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Quantification of HTLV-I proviral load in experimentally infected rabbits
BACKGROUND: Levels of proviral load in HTLV-1 infected patients correlate with clinical outcome and are reasonably prognostic. Adaptation of proviral load measurement techniques is examined here for use in an experimental rabbit model of HTLV-1 infection. Initial efforts sought to correlate proviral...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1156951/ https://www.ncbi.nlm.nih.gov/pubmed/15910683 http://dx.doi.org/10.1186/1742-4690-2-34 |
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author | Zhao, Tong-Mao Hague, Bishop Caudell, David L Simpson, R Mark Kindt, Thomas J |
author_facet | Zhao, Tong-Mao Hague, Bishop Caudell, David L Simpson, R Mark Kindt, Thomas J |
author_sort | Zhao, Tong-Mao |
collection | PubMed |
description | BACKGROUND: Levels of proviral load in HTLV-1 infected patients correlate with clinical outcome and are reasonably prognostic. Adaptation of proviral load measurement techniques is examined here for use in an experimental rabbit model of HTLV-1 infection. Initial efforts sought to correlate proviral load with route and dose of inoculation and with clinical outcome in this model. These methods contribute to our continuing goal of using the model to test treatments that alleviate virus infection. RESULTS: A real-time PCR assay was used to measure proviral load in blood and tissue samples from a series of rabbits infected using HTLV-1 inocula prepared as either cell-free virus particles, infected cells or blood, or by naked DNA injection. Proviral loads from asymptomatically infected rabbits showed levels corresponding to those reported for human patients with clinically silent HTLV-1 infections. Proviral load was comparably increased in 50% of experimentally infected rabbits that developed either spontaneous benign or malignant tumors while infected. Similarly elevated provirus was found in organs of rabbits with experimentally induced acute leukemia/lymphoma-like disease. Levels of provirus in organs taken at necropsy varied widely suggesting that reservoirs of infections exist in non-lymphoid organs not traditionally thought to be targets for HTLV-1. CONCLUSION: Proviral load measurement is a valuable enhancement to the rabbit model for HTLV-1 infection providing a metric to monitor clinical status of the infected animals as well as a means for the testing of treatment to combat infection. In some cases proviral load in blood did not reflect organ proviral levels, revealing a limitation of this method for monitoring health status of HTLV-1 infected individuals. |
format | Text |
id | pubmed-1156951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11569512005-06-22 Quantification of HTLV-I proviral load in experimentally infected rabbits Zhao, Tong-Mao Hague, Bishop Caudell, David L Simpson, R Mark Kindt, Thomas J Retrovirology Research BACKGROUND: Levels of proviral load in HTLV-1 infected patients correlate with clinical outcome and are reasonably prognostic. Adaptation of proviral load measurement techniques is examined here for use in an experimental rabbit model of HTLV-1 infection. Initial efforts sought to correlate proviral load with route and dose of inoculation and with clinical outcome in this model. These methods contribute to our continuing goal of using the model to test treatments that alleviate virus infection. RESULTS: A real-time PCR assay was used to measure proviral load in blood and tissue samples from a series of rabbits infected using HTLV-1 inocula prepared as either cell-free virus particles, infected cells or blood, or by naked DNA injection. Proviral loads from asymptomatically infected rabbits showed levels corresponding to those reported for human patients with clinically silent HTLV-1 infections. Proviral load was comparably increased in 50% of experimentally infected rabbits that developed either spontaneous benign or malignant tumors while infected. Similarly elevated provirus was found in organs of rabbits with experimentally induced acute leukemia/lymphoma-like disease. Levels of provirus in organs taken at necropsy varied widely suggesting that reservoirs of infections exist in non-lymphoid organs not traditionally thought to be targets for HTLV-1. CONCLUSION: Proviral load measurement is a valuable enhancement to the rabbit model for HTLV-1 infection providing a metric to monitor clinical status of the infected animals as well as a means for the testing of treatment to combat infection. In some cases proviral load in blood did not reflect organ proviral levels, revealing a limitation of this method for monitoring health status of HTLV-1 infected individuals. BioMed Central 2005-05-23 /pmc/articles/PMC1156951/ /pubmed/15910683 http://dx.doi.org/10.1186/1742-4690-2-34 Text en Copyright © 2005 Zhao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Zhao, Tong-Mao Hague, Bishop Caudell, David L Simpson, R Mark Kindt, Thomas J Quantification of HTLV-I proviral load in experimentally infected rabbits |
title | Quantification of HTLV-I proviral load in experimentally infected rabbits |
title_full | Quantification of HTLV-I proviral load in experimentally infected rabbits |
title_fullStr | Quantification of HTLV-I proviral load in experimentally infected rabbits |
title_full_unstemmed | Quantification of HTLV-I proviral load in experimentally infected rabbits |
title_short | Quantification of HTLV-I proviral load in experimentally infected rabbits |
title_sort | quantification of htlv-i proviral load in experimentally infected rabbits |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1156951/ https://www.ncbi.nlm.nih.gov/pubmed/15910683 http://dx.doi.org/10.1186/1742-4690-2-34 |
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