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Ancestral chytrid pathogen remains hypervirulent following its long coevolution with amphibian hosts
Author(s) -
Minjie Fu,
Bruce Waldman
Publication year - 2019
Publication title -
proceedings of the royal society b biological sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.342
H-Index - 253
eISSN - 1471-2954
pISSN - 0962-8452
DOI - 10.1098/rspb.2019.0833
Subject(s) - biology , amphibian , chytridiomycosis , zoology , host (biology) , emerging infectious disease , population , lineage (genetic) , pathogen , ecology , virulence , microbiology and biotechnology , genetics , outbreak , virology , demography , sociology , gene
Many amphibian species around the world, except in Asia, suffer morbidity and mortality when infected by the emerging infectious pathogenBatrachochytrium dendrobatidis (Bd). A lineage of the amphibian chytrid fungus isolated from South Korean amphibians (BdAsia-1) is evolutionarily basal to recombinant global pandemic lineages (BdGPL) associated with worldwide amphibian population declines. In Asia, the Bd pathogen and its amphibian hosts have coevolved over 100 years or more. Thus, resilience of Asian amphibian populations to infection might result from attenuated virulence of endemic Bd lineages, evolved immunity to the pathogen or both. We compared susceptibilities of an Australasian amphibian,Litoria caerulea , known to lack resistance to BdGPL, with those of three Korean species,Bufo gargarizans ,Bombina orientalis andHyla japonica , after inoculation with BdAsia-1, BdGPL or a blank solution. Subjects became infected in all experimental treatments but Korean species rapidly cleared themselves of infection, regardless of Bd lineage. They survived with no apparent secondary effects. By contrast,L. caerulea , after infection by either BdAsia-1 or BdGPL, suffered deteriorating body condition and carried progressively higher Bd loads over time. Subsequently, most subjects died. Comparing their effects onL. caerulea , BdAsia-1 induced more rapid disease progression than BdGPL. The results suggest that genomic recombination with other lineages was not necessary for the ancestral Bd lineage to evolve hypervirulence over its long period of coevolution with amphibian hosts. The pathogen's virulence may have driven strong selection for immune responses in endemic Asian amphibian host species.

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