David S Blehert
David Blehert is Chief of the National Wildlife Health Center's Laboratory Sciences Branch
David Blehert received a Ph.D. in Bacteriology from the University of Wisconsin-Madison in 1999, and he joined the USGS National Wildlife Health Center (NWHC) as a Diagnostic and Research Microbiologist in 2003. His research focuses on investigation of the ecology and pathobiology of bat white-nose syndrome. Today, Dr. Blehert is Chief of the NWHC's Laboratory Sciences Branch, which specializes in the investigation of unusual mortality events impacting our nation's wildlife. His laboratories also conduct surveillance for animal diseases of high consequence, such as white-nose syndrome in bats and highly pathogenic avian influenza viruses in wild waterfowl.
Professional Experience
2014 to present, Chief, Laboratory Sciences Branch, U.S. Geological Survey National Wildlife Health Center, Madison, Wisconsin
2003-2014, Diagnostic and Research Microbiologist, U.S. Geological Survey National Wildlife Health Center, Madison, Wisconsin
1999 to 2003, Intramural Research Training Associate Fellow, National Institutes of Health, Bethesda, Maryland
Education and Certifications
Ph.D. Bacteriology, University of Wisconsin-Madison, 1999
B.S. Biology, University of Minnesota-Minneapolis St. Paul, 1993
Affiliations and Memberships*
Fellow, American Academy of Microbiology. Elected in February, 2020.
Fellow, Canadian Institute for Advanced Research. CIFAR Program Fungal Kingdom: Threats and Opportunities. Elected in June, 2019.
Honorary Fellow, University of Wisconsin-Madison School of Veterinary Medicine, Department of Pathobiological Sciences. 2003-2018.
Member, Wildlife Disease Association. 2006-present.
Member, American Society for Microbiology. 1995-present.
Science and Products
Moving beyond too little, too late: managing emerging infectious diseases in wild populations requires international policy and partnerships
Nonlethal screening of bat-wing skin with the use of ultraviolet fluorescence to detect lesions indicative of white-nose syndrome
White-nose syndrome initiates a cascade of physiologic disturbances in the hibernating bat host
Acute pasteurellosis in wild big brown bats (Eptesicus fuscus)
Pathophysiology of white-nose syndrome in bats: A mechanistic model linking wing damage to mortality
White-nose syndrome in bats: Illuminating the darkness
Electrolyte depletion in white-nose syndrome bats
Distribution and environmental persistence of the causative agent of white-nose syndrome, Geomyces destructans, in bat hibernacula of the eastern United States
Epidemiology of a Salmonella enterica subsp. Enterica serovar Typhimurium strain associated with a songbird outbreak.
Inoculation of bats with European Geomyces destructans supports the novel pathogen hypothesis for the origin of white-nose syndrome
A culture-based survey of fungi in soil from bat hibernacula in the eastern United States and its implications for detection of Geomyces destructans, the causal agent of bat white-nose syndrome
Temperature-dependent growth of Geomyces destructans, the fungus that causes bat white-nose syndrome
Non-USGS Publications**
**Disclaimer: The views expressed in Non-USGS publications are those of the author and do not represent the views of the USGS, Department of the Interior, or the U.S. Government.
Science and Products
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Filter Total Items: 71
Moving beyond too little, too late: managing emerging infectious diseases in wild populations requires international policy and partnerships
Emerging infectious diseases (EIDs) are on the rise due to multiple factors, including human facilitated movement of pathogens, broad-scale landscape changes, and perturbations to ecological systems (Jones et al. 2008; Fisher et al. 2012). Epidemics in wildlife are problematic because they can lead to pathogen spillover to new host organisms, erode biodiversity and threaten ecosystems that sustainAuthorsJamie Voyles, A. Marm Kilpatrick, James P. Collins, Matthew C. Fisher, Winifred F. Frick, Hamish I. McCallum, Craig K. R. Willis, David S. Blehert, Kris A. Murray, Robert Puschendorf, Erica Bree Rosenblum, Benjamin M. Bolker, Tina L. Cheng, Kate E. Langwig, Daniel L. Linder, Mary Toothman, Mark Q. Wilber, Cheryl J. BriggsNonlethal screening of bat-wing skin with the use of ultraviolet fluorescence to detect lesions indicative of white-nose syndrome
Definitive diagnosis of the bat disease white-nose syndrome (WNS) requires histologic analysis to identify the cutaneous erosions caused by the fungal pathogen Pseudogymnoascus [formerly Geomyces] destructans (Pd). Gross visual inspection does not distinguish bats with or without WNS, and no nonlethal, on-site, preliminary screening methods are available for WNS in bats. We demonstrate that long-wAuthorsGregory G. Turner, Carol U. Meteyer, Hazel Barton, John F. Gumbs, DeeAnn M. Reeder, Barrie Overton, Hana Bandouchova, Tomáš Bartonička, Natália Martínková, Jiri Pikula, Jan Zukal, David S. BlehertWhite-nose syndrome initiates a cascade of physiologic disturbances in the hibernating bat host
Background The physiological effects of white-nose syndrome (WNS) in hibernating bats and ultimate causes of mortality from infection with Pseudogymnoascus (formerly Geomyces) destructans are not fully understood. Increased frequency of arousal from torpor described among hibernating bats with late-stage WNS is thought to accelerate depletion of fat reserves, but the physiological mechanisms thatAuthorsMichelle L. Verant, Carol U. Meteyer, John R. Speakman, Paul M. Cryan, Jeffrey M. Lorch, David S. BlehertAcute pasteurellosis in wild big brown bats (Eptesicus fuscus)
We report acute fatal pasteurellosis in wild big brown bats (Eptesicus fuscus) in Wisconsin, USA. Mortality of approximately 100 bats was documented over 4 wk, with no evidence for predatory injuries. Pasteurella multocida serotype 1 was isolated from multiple internal organs from four of five bats examined postmortem.AuthorsDavid S. Blehert, Ramón P. Maluping, David E. Green, Brenda M. Berlowski-Zier, Anne E. Ballmann, Julia LangenbergPathophysiology of white-nose syndrome in bats: A mechanistic model linking wing damage to mortality
White-nose syndrome is devastating North American bat populations but we lack basic information on disease mechanisms. Altered blood physiology owing to epidermal invasion by the fungal pathogen Geomyces destructans (Gd) has been hypothesized as a cause of disrupted torpor patterns of affected hibernating bats, leading to mortality. Here, we present data on blood electrolyte concentration, haematoAuthorsLisa Warnecke, James M. Turner, Trent K. Bollinger, Vikram Misra, Paul M. Cryan, David S. Blehert, Gudrun Wibbelt, Craig K. R. WillisWhite-nose syndrome in bats: Illuminating the darkness
Happy ten-year anniversary to BMC Biology! We can attest to the effectiveness of the journal in reaching a great diversity of scientists based on reader responses to our commentary [1] about bat white-nose syndrome (WNS) two years ago. WNS is still on course to rank among the most destructive wildlife diseases to emerge in recent history, and it has continued to have unprecedented effects on populAuthorsPaul M. Cryan, Carol U. Meteyer, Justin G. Boyles, David S. BlehertElectrolyte depletion in white-nose syndrome bats
The emerging wildlife disease white-nose syndrome is causing widespread mortality in hibernating North American bats. White-nose syndrome occurs when the fungus Geomyces destructans infects the living skin of bats during hibernation, but links between infection and mortality are underexplored. We analyzed blood from hibernating bats and compared blood electrolyte levels to wing damage caused by thAuthorsPaul M. Cryan, Carol Uphoff Meteyer, David S. Blehert, Jeffrey M. Lorch, DeeAnn M. Reeder, Gregory G. Turner, Julie Webb, Melissa Behr, Michelle L. Verant, Robin E. Russell, Kevin T. CastleDistribution and environmental persistence of the causative agent of white-nose syndrome, Geomyces destructans, in bat hibernacula of the eastern United States
White-nose syndrome (WNS) is an emerging disease of hibernating bats caused by the recently described fungus Geomyces destructans. First isolated in 2008, the origins of this fungus in North America and its ability to persist in the environment remain undefined. To investigate the correlation between manifestation of WNS and distribution of G. destructans in the U.S., we analyzed sediment samplesAuthorsJeffrey M. Lorch, Laura K. Muller, Robin E. Russell, Michael O'Connor, Daniel L. Lindner, David S. BlehertEpidemiology of a Salmonella enterica subsp. Enterica serovar Typhimurium strain associated with a songbird outbreak.
Salmonella enterica subsp. enterica serovar Typhimurium is responsible for the majority of salmonellosis cases worldwide. This Salmonella serovar is also responsible for die-offs in songbird populations. In 2009, there was an S. Typhimurium epizootic reported in pine siskins in the eastern United States. At the time, there was also a human outbreak with this serovar that was associated with contamAuthorsDavid S. Blehert, Sonia M. Hernandez, Kevin Keel, Susan Sanchez, Eija TreesInoculation of bats with European Geomyces destructans supports the novel pathogen hypothesis for the origin of white-nose syndrome
White-nose syndrome (WNS) is an emerging disease of hibernating bats associated with cutaneous infection by the fungus Geomyces destructans (Gd), and responsible for devastating declines of bat populations in eastern North America. Affected bats appear emaciated and one hypothesis is that they spend too much time out of torpor during hibernation, depleting vital fat reserves required to survive thAuthorsLisa Warnecke, James M. Turner, Trent K. Bollinger, Jeffrey M. Lorch, Vikram Misra, Paul M. Cryan, Gudrun Wibbelt, David S. Blehert, Craig K. R. WillisA culture-based survey of fungi in soil from bat hibernacula in the eastern United States and its implications for detection of Geomyces destructans, the causal agent of bat white-nose syndrome
The recent emergence of white-nose syndrome (WNS), a fungal disease causing unprecedented mortality among hibernating bats of eastern North America, has revealed a knowledge gap regarding fungal communities associated with bats and their hibernacula. We used culture-based techniques to investigate the diversity of fungi in soil samples collected from 24 bat hibernacula in the eastern United StatesAuthorsJeffrey M. Lorch, Daniel L. Lindner, Andrea Gargas, Laura K. Muller, Andrew M. Minnis, David S. BlehertTemperature-dependent growth of Geomyces destructans, the fungus that causes bat white-nose syndrome
White-nose syndrome (WNS) is an emergent disease estimated to have killed over five million North American bats. Caused by the psychrophilic fungus Geomyces destructans, WNS specifically affects bats during hibernation. We describe temperature-dependent growth performance and morphology for six independent isolates of G. destructans from North America and Europe. Thermal performance curves for allAuthorsMichelle L. Verant, Justin G. Boyles, William Waldrep, Gudrun Wibbelt, David S. BlehertNon-USGS Publications**
Rickard, A.H., R.J. Palmer, Jr., D.S. Blehert, S.R. Campagna, M.F. Semmelhack, P.G. Egland, B.L. Bassler, and P.E. Kolenbrander. 2006. Autoinducer 2: a concentration-dependent signal for mutualistic bacterial biofilm growth. Molecular Microbiology 60: 1446-1456.Orville, A. M., L. Manning, D.S. Blehert, J.M. Studts, B.W. Matthews, B.G. Fox, and G.H. Chambliss. 2004. Crystallization and preliminary analysis of xenobiotic reductase A and ligand complexes from Pseudomonas putida II-B. Acta Crystallographica 60: 957-961.Orville, A. M., L. Manning, D.S. Blehert, B.G. Fox, and G.H. Chambliss. 2004. Crystallization and preliminary analysis of xenobiotic reductase B from Pseudomonas fluorescens I-C. Acta Crystallographica 60: 1289-1291.Blehert, D.S., R.J. Palmer, Jr., J.B. Xavier, J.S. Almeida, and P.E. Kolenbrander. 2003. Autoinducer-2 production by Streptococcus gordonii DL1 and the biofilm phenotype of a luxS mutant are influenced by nutritional conditions. Journal of Bacteriology 185: 4851-4860.Kolenbrander, P.E., R.F. Lerud, D.S. Blehert, P.G. Egland, J.S. Foster, and R.J. Palmer, Jr. 2003. The role of coaggregation in oral biofilm formation. In V. O’Flaherty, A. Moran, P. Lens and P. Stoodley (eds.), Biofilms in Medicine, Industry and Environmental Biotechnology, IWA Publishing, London, UK. p. 32-46.Kolenbrander, P.E., R.N. Andersen, D.S. Blehert, P.G. Egland, J.S. Foster, and R.J. Palmer, Jr. 2002. Communication among oral bacteria. Microbiology and Molecular Biology Reviews 66: 486-505.Blehert, D.S., B.G. Fox, and G.H. Chambliss. 1999. Cloning and sequence analysis of two Pseudomonas flavoprotein xenobiotic reductases. Journal of Bacteriology 181: 6254-6263.Blehert, D.S., K.L. Knoke, B.G. Fox, and G.H. Chambliss. 1997. Regioselectivity of nitroglycerin denitration by flavoprotein nitroester reductases purified from two Pseudomonas species. Journal of Bacteriology 179: 6912-6920.**Disclaimer: The views expressed in Non-USGS publications are those of the author and do not represent the views of the USGS, Department of the Interior, or the U.S. Government.
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*Disclaimer: Listing outside positions with professional scientific organizations on this Staff Profile are for informational purposes only and do not constitute an endorsement of those professional scientific organizations or their activities by the USGS, Department of the Interior, or U.S. Government