| Literature DB >> 25445339 |
Jung-Mi Kim1, Ha-Yeon Song1, Hyo-Jin Choi1, Suk-Hyun Yun2, Kum-Kang So2, Han-Kyu Ko3, Dae-Hyuk Kim4.
Abstract
This study attempted to cure the edible mushroom Lentinula edodes strain FMRI0339 of the L. edodes mycovirus (LeV) in order to obtain an isogenic virus-free fungal strain as well as a virus-infected strain for comparison. Mycelial fragmentation, followed by being spread on a plate with serial dilutions resulted in a virus-free colony. Viral absence was confirmed with gel electrophoresis after dsRNA-specific virus purification, Northern blot analysis, and PCR using reverse transcriptase (RT-PCR). Once cured, all of fungal cultures remained virus-free over the next two years. Interestingly, the viral titer of LeV varied depending on the culture condition. The titer from the plate culture showed at least a 20-fold higher concentration than that grown in the liquid culture. However, the reduced virus titer in the liquid culture was recovered by transferring the mycelia to a plate containing the same medium. In addition, oxygen-depleted culture conditions resulted in a significant decrease of viral concentration, but not to the extent seen in the submerged liquid culture. Although no discernable phenotypic changes in colony morphology were observed, virus-cured strains showed significantly higher growth rates and mycelial mass than virus-infected strains. These results indicate that LeV infection has a deleterious effect on mycelial growth.Entities:
Keywords: Isogenic strain; Lentinula edodes; Mycovirus; dsRNA
Mesh:
Year: 2014 PMID: 25445339 DOI: 10.1016/j.virusres.2014.11.016
Source DB: PubMed Journal: Virus Res ISSN: 0168-1702 Impact factor: 3.303