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Context. Chlamydia species impose major global burdens on both human and animal health. However, chlamydial infections of wild rodents have been understudied, posing limitations on assessments of disease risks for rodent conservation translocations. This is particularly true when there is evidence of infection in proposed source populations, as occurred for the Shark Bay mouse (Pseudomys gouldii) translocations to Dirk Hartog Island. Aims. The aim of this study was to reduce uncertainty surrounding the risks posed by Chlamydia for these translocations by: (1) determining the presence, prevalence and diversity of Chlamydia in rodent populationsin the Shark Bay region of Western Australia; (2) identifying associations with health parameters; and (3) assessing for evidence of cross-species transmission. Methods. Swab, faecal and tissue samples from 110 wildcaught individuals (comprising five rodent and two marsupial species) were collected across four islands in Western Australia. These samples were analysed by a Chlamydiaceae 23s rRNA qPCR in a 14-month cross-sectional study conducted between 2020 and 2021. Key results. In total, 20% of all individuals (22/110; 95%CI 13.6–28.4) from five species, including 19% (19/100; 95% CI 12.5–27.8) of rodents, were positive by the Chlamydiaceae qPCR, although in low loads. Further attempts at species identification of the Chlamydiaceae were unsuccessful. Our results found no detectable adverse health associations, or significant associated pathological findings, with low molecularloadssupporting an asymptomatic infection state. Additionally, there were no disease associationsin Shark Bay bandicoots(Perameles bougainville) despite the presence of an ocular disease syndrome previously linked to chlamydial infection in this species. Conclusions and implications. Our findings suggest that sub-clinical chlamydial infections in wild Australian rodents may be widespread, but for the Dirk Hartog Island translocations, the risks of Chlamydia associated with movement of Shark Bay mice are likely low. The results highlight how current knowledge gaps pertaining to wildlife health can be addressed through collaborative approaches to translocation planning and implementation. [ABSTRACT FROM AUTHOR]

Cetacean morbillivirus (CeMV; family Paramyxoviridae) has caused several epizootics globally during the past 25 years. Three strains of CeMV--porpoise, dolphin, and pilot whale morbillivirus--are classified as 1 species (1). CeMV [...]

Streptococcus iniae causes high mortality in cultured and wild fish stocks globally. Since the first report in captive Amazon river dolphins Inia geoffrensis in 1976, it has emerged in finfish across all continents except Antarctica. In March 2016, an estimated 17000 fish were observed dead and dying along a remote 70 km stretch of the Kimberley coastline north of Broome, Western Australia. Affected species included finfish (lionfish Pterois volitans, angelfish Pomacanthus sp., stripey snapper Lutjanus carponotatus, sand bass Psammoperca waigiensis, yellowtail grunter Amniataba caudavittata, damselfish Pomacentridae sp.), flatback sea turtles Natator depressus, and olive (Aipysurus laevis) and black-ringed (Hydrelaps darwiniensis) sea snakes. Moribund fish collected during the event exhibited exophthalmia and abnormal behaviour, such as spiralling on the surface or within the water column. Subsequent histopathological examination of 2 fish species revealed bacterial septicaemia with chains of Gram-positive cocci seen in multiple organs and within brain tissue. S. iniae was isolated and identified by bacterial culture, species-specific PCR, Matrix-Assisted Laser Desorption Ionisation Time-Of-Flight (MALDI-TOF) and biochemical testing. This is the first report of S. iniae associated with a major multi-species wild marine fish kill in Australia. Extreme weather events in the region including a marked decrease in water temperatures, followed by an extended period of above-average coastal water temperatures, were implicated as stressors potentially contributing to this outbreak.