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A Retrospective Examination of Feline Leukemia Subgroup Characterization: Viral Interference Assays to Deep Sequencing

Feline leukemia virus (FeLV) was the first feline retrovirus discovered, and is associated with multiple fatal disease syndromes in cats, including lymphoma. The original research conducted on FeLV employed classical virological techniques. As methods have evolved to allow FeLV genetic characterizat...

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Autores principales: Chiu, Elliott S., Hoover, Edward A., VandeWoude, Sue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795442/
https://www.ncbi.nlm.nih.gov/pubmed/29320424
http://dx.doi.org/10.3390/v10010029
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author Chiu, Elliott S.
Hoover, Edward A.
VandeWoude, Sue
author_facet Chiu, Elliott S.
Hoover, Edward A.
VandeWoude, Sue
author_sort Chiu, Elliott S.
collection PubMed
description Feline leukemia virus (FeLV) was the first feline retrovirus discovered, and is associated with multiple fatal disease syndromes in cats, including lymphoma. The original research conducted on FeLV employed classical virological techniques. As methods have evolved to allow FeLV genetic characterization, investigators have continued to unravel the molecular pathology associated with this fascinating agent. In this review, we discuss how FeLV classification, transmission, and disease-inducing potential have been defined sequentially by viral interference assays, Sanger sequencing, PCR, and next-generation sequencing. In particular, we highlight the influences of endogenous FeLV and host genetics that represent FeLV research opportunities on the near horizon.
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spelling pubmed-57954422018-02-09 A Retrospective Examination of Feline Leukemia Subgroup Characterization: Viral Interference Assays to Deep Sequencing Chiu, Elliott S. Hoover, Edward A. VandeWoude, Sue Viruses Review Feline leukemia virus (FeLV) was the first feline retrovirus discovered, and is associated with multiple fatal disease syndromes in cats, including lymphoma. The original research conducted on FeLV employed classical virological techniques. As methods have evolved to allow FeLV genetic characterization, investigators have continued to unravel the molecular pathology associated with this fascinating agent. In this review, we discuss how FeLV classification, transmission, and disease-inducing potential have been defined sequentially by viral interference assays, Sanger sequencing, PCR, and next-generation sequencing. In particular, we highlight the influences of endogenous FeLV and host genetics that represent FeLV research opportunities on the near horizon. MDPI 2018-01-10 /pmc/articles/PMC5795442/ /pubmed/29320424 http://dx.doi.org/10.3390/v10010029 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chiu, Elliott S.
Hoover, Edward A.
VandeWoude, Sue
A Retrospective Examination of Feline Leukemia Subgroup Characterization: Viral Interference Assays to Deep Sequencing
title A Retrospective Examination of Feline Leukemia Subgroup Characterization: Viral Interference Assays to Deep Sequencing
title_full A Retrospective Examination of Feline Leukemia Subgroup Characterization: Viral Interference Assays to Deep Sequencing
title_fullStr A Retrospective Examination of Feline Leukemia Subgroup Characterization: Viral Interference Assays to Deep Sequencing
title_full_unstemmed A Retrospective Examination of Feline Leukemia Subgroup Characterization: Viral Interference Assays to Deep Sequencing
title_short A Retrospective Examination of Feline Leukemia Subgroup Characterization: Viral Interference Assays to Deep Sequencing
title_sort retrospective examination of feline leukemia subgroup characterization: viral interference assays to deep sequencing
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795442/
https://www.ncbi.nlm.nih.gov/pubmed/29320424
http://dx.doi.org/10.3390/v10010029
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