TY - JOUR
T1 - A heteroduplex assay for the rapid detection of dual Human Immunodeficiency Virus Type 1 infections
AU - Powell, Rebecca L.R.
AU - Urbanski, Mateusz M.
AU - Nyambi, Phillipe N.
N1 - Funding Information:
Supported by grant number AI47053 from the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Fogarty International Center (TW01409), Center for AIDS Research (AI027742-17), and funds from the Department of Veterans Affairs (Merit Review Award and the Research Enhancement Program). The authors are grateful to the individuals who have donated their blood for these studies, and wish to acknowledge the continued support of the Ministry of Public Health, Cameroon.
PY - 2008/4
Y1 - 2008/4
N2 - The predominance of circulating and unique recombinant forms (URFs) of Human Immunodeficiency Virus Type 1 (HIV-1) in Cameroon suggests that dual infection occurs frequently in this region. Despite the potential impact of these infections on the evolution of HIV diversity, relatively few have been detected. The failure to detect dual infections may be attributable to the laborious and costly sequence analysis involved in their identification. As such, there is a need for a cost-effective, more rapid method to efficiently distinguish this subset of HIV-positive individuals, particularly in regions where HIV diversity is broad. In the present study, the heteroduplex assay (HDA) was developed to detect dual HIV-1 infection. This assay was validated on sequential specimens obtained from 20 HIV+ study subjects, whose single or dual infection status was determined by standard sequence analysis. By mixing gag fragments amplified from the sequential specimens from each study subject in HDA reactions, it was shown that single and dual infection status correlated with the absence and presence, respectively, of heteroduplex bands upon gel electrophoresis. Therefore, this novel assay is capable of identifying dual infections with a sensitivity and specificity equivalent to that of sequence analysis. Given the impact of dual infection on viral recombination and diversity, this simple technique will be beneficial to understanding HIV-1 evolution within an individual, as well as at a population level, in West-Central Africa and globally.
AB - The predominance of circulating and unique recombinant forms (URFs) of Human Immunodeficiency Virus Type 1 (HIV-1) in Cameroon suggests that dual infection occurs frequently in this region. Despite the potential impact of these infections on the evolution of HIV diversity, relatively few have been detected. The failure to detect dual infections may be attributable to the laborious and costly sequence analysis involved in their identification. As such, there is a need for a cost-effective, more rapid method to efficiently distinguish this subset of HIV-positive individuals, particularly in regions where HIV diversity is broad. In the present study, the heteroduplex assay (HDA) was developed to detect dual HIV-1 infection. This assay was validated on sequential specimens obtained from 20 HIV+ study subjects, whose single or dual infection status was determined by standard sequence analysis. By mixing gag fragments amplified from the sequential specimens from each study subject in HDA reactions, it was shown that single and dual infection status correlated with the absence and presence, respectively, of heteroduplex bands upon gel electrophoresis. Therefore, this novel assay is capable of identifying dual infections with a sensitivity and specificity equivalent to that of sequence analysis. Given the impact of dual infection on viral recombination and diversity, this simple technique will be beneficial to understanding HIV-1 evolution within an individual, as well as at a population level, in West-Central Africa and globally.
KW - Dual infection
KW - HIV-1
KW - Heteroduplex assay
UR - http://www.scopus.com/inward/record.url?scp=40849140481&partnerID=8YFLogxK
U2 - 10.1016/j.jviromet.2008.01.015
DO - 10.1016/j.jviromet.2008.01.015
M3 - Article
C2 - 18314205
AN - SCOPUS:40849140481
SN - 0166-0934
VL - 149
SP - 20
EP - 27
JO - Journal of Virological Methods
JF - Journal of Virological Methods
IS - 1
ER -