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Biochemical and Molecular Profiling of Indigenous Xenorhabdus Isolates Associated with Steinernema Spp


Affiliations
1 Project Directorate of Biological Control, Post Box No.2491, H. A. Farm Post, Bellary Road, Bangalore - 560024, Karnataka, India
 

Bacterial symbionts were obtained from entomopathogenic nematodes Steinernema carpocapsae, S, riobrave, S. feltiae and S. tami, and identified as belonging to Xenorhabdus species by subjecting to biochemical characterization. The Xenorhabdus isolates were further characterized for their interspecific variation by protein profiling and RFLP analysis of 16S rDNA. The protein profiles recorded discernible differences with protein distribution ranging from 97Kda to 14Kda, but most of the fragments were common to all isolates. RFLP analysis of 16S rDNA of the isolates using eight restriction enzymes showed the distinctness of isolates and based on the restriction enzyme patterns, the isolates were grouped into two clusters. The study showed that a combination of biochemical and molecular techniques could be used for the identification and characterization of Xenorhabdus isolates.

Keywords

Indigenous Isolates, PCR-RFLP, Steinernema, Xenorhabdus, 16S rDNA.
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  • Biochemical and Molecular Profiling of Indigenous Xenorhabdus Isolates Associated with Steinernema Spp

Abstract Views: 251  |  PDF Views: 130

Authors

H. S. Vidya
Project Directorate of Biological Control, Post Box No.2491, H. A. Farm Post, Bellary Road, Bangalore - 560024, Karnataka, India
M. Nagesh
Project Directorate of Biological Control, Post Box No.2491, H. A. Farm Post, Bellary Road, Bangalore - 560024, Karnataka, India

Abstract


Bacterial symbionts were obtained from entomopathogenic nematodes Steinernema carpocapsae, S, riobrave, S. feltiae and S. tami, and identified as belonging to Xenorhabdus species by subjecting to biochemical characterization. The Xenorhabdus isolates were further characterized for their interspecific variation by protein profiling and RFLP analysis of 16S rDNA. The protein profiles recorded discernible differences with protein distribution ranging from 97Kda to 14Kda, but most of the fragments were common to all isolates. RFLP analysis of 16S rDNA of the isolates using eight restriction enzymes showed the distinctness of isolates and based on the restriction enzyme patterns, the isolates were grouped into two clusters. The study showed that a combination of biochemical and molecular techniques could be used for the identification and characterization of Xenorhabdus isolates.

Keywords


Indigenous Isolates, PCR-RFLP, Steinernema, Xenorhabdus, 16S rDNA.