Ixodes scapularis (Ixodida: Ixodidae) Parasitizing an Unlikely Host: Big Brown Bats, Eptesicus fuscus (Chiroptera: Vespertilionidae), in New York State, USA

Ixodes scapularis Say is a three-host tick that has been recorded feeding on over 150 different species of terrestrial vertebrates (mammals, birds, and reptiles). This tick is found throughout the northeastern, coastal southeastern, and upper midwestern United States and is considered the most significant vector of tick-borne pathogens to humans in North America. Despite its ubiquity and broad host range, I. scapularis previously has not been reported feeding on bats (Chiroptera). However, during 2019 and 2020, larvae and nymphs of I. scapularis were recovered from big brown bats, Eptesicus fuscus (Palisot de Beauvois), at four locations in rural New York State, USA. All Ixodes infested bats were injured and found on the ground; therefore, parasitism by I. scapularis was likely opportunistic. Nonetheless, the large number of pathogens known to be associated with bats and the frequency with which I. scapularis bites people suggest that this host–tick relationship is of at least potential epidemiological significance.

Humidity, huddling & the hibernation energetics of big brown bats (Eptesicus fuscus)

During winter, many mammals hibernate and lower their body temperature and metabolic rate (MR) in prolonged periods of torpor. Hibernators will use energetically expensive arousals (i.e., restore body temperature and MR) presumably to re-establish water balance. Some hibernating mammals however will huddle in groups, possibly to decrease energetic costs and total evaporative water loss (EWL), although the benefit is not fully understood. Research on the relationship between behaviour, physiology, water loss, and energy expenditure of bats during hibernation is especially important because of a fungal disease called white-nose syndrome (WNS). To date, 12 North American bat species are affected by WNS, however big brown bats (Eptesicus fuscus) appear resistant, although the underlying mechanism is poorly understood. The overall objective of my thesis was to understand the influence of humidity and huddling on the behavioural and physiological responses of hibernating big brown bats. To test my hypotheses, I used a captive colony of hibernating big brown bats (n = 20). Specifically, for Chapter 2, I first tested the hypothesis that big brown bats adjust huddling and drinking behaviour depending on humidity, to maintain a consistent pattern of periodic arousals, and therefore energy balance during hibernation. I found that bats hibernating in a dry environment did not differ in arousal/torpor bout frequency, or torpor bout duration throughout hibernation but drank at twice the rate as bats in a humid environment. Bats in the dry treatment also had shorter arousals, and huddled in a denser huddle, potentially to reduce rates of total EWL. During late hibernation, for Chapter 3, I used open-flow respirometry to test two additional hypotheses, first that phenotypic flexibility in total EWL helps explain the tolerance of hibernating big brown bats for a wide range of humidity relative to other bat species. I found that dry-acclimated bats had lower rates of total EWL, compared to bats acclimated to humid conditions. I then tested the second hypothesis that big brown bats can use huddling to mitigate the challenge of dry conditions. I found that, for humid-acclimated bats, rates of total EWL were reduced with huddling bats but there was no effect of huddling on EWL for bats acclimated to dry conditions. These results suggest that the ability of big brown bats to reduce rates of total EWL through acclimation may reduce the need to huddle with conspecifics to avoid water loss and thus dehydration. Overall, my thesis suggests that big brown bats use both behavioural and physiological mechanisms to reduce water loss which could allow them to exploit habitats for hibernation that are unavailable to other bat species and could also help explain their apparent resistance to WNS.

Evaluating odour and urinary sex preferences in the big brown bat (Eptesicus fuscus)

Olfactory cues provide detailed information to mammals regarding conspecifics. Bats may identify species, colony membership, and individual’s using olfaction. Big brown bats (Eptesicus fuscus (Palisot de Beauvois, 1976)) live in mixed-sex colonies and must differentiate between sexes to locate mates. We hypothesized that odour cues convey information about sex. In Experiment 1, adult E. fuscus were recorded exploring a Y-maze that contained general body odours sampled from male or female conspecifics. One group of subjects was habituated to the Y-maze prior to experimental trials, whereas a second group was not. Bat exploration and the proportion of time spent near each scent were used as preference indicators for the body odour of a particular sex. Experiment 2 followed similar procedures except the odour cue tested was urine from either male or female conspecifics and without Y-maze habituation. Results found no evidence that E. fuscus prefer the body odours of a given sex, but females did prefer the odour of male urine. Non-habituated animals in Experiment 1 were more likely to explore the Y-maze and approach a stimulus scent compared to habituated bats. These findings have important implications for courtship and mating behaviour in bats, as well for designing future behavioural studies.

Predation of a brown bat (Vespertilionidae) by a Green Frog (Lithobates clamitans) in Ontario, Canada

On 31 July 2019, a Green Frog (Lithobates clamitans) was observed consuming a Big Brown Bat (Eptesicus fuscus) at Meux Creek, Neustadt, Ontario. The bat was likely roosting at a nearby undercut bank when it was predated by the frog, which required nearly 90 min to consume its prey. This is the first record of a Green Frog consuming a bat species in Canada.

Hepatic lipid signatures of little brown bats (Myotis lucifugus) and big brown bats (Eptesicus fuscus) at early stages of white-nose syndrome

White-nose syndrome (WNS) is an emergent wildlife fungal disease of cave-dwelling, hibernating bats that has led to unprecedented mortalities throughout North America. A primary factor in WNS-associated bat mortality includes increased arousals from torpor and premature fat depletion during winter months. Details of species and sex-specific changes in lipid metabolism during WNS are poorly understood and may play an important role in the pathophysiology of the disease. Given the likely role of fat metabolism in WNS and the fact that the liver plays a crucial role in fatty acid distribution and lipid storage, we assessed hepatic lipid signatures of little brown bats (Myotis lucifugus) and big brown bats (Eptesicus fuscus) at an early stage of infection with the etiological agent, Pseudogymnoascus destructans (Pd). Differences in lipid profiles were detected at the species and sex level in the sham-inoculated treatment, most strikingly in higher hepatic triacylglyceride (TG) levels in E. fuscus females compared to males. Interestingly, several dominant TGs (storage lipids) decreased dramatically after Pd infection in both female M. lucifugus and E. fuscus. Increases in hepatic glycerophospholipid (structural lipid) levels were only observed in M. lucifugus, including two phosphatidylcholines (PC [32:1], PC [42:6]) and one phosphatidylglycerol (PG [34:1]). These results suggest that even at early stages of WNS, changes in hepatic lipid mobilization may occur and be species and sex specific. As pre-hibernation lipid reserves may aid in bat persistence and survival during WNS, these early perturbations to lipid metabolism could have important implications for management responses that aid in pre-hibernation fat storage.