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2 Journal of Plant Protection Research

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Multigene phylogeny reveals three new records of Colletotrichum spp. and several new host records for the mycobiota of Iran

100%

Arzanlou M. , Bakhshi M. , Karimi K. , Torbati M.

Journal of Plant Protection Research

2015

tom 55

nr 2

The genus Colletotrichum comprises a number of plant pathogens of major importance which cause anthracnose diseases on a wide range of woody and herbaceous plants worldwide. With the advent of molecular studies, it has been shown that most of the previously known species e.g. C. boninense, C. acutatum, and C. gloeosporioides have been split into several species. In the present study, the identity of Colletotrichum isolates from the northern and northwestern zone of Iran were determined based on multi-gene phylogenetic analyses. Phylogenetic analysis based on a combination of internal transcribed spacer (ITS), beta tubulin (TUB), histone H3 (HIS), calmodulin (CAL), and actin (ACT) loci, clustered our isolates into three clades, including C. salicis on Salix sp., Colletotrichum sp. (C. fuscum sensu lato) within the C. destructivum species complex on Viola sp., and C. fructicola on Citrus sinensis, Malus domestica, Gleditsia caspica, and Sambucus ebulus. These three species are new for mycobiota of Iran. According to these results, Viola sp. from West Azerbaijan (Khoy-Firouragh) is a new host for Colletotrichum sp. in the C. destructivum species complex. Furthermore, C. sinensis from Mazandaran (Behshahr), and G. caspica, and S. ebulus from Guilan (Talesh), are new host records for C. fructicola.

Inhibitory effects of antagonistic bacteria inhabiting the rhizosphere of the sugarbeet plants, on Cercospora beticola Sacc., the causal agent of Cercospora leaf spot disease on sugarbeet

88%

Arzanlou M. , Mousavi S. , Bakhshi M. , Khakvar R. , Bandehagh A.

nr 1

In the present study, the antagonistic capability of bacterial agents inhabiting the rhizosphere of sugarbeet plants were evaluated against Cercospora beticola Sacc. under laboratory and greenhouse conditions. After preliminary screening using the dual culture method, 14 strains with higher antagonistic capability were selected for further inhibitory assays against C. beticola. Bacterial strains were identified based on the sequence data of the small subunit-rDNA (SSU-rDNA) gene. Based on the SSU sequence data, the identity of bacterial strains were determined as Bacillus (10 strains: RB1, RB2, RB3, RB4, RB5, RB6, RB7, RB8, RB9, RB10), Paenibacillus (two strains: RP1, RP2), Enterobacter (one strain: RE), and Pseudomonas (one strain: RPs). The results obtained in this study showed that in all of the assays (dual culture, volatile and non-volatile metabolites) bacterial antagonists significantly inhibited the growth of C. beticola compared to the control. Bacillus (RB2) showed the highest inhibition rate on C. beticola in all of the assays. Based on the results of the laboratory assays, three bacterial strains RB2 (Bacillus), RPs (Pseudomonas), and RE (Paenibacillus) were selected for greenhouse assays. The experiment was designed based on a completely randomised design (CRD) with the application of antagonists prior to, simultaneously, and after inoculation with C. beticola on sugarbeet leaves. The reduction in disease severity was evaluated seven days after inoculation. The results of greenhouse assays were consistent with the results of laboratory studies. The obtained results showed that bacterial antagonists significantly reduced the disease severity when compared to the control.