Abstract

Simple SummarySugarcane is an important agro-industrial crop because it is one of the major sources of white sugar. Red rot which is caused by Colletotrichum falcatum is the most devastating disease of sugarcane because its infestation results in significant sugarcane yield loss. The intra- and inter-specific genetic diversity, population structure and phylogenetic relationship amongst C. falcatum isolates from Bangladesh remain unclear. This information is essential for the effective management of red rot and to also develop resistant sugarcane varieties through plant breeding programmes. This paper demonstrates the phylogenetic relationship and genetic diversity of C. falcatum isolates from Bangladesh. Also, it provides baseline information that can be used to establish red rot disease management strategies for future application.Colletotrichum falcatum Went causes red rot disease in sugarcane farming in the tropical and sub-tropical regions. This disease causes significant economic loss to the sugarcane production industry. Successful disease management strategies depend on understanding the evolutionary relationship between pathogens, genetic diversity, and population structure, particularly at the intra-specific level. Forty-one isolates of C. falcatum were collected from different sugarcane farms across Bangladesh for molecular identification, phylogeny and genetic diversity study. The four genes namely, ITS-rDNA, β-tubulin, Actin and GAPDH sequences were conducted. All the 41 C. falcatum isolates showed a 99–100% similarity index to the conserved gene sequences in the GenBank database. The phylogram of the four genes revealed that C. falcatum isolates of Bangladesh clustered in the same clade and no distinct geographical structuring were evident within the clade. The four gene sequences revealed that C. falcatum isolates from Bangladesh differed from other countries´ isolates because of nucleotides substitution at different loci. The genetic structure of C. falcatum isolates were determined using ISSR marker generated 404 polymorphic loci from 10 selected markers. The percentage of polymorphic loci was 99.01. The genetic variability at species level was slightly higher than at population level. Total mean gene diversity at the species level was 0.1732 whereas at population level it was 0.1521. The cluster analysis divided 41 isolates into four main genetic groups and the principal component analysis was consistent with cluster analysis. To the best of our knowledge, this is the first finding on characterizing C. falcatum isolates infesting sugarcane in Bangladesh. The results of this present study provide important baseline information vis a vis C. falcatum phylogeny analysis and genetic diversity study.

Highlights

  • Sugarcane (Saccharum officinarum L.) is widely cultivated in the tropics and sub-tropics

  • The molecular approach is the best alternative methods used to overcome the problem in C. falcatum identification and characterization

  • The sequence analysis of ITS, β-tubulin, actin, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) genes region provides accurate information on the characterization and phylogenetic understanding of C. falcatum isolates from Bangladesh

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Summary

Introduction

Sugarcane (Saccharum officinarum L.) is widely cultivated in the tropics and sub-tropics. It is one of the main sources of sugar in the world [1]. Sugarcane covers approximately 26.3 million hectares of the global arable land. In Bangladesh (North West and South East of Bangladesh), sugarcane is cultivated on 0.11 million hectares of land for white sugar, ethanol, juice production, chewing, and brown sugar [3]. Sugarcane plants are susceptible to several diseases, of which red rot which is caused by Colletotrichum falcatum is one of the devastating diseases (Glomerallacae of Ascomycota). Sugarcane red rot is endemic in the tropics and subtropics and it poses a serious challenge to sugarcane production in Bangladesh [6]. Environment, and pathogen strain, it reduces sugarcane weight up to 29% with sugar recovery loss up to 31% [7]

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