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Detection of HIV-1 p24 at Attomole Level by Ultrasensitive ELISA with Thio-NAD Cycling

To reduce the window period between HIV-1 infection and the ability to diagnose it, a fourth-generation immunoassay including the detection of HIV-1 p24 antigen has been developed. However, because the commercially available systems for this assay use special, high-cost instruments to measure, for e...

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Autores principales: Nakatsuma, Akira, Kaneda, Mugiho, Kodama, Hiromi, Morikawa, Mika, Watabe, Satoshi, Nakaishi, Kazunari, Yamashita, Masakane, Yoshimura, Teruki, Miura, Toshiaki, Ninomiya, Masaki, Ito, Etsuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476629/
https://www.ncbi.nlm.nih.gov/pubmed/26098695
http://dx.doi.org/10.1371/journal.pone.0131319
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author Nakatsuma, Akira
Kaneda, Mugiho
Kodama, Hiromi
Morikawa, Mika
Watabe, Satoshi
Nakaishi, Kazunari
Yamashita, Masakane
Yoshimura, Teruki
Miura, Toshiaki
Ninomiya, Masaki
Ito, Etsuro
author_facet Nakatsuma, Akira
Kaneda, Mugiho
Kodama, Hiromi
Morikawa, Mika
Watabe, Satoshi
Nakaishi, Kazunari
Yamashita, Masakane
Yoshimura, Teruki
Miura, Toshiaki
Ninomiya, Masaki
Ito, Etsuro
author_sort Nakatsuma, Akira
collection PubMed
description To reduce the window period between HIV-1 infection and the ability to diagnose it, a fourth-generation immunoassay including the detection of HIV-1 p24 antigen has been developed. However, because the commercially available systems for this assay use special, high-cost instruments to measure, for example, chemiluminescence, it is performed only by diagnostics companies and hub hospitals. To overcome this limitation, we applied an ultrasensitive ELISA coupled with a thio-NAD cycling, which is based on a usual enzyme immunoassay without special instruments, to detect HIV-1 p24. The p24 detection limit by our ultrasensitive ELISA was 0.0065 IU/assay (i.e., ca. 10(-18) moles/assay). Because HIV-1 p24 antigen is thought to be present in the virion in much greater numbers than viral RNA copies, the value of 10(-18) moles of the p24/assay corresponds to ca. 10(3) copies of the HIV-1 RNA/assay. That is, our ultrasensitive ELISA is chasing the detection limit (10(2) copies/assay) obtained by PCR-based nucleic acid testing (NAT) with a margin of only one different order. Further, the detection limit by our ultrasensitive ELISA is less than that mandated for a CE-marked HIV antigen/antibody assay. An additional recovery test using blood supported the reliability of our ultrasensitive ELISA.
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spelling pubmed-44766292015-06-25 Detection of HIV-1 p24 at Attomole Level by Ultrasensitive ELISA with Thio-NAD Cycling Nakatsuma, Akira Kaneda, Mugiho Kodama, Hiromi Morikawa, Mika Watabe, Satoshi Nakaishi, Kazunari Yamashita, Masakane Yoshimura, Teruki Miura, Toshiaki Ninomiya, Masaki Ito, Etsuro PLoS One Research Article To reduce the window period between HIV-1 infection and the ability to diagnose it, a fourth-generation immunoassay including the detection of HIV-1 p24 antigen has been developed. However, because the commercially available systems for this assay use special, high-cost instruments to measure, for example, chemiluminescence, it is performed only by diagnostics companies and hub hospitals. To overcome this limitation, we applied an ultrasensitive ELISA coupled with a thio-NAD cycling, which is based on a usual enzyme immunoassay without special instruments, to detect HIV-1 p24. The p24 detection limit by our ultrasensitive ELISA was 0.0065 IU/assay (i.e., ca. 10(-18) moles/assay). Because HIV-1 p24 antigen is thought to be present in the virion in much greater numbers than viral RNA copies, the value of 10(-18) moles of the p24/assay corresponds to ca. 10(3) copies of the HIV-1 RNA/assay. That is, our ultrasensitive ELISA is chasing the detection limit (10(2) copies/assay) obtained by PCR-based nucleic acid testing (NAT) with a margin of only one different order. Further, the detection limit by our ultrasensitive ELISA is less than that mandated for a CE-marked HIV antigen/antibody assay. An additional recovery test using blood supported the reliability of our ultrasensitive ELISA. Public Library of Science 2015-06-22 /pmc/articles/PMC4476629/ /pubmed/26098695 http://dx.doi.org/10.1371/journal.pone.0131319 Text en © 2015 Nakatsuma et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nakatsuma, Akira
Kaneda, Mugiho
Kodama, Hiromi
Morikawa, Mika
Watabe, Satoshi
Nakaishi, Kazunari
Yamashita, Masakane
Yoshimura, Teruki
Miura, Toshiaki
Ninomiya, Masaki
Ito, Etsuro
Detection of HIV-1 p24 at Attomole Level by Ultrasensitive ELISA with Thio-NAD Cycling
title Detection of HIV-1 p24 at Attomole Level by Ultrasensitive ELISA with Thio-NAD Cycling
title_full Detection of HIV-1 p24 at Attomole Level by Ultrasensitive ELISA with Thio-NAD Cycling
title_fullStr Detection of HIV-1 p24 at Attomole Level by Ultrasensitive ELISA with Thio-NAD Cycling
title_full_unstemmed Detection of HIV-1 p24 at Attomole Level by Ultrasensitive ELISA with Thio-NAD Cycling
title_short Detection of HIV-1 p24 at Attomole Level by Ultrasensitive ELISA with Thio-NAD Cycling
title_sort detection of hiv-1 p24 at attomole level by ultrasensitive elisa with thio-nad cycling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476629/
https://www.ncbi.nlm.nih.gov/pubmed/26098695
http://dx.doi.org/10.1371/journal.pone.0131319
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