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Open Access. Powered by Scholars. Published by Universities.®

Genetics

2012

David B. Taylor

Muscidifurax

Articles 1 - 2 of 2

Full-Text Articles in Life Sciences

Mitochondrial Dna Variation Among Muscidifurax Spp. (Hymenoptera: Pteromalidae), Pupal Parasitoids Of Filth Flies (Diptera), David B. Taylor, Richard D. Peterson Ii, Allen L. Szalanski, James J. Petersen Feb 2012

Mitochondrial Dna Variation Among Muscidifurax Spp. (Hymenoptera: Pteromalidae), Pupal Parasitoids Of Filth Flies (Diptera), David B. Taylor, Richard D. Peterson Ii, Allen L. Szalanski, James J. Petersen

David B. Taylor

Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and sequencing analyses were used to characterize an amplicon of ~625 bp in 4 of the 5 nominate species of Muscidifurax Girault & Sanders, pupal parasitoids of muscoid flies. A single polymorphic nucleotide site was observed among 2 samples of M. raptor Girault & Sanders. No sequence variation was observed among 3 samples of M. raptorellus Kogan & Legner. The sequence of M. uniraptor Kogan & Legner was identical to that of M. raptorellus. Nucleotide divergence among the Muscidifurax spp. ranged from 0.14 to 0.18 substitutions per nucleotide. Muscidifurax zaraptor Kogan & Legner …


Identification Of Muscidifurax Spp. By Polymerase Chain Reaction-Restriction Fragment Length Polymorphism, David Taylor, Allen Szalanski Feb 2012

Identification Of Muscidifurax Spp. By Polymerase Chain Reaction-Restriction Fragment Length Polymorphism, David Taylor, Allen Szalanski

David B. Taylor

Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis of the nuclear ribosomal ITS1 region was used to differentiate Muscidifurax (Hymenoptera: Pteromalidae) species which are parasitoids of filth fly pupae. Three restriction enzymes, Dpn 11, Mse I, and Taq I, produced restriction patterns which were diagnostic for the four species analyzed, M. raptor, M. raptorellus, M. uniraptor, and M. zaraptor. Seven other restriction enzymes were able to differentiate one or more of the species and can be used alone, or in combination with other enzymes, to verify identifications. No intraspecific variation was observed among the populations examined. The utility of the …