacterium tuberculosis strains from eastern India.
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