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
Bat white-nose syndrome: a real-time TaqMan polymerase chain reaction test targeting the intergenic spacer region of Geomyces destructanstructans.
Fungal disease and the developing story of bat white-nose syndrome
Frequent arousal from hibernation linked to severity of infection and mortality in bats with white-nose syndrome
Confirmation of white-nose syndrome in bats of Europe and implications of this discovery toward understanding the disease in bats of North America
Recovery of little brown bats (Myotis lucifugus) from natural infection with Geomyces destructans, white-nose syndrome
Bat white-nose syndrome in North America
Experimental infection of bats with Geomyces destructans causes white-nose syndrome
In vitro detection and quantification of botulinum neurotoxin type E activity in avian blood
In vitro detection and quantification of botulinum neurotoxin type E activity in avian blood
Links between type E botulism outbreaks, lake levels, and surface water temperatures in Lake Michigan, 1963-2008
DNA-based detection of the fungal pathogen Geomyces destructans in soil from bat hibernacula
White-nose syndrome fungus (Geomyces destructans) in bats, Europe
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
Bat white-nose syndrome: a real-time TaqMan polymerase chain reaction test targeting the intergenic spacer region of Geomyces destructanstructans.
The fungus Geomyces destructans is the causative agent of white-nose syndrome (WNS), a disease that has killed millions of North American hibernating bats. We describe a real-time TaqMan PCR test that detects DNA from G. destructans by targeting a portion of the multicopy intergenic spacer region of the rRNA gene complex. The test is highly sensitive, consistently detecting as little as 3.3 fg ofAuthorsLaura K. Muller, Jeffrey M. Lorch, Daniel L. Lindner, Michael O'Connor, Andrea Gargas, David S. BlehertFungal disease and the developing story of bat white-nose syndrome
Two recently emerged cutaneous fungal diseases of wildlife, bat white-nose syndrome (WNS) and amphibian chytridiomycosis, have devastated affected populations. Fungal diseases are gaining recognition as significant causes of morbidity and mortality to plants, animals, and humans, yet fewer than 10% of fungal species are known. Furthermore, limited antifungal therapeutic drugs are available, antifuAuthorsDavid S. BlehertFrequent arousal from hibernation linked to severity of infection and mortality in bats with white-nose syndrome
White-nose syndrome (WNS), an emerging infectious disease that has killed over 5.5 million hibernating bats, is named for the causative agent, a white fungus (Geomyces destructans (Gd)) that invades the skin of torpid bats. During hibernation, arousals to warm (euthermic) body temperatures are normal but deplete fat stores. Temperature-sensitive dataloggers were attached to the backs of 504 free-rAuthorsDeeAnn M. Reeder, Craig L. Frank, Gregory G. Turner, Carol U. Meteyer, Allen Kurta, Eric R. Britzke, Megan E. Vodzak, Scott R. Darling, Craig W. Stihler, Alan C. Hicks, Roymon Jacob, Laura E. Grieneisen, Sarah A. Brownlee, Laura K. Muller, David S. BlehertConfirmation of white-nose syndrome in bats of Europe and implications of this discovery toward understanding the disease in bats of North America
No abstract available.AuthorsCarol U. Meteyer, David S. Blehert, Paul M. CryanRecovery of little brown bats (Myotis lucifugus) from natural infection with Geomyces destructans, white-nose syndrome
Geomyces destructans produces the white fungal growth on the muzzle and the tacky white discoloration on wings and ears that characterize white-nose syndrome (WNS) in cave-hibernating bats. To test the hypothesis that postemergent WNS-infected bats recover from infection with G. destructans, 30 little brown bats (Myotis lucifugus) were collected in May 2009 from a WNS-affected hibernation site inAuthorsCarol Uphoff Meteyer, Mick Valent, Jackie Kashmer, Elizabeth L. Buckles, Jeffrey M. Lorch, David S. Blehert, Amanda Lollar, Douglas Berndt, Emily Wheeler, C. LeAnn White, Anne E. BallmannBat white-nose syndrome in North America
* The newly described fungus, Geomyces destructans, causes an invasive skin infection in bats and is the likely agent of white-nose syndrome (WNS). * With immune system functions and body temperatures reduced during hibernation, bats may be unusually susceptible to a pathogenic fungus such as G. destructans. * WNS was first observed in a popular show cave near Albany, New York, leading some investAuthorsDavid S. Blehert, Jeffrey M. Lorch, Anne E. Ballmann, Paul M. Cryan, Carol U. MeteyerExperimental infection of bats with Geomyces destructans causes white-nose syndrome
White-nose syndrome (WNS) has caused recent catastrophic declines among multiple species of bats in eastern North America. The disease's name derives from a visually apparent white growth of the newly discovered fungus Geomyces destructans on the skin (including the muzzle) of hibernating bats. Colonization of skin by this fungus is associated with characteristic cutaneous lesions that are the onlAuthorsJ.M. Lorch, C.U. Meteyer, M.J. Behr, J.G. Boyles, P.M. Cryan, A.C. Hicks, A.E. Ballmann, J.T.H. Coleman, D.N. Redell, D.M. Reeder, D.S. BlehertIn vitro detection and quantification of botulinum neurotoxin type E activity in avian blood
Botulinum neurotoxin serotype E (BoNT/E) outbreaks in the Great Lakes region cause large annual avian mortality events, with an estimated 17,000 bird deaths reported in 2007 alone. During an outbreak investigation, blood collected from bird carcasses is tested for the presence of BoNT/E using the mouse lethality assay. While sensitive, this method is labor-intensive and low throughput and can takeAuthorsTimothy M. Piazza, David S. Blehert, F. Mark Dunning, Brenda M. Berlowski-Zier, Fusun N. Zeytin, Michael D. Samuel, Ward C. TuckerIn vitro detection and quantification of botulinum neurotoxin type E activity in avian blood
Botulinum neurotoxin serotype E (BoNT/E) outbreaks in the Great Lakes region cause large annual avian mortality events, with an estimated 17,000 bird deaths reported in 2007 alone. During an outbreak investigation, blood collected from bird carcasses is tested for the presence of BoNT/E using the mouse lethality assay. While sensitive, this method is labor-intensive and low throughput and can takeAuthorsTimothy M. Piazza, David S. Blehert, F. Mark Dunning, Brenda M. Berlowski-Zier, Fusun N. Zeytin, M. D. Samuel, Ward C. TuckerLinks between type E botulism outbreaks, lake levels, and surface water temperatures in Lake Michigan, 1963-2008
Relationships between large-scale environmental factors and the incidence of type E avian botulism outbreaks in Lake Michigan were examined from 1963 to 2008. Avian botulism outbreaks most frequently occurred in years with low mean annual water levels, and lake levels were significantly lower in outbreak years than in non-outbreak years. Mean surface water temperatures in northern Lake Michigan duAuthorsBrenda Moraska Lafrancois, Stephen C. Riley, David S. Blehert, Anne E. BallmannDNA-based detection of the fungal pathogen Geomyces destructans in soil from bat hibernacula
White-nose syndrome (WNS) is an emerging disease causing unprecedented morbidity and mortality among bats in eastern North America. The disease is characterized by cutaneous infection of hibernating bats by the psychrophilic fungus Geomyces destructans. Detection of G. destructans in environments occupied by bats will be critical for WNS surveillance, management and characterization of the fungalAuthorsDaniel L. Lindner, Andrea Gargas, Jeffrey M. Lorch, Mark T. Banik, Jessie Glaeser, Thomas H. Kunz, David S. BlehertWhite-nose syndrome fungus (Geomyces destructans) in bats, Europe
White-nose syndrome is an emerging disease in North America that has caused substantial declines in hibernating bats. A recently identified fungus (Geomyces destructans) causes skin lesions that are characteristic of this disease. Typical signs of this infection were not observed in bats in North America before white-nose syndrome was detected. However, unconfirmed reports from Europe indicated whAuthorsG. Wibbelt, A. Kurth, D. Hellmann, M. Weishaar, A. Barlow, M. Veith, J. Pruger, T. Gorfol, T. Grosche, F. Bontadina, U. Zophel, Hans-Peter Seidl, P.M. Cryan, D.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