ArticlePloS one2015
Phylogeographical Structure in Mitochondrial DNA of Legume Pod Borer (Maruca vitrata) Population in Tropical Asia and Sub-Saharan Africa.
Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Hi-C guided genome assembly and karyotype analysis of the Indian population of Maruca vitrata (Lepidoptera: Crambidae) set the stage for structural and functional genomic insights.BMC genomic data · 2026Article
- De Novo Mining and Validating Novel Microsatellite Markers to Assess Genetic Diversity inGenes · 2023Article
- Genetic Diversity and Population Structure of Head Blight Disease Causing FungusJournal of fungi (Basel, Switzerland) · 2022Article
- Functional characteristics of a novel odorant binding protein in the legume pod borer, Maruca vitrata.Scientific reports · 2021Article
- Article
- Diversity analysis reveals genetic homogeneity among Indian populations of legume pod borer,3 Biotech · 2019Article
- Pheromone-binding proteins based phylogenetics and phylogeography ofEcology and evolution · 2019Article
- Volatiles fromBiological control : theory and applications in pest management · 2019Article
- An Insight in the Reproductive Biology ofPsyche; a journal of entomology · 2017Article
- Pheromone Blend Analysis and Cross-Attraction among Populations of Maruca vitrata from Asia and West Africa.Journal of chemical ecology · 2015Article
- A study on Maruca vitrata infestation of Yard-long beans (Vigna unguiculata subspecies sesquipedalis).Heliyon · 2015Article
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4 authors.
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Abstract
This study was undertaken to assess the genetic diversity and host plant races of M. vitrata population in South and Southeast Asia and sub-Saharan Africa. The cytochrome c oxidase subunit 1 (cox1) gene was used to understand the phylogenetic relationship of geographically different M. vitrata population, but previous studies did not include population from Southeast Asia, the probable center of origin for Maruca, and from east Africa. Extensive sampling was done from different host plant species in target countries. Reference populations from Oceania and Latin America were used. An amplicon of 658 bp was produced by polymerase chain reaction, and 64 haplotypes were identified in 686 M. vitrata individuals. Phylogenetic analysis showed no difference among the M. vitrata population from different host plants. However, the results suggested that M. vitrata has formed two putative subspecies (which cannot be differentiated based on morphological characters) in Asia and sub-Saharan Africa, as indicated by the high pairwise FST values (0.44-0.85). The extremely high FST values (≥ 0.93) of Maruca population in Latin America and Oceania compared to Asian and African population seem to indicate a different species. On the continental or larger geographical region basis, the genetic differentiation is significantly correlated with the geographical distance. In addition, two putative species of Maruca, including M. vitrata occur in Australia, Indonesia and Papua New Guinea. The negative Tajima's D and Fu's FS values showed the recent demographic expansion of Maruca population. The haplotype network and Automatic Barcode Gap Discovery analyses confirmed the results of phylogenetic analysis. Thus, this study confirmed the presence of three putative Maruca species, including one in Latin America, one in Oceania (including Indonesia) and M. vitrata in Asia, Africa and Oceania. Hence, the genetic differences in Maruca population should be carefully considered while designing the pest management strategies in different regions.
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