Characterization and PCR-based detection of benzimidazole-resistant isolates of Monilinia laxa in California

被引:84
作者
Ma, ZH
Yoshimura, MA
Holtz, BA
Michailides, TJ
机构
[1] Univ Calif Davis, Kearney Agr Ctr, Dept Plant Pathol, Parlier, CA 93648 USA
[2] Calif Polytech State Univ San Luis Obispo, Dept Biol Sci, San Luis Obispo, CA 93407 USA
[3] Univ Calif Cooperat Extens, Madera, CA 93637 USA
关键词
allele-specific PCR; brown rot; Monilinia laxa; PCR-restriction fragment length polymorphism (PCR-RFLP); Prunus spp;
D O I
10.1002/ps.982
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Monilinia laxa is a pathogen of brown rot of stone fruit and almond in California, causing blossom blights and fruit rots. In this study, low-level resistance to the benzimidazole fungicides benomyl and thiophanate-methyl was detected in field isolates of M laxa collected from stone fruits and almonds in California. Low-resistant (LR) isolates grew in potato dextrose agar (PDA) plates amended with benomyl and thiophanate-methyl at I and 5 mu g ml(-1), respectively, but not in plates amended with benomyl at 5 mu g ml(-1) or thiophanate-methyl at 50 mu g ml(-1). The benzimidazole LR isolates were characterized by temperature sensitivity and the DNA sequence of the beta-tubulin gene. The LR isolates showed high-temperature sensitivity, being sensitive to 1 mu g ml(-1) of benomyl at 28 degrees C but resistant at 8-24 degrees C. Analysis of the DNA sequence of the beta-tubulin gene showed that the LR isolates had a point mutation at the amino-acid position 240, causing substitution of leucine by phenylalanine. Based on the point mutation, a pair of allele-specific PCR primers was developed for rapid detection of LR isolates of M laxa. In addition, a pair of PCR primers specific to M laxa was developed on the basis of the differences in the DNA sequence of the intron 6 of beta-tubulin gene from M laxa, M fructicola and other fungal species. The primer pair amplified the expected 376-bp DNA fragment from all M laxa isolates tested, but not from 14 other fungal species isolated from stone fruit and almond crops. The restriction endonuclease BsmA I recognized the sequence GTCTCC in the PCR products from sensitive (S) isolates only, but not the GTTTCC sequence in the PCR products from LR isolates. The endonuclease digested the 376-bp PCR products from S isolates to produce two bands (111 and 265bp) on agarose gels. Thus, both allele-specific PCR and the PCR-restriction fragment length polymorphism (PCR-RFLP) methods could be useful for rapidly detecting benzimidazole-resistant isolates of M laxa from stone fruit and almond crops in California. (c) 2004 Society of Chemical Industry.
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页码:449 / 457
页数:9
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