Disruption of Botrytis cinerea class I chitin synthase gene Bcchs1 results in cell wall weakening and reduced virulence
To get a better insight into the relationship between cell wall integrity and pathogenicity of the fungus Botrytis cinerea, we have constructed chitin synthase mutants. A 620 bp class I chitin synthase gene fragment ( Bcchs1) obtained by PCR amplification was used to disrupt the corresponding gene i...
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Published in | Fungal genetics and biology Vol. 40; no. 1; pp. 38 - 46 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.10.2003
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Subjects | |
Online Access | Get full text |
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Summary: | To get a better insight into the relationship between cell wall integrity and pathogenicity of the fungus
Botrytis cinerea, we have constructed chitin synthase mutants. A 620 bp class I chitin synthase gene fragment (
Bcchs1) obtained by PCR amplification was used to disrupt the corresponding gene in the genome. Disruption of
Bcchs1 occurred at a frequency of 8%. Nine independent mutants were obtained and the
Bcchs1 mutant phenotype compared to that of transformants in which the gene was not disrupted. These disruption mutants were dramatically reduced in their in vitro Mg
2+, Mn
2+, and Co
2+-dependent chitin synthase activity. Chitin content was reduced by 30%, indicating that Bcchs1p contributes substantially to cell wall composition. Enzymatic degradation by a cocktail of glucanases revealed cell wall weakening in the mutant.
Bcchs1 was transcribed at a constant level during vegetative exponential growth, suggesting that it was necessary throughout hyphal development.
Bcchs1 mutant growth was identical to undisrupted control transformant growth, however, the mutant exhibited reduced pathogenicity on vine leaves. It can be assumed that disruption of
Bcchs1 leads to cell wall weakening which might slow down
in planta fungal progression. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1087-1845 1096-0937 |
DOI: | 10.1016/S1087-1845(03)00065-3 |