Genome-Wide Transcriptional Response of Silurana (Xenopus) tropicalis to Infection with the Deadly Chytrid Fungus

被引:83
作者
Rosenblum, Erica Bree
Poorten, Thomas J.
Settles, Matthew
Murdoch, Gordon K.
Robert, Jacques
Maddox, Nicole
Eisen, Michael B.
机构
[1] Department of Biological Sciences, University of Idaho, Moscow, ID
[2] Department of Molecular and Cell Biology, Department of Integrative Biology, University of California, Berkeley, CA
[3] School of Molecular Bioscience, Department of Animal Sciences, Washington State University, Pullman, WA
[4] Department of Animal and Veterinary Science, University of Idaho, Moscow, ID
[5] Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY
[6] Howard Hughes Medical Institute, University of California, Berkeley, CA
来源
PLOS ONE | 2009年 / 4卷 / 08期
关键词
D O I
10.1371/journal.pone.0006494
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Emerging infectious diseases are of great concern for both wildlife and humans. Several highly virulent fungal pathogens have recently been discovered in natural populations, highlighting the need for a better understanding of fungal-vertebrate host-pathogen interactions. Because most fungal pathogens are not fatal in the absence of other predisposing conditions, host-pathogen dynamics for deadly fungal pathogens are of particular interest. The chytrid fungus Batrachochytrium dendrobatidis (hereafter Bd) infects hundreds of species of frogs in the wild. It is found worldwide and is a significant contributor to the current global amphibian decline. However, the mechanism by which Bd causes death in amphibians, and the response of the host to Bd infection, remain largely unknown. Here we use whole-genome microarrays to monitor the transcriptional responses to Bd infection in the model frog species, Silurana (Xenopus) tropicalis, which is susceptible to chytridiomycosis. To elucidate the immune response to Bd and evaluate the physiological effects of chytridiomycosis, we measured gene expression changes in several tissues (liver, skin, spleen) following exposure to Bd. We detected a strong transcriptional response for genes involved in physiological processes that can help explain some clinical symptoms of chytridiomycosis at the organismal level. However, we detected surprisingly little evidence of an immune response to Bd exposure, suggesting that this susceptible species may not be mounting efficient innate and adaptive immune responses against Bd. The weak immune response may be partially explained by the thermal conditions of the experiment, which were optimal for Bd growth. However, many immune genes exhibited decreased expression in Bd-exposed frogs compared to control frogs, suggesting a more complex effect of Bd on the immune system than simple temperature-mediated immune suppression. This study generates important baseline data for ongoing efforts to understand differences in response to Bd between susceptible and resistant frog species and the effects of chytridiomycosis in natural populations.
引用
收藏
页数:10
相关论文
共 51 条
[1]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[2]   Virulence of the amphibian chytrid fungus Batrachochytrium dendrobatidis varies with the strain [J].
Berger, L ;
Marantelli, G ;
Skerratt, LL ;
Speare, R .
DISEASES OF AQUATIC ORGANISMS, 2005, 68 (01) :47-50
[3]   Chytridiomycosis causes amphibian mortality associated with population declines in the rain forests of Australia and Central America [J].
Berger, L ;
Speare, R ;
Daszak, P ;
Green, DE ;
Cunningham, AA ;
Goggin, CL ;
Slocombe, R ;
Ragan, MA ;
Hyatt, AD ;
McDonald, KR ;
Hines, HB ;
Lips, KR ;
Marantelli, G ;
Parkes, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :9031-9036
[4]   Effect of season and temperature on mortality in amphibians due to chytridiomycosis [J].
Berger, L ;
Speare, R ;
Hines, HB ;
Marantelli, G ;
Hyatt, AD ;
McDonald, KR ;
Skerratt, LF ;
Olsen, V ;
Clarke, JM ;
Gillespie, G ;
Mahony, M ;
Sheppard, N ;
Williams, C ;
Tyler, MJ .
AUSTRALIAN VETERINARY JOURNAL, 2004, 82 (07) :434-439
[5]   Immune response to fungal infections [J].
Blanco, Jose L. ;
Garcia, Marta E. .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2008, 125 (1-2) :47-70
[6]   Bat White-Nose Syndrome: An Emerging Fungal Pathogen? [J].
Blehert, David S. ;
Hicks, Alan C. ;
Behr, Melissa ;
Meteyer, Carol U. ;
Berlowski-Zier, Brenda M. ;
Buckles, Elizabeth L. ;
Coleman, Jeremy T. H. ;
Darling, Scott R. ;
Gargas, Andrea ;
Niver, Robyn ;
Okoniewski, Joseph C. ;
Rudd, Robert J. ;
Stone, Ward B. .
SCIENCE, 2009, 323 (5911) :227-227
[7]   A comparison of normalization methods for high density oligonucleotide array data based on variance and bias [J].
Bolstad, BM ;
Irizarry, RA ;
Åstrand, M ;
Speed, TP .
BIOINFORMATICS, 2003, 19 (02) :185-193
[8]   Rapid quantitative detection of chytridiomycosis (Batrachochytrium dendrobatidis) in amphibian samples using real-time Taqman PCR assay [J].
Boyle, DG ;
Boyle, DB ;
Olsen, V ;
Morgan, JAT ;
Hyatt, AD .
DISEASES OF AQUATIC ORGANISMS, 2004, 60 (02) :141-148
[9]  
Daszak P, 2004, HERPETOL J, V14, P201
[10]   Hypoxia-inducible factor 1:: regulation by hypoxic and non-hypoxic activators [J].
Déry, MAC ;
Michaud, MD ;
Richard, DE .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2005, 37 (03) :535-540