Publication:
Identification of catalase as an early up-regulated gene in Beauveria bassiana and its role in entomopathogenic fungal virulence

dc.contributor.authorDuriya Chantasinghen_US
dc.contributor.authorSupattra Kitikhunen_US
dc.contributor.authorNemat O. Keyhanien_US
dc.contributor.authorKatewadee Boonyapakronen_US
dc.contributor.authorHonglada Thoetkiattikulen_US
dc.contributor.authorKusol Pootanakiten_US
dc.contributor.authorLily Eurwilaichitren_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Floridaen_US
dc.date.accessioned2018-10-19T04:28:51Z
dc.date.available2018-10-19T04:28:51Z
dc.date.issued2013-11-01en_US
dc.description.abstractThe ability of entomopathogenic fungi to infect insects is a complex process involving differential expression of numerous genes some of which are up-regulated when the fungus is in contact with or exposed to insect cuticles. In this report, we identified a set of differentially expressed genes in the entomopathogenic fungus Beauveria bassiana BCC2659 in response to Spodoptera exigua larvae. PCR-select suppression subtractive hybridization (PCR-SSH) was used to identify genes differentially expressed during the initial aspects of the fungal-insect interaction, i.e. up to a 2h post-infection model. Ten fungal genes identified by PCR-SHH were confirmed to be up-regulated by semi-quantitative RT-PCR. Of these genes, a catalase (catE7), implicated in stress resistance, was chosen for further characterization in order to probe its role in B. bassiana pathogenesis and to determine whether over-expression would result in a more virulent strain. To investigate this, a transgenic B. bassiana strain, overexpressing CatE7 was constructed. Fungal transformant lines with extra catE7 copies (Bb::BbcatE7) showed ~2-fold higher catalase activity than the wild type. Bb::BbcatE7 strains germinated faster than the wild-type parent and exhibited significantly higher virulence against S. exigua larvae. Although the Bb::BbcatE7 strains were no better than wild type in terms of vegetative growth in the presence of exogenous H2O2concentrations, conidial germination rates were higher in the Bb::BbcatE7 strain in the presence of H2O2. These results suggest that responses mediated by catalases play an important role in the fungal-insect infection process and the manipulation of catalase expression can lead to more effective fungal strains for insect control. © 2013 Elsevier Inc.en_US
dc.identifier.citationBiological Control. Vol.67, No.2 (2013), 85-93en_US
dc.identifier.doi10.1016/j.biocontrol.2013.08.004en_US
dc.identifier.issn10499644en_US
dc.identifier.other2-s2.0-84883442967en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/30959
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883442967&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleIdentification of catalase as an early up-regulated gene in Beauveria bassiana and its role in entomopathogenic fungal virulenceen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883442967&origin=inwarden_US

Files

Collections