ABSTRACT:The emergence of antimicrobial resistance is arguably the most important threat to human and animal health. The impacts of antimicrobial use can reach far from the site of prescription and wildlife may serve as a conduit for the movement of resistance across landscapes, contributing to the spread of antimicrobial resistance within and between different reservoirs. We compared antimicrobial resistance and life history among wild and domestic species in Chobe, Botswana to explore key attributes and behaviors that may increase exposure and allow resistance to move between humans, animals, and ecosystems. Among 150 fecal samples evaluated from African animals, 41.3% contained Escherichia coli isolates that were resistant to one or two of 10 tested antibiotics, and 13.3% of isolates demonstrated multidrug resistance (three or more antibiotics). Resistance to each of the 10 tested antibiotics was detected among wildlife fecal samples. Resistance was widespread, but not ubiquitous, and isolates from wildlife demonstrated similar patterns of resistance to human E. coli from environmental and clinical sources in the study area. Multidrug resistance was significantly higher in carnivores, water-associated species, and species inhabiting urban areas, suggesting that life history may be key to understanding exposure patterns and transmission dynamics in heterogeneous landscapes.

Cryptococcosis caused by Cryptococcus gattii is a devastating disease of immunocompetent hosts with an incompletely understood pathogenesis. Utilizing an immunoproteomic approach in a naturally occurring koala model of disease, a number of key proteins and pathways are identified in the early and late pathogenesis of cryptococcosis for the first time. In particular, the thioredoxin system appears important in the pathogenesis of cryptococcosis caused by C. gattii VGII.

Major histocompatibility complex (MHC) class II molecules have an integral role in the adaptive immune response, as they bind and present antigenic peptides to T helper lymphocytes. In this study of koalas, species-specific primers were designed to amplify exon 2 of the MHC class II DA and DB genes, which contain much of the peptide-binding regions of the α and β chains. A total of two DA α1 domain variants and eight DA β1 (DAB), three DB α1 and five DB β1 variants were amplified from 20 koalas from two free-living populations from South East Queensland and the Port Macquarie region in northern New South Wales. We detected greater variation in the β1 than in the α1 domains as well as evidence of positive selection in DAB. The present study provides a springboard to future investigation of the role of MHC in disease susceptibility in koalas.

Leptospiral surveillance is often limited to the usual suspects: rodents and domestic animals. We identify Leptospira in a wide range of African wildlife, suggesting that leptospirosis transmission and persistence may also involve hosts not normally considered.