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Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses

In vitro fitness assays are essential tools for determining viral replication fitness for viruses such as HIV-1. Various measurements have been used to extrapolate viral replication fitness, ranging from the number of viral particles per infectious unit, growth rate in cell culture, and relative fit...

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Autores principales: Manocheewa, Siriphan, Lanxon-Cookson, Erinn C., Liu, Yi, Swain, J. Victor, McClure, Jan, Rao, Ushnal, Maust, Brandon, Deng, Wenjie, Sunshine, Justine E., Kim, Moon, Rolland, Morgane, Mullins, James I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542137/
https://www.ncbi.nlm.nih.gov/pubmed/25993602
http://dx.doi.org/10.3791/52610
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author Manocheewa, Siriphan
Lanxon-Cookson, Erinn C.
Liu, Yi
Swain, J. Victor
McClure, Jan
Rao, Ushnal
Maust, Brandon
Deng, Wenjie
Sunshine, Justine E.
Kim, Moon
Rolland, Morgane
Mullins, James I.
author_facet Manocheewa, Siriphan
Lanxon-Cookson, Erinn C.
Liu, Yi
Swain, J. Victor
McClure, Jan
Rao, Ushnal
Maust, Brandon
Deng, Wenjie
Sunshine, Justine E.
Kim, Moon
Rolland, Morgane
Mullins, James I.
author_sort Manocheewa, Siriphan
collection PubMed
description In vitro fitness assays are essential tools for determining viral replication fitness for viruses such as HIV-1. Various measurements have been used to extrapolate viral replication fitness, ranging from the number of viral particles per infectious unit, growth rate in cell culture, and relative fitness derived from multiple-cycle growth competition assays. Growth competition assays provide a particularly sensitive measurement of fitness since the viruses are competing for cellular targets under identical growth conditions. There are several experimental factors to consider when conducting growth competition assays, including the multiplicity of infection (MOI), sampling times, and viral detection and fitness calculation methods. Each factor can affect the end result and hence must be considered carefully during the experimental design. The protocol presented here includes steps from constructing a new recombinant HIV-1 clone to performing growth competition assays and analyzing the experimental results. This protocol utilizes experimental parameter values previously shown to yield consistent and robust results. Alternatives are discussed, as some parameters need to be adjusted according to the cell type and viruses being studied. The protocol contains two alternative viral detection methods to provide flexibility as the availability of instruments, reagents and expertise varies between laboratories.
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spelling pubmed-45421372015-08-31 Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses Manocheewa, Siriphan Lanxon-Cookson, Erinn C. Liu, Yi Swain, J. Victor McClure, Jan Rao, Ushnal Maust, Brandon Deng, Wenjie Sunshine, Justine E. Kim, Moon Rolland, Morgane Mullins, James I. J Vis Exp Immunology In vitro fitness assays are essential tools for determining viral replication fitness for viruses such as HIV-1. Various measurements have been used to extrapolate viral replication fitness, ranging from the number of viral particles per infectious unit, growth rate in cell culture, and relative fitness derived from multiple-cycle growth competition assays. Growth competition assays provide a particularly sensitive measurement of fitness since the viruses are competing for cellular targets under identical growth conditions. There are several experimental factors to consider when conducting growth competition assays, including the multiplicity of infection (MOI), sampling times, and viral detection and fitness calculation methods. Each factor can affect the end result and hence must be considered carefully during the experimental design. The protocol presented here includes steps from constructing a new recombinant HIV-1 clone to performing growth competition assays and analyzing the experimental results. This protocol utilizes experimental parameter values previously shown to yield consistent and robust results. Alternatives are discussed, as some parameters need to be adjusted according to the cell type and viruses being studied. The protocol contains two alternative viral detection methods to provide flexibility as the availability of instruments, reagents and expertise varies between laboratories. MyJove Corporation 2015-05-04 /pmc/articles/PMC4542137/ /pubmed/25993602 http://dx.doi.org/10.3791/52610 Text en Copyright © 2015, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Immunology
Manocheewa, Siriphan
Lanxon-Cookson, Erinn C.
Liu, Yi
Swain, J. Victor
McClure, Jan
Rao, Ushnal
Maust, Brandon
Deng, Wenjie
Sunshine, Justine E.
Kim, Moon
Rolland, Morgane
Mullins, James I.
Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses
title Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses
title_full Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses
title_fullStr Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses
title_full_unstemmed Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses
title_short Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses
title_sort pairwise growth competition assay for determining the replication fitness of human immunodeficiency viruses
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542137/
https://www.ncbi.nlm.nih.gov/pubmed/25993602
http://dx.doi.org/10.3791/52610
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