Intensity of infection with intracellular Eimeria spp. and pinworms is reduced in hybrid mice compared to parental subspecies

Genetic diversity in animal immune systems is usually beneficial. In hybrid recombinants, this is less clear, as the immune system could also be impacted by genetic conflicts. In the European house mouse hybrid zone, the long‐standing impression that hybrid mice are more highly parasitized and less fit than parentals persists despite the findings of recent studies. Working across a novel transect, we assessed infections by intracellular protozoans, Eimeria spp., and infections by extracellular macroparasites, pinworms. For Eimeria, we found lower intensities in hybrid hosts than in parental mice but no evidence of lowered probability of infection or increased mortality in the centre of the hybrid zone. This means ecological factors are very unlikely to be responsible for the reduced load of infected hybrids. Focusing on parasite intensity (load in infected hosts), we also corroborated reduced pinworm loads reported for hybrid mice in previous studies. We conclude that intensity of diverse parasites, including the previously unstudied Eimeria, is reduced in hybrid mice compared to parental subspecies. We suggest caution in extrapolating this to differences in hybrid host fitness in the absence of, for example, evidence for a link between parasitemia and health.Peer Reviewe

Shrews (Mammalia, Eulipotyphla) from a biodiversity hotspot, Mount Nimba (West Africa), with a field identification key to species

In this study, we collected 226 shrew specimens originating from 16 localities on the Guinean and Liberian sides of Mount Nimba. We surveyed all major vegetation zones from 400 to 1600 m above sea level (asl), including forest and savannah habitats. We recorded 11 species, whose identifications were confirmed by genetic analyses and classical morphometrics. Furthermore, we provide cytogenetic data for five of these species. The shrew community at Mount Nimba is composed of a mix of both savannah- and forest-dependent species, which is related to the peculiar position of Mount Nimba situated at the transition between lowland rainforest to the south and Guinean woodlands to the north. We recorded 11 species of shrews in syntopy in lowland rainforest, seven in edaphic savannah and mountain forest, and five in high-altitude savannah at 1600 m asl. Based on morphometric analyses, we show that these syntopic species separate along a size axis, allowing species to occupy different ecological niches, which we speculate allows them to access different food resources. We also highlight that Crocidura theresae Heim de Balsac, 1968 from Mount Nimba has a different karyotype from that described in Côte d’Ivoire. Finally, we develop a novel identification key for shrews from Mount Nimba using external characters and standard body measurements, allowing it to be used in the field on live specimens. In total 12 shrew species are now known from Mount Nimba, which highlights its exceptional position as a tropical African biodiversity hotspot.https://sciencepress.mnhn.fr/en/periodiques/zoosystemadm2022Mammal Research InstituteZoology and Entomolog

Annual (2023) taxonomic update of RNA-directed RNA polymerase-encoding negative-sense RNA viruses (realm Riboviria: kingdom Orthornavirae: phylum Negarnaviricota)

55 Pág.In April 2023, following the annual International Committee on Taxonomy of Viruses (ICTV) ratification vote on newly proposed taxa, the phylum Negarnaviricota was amended and emended. The phylum was expanded by one new family, 14 new genera, and 140 new species. Two genera and 538 species were renamed. One species was moved, and four were abolished. This article presents the updated taxonomy of Negarnaviricota as now accepted by the ICTV.This work was supported in part through the Laulima Government Solutions, LLC, prime contract with the U.S. National Institute of Allergy and Infec tious Diseases (NIAID) under Contract No. HHSN272201800013C. J.H.K. performed this work as an employee of Tunnell Government Services (TGS), a subcontractor of Laulima Government Solutions, LLC, under Contract No. HHSN272201800013C. U.J.B. was supported by the Division of Intramural Resarch, NIAID. This work was also funded in part by Contract No. HSHQDC15-C-00064 awarded by DHS S and T for the management and operation of The National Biodefense Analysis and Countermeasures Centre, a federally funded research and development centre operated by the Battelle National Biodefense Institute (V.W.); and NIH contract HHSN272201000040I/HHSN27200004/D04 and grant R24AI120942 (N.V., R.B.T.). S.S. acknowl edges support from the Mississippi Agricultural and Forestry Experiment Station (MAFES), USDA-ARS project 58-6066-9-033 and the National Institute of Food and Agriculture, U.S. Department of Agriculture, Hatch Project, under Accession Number 1021494. The funders had no role in the design of the study; in the collection, analysis, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results. The views and conclusions contained in this document are those of the authors and should not be interpreted as necessarily representing the official policies, either expressed or implied, of the U.S. Department of the Army, the U.S. Department of Defence, the U.S. Department of Health and Human Services, including the Centres for Disease Control and Prevention, the U.S. Department of Homeland Security (DHS) Science and Technology Directorate (S and T), or of the institutions and companies affiliated with the authors. In no event shall any of these entities have any responsibility or liability for any use, misuse, inability to use, or reliance upon the information contained herein. The U.S. departments do not endorse any products or commercial services mentioned in this publication. The U.S. Government retains and the publisher, by accepting the article for publication, acknowledges that the U.S.Government retains a non-exclusive, paid up, irrevocable, world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so, for U.S. Government purposes.Peer reviewe

STRUCTURE parameter settings

Parameter settings used in the software STRUCTURE, to infer population genetic structure of Mastomys natalensis based on microsatellite genotypes

MrBayes input files

Input files for the software MrBayes of arenavirus partial L, NP and GPC sequences, containing the used alignments and parameter settings to infer the phylogenetic trees displayed in the manuscript

Microsatellite genotypes_GryseelsPLoSPathogens2016

Genotypes of 15 microsatellite loci of 760 Mastomys natalensis individuals from Tanzania

Landscape cost values for GIS and Circuitscape analyses_GryseelsPLoSPathogens2016

Cost values of land use elements that occurred in our study area in terms of Mastomys natalensis habitat quality

When Viruses Don’t Go Viral: The Importance of Host Phylogeographic Structure in the Spatial Spread of Arenaviruses

<div><p>Many emerging infections are RNA virus spillovers from animal reservoirs. Reservoir identification is necessary for predicting the geographic extent of infection risk, but rarely are taxonomic levels below the animal species considered as reservoir, and only key circumstances in nature and methodology allow intrinsic virus-host associations to be distinguished from simple geographic (co-)isolation. We sampled and genetically characterized in detail a contact zone of two subtaxa of the rodent <i>Mastomys natalensis</i> in Tanzania. We find two distinct arenaviruses, Gairo and Morogoro virus, each spatially confined to a single <i>M</i>. <i>natalensis</i> subtaxon, only co-occurring at the contact zone’s centre. Inter-subtaxon hybridization at this centre and a continuum of quality habitat for <i>M</i>. <i>natalensis</i> show that both viruses have the ecological opportunity to spread into the other substaxon’s range, but do not, strongly suggesting host-intrinsic barriers. Such barriers could explain why human cases of another <i>M</i>. <i>natalensis</i>-borne arenavirus, Lassa virus, are limited to West Africa.</p></div

Phylogenomic characterization of Lopma virus and Praja virus, two novel rodent-borne arteriviruses

Recent years have witnessed the discovery of several new viruses belonging to the family Arteriviridae, expanding the known diversity and host range of this group of complex RNA viruses. Although the pathological relevance of these new viruses is not always clear, several well-studied members of the family Arteriviridae are known to be important animal pathogens. Here, we report the complete genome sequences of four new arterivirus variants, belonging to two putative novel species. These new arteriviruses were discovered in African rodents and were given the names Lopma virus and Praja virus. Their genomes follow the characteristic genome organization of all known arteriviruses, even though they are only distantly related to currently known rodent-borne arteriviruses. Phylogenetic analysis shows that Lopma virus clusters in the subfamily Variarterivirinae, while Praja virus clusters near members of the subfamily Heroarterivirinae: the yet undescribed forest pouched giant rat arterivirus and hedgehog arterivirus 1. A co-divergence analysis of rodent-borne arteriviruses confirms that they share similar phylogenetic patterns with their hosts, with only very few cases of host shifting events throughout their evolutionary history. Overall, the genomes described here and their unique clustering with other arteriviruses further illustrate the existence of multiple rodent-borne arterivirus lineages, expanding our knowledge of the evolutionary origin of these viruses

Development of eight polymorphic microsatellite markers in the Black and Rufous sengi, Rhynchocyon petersi

MICROSATELLITE LETTERSThe Black and Rufous sengi, Ryhnchocyon petersi, is endemic to a limited range in East Africa. We report the development of eight polymorphic microsatellites using next generation sequencing technology. Eighteen individuals from Zaraninge forest (Saadani National Park, Tanzania) were genotyped. The number of alleles per locus ranged from 2 to 6, while the observed and expected heterozygosities varied from 0.17 to 0.82 and from 0.25 to 0.81, respectively. No locus deviated from Hardy–Weinberg equilibrium. These microsatellite markers will be useful tools to study the effect of habitat fragmentation on the population genetic structure of R. petersi