Browsing by Author "Gryseels, Sophie"

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Arenavirus dynamics in experimentally and naturally infected rodents
(EcoHealth Alliance, 2017-06) Marien, Joachim; Borremans, Benny; Gryseels, Sophie; Broecke, Bram Vanden; Becker-Ziaja, Beate; Makundi, Rhodes; Massawe, Apia; Reijniers, Jonas; Leirs, Herwig
Infectious diseases of wildlife are typically studied using data on antibody and pathogen levels. In order to interpret these data, it is necessary to know the course of antibodies and pathogen levels after infection. Such data are typically collected using experimental infection studies in which host individuals are inoculated in the laboratory and sampled over an extended period, but because laboratory conditions are controlled and much less variable than natural conditions, the immune response and pathogen dynamics may differ. Here, we compared Morogoro arenavirus infection patterns between naturally and experimentally infected multimammate mice (Mastomys natalensis). Longitudinal samples were collected during three months of bi-weekly trapping in Morogoro, Tanzania, and antibody titer and viral RNA presence were determined. The time of infection was estimated from these data using a recently developed Bayesian approach, which allowed us to assess whether the natural temporal patterns match the previously observed patterns in the laboratory. A good match was found for 52% of naturally infected individuals, while most of the mismatches can be explained by the presence of chronically infected individuals (35%), maternal antibodies (10%), and an antibody detection limit (25%). These results suggest that while laboratory data are useful for interpreting field samples, there can still be differences due to conditions that were not tested in the laboratory.
Density dependence and persistence of Morogoro arenavirus transmission in a fluctuating population of its reservoir host
(British Ecological Society, 2019-07-21) Mariën, Joachim; Borremans, Benny; Verhaeren, Christophe; Kirkpatrick, Lucinda; Gryseels, Sophie; Bellocq, Joëlle Goüy de; Günther, Stephan; Sabuni, Christopher A.; Massawe, Apia W.; Reijniers, Jonas; Leirs, Herwig
A key aim in wildlife disease ecology is to understand how host and parasite characteristics influence parasite transmission and persistence. Variation in host population density can have strong impacts on transmission and outbreaks, and theory predicts particular transmission–density patterns depending on how para- sites are transmitted between individuals. Here, we present the results of a study on the dynamics of Morogoro arenavirus in a population of multimammate mice (Mastomys natalensis). This widespread African rodent, which is also the reservoir host of Lassa arenavirus in West Africa, is known for its strong seasonal density fluctuations driven by food availability. We investigated to what degree virus transmission changes with host population density and how the virus might be able to persist during periods of low host density.A seven‐year capture–mark–recapture study was conducted in Tanzania where rodents were trapped monthly and screened for the presence of antibodies against Morogoro virus. Observed seasonal seroprevalence patterns were com- pared with those generated by mathematical transmission models to test different hypotheses regarding the degree of density dependence and the role of chroni- cally infected individuals. We observed that Morogoro virus seroprevalence correlates positively with host density with a lag of 1–4 months. Model results suggest that the observed sea- sonal seroprevalence dynamics can be best explained by a combination of verti- cal and horizontal transmission and that a small number of animals need to be infected chronically to ensure viral persistence. Transmission dynamics and viral persistence were best explained by the existence of both acutely and chronically infected individuals and by seasonally changing transmission rates. Due to the presence of chronically infected rodents, rodent control is unlikely to be a feasible approach for eliminating arenaviruses such as Lassa virus from Mastomys populations.
"Gairovirus,anovelarena virusof the widespread Mastomys natalensis: genetically divergent,but ecologically similar to Lassa and Morogoro viruses
(ElsevierInc, 2015) Gryseels, Sophie; Rieger, Toni; Oestereich, Lisa; Cuypers, Bart; Borremans, Benny; Makundi, Rhodes; Leirs, Herwig; Günther, Stephan; Goüy de Bellocq, Joëlle
Despite itsnearpan-Africanrange,theNatalmultimammatemouse, Mastomysnatalensis, carriesthe human pathogenLassavirusonlyinWestAfrica,whiletheseeminglynon-pathogenicarenaviruses Mopeia, Morogoro,andLunahavebeendetectedinthissemi-commensalrodentinMozambique/ Zimbabwe,TanzaniaandZambia,respectively.Here,wedescribeanovelarenavirusin M. natalensis from Gairo districtofcentralTanzania,forwhichweproposethename “Gairo virus”. Surprisingly,thevirusis not closelyrelatedwithMorogorovirusthatinfects M. natalensis only 90kmsouthofGairo,butclusters phylogeneticallywithMobala-likevirusesthatinfectnon-M. natalensis host speciesinCentralAfrican RepublicandEthiopia.Despitetheevolutionarydistance,Gairovirussharesbasicecologicalfeatures with theother M. natalensis-borne virusesLassaandMorogoro.Ourdatashowthat M. natalensis, carrying distantlyrelatedviruseseveninthesamegeographicalarea,isapotentreservoirhostfora varietyofarenaviruses.
Presence of Mopeia Virus, an African Arenavirus, Related to Biotope and Individual Rodent Host Characteristics: Implications for Virus Transmission
(2011) Borremans, Benny; Leirs, Herwig; Gryseels, Sophie; Gu¨ nther, Stephan; Makundi, Rhodes; de Bellocq, Joe¨ lle Gou¨ y
The East African Mopeia virus (MOPV) is an arenavirus closely related to the highly pathogenic West African Lassa virus, even sharing the same reservoir rodent host Mastomys natalensis. Because MOPV is not known to cause human disease, it offers a unique alternative for studying Lassa virus transmission. We investigated how habitat, population density, and host characteristics are related to MOPV occurrence in M. natalensis populations in Morogoro, Tanzania. In 3 contrasting habitats, 511 M. natalensis individuals were trapped, 12.1% (58/480 tested individuals) of which tested seropositive for antibodies and 8.4% (41/489 tested individuals) for MOPVRNA. Although population densities differ among habitats, density and habitat were not significantly correlated to MOPV-RNA or antibody presence. Antibody presence was not significantly correlated with any host characteristics. In contrast, MOPV-RNA presence was inversely related to weight, age, sexual maturity, and body mass index. The model with body mass index as predictor was the best at predicting infection probability. Thirty-five individuals were exclusively MOPV-RNA positive, 52 were exclusively antibody positive, and 6 were both MOPV-RNA and antibody positive. Interpreting these data using experimental infection results from studies on other arenaviruses, this would mean that these infections were very recent, old, and roughly 1–3 weeks after infection, respectively. The higher RNA prevalence in juveniles implies vertical transmission, or that horizontal transmission occurs mainly in this age group due to lack of immunity, higher susceptibility, and/or higher juvenile contact rates. This study demonstrates the strength of combining information on antibody and RNA presence with host characteristics, and how this information can provide valuable insights into transmission dynamics.
Subspecific rodent taxa as the relevant host taxonomic level for mammarenavirus host specificity
(Elsevier Inc., 2023) Cuypers, Laura N.; Gryseels, Sophie; Baird, Stuart J.E.; Sabuni, Christopher A.; Katakweba, Abdul S.; van den Burg, Sebastiaan R.M.; Bryja, Josef; Leirs, Herwig; de Bellocq, Joëlle Goüy
Mastomys natalensis-borne mammarenaviruses appear specific to subspecific M. natalensis taxa rather than to the whole species. Yet mammarenaviruses carried by M. natalensis are known to spill over and jump hosts in northern sub-Saharan Africa. Phylogeographic studies increasingly show that, like M. natalensis, small mammals in sub- Saharan Africa are often genetically structured into several subspecific taxa. Other mammarenaviruses may thus also form virus-subspecific host taxon associations. To investigate this, and if mammarenaviruses carried by M. natalensis in southern Africa are less prone to spill-over, we screened 1225 non-M. natalensis samples from Tanzania where many small mammal taxa meet. We found mammarenavirus RNA in 6 samples. Genetic/genomic characterisation confirmed they were not spill-over from M. natalensis. We detected host jumps among rodent tribe members and an association between mammarenaviruses and subspecific taxa of Mus minutoides and Grammomys surdaster, indicating host genetic structure may be crucial to understand virus distribution and host specificity.