Characterization of Heterorhabditis Isolates by PCR Amplification of Segments of mtDNA and rDNA Genes

Authors

Susan A. Joyce, St. Patrick's College, Maynooth (Pontificial University)
Ann M. Burnell, St. Patrick's College, Maynooth (Pontificial University)
Thomas O. Powers, University of Nebraska-LincolnFollow

Document Type

Article

Date of this Version

1994

Comments

Published in Journal of Nematology (1994) 26(3):260-270; © The Society of Nematologists 1994; Used by Permission

Abstract

Restriction digests of amplified DNA from the mitochondrial genome and the nuclear ribosomal internally transcribed spacer region have been evaluated as genetic markers for species groups in Heterorhabditis. Six RFLP profiles have been identified. These profiles supported groupings determined by cross-breeding studies and were in agreement with less definitive groupings based on other biochemical and molecular methods. Digestion patterns of both amplification products provided strong evidence for the recognition of species groups, which include Irish, NW European, tropical, and a H. bacteriophora complex. The H. bacteriophora complex could be further resolved into three genotypes represented by H. zealandica, the H. bacteriophora, Brecon (Australian) type isolate for H. bacteriophora, and a grouping composed of isolates NC1, V16, HI82, and HP88. All cultures obtained of the H. megidis isolate were identical to the NW European group. These results could be used to aid monitoring of field release of Heterorhabditis as well as allowing a rapid initial assessment of taxonomic grouping.