Open access peer-reviewed chapter

The Physiological Ecology of White-Nose Syndrome (WNS) in North American Bats

Written By

Craig L. Frank

Submitted: 01 September 2021 Reviewed: 08 September 2021 Published: 15 October 2021

DOI: 10.5772/intechopen.100369

From the Edited Volume

Bats - Disease-Prone but Beneficial

Edited by Heimo Mikkola

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White-nose Syndrome (WNS) is an emergent mycosis in North America that is caused by a severe cutaneous infection with the fungus Pseudogymnoascus destructans (Pd) during hibernation. Pseudogymnoascus destructans (Pd) was first observed in North America at a single site during the winter of 2006–2007 and has since spread to 39 U.S. States and 7 Canadian provinces. This fungus was introduced to North America from Europe, where it is endemic. WNS has thus far been observed to occur only in hibernating bats and has caused the populations of 4 North American bat species to decline by more than 84% within 7 years. Field studies have revealed that 4 other North American bat species are not afflicted with WNS when hibernating in areas where Pd occurs. The physiological and biochemical adaptations that permit some bat species to resist Pd infections are starting to be elucidated but are still poorly understood. A total of 47 different bat species are found in North America, about half of which hibernate during the winter. The potential future effects of WNS on 13 of these hibernating bat species remains to be determined.


  • mycosis
  • hibernation
  • immunity
  • Pseudogymnoascus destructans
  • lipids

1. Introduction

White-nose Syndrome (WNS) is an emergent mycosis that affects some bat species in North America and is caused by an extensive cutaneous infection with the fungus Pseudogymnoascus destructans (Pd) during hibernation. It was first observed at a single cave in New York State during the winter of 2006–2007, and then spread to 5 more caves/mines in New York State during the winter of 2007–2008 [1]. Pseudogymnoascus destructans (Pd) has since spread to 39 U.S. States and 7 Canadian provinces, and it was introduced to North America from Europe [2]. This fungus grows on the muzzle, wings, and ears of afflicted bats during hibernation, with hyphae penetrating both the epidermis and dermis, consuming hair follicles, sebaceous and sweat glands [3, 4, 5]. Pseudogymnoascus destructans grows at ambient temperatures ranging from 1.9 to 15°C, although the hyphal morphology of this fungus exhibits heat stress at an ambient temperature (Ta) > 12°C, and growth ceases altogether at Ta > 19°C [6]. The arrival of Pd has led to severe population declines for 4 of the 6 bat species that hibernate in the Northeastern United States and Canada. Within 1–2 years after the arrival of Pd at a hibernation site, the number of little brown (Myotis lucifugus), northern long-eared (Myotis septentrionalis), Indiana (Myotis sodalis), and tricolored (Perimyotis subflavus) bats decreases by 75–95% due to high over-winter mortality during the hibernation period [7]. Extensive cutaneous infections with Pd have been shown to be the cause of WNS in laboratory inoculation/hibernation experiments with captive M. lucifugus [8]. Bats suffering from WNS have numerous skin lesions caused by Pd infections on their wings, face, and ears. These Pd lesions display an orange-yellow fluorescence when illuminated by long-wave (365–385 nm) UV light [9]. The mechanism by which an extensive cutaneous infection with Pd leads to WNS and subsequent death during hibernation in some North American bat species is due to the effects of these infections on the hibernation energetics of small bats.


2. Hibernation physiology and white-nose syndrome

Mammals and birds are unique among animals in that they are homeothermic endotherms, maintaining a constant core body temperature (Tb) over a wide range of ambient temperatures (Ta) through a high metabolic rate [10]. Prolonged periods of high metabolic heat production by mammals and birds requires high rates of energy intake. Food availability in the wild often fluctuates, and consequently the energetic costs of maintaining a high Tb (32–42°C) via endothermy becomes prohibitively expensive during certain environmental conditions. Not all mammals and birds are permanently homeothermic, but instead enter periods of torpor [11]. Torpor is a period when metabolic rate and Tb are greatly reduced. It involves the regulation of Tb at a new and substantially lower level, with a new minimum Tb being maintained. Torpor is a controlled reduction in metabolic rate, Tb, and a suite of physiological processes in endotherms [12]. Mammalian and avian species that employ torpor are therefore classified as heterothermic endotherms [11]. Metabolic rates during torpor can be less than 5% of basal metabolic rate with a corresponding Tb of just 0.5–1.0°C above ambient temperature (Ta) in most instances [13]. Mammals and birds generally employ one of two common patterns of torpor, depending upon species: prolonged torpor during hibernation, and daily torpor. Daily torpor occurs when a heterotherm has torpor bouts that are 3–12 h in duration. Hibernation is seasonal, usually from late summer/autumn to the following spring. Hibernators do not remain torpid continuously throughout the hibernation season; instead, bouts of torpor last from days to weeks, interrupted by brief periods of high metabolic rates and high Tb called arousal episodes. Hibernation is the most common pattern of torpor found in mammals. Numerous studies have revealed that daily torpor occurs in at least 42 bird species, and 78 mammalian species as well. At present, only 1 bird species (the Common Poorwill, Phalaenoptilus nuttallii) is known to hibernate, whereas hibernation has been document in about 100 mammalian species [14].

Stored triacylglycerols mobilized from white adipose tissue (WAT) are the primary energy source utilized during mammalian hibernation [15]. The periods of high metabolic rates and Tb known as arousal episodes normally account for 80–90% of stored lipids (energy) utilized during hibernation [16, 17], but their physiological function is poorly understood. A number of physiological/biochemical alterations that occur during torpor are reversed during arousal episodes. These alterations include dendritic retraction, leukocyte sequestration in secondary lymphatic organs, endocytosis, and protein degradation [18]. Periodic arousals from torpor thus serve to rectify physiological/biochemical imbalances that occur during torpor. Heterothermic mammals typically undergo an extensive period of feeding and fattening for several weeks prior to the onset of hibernation, during which body fat levels increase by 4 to 7-fold. The body fat content of M. lucifugus increases from 7 to 27% body mass during the 2 months prior to hibernation [19, 20], for example.

The energetic constraints that normal arousal episodes place on the physiological ecology of hibernating bats are illustrated by examining the winter physiological ecology of one bat species that is now severely impacted by WNS, M. lucifugus. Although the normal arousal episodes of hibernating M. lucifugus are usually less than 1 h in duration, they nonetheless account for 80–90% of all energy utilized during hibernation by this species [21]. Each of these arousal episodes requires the utilization of about 110 mg of stored depot lipids [22]. The body mass of M. lucifugus at the onset hibernation averages 8.5 g, indicating that about 2.0 g of depot lipids (triacylglycerols) are stored by each bat to support the entire 190-d hibernation period [23]. If arousal episodes consume a total of at least 80% of the lipids utilized during the entire hibernation period, then about 1.6 g of the 2.0 g stored by M. lucifugus are required to fuel them. Hibernating M. lucifugus thus have enough stored energy to support only about 14–15 arousal episodes during the entire period. Free-ranging M. lucifugus hibernating at ambient temperatures of 5.5 to 12.0°C consequently have normal torpor bouts averaging 12.4 to 19.7 d in length [22, 24] which enables them to survive a 190-d hibernation period without depleting their energy reserves prior to the spring.

Studies on free-ranging M. lucifugus revealed that bats with extensive Pd infections arouse more frequently from torpor during hibernation, and consequently their torpor bouts were much shorter than the normal range of 12.4 to 19.7 d previously reported for this species. Individuals with extensive cutaneous Pd infections (lesions) had a mean (± SE) torpor bout duration of 7.93 ± 2.49 d between arousal episodes, whereas those with no Pd lesions had a mean torpor duration of 16.32 ± 6.65 d which was significantly longer [25]. This 51% reduction in torpor bout duration produced by extensive cutaneous Pd infections made arousal episodes more frequent, which increased the rate of energy expenditure during the entire hibernation period. This increased rate of energy expenditure during hibernation is WNS, which leads to the premature depletion of body fat reserves prior to the normal spring emergence from hibernation when food (arthropods) first becomes available, which in turn causes of death [26]. The mechanism by which a severe cutaneous infection with Pd increases the frequently of arousal episodes during hibernation is related to the degree of evaporative water loss from the skin surface. The normal rate of evaporative water loss (EWL) of bats is considerable during torpor, and it is thought that they periodically arouse from torpor to drink in order to restore their water balance [27]. Hibernating bats have been observed drinking during arousal episodes [28]. It thus has been proposed that the numerous skin lesions caused by severe Pd infections may increase the EWL of affected bats, which in turn would cause them to arouse from torpor more frequently to drink. Analyses of blood samples collected from both Pd infected and uninfected M. lucifugus during hibernation support this hypothesis [29, 30]. Laboratory inoculation/hibernation experiments with M. lucifugus revealed that the mean EWL rate of individuals with numerous cutaneous Pd lesions was 1.6-fold greater than that for bats with no Pd lesions [31]. Interpreting these findings together reveals that when cutaneous Pd infections result in numerous skin lesions, WNS is caused by a corresponding increase in the rate of cutaneous EWL, which in turns leads to both reduced torpor bout lengths and more frequent arousal episodes. This subsequently results in a greater rate of energy expenditure during hibernation that produces a premature depletion of body fat reserves during hibernation, before feeding can occur in the spring.


3. The susceptibility to Pseudogymnoascus destructans

Field studies on hibernating bats demonstrated that P. destructans is found throughout both Europe and Asia, appearing on the skin of these bat species with no apparent increases in over-winter mortality or WNS [32, 33]. The greater mouse-eared bat (Myotis myotis) of Europe has been shown to be highly resistant to cutaneous Pd infections in both field [34] and laboratory studies [35]. Examination of hibernation sites in Europe revealed Pd growing on the muzzles of 5 different European species during torpor: pond (Myotis dasycneme), greater mouse-eared bat (M. myotis), Daubenton’s (Myotis duabentonii), Brandt’s (Myotis brandtii), and lesser mouse-eared (Myotis oxygnathus) bats. Mass deaths were not observed at these sites, however, and there were no apparent disruptions in torpor bout duration [34]. Histological analyses of infected M. myotis revealed that the hyphae of Pd do not extend beyond the epidermis of this bat species, even after several months of hibernation [36]. Some bat species are thus more resistant to Pd infections than others, thereby avoiding WNS. Cutaneous Pd infections and some associated skin lesions have subsequently been observed in 11 different European and 2 Asia bat species during hibernation [32, 33], with no apparent disruptions in torpor bout length or mortality. These studies indicate that European and Asian species of hibernating bats have evolved a resistance to Pd that greatly reduces the extent to which this fungus can infect the skin, thereby reducing the number of lesions that appear during hibernation to the point where torpor bout length is not significantly affected.

A similar resistance to both Pd infections and subsequent WNS is displayed by 4 species of North American bats as well. Field studies demonstrated that big brown bats (Eptesicus fuscus) hibernating where Pd occurs have torpor bouts of normal duration, and usually survive the winter with depot fat remaining [37]. Laboratory hibernation experiments with E. fuscus also revealed that Pd does not extensively grow in the skin of this species during hibernation [38]. The Eastern small-footed bat (Myotis leibii) is also highly resistant to cutaneous infections with Pd. A survey of 42 bat hibernation sites in the USA revealed that the number of M. leibii at these locations declined on average by only 12% during the first several years since the first appearance of Pd, whereas the number of M. lucifugus, M. septentrionalis, and P. subflavus at these sites decreased by 75–98% during this same period [39]. The Southeastern myotis (Myotis austroriparius) is a hibernating species found in Southern USA. Examinations of hibernation sites for this species in Alabama reveal although P. destructans first appeared in this area during 2011, no increases in the over-winter mortality of M. austroriparius have been observed. The skin of 99 hibernating M. austroriparius was examined for both the presence P. destructans DNA on it, and the UV-florescent skin lesions characteristic of Pd infections. Although 77% of the bats tested had Pd DNA on their skin, none of them had Pd skin lesions [40]. These findings indicate that although M. austroriparius was exposed to propagules (spores) of Pd, this fungus did not invade the skin of this bat species during hibernation, thus WNS does not develop. The gray bat (Myotis grisescens) is listed as an endangered species by the U.S. Fish & Wildlife Service, and some populations hibernate in caves located in the U.S. state of Tennessee. Pseudogymnoascus destructans first appeared in these caves during 2013, and some of the M. grisescens hibernating in these areas were found to have Pd skin lesions. No mass mortality has been observed for this species during hibernation, however, and the number of M. grisescens hibernating in these caves has been increasing since 2013. The total number of M. grisescens hibernating at 3 Tennessee caves increased by 15.4% during between 2016–2017 and 2018–2019, and it increased by 2.9-fold at another cave during this same period [41]. It therefore appears that the degree of Pd infection that occurs during hibernation by M. grisescens is not sufficient to cause WNS.

There is ample evidence that some populations of M. lucifugus in the Northeastern United States have evolved a greater resistance to cutaneous infections with Pd, thereby avoiding WNS. A mark/recapture study conducted by Reichard et al. [42] revealed that the over-winter survival rate of M. lucifugus at 8 hibernation sites where Pd occurs in the Northeastern USA was at least 5.4%, with some individuals surviving 4 consecutive winters. Another mark and recapture study with M. lucifugus hibernating at a site in Michigan revealed that some individuals have survived 7 consecutive winters at a site where Pd occurs [43]. Studies on hibernating free-ranging M. lucifugus conducted during the first several years after the appearance of Pd revealed that although most individuals developed severe Pd infections with a high density of skin lesions that resulted in WNS, some individuals developed only moderate Pd infections that produced far fewer skin lesions, avoiding WNS and surviving the winter. Furthermore, the mean (± SE) torpor bout duration of these individuals with fewer lesions was 13.96 ± 4.30 d, which was not significantly different from that observed for M. lucifugus hibernating with no cutaneous Pd infections [25]. The differences in torpor bout lengths between individual M. lucifugus hibernating at the same site where Pd is found is illustrated by the skin temperature (Tskin) recordings of 2 adult females hibernating at the Williams Preserve Mine in New York State during the November–December period of 2008 (Figure 1). Skin temperature is equivalent to body temperature in small bats [44]. The first bat (Figure 1A) began hibernation with torpor bouts that were normal in length (15–20 d), but torpor bout length decreased to just 7–9 d during December 2008, indicating that this individual had succumbed to WNS. The second M. lucifugus (Figure 1B) examined, however, maintained torpor bouts that were 15–20 d long throughout the study period, demonstrating that it was not afflicted with WNS.

Figure 1.

(A) Skin temperatures of two different female Myotis lucifugus hibernating at the Williams preserve mine during November and December 2008. (B) Recordings of Tskin began 45 min after a temperature-sensitive radio transmitter was placed on each bat during Julian day 305. Radio signals were continuously recorded at 10–15 min intervals, torpor is defined as when Tskin < 24°C. *indicates a period when the bat was out of the range of the automated radio receiver during an arousal episode. Data are from Frank et al. [23].

These studies indicate that for M. lucifugus, some individuals within certain populations are more resistant to Pd infections than others, and these are the bats that are surviving consecutive winters despite the presence of Pd. The consistent survival of some M. lucifugus in the presence of Pd has led to a partial recovery of some populations in New York State. A small maternity colony of M. lucifugus in NY examined by Dobony and Johnson [45] during the summers of 2006 through 2017 demonstrated that the size of it decreased by 88% after the first appearance of Pd, then stabilized during 2010–2014, and has been increasing since 2014. The New York Department of Environmental Conservation has been conducting annual counts of hibernating bats at the Williams Preserve Mine and Hailes Cave since 1999. These are 2 of the 6 bat hibernation sites where Pd first appeared during the winter 2007–2008. The number of M. lucifugus hibernating at the Williams Preserve Mine during the winter of 2008–2009 was just 12% of that observed prior to the first appearance of Pd, and the number at Hailes Cave was just 9% of the pre-Pd level for this site. The number of M. lucifugus observed at these sites during subsequent hibernation periods has since consistently increased, however. The number of M. lucifugus increased to 41% of pre-Pd levels by 2017 at the Williams Preserve Mine, and increased to 31% of pre-Pd levels at Hailes Cave by 2017 [23]. Another field study conducted at the Williams Preserve Mine indicates that this M. lucifugus population has evolved a higher resistance to Pd growth on their wings [46].

A field study conducted at a single hibernation site in NY during the winter of 2014–2015, about 6 years after Pd had arrived, indicated that the mean (± SE) torpor bout duration of M. lucifugus surviving the winter was 12.0 ± 10.8 d [47], which is close to the normal torpor bout duration of 15–20 d previously reported for this species, thus indicating that most were hibernating normally. Another field study on M. lucifugus hibernating in the Williams Preserve Mine revealed that the bats hibernating at this site 1 year after the arrival of Pd (2008–2009) had: a) a mean torpor bout duration of 7.6 d, b) no depot fat reserves remaining by March, and c) an apparent over-winter mortality rate of 88%. The M. lucifugus hibernating at this same site 6–9 years after the arrival of Pd, in contrast, had: a) a mean torpor bout duration of 14.7 d, b) depot fat remaining in March, and c) an apparent over-winter mortality rate of 50% [23]. Interpreting these studies together reveals that some populations of M. lucifugus have recently evolved a greater resistance to cutaneous infections with Pd, thus reducing the frequency of WNS.


4. Impacts of WNS

The impact of WNS on the total number of M. lucifugus in North America has been drastic, despite the partial recovery of some populations in New York State. A recent analysis of winter hibernaculum counts for 5 bat species performed in 27 U.S. states and 2 Canadian over a 23-year period was performed by Cheng et al. [48]. Their analysis revealed that the total number of M. lucifugus, M. septentrionalis, and P. subflavus hibernating at these sites decreased by over 90% with the first 7 years after the arrival of Pd, and the number of M. sodalis decreased by 84%. The decline in the number of M. septentrionalis was so great that the U.S. Fish and Wildlife Service designated it a threatened species in 2016. A total of 47 different bat species are found in North America, and about half of them are known to hibernate during the winter [49]. Although the susceptibility of 8 of these hibernating bat species to WNS is well understood, the ability of Pd infections to cause WNS in other species of hibernating North American bats is virtually unknown. The National Wildlife Health Center of the U.S. Geological Survey thus began a WNS surveillance program in 2013 to address the potential effects of Pd as it spreads across the USA. Each year the wildlife agencies of 22 U.S. states submit thousands skin surface swabs collected from free-ranging bats during either the fall or hibernation to the National Wildlife Health Center which are examined for Pd DNA. Skin biopsies collected from bats showing signs of fungal infection are also submitted for histological analyses [A. Ballman, personal communication]. The result of these surveys are summarized in the WNS webpage maintained by the U.S. Fish & Wildlife Service [50]. The degree to which each species of hibernating North America bat is susceptible to cutaneous Pd infections and WNS has been compiled in Table 1 using both the results of both the surveys conducted by National Wildlife Health Center as well as the published studies cited previously. The susceptibility of 7 of the 21 bat species listed in Table 1 to Pd infections during hibernation is currently unknown due to a lack of data for these species. The DNA of Pd has been found on the skin surface of Myotis ciliolabrum, Corynorhinus townsendii, and Lasionycteris noctivagans indicating that Pd now occurs with the range of these species, but it is not known if Pd can invade their skin and produce lesions. Skin lesions caused by Pd infections have been documented in hibernating Myotis yumanensis, M. volans, and Myotis velifer, but it is not known if the density of Pd lesions that appear during this period is sufficient to cause WNS. The degree of Pd infection that occurs in Myotis austroriparius, M. grisescens, Myotis leibii, and E. fuscus is not sufficient to cause WNS in these species.

Scientific nameCommon namePd susceptibility
Myotis lucifugusLittle brown myotisWNS
Myotis septentrionalisN. Long-eared myotisWNS
Myotis sodalisIndiana myotisWNS
Perimyotis subflavusTricolored batWNS
Myotis californicusCalifornia myotisUnknown
Myotis thysanodesFringed myotisUnknown
Myotis evotisW. Long-eared myotisUnknown
Antrozous pallidusPallid batUnknown
Parastrellus hesperusCanyon batUnknown
Myotis auriculusSouthwestern myotisUnknown
Idionycteris phyllotisAllen’s big-eared batUnknown
Myotis leibiiSmall-footed myotisNo WNS
Myotis austroripariusSoutheastern myotisNo WNS
Eptesicus fuscusBig brown batNo WNS
Myotis grisescensGray myotisNo WNS
Myotis ciliolabrumSmall-footed myotisPd DNA
Corynorhinus townsendiiTownsend’s batPd DNA
Lasionycteris noctivagansSilver-haired batPd DNA
Myotis yumanensisYuma myotisPd infection
Myotis volansLong-legged myotisPd infection
Myotis veliferCave myotisPd infection

Table 1.

North American species of hibernating bats and their known levels of susceptibility to cutaneous infection with Pseudogymnoascus destructans.


5. Cutaneous lipids

Four of the hibernating bat species found in North America as well as 11 hibernating bat species in Europe limit the degree of cutaneous Pd infection to the point where it does not result in WNS during hibernation. The physiological and biochemical mechanisms that enable these bat species to reduce Pd infections are poorly understood. Several recent studies have revealed that one factor which confers a resistance to Pd infections is the lipid composition of the epidermis. The outermost stratum of the epidermis is the first defense against fungal skin infections because the mycelium must initially invade it, and leukocytes are not present in these epidermal layers. The epidermis is composed chiefly of special epithelial cells called keratinocytes that occur in 4 strata; they are produced in the deepest stratum (the stratum basale) and migrate to the top stratum (the stratum corneum) as they age. Epidermal surface lipids are a mixture of compounds secreted by keratinocytes into the intracellular matrix, and sebum secreted onto it by the sebaceous glands. The lipid mixture secreted by keratinocytes contains free sphingosine bases, ceramides, cholesterol, and free fatty acids (FFAs), whereas the sebum is composed of triacylglycerols, diacylglycerols, FFAs, wax esters, squalene, cholesterol, and cholesterol esters [51, 52]. The epidermal lipids of bats also have cerebrosides and monoacylglycerols [53, 54]. Some free fatty acids (FFAs) are known to have anti-microbial effects [55].

It has been demonstrated that the wing epidermis of both M. lucifugus and E. fuscus contain the same 7 fatty acids: Myristic (14:0), pentadecanoic (15:0), palmitic (16:0), palmitoleic (16:1), stearic (18:0), oleic (18:1), and linoleic (18:2) acids. The wing epidermis of hibernating E. fuscus contains about twice as much myristic, palmitoleic, oleic, and linoleic acids than that of M. lucifugus, as well. Laboratory experiments with Pd cultures revealed that pentadecanoic, palmitoleic, oleic, and linoleic acids in the free fatty acid (FFA) form inhibit the growth of Pd [56, 57], with linoleic acid reducing it by more than 99%. The results of one of these experiments are summarized in Figure 2.

Figure 2.

Mean (± SE) surface areas of Pd colonies at various growth stages on media containing 1% of either oleic (18:1), linoleic (18:2) or stearic (18:0) acids, while being incubated at 5.0 (blue symbols) and 10.6°C (red symbols). Mean within the same temperature treatment sharing a common lower-case letter are not significantly different at the P < 0.05 level. Data are from Frank et al. [56].

Epidermal free fatty acid composition thus appears to be one of the factors that enables E. fuscus to better resist Pd infections than Myotis lucifugus.

Wax esters consist of an alcohol linked to a fatty acid molecule with an ester bond [58]. About 120 different wax esters have been found in the sebum of Myotis myotis during hibernation [59]. A recent study used laboratory Pd culture experiments to determine the effects of some of these wax esters on Pd growth [60]. These experiments have revealed that 4 of the wax esters found in the sebum of M. myotis inhibit Pd growth by over 90%. These anti-Pd wax esters are: behenyl linoleate, palmityl linoleate, arachidyl linoleate, and behenyl palmitoleate. One factor that enables M. myotis to resist Pd infections is therefore presence of these anti-Pd wax esters in their epidermis. Changes in epidermal lipid composition may also be one of the adaptations that permit some populations of M. lucifugus to now have a higher resistance to cutaneous Pd infections.


6. Conclusions

Four species of North American bats develop severe Pd infections during hibernation which result in WNS, whereas 4 other bat species develop only moderate Pd infections during this period and do not display the abnormal torpor patterns and mortality associated with WNS. It has been also demonstrated that within the same population of M. lucifugus, individuals with a high density of Pd lesion in their skin suffer from WNS, whereas those with a much lower density of Pd lesions do not. Cutaneous infections with Pd thus do not always result in WNS, and a certain density of Pd lesions must be present in the skin before WNS develops. The precise minimum Pd lesion density for WNS is not known, and it should be determined to better understand both the ecology and potential impacts of WNS on the hibernating bat populations of North America, as the mere presence of some Pd lesions alone does not indicate that a bat species/population is afflicted with WNS. The effects of these lesions on torpor bout length must be taken into consideration when assessing potential WNS. The full extent to which Pd can infect the skin and causes WNS in 13 of 21 bat species listed in Table 1 is not known. Most of these 13 bat species occur in Western North America. It is thus unclear how WNS will affect most Western bat species as Pd spreads across North America. If current trends in Pd susceptibility continue, then it is likely that WNS will severely affect 7–8 additional bat species in North America. Analyses of preserved museum specimens suggest that Pd has been associated with hibernating bats in Europe for over 100 years, whereas they reveal no evidence that Pd was present in North America bats between 1861 and 1971 [61]. It therefore appears that bats across Europe have adapted to Pd for over 100 years, and they are now highly resistant to Pd infections, thereby avoiding WNS. The physiological/biochemical basis of this resistance is largely unknown but warrants further investigation to better predict which New World bat species will be severely affected by WNS.



I thank April Davis, Carl Herzog, Alan Hicks, and Melissa Ingala for helpful discussions which greatly improved this review.


Conflict of interest

The author declares no conflict of interest.


  1. 1. Keller S, Lorch JM, Berlowski-Zier BM, Ballman A, Blehert DS. Analysis of archival specimens confirms White-Nose Syndrome in little brown bats (Myotis lucifugus) from New York, USA, in spring 2007. Journal of Wildlife Diseases. 2021;57 (2): 457-460. DOI:DOI:10.7589/JWD-D-20-00137
  2. 2. Trivedi J, Lachapelle J, Vanderwolf KJ, Misra V, Willis CKR, Ratcliffe JM, et al. Fungus causing white-nose syndrome in bats accumulates genetic variability in North America with no sign of recombination. mSphere. 2017;2:e00271-e00217. DOI:10.1128/mSphereDirect.00271-17
  3. 3. Blehert DS, Hicks AC, Behr M, Meteyer CU, Berlowski-Zier BM, Buckles EL, et al. Bat white-nose syndrome: an emerging fungal pathogen? Science. 2009;323(5911):227
  4. 4. Gargas A, Trest MT, Christensen M, Volk TJ, Blehert DS. Geomyces destructans sp. Nov. associated with bat white nose syndrome. Mycotaxon. 2009;108:147-154
  5. 5. Chaturvedi V, Springer DJ, Behr MJ, Ramani R, Li, X, Peck MK, et al. Morphological and molecular characterizations of psychrophilic fungus Geomyces destructans from New York bats with White Nose Syndrome (WNS). PLoS ONE. 2010;5(5):e10783
  6. 6. Verant ML, Boyles JG, Waldrep W Jr, Wibbelt G, Blehert DS. Temperature-dependent growth of Geomyces destructans, the fungus that causes bat white-nose syndrome. PLoS ONE. 2012;7(9):e46280. DOI:10.1371/journal.pone.0046280
  7. 7. Langwig KE, Hoyt JR, Parise KL, Kath J, Kirk D, Frick WF, et al. Invasion dynamics of white-nose syndrome fungus, midwestern United States. Emerging Infectious Diseases. 2015;21:1023-1026
  8. 8. Warnecke L, Turner JM, Bollinger TK, Lorch JM, Misra V, Cryan PM, Wibbelt G, Blehert DS, Willis CK. Inoculation of bats with European Geomyces destructans supports the novel pathogen hypothesis for the origin of White-nose syndrome. PNAS. 2012;109:6999-7003
  9. 9. Turner GG, Meteyer CU, Barton H, Gumbs JF, Reeder DM, Overton B, et al. Nonlethal screening of bat-wing skin with the use of ultraviolet fluorescence to detect lesions indicative of white-nose syndrome. Journal of Wildlife Diseases. 2014;50(3):566-573
  10. 10. Hill RW, Wyse GA, Anderson M. Animal Physiology, 4th ed. New York: Sinauer Associates; 2016. 440 p
  11. 11. Geiser, F. Metabolic rate and body temperature. Annual Review of Physiology. 2004;66:239-274
  12. 12. Somero GN, Lockwood BL, Tomanek L. Biochemical Adaptation: Response to Environmental Challenges from Life’s Origins to the Anthropocene. New York: Oxford University Press; 2017. 572 p
  13. 13. Geiser F, Ruf T. Hibernation versus Daily Torpor in Mammals and Birds: Physiological variables and classification of torpor patterns. Physiological Zoology. 1995;68(6), 935-966
  14. 14. Ruf T, Geiser F. Daily torpor and hibernation in birds and mammals. Biological Reviews. 2015;90: 891-926. DOI:10.1111/brv.12137
  15. 15. Dark J. Annual lipid cycles in hibernators: integration of physiology and behavior. Annual Review of Nutrition. 2005;25: 469-497
  16. 16. Kayser C. Hibernation. In: Mayer W, Van Gelder R, editors. Physiological Mammalogy, volume II. New York: Academic Press; 1965. p. 180-296
  17. 17. Karpovich SA, Tøien Ø, Buck CL, Barnes BM. Energetics of arousal episodes in hibernating arctic ground squirrels. Journal of Comparative Physiology B. 2009;179:691-700
  18. 18. van Breukelen, F, Martin SL. The Hibernation Continuum: physiological and molecular aspects of metabolic plasticity in Mammals. Physiology. 2015;30: 273-281. DOI:10.1152/physiol.00010.2015
  19. 19. Kunz TH, Wrazen JA, Burnett CD. Changes in body mass and body composition in pre-hibernating little brown bats (Myotis lucifugus). Ecoscience. 1998;5:8-17
  20. 20. Reynolds RS, Kunz TH. Changes in body composition during reproduction and postnatal growth in the little brown bat, Myotis lucifugus (Chiroptera: Vespertilionidae). Ecoscience. 2000;7: 10-17
  21. 21. Thomas DW. The physiological ecology of hibernation in vespertilionid bats. Symposia of the Zoological Society of London. 1995;67:233-244
  22. 22. Thomas DW, Dorais J, Bergeron J-M. Winter energy budgets and cost of arousals for hibernating little brown bats, Myotis lucifugus. Journal of Mammalogy. 1990;71:475-479
  23. 23. Frank CL, Davis AD, Herzog, C. The evolution of a bat population with white-nose syndrome (WNS) reveals a shift from an epizootic to an enzootic phase. Frontiers in Zoology. 2019;16:40. DOI:10.1186/s12983-019-0340-y
  24. 24. Brack V, Twente JW. The duration of the period of hibernation of three species of vestertilionid bats I. Field studies. Canadian Journal of Zoology. 1985;63:2952-2954
  25. 25. Reeder DM, Frank CL, Turner GC, Meteyer CU, Kurta A, Britzke ER, et al. Frequent arousal from hibernation linked to severity of infection and mortality in bats with White-nose Syndrome. PLoS ONE. 2012;7(6):e38920. DOI:10.1371/journal.pone.0038920
  26. 26. Frank CL, Diaz P, Kunz TH. The relationship between White-nose Syndrome and dietary PUFA levels in bats. In: Ruf T, Bieber C, Arnold W, Millesi E, editors. Living in a seasonal world: thermoregulatory and metabolic adaptations. Germany: Springer-Verlag; 2012. p. 271-279
  27. 27. Thomas DW, Geiser F. Periodic arousals in hibernating mammals: is evaporative water loss involved? Functional Ecology. 1997;11:585-591
  28. 28. Wilcox A, Warnecke L, Turner JM, McGuire LP, Jameson JW, Misra V, Bollinger TC, Willis CK. Behaviour of hibernating little brown bats experimentally inoculated with the pathogen that causes White-nose Syndrome. Animal Behavior. 2014;88:157-164
  29. 29. Cryan PM, Meteyer CU, Blehert DS, Lorch JM, Reeder DM, Turner GG, Webb J, Behr M, Verant M, Russell RE, Castle KT. Electrolyte depletion in white-nose syndrome bats. Journal of Wildlife Diseases. 2013;49(2):398-343
  30. 30. Warnecke L, J. Turner JM, Bollinger TK, Misra V, Cryan PM, Blehert DS, Willis CK. Pathophysiology of white-nose syndrome in bats: a mechanistic model linking wing damage to mortality. Biology Letters. 2013;9:20130177
  31. 31. McGuire LP, Mayberry HW, Willis CKR. White-nose syndrome increases torpid metabolic rate and evaporative water loss in hibernating bats. American Journal of Physiology. 2017;313:R680-R686. DOI:10.1152/ajpregu.00058.2017
  32. 32. Zukal, J. et al. White-nose syndrome without borders: Pseudogymnoascus destructans infection tolerated in Europe and Palearctic Asia but not in North America. Scientific Reports. 2016;6:19829; DOI:10.1038/srep19829 (2016)
  33. 33. Hoyt JR, Sun K, Parise KL, Lu G, Langwig KE, Jiang T, et al. Widespread bat white-nose syndrome fungus, Northeastern China. Emerging Infectious Disease. 2016;22(1):140-142. DOI:10.3201/eid2201.151314
  34. 34. Wibbelt G, Kurth D, Hellmann M, Weishaur A, Barlow M, Veith J, Pruger T, Gorfol L, Grosche F, Bontadina V, Zophel HP, Seidl P, Cryan PM, Belhert DS. White-nose syndrome fungus (Geomyces destructans) in bats, Europe. Emerging Infectious Diseases. 2010;16:1237-1242
  35. 35. Davy C, Donaldson M, Willis CKR, Saville B, McGuire L, Mayberry H, Wilcox A, Wibbelt G, Misra V, Bollinger T, Christopher JK. The other white-nose syndrome transcriptome: Tolerant and susceptible hosts respond differently to the pathogen Pseudogymnoascus destructans. Ecology and Evolution. 2017;7: 10.1002/ece3.3234
  36. 36. Wibbelt G, Puechmaille SJ, Ohlendorf B, Mu¨ hldorfer K, Bosch T, et al. Skin lesions in European hibernating bats associated with Geomyces destructans, the etiologic agent of White-Nose Syndrome. PLoS ONE 2013;8(9): e74105. DOI:10.1371/journal.pone.0074105
  37. 37. Frank CL, Michalski A, McDonough AA, Rahimian M, Rudd RJ, Herzog CJ, et al. The resistance of a North American bat species (Eptesicus fuscus) to White-nose Syndrome (WNS). PLoS ONE. 2014;9(12):e113958; DOI:10.1371/journal.pone.0113958
  38. 38. Moore MS, Field KA, Behr MJ, et al. Energy conserving thermoregulatory patterns and lower disease severity in a bat resistant to the impacts of white-nose syndrome. Journal of Comparative Physiology B. 2018;88: 163. DOI:10.1007/s00360-017-1109-2
  39. 39. Turner GG, Reeder D, Coleman J. A five-year assessment of mortality and geographic spread of white-nose syndrome in North American bats and a look to the future. Bat Research News. 2011;52:13-27
  40. 40. Johnson JS, Sharp NW, Monarchino MN, Lilley TM, Edelman AJ. No Sign of infection in free-ranging Myotis austroriparius hibernating in the presence of Pseudogymnoascus destructans in Alabama. Southeastern Naturalist. 2021;20(1):20-28. DOI:10.1656/058.020.0102
  41. 41. Campbell J. Tennessee winter bat population and White-nose Syndrome monitoring report for 2018-2019. TWRA Technical Report. 2019;19:6
  42. 42. Reichard JD, Fuller NW, Bennett AB, Darling SR, Moore MS, Langwig KE, et al. Interannual survival of Myotis lucifugus (Chiroptera: Vespertilionidae) near the epicenter of White-nose Syndrome. Northeastern Naturalist. 2014;21(4):N56-N59
  43. 43. Kurta A, Foster RW, Daly BA, Wilson AK, Slider RM, Rockey CD, Rockey JM, Long BL, Auteri GG, Collins JD, White JP, Kaarakka HM, Redell JA, Reeder DM. Exceptional longevity in little brown bats still occurs, despite presence of White-Nose Syndrome. Journal of Fish and Wildlife Management. 1 2020;11(2): 583-587. DOI:DOI:10.3996/JFWM-20-039
  44. 44. Willis CKR, Brigham RM. Defining torpor in free-ranging bats: experimental evaluation of external temperature sensitive radio transmitters and the concept of active temperature. Journal of Comparative Physiology B. 2003;173:379-389
  45. 45. Dobony CA, Johnson JB. Observed resiliency of little brown myotis to long-term white-nose syndrome exposure. Journal of Fish and Wildlife Management. 2018;9(1):168-179
  46. 46. Langwig KE, Hoyt JR, Parise KL, Frick WF, Foster JT, Kilpatrick AM. Resistance in persisting bat populations after white-nose syndrome invasion. Philosophical Transactions of the Royal Society B. 2017;372:20160044
  47. 47. Lilley T, Johnson J, Ruokolainen L, Rogers E, Wilson C, Mead Schell S, et al. White-nose syndrome survivors do not exhibit frequent arousals associated with Pseudogymnoascus destructans infection. Frontiers in Zoology. 2016;13. 10.1186/s12983-016-0143-3
  48. 48. Cheng TL, et al. The scope and severity of white-nose syndrome on hibernating bats in North America Conservation Biology. 2021;1-12. DOI:10.1002/cobi.13739
  49. 49. Feldhamer GA, Drickamer LC, Vessey SH, Merrit JF, Krajewski C. Mammalogy, Adaptation, Diversity, Ecology. New York: McGraw Hill; 2007. 625 p
  50. 50. Bats Affected by WNS [Internet]. 2021. Available from: [Accessed: 2021-09-01]
  51. 51. Camera E; Ludovici M; Galante M; Singagra J-L; Picardo M. Comprehensive analysis of the major lipid classes in sebum by rapid resolution high performance liquid chromatography and electrospray mass spectrometry. Journal of Lipid Research. 2010;51: 3377-3388
  52. 52. Feingold KK. The role of epidermal lipids in cutaneous permeability barrier homeostasis. Journal of Lipid Research. 2007;48: 2531-2546
  53. 53. Ben-Hamo M, Munoz-Garcia A; Larrain, P; Pinshaw B, Korine C, Williams JB. The cutaneous lipid composition of bat wing and tail membranes: a case of convergent evolution with birds. Proceedings of the Royal Society B. 2016;283:20160636. DOI:10.1098/rspb.2016.0636
  54. 54. Pannkuk EL, Gilmore DE, Fuller NW, Savary BJ, Risch TS. Sebaceous lipid profiling of bat integumentary tissues: quantitative analysis of free fatty acids, monacylglycerides, squalene and sterols. Chemistry and Biodiversity. 2013;10:2122-2132
  55. 55. Fisher CL, Blanchette DR, Brogden KA, Dawson DV, Drake DR, Hill JR, Wertz PW. The roles of cutaneous lipids in host defense. Biochimica et Biophysica Acta. 2014;1841(3): 319-322
  56. 56. Frank CL, Ingala MR, Ravenelle RE, Dougherty-Howard K, Wicks SO, Herzog C, et al. The effects of cutaneous fatty acids on the growth of Pseudogymnoascus destructans, the etiological agent of White-nose Syndrome (WNS). PLoS ONE. 2016;11(4):e0153535. DOI:10.1371/journal.pone.0153535
  57. 57. Ingala, MR, Monro, JJ, Ravenelle, RE, Frank CL. The effects of epidermal fatty acid profiles, 1-oleoglycerol, and triacylglycerols on the susceptibility of hibernating bats to Pseudogymnoascus destructans. PLoS ONE. 2017;12(10):e0187195. DOI:10.1371/journal.pone.0187195
  58. 58. Gunstone FD. Fatty Acid and Lipid Chemistry. New York: Chapman and Hall; 1996. 375 p
  59. 59. Řezanka T, Viden I, Nováková A, Bandouchová H, Sigler K. Wax ester analysis of bats suffering from White Nose Syndrome in Europe. Lipids. 2015;50:633-645. DOI:10.1007/s11745-015-4027-7
  60. 60. Frank CL, Sitler-Elbel KG, Hudson AJ, Ingala MR. The antifungal properties of epidermal fatty acid esters: insights from White-Nose Syndrome (WNS) in bats. Molecules. 2018;23:1986. DOI:10.3390/molecules23081986
  61. 61. Campana MG, Kurata NP, Foster JT, Helgen LE, Reeder DM, Fleischer RC, et al. White-Nose Syndrome fungus in a 1918 bat specimen from France. Emerging Infectious Diseases 2017;23(9):1611-1612. DOI:10.3201/eid2309.170875

Written By

Craig L. Frank

Submitted: 01 September 2021 Reviewed: 08 September 2021 Published: 15 October 2021