Audrey L. Dikkeboom
Research Subjects
Research Interests
Audrey L. Dikkeboom has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Ae Goodwin
Aquaculture/Fisheries Center, University of Arkansas at Pine Bluff, Pine Bluff, AR 71601, USA
1 shared publication - Janet V. Warg
Diagnostic Virology Laboratory, National Veterinary Services Laboratories, VS, APHIS, USDA, Ames, Iowa 50010, USA
1 shared publication - John Whitney
LaCrosse Fish Health Center
1 shared publication - Kevin Snekvik
Department of Veterinary Microbiology and Pathology, College of Veterinary Medicine, Washington State University, Pullman, Washington, USA
1 shared publication
Latest Publications
- 18 October 2006
- Published by Springer Nature in Virus Genes
- Vol. 35 (1) , 87-95
Comparison of multiple genes of spring viremia of carp viruses isolated in the United States
Five spring viremia of carp viruses (SVCV), Rhabdovirus carpio, were isolated in the United States (US) between 2002 and 2004. Single tube reverse transcription-polymerase chain reaction (RT-PCR) was used to generate overlapping cDNA fragments from the US isolates of SVCV. Multiple pairs of specific primers were designed to amplify a portion of the phosphoprotein gene, the matrix gene, and the glycoprotein gene of SVCV genogroup Id (corresponding to nucleotides 2174–4942 of GenBank accession NC_002803). Sequences were proofread and aligned to generate a consensus sequence for each isolate. Phylogenetic analysis of the 2705 nucleotide consensus sequence revealed that all five US isolates belong to SVCV genogroup Ia, Asian origin isolates, and a PCR primer binding site unique to SVCV genogroup Ia was identified.
- 18 October 2006
- Published by Springer Nature in Virus Genes
- Vol. 35 (1) , 87-95
Comparison of multiple genes of spring viremia of carp viruses isolated in the United States
Five spring viremia of carp viruses (SVCV), Rhabdovirus carpio, were isolated in the United States (US) between 2002 and 2004. Single tube reverse transcription-polymerase chain reaction (RT-PCR) was used to generate overlapping cDNA fragments from the US isolates of SVCV. Multiple pairs of specific primers were designed to amplify a portion of the phosphoprotein gene, the matrix gene, and the glycoprotein gene of SVCV genogroup Id (corresponding to nucleotides 2174–4942 of GenBank accession NC_002803). Sequences were proofread and aligned to generate a consensus sequence for each isolate. Phylogenetic analysis of the 2705 nucleotide consensus sequence revealed that all five US isolates belong to SVCV genogroup Ia, Asian origin isolates, and a PCR primer binding site unique to SVCV genogroup Ia was identified.