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Imlau, M.

Publications and source records attributed to Imlau, M..

3 recordsLinked to original sources

Evolutionary dynamics of a lethal recessive allele in reintroduced fragmented lynx populations

Conservation programs worldwide use reintroductions and translocations as management tools to support endangered species. Such efforts often face genetic challenges, as small populations and restricted gene flow can lead to inbreeding and loss of genetic diversity. Inbreeding depression is a well-known risk in small, isolated populations, where reduced genetic diversity can compromise fitness and threaten population persistence. While correlations between inbreeding and reduced fitness are well documented, so far, no causal variant for a fitness-relevant phenotype has been described in a wild population. Here, we combine long-term health and population data with genomic analyses to identify a recessive lethal allele responsible for extensive organ mineralization in young Eurasian lynx (Lynx lynx) from a reintroduced population in Switzerland. The causal variant is located in FGF23 and predicted to impair secretion of fibroblast growth factor 23, an important regulator of phosphate homeostasis. The deleterious allele was likely introduced from one of the lynx source populations and subsequently increased in frequency through founder effects and inbreeding. All three Swiss lynx populations show high inbreeding levels (FROH > 0.4), reflecting substantial loss of genetic diversity. Our findings uniquely demonstrate how demographic history, founder effects, genetic drift, and inbreeding interact to shape the fate of a recessive deleterious allele, highlighting the importance of multiscale monitoring in wildlife conservation.

evolutionary biology↗

Pathologic and phylogenetic characterization of Usutu virus infections in free-ranging wild birds in Switzerland (2015-2020)

Usutu Virus (USUV) is an emerging flavivirus causing fatal disease in free-ranging and captive birds but also infecting mammals and representing a significant zoonotic agent in Europe, making monitoring and investigations of this viral agent crucial both for conservation and public health. We carried out a retrospective investigation focusing on free-ranging wild birds confirmed to be USUV infected examined at the Institute for Fish and Wildlife Health (FIWI), Switzerland. The pathology and virology findings together with the phylogeographic and environmental data were examined for underlying factors to the dynamics of the USUV infection in Switzerland, between 2015 and 2020, with particular focus to the major peak of 2018. USUV infection was confirmed by reverse transcription-PCR in 67 birds, with common blackbirds (Turdus merula, 73%; 49/67) being overrepresented, showing signs of diseases including poor body condition (84%; 56/67) and splenomegaly (75%; 50/67). Histology (n=34) revealed changes in the heart (58%; 19/33), the central nervous system (67%; 22/33) and the liver (62%; 21/34). Of interest, the splenic changes (86%, 25/29) showed different, but likely correlated phenotypes, characterized by the presence of discrete and/or diffuse histiocytic infiltrates in the congested and lymphoid depleted spleen parenchyma, possibly reflecting different stages of the disease. Phylogenetic analysis unambiguously revealed that the recent USUV infections were predominantly caused by strains of the Europe 3 lineage. USUV Africa 3 strains were detected exclusively from southern Switzerland in one location (two blackbirds). Our investigation revealed intralesional Usutu viral RNA consistent with infection in previously undescribed hosts (Corvus frugilegus, Cygnus olor) and provided new insights into the pathogenesis and the ecology of the disease. The environmental data suggested the occurrence of unique weather conditions, possibly boosting the mosquito population and favoring an unprecedented increase of cases in 2018. Finally, the increase in genetic diversity of the circulating strains might have contributed to the recorded high mortality in 2018. Author SummaryAt the end of the 20th century, Usutu virus (USUV) was associated for the first time with mass mortality in wild black birds in Italy. Shortly after, reports on avian fatalities associated with USUV all over Europe appeared. In 2018 an unprecedented high occurrence of Usutu virus disease (UVD) caused high mortalities in wild birds in Switzerland and other European countries. Here we examined deceased wild birds with UVD with an emphasis on pathological examination and identification of USUV strains. The spleen is one of the main organs affected and we propose a timeline of lesion progression correlating with early, intermediate and late changes. Whereas we mainly identified strains of the European 3 lineage, we also found a hotspot of African 3 lineage strains. This indicates multiple entries of USUV into Switzerland. Although the disease is especially fatal in Strigiformes and Passeriformes, we expanded the spectrum of bird species (mute swans, rooks) naturally infected with the USUV. Usutu virus is an arthropod-borne virus and transmission occurs mainly via blood feeding vectors such as mosquitoes. We discuss the influence of weather conditions on mosquito population and the potential role of invasive mosquito species, such as the Asian tiger mosquito and other Aedes spp., as additional vectors for disease.

microbiology↗

Ca2+-activated sphingomyelin scrambling and turnover mediate ESCRT-independent lysosomal repair

Lysosomes are vital organelles vulnerable to injuries from diverse materials. Failure to repair or sequester damaged lysosomes poses a threat to cell viability. Here we report that cells exploit a sphingomyelin-based lysosomal repair pathway that operates independently of ESCRT to reverse potentially lethal membrane damage. Various conditions perturbing organelle integrity trigger a rapid calcium-activated scrambling and cytosolic exposure of sphingomyelin. Subsequent metabolic conversion of sphingomyelin by neutral sphingomyelinases on the cytosolic surface of injured lysosomes promotes their repair, also when ESCRT function is compromised. Conversely, blocking turnover of cytosolic sphingomyelin renders cells more sensitive to lysosome-damaging drugs. Our data indicate that calcium-activated scramblases, sphingomyelin, and neutral sphingomyelinases are core components of a previously unrecognized membrane restoration pathway by which cells preserve the functional integrity of lysosomes.

cell biology↗