Breeding systems exert profound effects on the amount and distribution of genetic diversity within and among populations. Knowledge of breeding systems is also important for understanding dynamics between coevolving organisms, e.g., pathogen-host interactions. Here we study the breeding system of the obligate anther smut Microbotryum violaceum on Silene dioica. Microbotryum violaceum is capable of both inbreeding and outcrossing, but several recent studies on other host races have indicated that automixis via intrapromycelial mating is the predominant breeding system. Compared with conjugations between cells from different meioses, automixis results in slower loss of heterozygosity and faster production of infectious hypha. However, high rates of intrapromycelial matings have been suggested to invoke a fitness cost due to production of fewer infectious dikaryons. Working with single strains under standardized laboratory conditions, we studied traits that could influence the distribution of genetic variability and pathogen fitness. We found that intrapromycelial mating is the dominant conjugation form for M. violaceum var. dioica but that the breeding system varies, partly because of genetic differences, both within and among populations. Further, we did not find the predicted fitness reduction for intrapromycelial matings, suggesting that intrapromycelial mating is a highly favorable breeding system for M. violaceum.

In 2012, Tigray orthohantavirus was discovered in Ethiopia, but its seasonal infection in small mammals, and whether it poses a risk to humans was unknown. The occurrence of small mammals, rodents and shrews, in human inhabitations in northern Ethiopia is affected by season and presence of stone bunds. We sampled small mammals in two seasons from low- and high-density stone bund fields adjacent to houses and community-protected semi-natural habitats in Atsbi and Hagere Selam, where Tigray orthohantavirus was first discovered. We collected blood samples from both small mammals and residents using filter paper. The presence of orthohantavirus-reactive antibodies in blood was then analyzed using immunofluorescence assay (human samples) and enzyme linked immunosorbent assays (small mammal samples) with Puumala orthohantavirus as antigen. Viral RNA was detected by RT-PCR using small mammal blood samples. Total orthohantavirus prevalence (antibodies or virus RNA) in the small mammals was 3.37%. The positive animals were three Stenocephalemys albipes rats (prevalence in this species = 13.04%). The low prevalence made it impossible to determine whether season and stone bunds were associated with orthohantavirus prevalence in the small mammals. In humans, we report the first detection of orthohantavirus-reactive IgG antibodies in Ethiopia (seroprevalence = 5.26%). S. albipes lives in close proximity to humans, likely increasing the risk of zoonotic transmission.

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