Distributed under Creative Commons Cc-by 4.0 Epidermal Cell Death in Frogs with Chytridiomycosis
Distributed under Creative Commons Cc-by 4.0 Epidermal Cell Death in Frogs with Chytridiomycosis
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根据知识共享 Cc-by 4.0 患有壶菌病的青蛙表皮细胞死亡分发
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通讯作者:
L. Berger
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作者:
L. Brannelly;A. Roberts;L. Skerratt;L. Berger
Background. Amphibians are declining at an alarming rate, and one of the major causes of decline is the infectious disease chytridiomycosis. Parasitic fungal sporangia occur within epidermal cells causing epidermal disruption, but these changes have not been well characterised. Apoptosis (planned cell death) can be a damaging response to the host but may alternatively be a mechanism of pathogen removal for some intracellular infections. Methods. In this study we experimentally infected two endangered amphibian species Pseudophryne corroboree and Litoria verreauxii alpina with the causal agent of chytrid-iomycosis. We quantified cell death in the epidermis through two assays: terminal transferase-mediated dUTP nick end-labelling (TUNEL) and caspase 3/7. Results. Cell death was positively associated with infection load and morbidity of clinically infected animals. In infected amphibians, TUNEL positive cells were concentrated in epidermal layers, correlating to the localisation of infection within the skin. Caspase activity was stable and low in early infection, where pathogen loads were light but increasing. In animals that recovered from infection, caspase activity gradually returned to normal as the infection cleared. Whereas, in amphibians that did not recover, caspase activity increased dramatically when infection loads peaked. Discussion. Increased cell death may be a pathology of the fungal parasite, likely contributing to loss of skin homeostatic functions, but it is also possible that apoptosis suppression may be used initially by the pathogen to help establish infection. Further research should explore the specific mechanisms of cell death and more specifically apoptosis regulation during fungal infection.
影响因子:
15.9
作者:
Kim, JM;Eckmann, L;Kagnoff, MF
通讯作者:
Kagnoff, MF