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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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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. |
format | Online Article Text |
id | pubmed-4476629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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