Evidence map›Paper›PMID 41299624›Full record

ArticleMicrobiome2025

Virome characterization of wild small mammals provides new insight into zoonotic pathogens in West Africa.

Xiao-Ai Zhang, Mei-Qi Zhang, Ya-Wen Liu, Lei Lin, Jing-Tao Zhang, Thomoshire George, Mohamed Boie Jalloh, Stephen Sevalie, Kandeh Bassie Kargbo, Bao-Gui Jiang and 9 more

Abstract read
In one paragraph

Article in Microbiome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Xiao-Ai Zhang *State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Mei-Qi Zhang *State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Ya-Wen Liu *Division of HIV/AIDS and Sex-Transmitted Virus Vaccines, National Institutes for Food and Drug Control (NIFDC), Beijing, 102629, China.
Lei Lin *State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Jing-Tao ZhangState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Thomoshire GeorgeDefense Medical Services (34 Military Hospital), Republic of Sierra Leone Armed Forces, Wilberforce, Freetown, Sierra Leone.
Mohamed Boie JallohDefense Medical Services (34 Military Hospital), Republic of Sierra Leone Armed Forces, Wilberforce, Freetown, Sierra Leone.
Stephen SevalieDefense Medical Services (34 Military Hospital), Republic of Sierra Leone Armed Forces, Wilberforce, Freetown, Sierra Leone.
Kandeh Bassie KargboDefense Medical Services (34 Military Hospital), Republic of Sierra Leone Armed Forces, Wilberforce, Freetown, Sierra Leone.
Bao-Gui JiangState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Zhi-Qiang MiState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Shu-Chao WangChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, 130122, China.
Guang-Qian SiState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Lei ZhangState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Li-Qun FangState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China.
Wei-Wei ChenFifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China. cww302@126.com.
Gang DongState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China. donggang@bmi.ac.cn.
Wei-Jin HuangDivision of HIV/AIDS and Sex-Transmitted Virus Vaccines, National Institutes for Food and Drug Control (NIFDC), Beijing, 102629, China. huangweijin@nifdc.org.cn.
Wei LiuState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, 100071, China. lwbime@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA significant number of infectious diseases affecting humans have been associated with zoonotic viruses. Wild small mammals, such as bats, rodents, and shrews, serve as natural reservoirs for a multitude of zoonotic viruses, particularly in Africa, where zoonosis is prevalent. Nevertheless, our knowledge of the virome composition within these hosts remains limited, impeding a more profound understanding of spillover events into human populations.

resultsWe employed a viral metagenomics approach to characterize the virome in 846 wild small mammals sampled from Sierra Leone. Based on the complete RNA-dependent RNA polymerase genome, a total of 39 RNA viruses infecting mammals were identified, comprising 13 known viruses and 26 novel viruses. Notably, the Paramyxoviridae family exhibited the highest diversity of viral species across all three orders of wild mammal. The animal species Hipposideros jonesi and Lophuromys chrysopus were found to harbor the highest viral richness. Among these viral species, 15 were identified as cross-species transmitted viruses shared among different animal species, 3 were classified as zoonotic (Encephalomyocarditis virus, Rocahepevirus sp., and Lassa virus), while 3 others posed a potential risk for spillover (melian virus, Rodent hepacivirus, Hunnivirus A). Cross-species transmission analysis revealed that rodents played central roles in virus sharing, while cross-order viral transmission was less likely to occur in bats. Among 26 newly identified viruses, four viruses (Bat ledantevirus 2, Rattus rattus jeilongvirus, Miniopterus inflatus ribovirus, and Rat mamastrovirus) were predicted to have high zoonotic potential. Among them, Bat ledantevirus 2 exhibited the highest zoonotic potential and phylogenetic relatedness to the known human-infecting virus (Le Dantec virus). Further seroepidemiological analysis in patients, using single-round infectious virus particles as antigens, revealed the presence of neutralizing antibodies against Bat ledantevirus 2, a novel virus belonging to the Rhabdoviridae family.

conclusionsThese findings highlight the critical need for enhanced surveillance at the human-animal interface in order to identify viruses with cross-species transmission potential prior to their spillover into human population. Video Abstract.

Indexed as

Animals, WildMammalsRNA VirusesViral ZoonosesViromeZoonosesAfrica, WesternAnimalsChiropteraDisease ReservoirsGenome, ViralHumansMetagenomicsPhylogenyRodentiaShrewsMammalViromeVirusWest AfricaZoonotic pathogens

Identifiers

PMID41299624
PMCPMC12659560

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.