House flies are well recognized as filth-associated organisms and public nuisances. House flies create sanitation issues when they bridge the gap between microbe-rich breeding environments and animal/human habitations. Numerous scientific surveys have demonstrated that house flies harbor bacterial pathogens that pose a threat to humans and animals. More extensive and informative surveys incorporating next-generation sequencing technologies have shown that house fly carriage of pathogens and harmful genetic elements, such as antimicrobial resistance genes, is more widespread and dangerous than previously thought. Further, there is a strong body of research confirming that flies not only harbor but also transmit viable, and presumably infectious, bacterial pathogens. Some pathogens replicate and persist in the fly, permitting prolonged shedding and dissemination. Finally, although the drivers still have yet to be firmly determined, the potential range of dissemination of flies and their associated pathogens can be extensive. Despite this evidence, the house flies’ role as reservoirs, disseminators, and true, yet facultative, vectors for pathogens have been greatly underestimated and underappreciated. In this review, we present key studies that bolster the house fly’s role both an important player in microbial ecology and population biology and as transmitters of microbial threats to animal and human health.

House flies (Musca domestica L.) are filth-breeding pests of urban and rural environments around the world. Frequenting microbe-rich substrates for nutritional and reproductive needs, house flies pose a risk to human and animal health through their carriage and transmission of pathogenic and antimicrobial resistant bacteria (AMR). Adult house flies were collected from Kansas beef and dairy cattle operations to assess factors influencing bacterial abundance and AMR incidence flies. Aerobic culturable bacteria and suspected coliforms (SC) were enumerated from fly homogenate cultured on nonselective (tryptic soy agar) and selective (violet-red bile agar VRBA) media, respectively. Unique morphotypes of SC isolates were screened for tetracycline resistance and tested for resistance to 4 additional antibiotics to identify multi-drug resistant (MDR) isolates. Female house flies carried greater abundances of both culturable bacteria and SC than male flies. Abiotic factors such as ambient and soil temperatures correlated with culturable bacteria and SC abundances in flies, but farm type correlated only with SC abundance and trends of resistance phenotypes observed in SC isolates. Male and female flies from both farm types carried one or more AMR and MDR SC isolates (73.02% AMR and 31.09% MDR). The majority of AMR and MDR bacteria were Escherichia/Shigella sp., which possessed the widest range of phenotypic resistance variability found in our study. Our results further emphasize the role house flies play in harboring bacteria of risk to human and animal health and identified factors of potential use for the development of strategies to mitigate house fly transmission of bacterial pathogens and AMR within confined cattle operations.

Animals encounter diverse microbial communities throughout their lifetime, which exert varying selection pressures. Antimicrobial peptides (AMPs), which lyse or inhibit microbial growth, are a first line of defense against some of these microbes. Here we examine how developmental variation in microbial exposure has affected the evolution of expression and amino acid sequences of Defensins (an ancient class of AMPs) in the house fly ( Musca domestica). The house fly is a well-suited model for this work because it trophically associates with varying microbial communities throughout its life history and its genome contains expanded families of AMPs, including Defensins. We identified two subsets of house fly Defensins: one expressed in larvae or pupae, and the other expressed in adults. The amino acid sequences of these two Defensin subsets form distinct monophyletic clades, and they are located in separate gene clusters in the genome. The adult-expressed Defensins evolve faster than larval/pupal Defensins, consistent with different selection pressures across developmental stages. Our results therefore suggest that varied microbial communities encountered across life history can shape the evolutionary trajectories of immune genes.