ArticleEcology and evolution2015
Antibodies to Pseudogymnoascus destructans are not sufficient for protection against white-nose syndrome.
Article in Ecology and evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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Who cites it
19 citing papers in PubMed, 41 citations in OpenAlex.
- Diverse hosts, diverse immune systems: Evolutionary variation in bat immunology.Annals of the New York Academy of Sciences · 2025Review
- Strategies and limitations of the bat immune response toFrontiers in immunology · 2025Review
- Signals of positive selection in genomes of palearctic Myotis-bats coexisting with a fungal pathogen.BMC genomics · 2024Article
- What are the 100 most cited fungal genera?Studies in mycology · 2024Article
- Levels of pathogen virulence and host resistance both shape the antibody response to an emerging bacterial disease.Scientific reports · 2021Article
- Ecology and impacts of white-nose syndrome on bats.Nature reviews. Microbiology · 2021Review
- Applied ecoimmunology: using immunological tools to improve conservation efforts in a changing world.Conservation physiology · 2021Article
- Major histocompatibility complex variation is similar in little brown bats before and after white-nose syndrome outbreak.Ecology and evolution · 2020Article
- Population Connectivity Predicts Vulnerability to White-Nose Syndrome in the Chilean Myotis (G3 (Bethesda, Md.) · 2020Article
- Article
- Virally-vectored vaccine candidates against white-nose syndrome induce anti-fungal immune response in little brown bats (Myotis lucifugus).Scientific reports · 2019Article
- Phenotypic Divergence along Geographic Gradients Reveals Potential for Rapid Adaptation of the White-Nose Syndrome Pathogen, Pseudogymnoascus destructans, in North America.Applied and environmental microbiology · 2018Article
- Energy conserving thermoregulatory patterns and lower disease severity in a bat resistant to the impacts of white-nose syndrome.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2018Article
- Pseudogymnoascus destructans transcriptome changes during white-nose syndrome infections.Virulence · 2017Article
- Immune responses in hibernating little brown myotis (Proceedings. Biological sciences · 2017Article
- Host persistence or extinction from emerging infectious disease: insights from white-nose syndrome in endemic and invading regions.Proceedings. Biological sciences · 2016Article
- White-nose syndrome survivors do not exhibit frequent arousals associated with Pseudogymnoascus destructans infection.Frontiers in zoology · 2016Article
- The White-Nose Syndrome Transcriptome: Activation of Anti-fungal Host Responses in Wing Tissue of Hibernating Little Brown Myotis.PLoS pathogens · 2015Article
- Article
Corrections and comments
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Authors and funding
12 authors at 3 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
White-nose syndrome (WNS) is a fungal disease caused by Pseudogymnoascus destructans (Pd) that affects bats during hibernation. Although millions of bats have died from WNS in North America, mass mortality has not been observed among European bats infected by the fungus, leading to the suggestion that bats in Europe are immune. We tested the hypothesis that an antibody-mediated immune response can provide protection against WNS by quantifying antibodies reactive to Pd in blood samples from seven species of free-ranging bats in North America and two free-ranging species in Europe. We also quantified antibodies in blood samples from little brown myotis (Myotis lucifugus) that were part of a captive colony that we injected with live Pd spores mixed with adjuvant, as well as individuals surviving a captive Pd infection trial. Seroprevalence of antibodies against Pd, as well as antibody titers, was greater among little brown myotis than among four other species of cave-hibernating bats in North America, including species with markedly lower WNS mortality rates. Among little brown myotis, the greatest titers occurred in populations occupying regions with longer histories of WNS, where bats lacked secondary symptoms of WNS. We detected antibodies cross-reactive with Pd among little brown myotis naïve to the fungus. We observed high titers among captive little brown myotis injected with Pd. We did not detect antibodies against Pd in Pd-infected European bats during winter, and titers during the active season were lower than among little brown myotis. These results show that antibody-mediated immunity cannot explain survival of European bats infected with Pd and that little brown myotis respond differently to Pd than species with higher WNS survival rates. Although it appears that some species of bats in North America may be developing resistance to WNS, an antibody-mediated immune response does not provide an explanation for these remnant populations.
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