Cargando…

Development of Multiplex RT-PCR with Immobilized Primers for Identification of Infectious Human Pneumonia Pathogens

A prototype of a system for the detection of infectious human pneumonia pathogens based on multiplex solid-phase reverse transcription PCR (RT-PCR) was developed. Primers were designed to identify the DNA of six bacterial pneumonia pathogen strains, and the RNA of two viral pathogens of pneumonia: i...

Descripción completa

Detalles Bibliográficos
Autores principales: Lapa, S. A., Miftakhov, R. A., Klochikhina, E. S., Ammur, Yu. I., Blagodatskikh, S. A., Shershov, V. E., Zasedatelev, A. S., Chudinov, A. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pleiades Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682033/
https://www.ncbi.nlm.nih.gov/pubmed/34955557
http://dx.doi.org/10.1134/S0026893321040063
_version_ 1784617118645354496
author Lapa, S. A.
Miftakhov, R. A.
Klochikhina, E. S.
Ammur, Yu. I.
Blagodatskikh, S. A.
Shershov, V. E.
Zasedatelev, A. S.
Chudinov, A. V.
author_facet Lapa, S. A.
Miftakhov, R. A.
Klochikhina, E. S.
Ammur, Yu. I.
Blagodatskikh, S. A.
Shershov, V. E.
Zasedatelev, A. S.
Chudinov, A. V.
author_sort Lapa, S. A.
collection PubMed
description A prototype of a system for the detection of infectious human pneumonia pathogens based on multiplex solid-phase reverse transcription PCR (RT-PCR) was developed. Primers were designed to identify the DNA of six bacterial pneumonia pathogen strains, and the RNA of two viral pathogens of pneumonia: influenza A and SARS-CoV-2. The signal accumulation of elongated immobilized primers occurs due to the incorporation of fluorescently labeled nucleotides in the chain. The signal is detected after all the components of the mixture are removed, which significantly reduces the background signal and increases the sensitivity of the analysis. The use of a specialized detector makes it possible to read the signals of elongated primers directly through the transparent cover film of the reaction chamber. This solution is designed to prevent cross-contamination and is suitable for simultaneous testing of a large number of test samples. The proposed platform is able to detect the presence of several pathogens of pneumonia in a sample and has an open architecture that allows expansion of the range of pathogenic bacteria and viruses that can be detected.
format Online
Article
Text
id pubmed-8682033
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Pleiades Publishing
record_format MEDLINE/PubMed
spelling pubmed-86820332021-12-20 Development of Multiplex RT-PCR with Immobilized Primers for Identification of Infectious Human Pneumonia Pathogens Lapa, S. A. Miftakhov, R. A. Klochikhina, E. S. Ammur, Yu. I. Blagodatskikh, S. A. Shershov, V. E. Zasedatelev, A. S. Chudinov, A. V. Mol Biol Genomics. Transcryptomics A prototype of a system for the detection of infectious human pneumonia pathogens based on multiplex solid-phase reverse transcription PCR (RT-PCR) was developed. Primers were designed to identify the DNA of six bacterial pneumonia pathogen strains, and the RNA of two viral pathogens of pneumonia: influenza A and SARS-CoV-2. The signal accumulation of elongated immobilized primers occurs due to the incorporation of fluorescently labeled nucleotides in the chain. The signal is detected after all the components of the mixture are removed, which significantly reduces the background signal and increases the sensitivity of the analysis. The use of a specialized detector makes it possible to read the signals of elongated primers directly through the transparent cover film of the reaction chamber. This solution is designed to prevent cross-contamination and is suitable for simultaneous testing of a large number of test samples. The proposed platform is able to detect the presence of several pathogens of pneumonia in a sample and has an open architecture that allows expansion of the range of pathogenic bacteria and viruses that can be detected. Pleiades Publishing 2021-12-17 2021 /pmc/articles/PMC8682033/ /pubmed/34955557 http://dx.doi.org/10.1134/S0026893321040063 Text en © Pleiades Publishing, Inc. 2021, ISSN 0026-8933, Molecular Biology, 2021, Vol. 55, No. 6, pp. 828–838. © Pleiades Publishing, Inc., 2021.Russian Text © The Author(s), 2021, published in Molekulyarnaya Biologiya, 2021, Vol. 55, No. 6, pp. 944–955. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Genomics. Transcryptomics
Lapa, S. A.
Miftakhov, R. A.
Klochikhina, E. S.
Ammur, Yu. I.
Blagodatskikh, S. A.
Shershov, V. E.
Zasedatelev, A. S.
Chudinov, A. V.
Development of Multiplex RT-PCR with Immobilized Primers for Identification of Infectious Human Pneumonia Pathogens
title Development of Multiplex RT-PCR with Immobilized Primers for Identification of Infectious Human Pneumonia Pathogens
title_full Development of Multiplex RT-PCR with Immobilized Primers for Identification of Infectious Human Pneumonia Pathogens
title_fullStr Development of Multiplex RT-PCR with Immobilized Primers for Identification of Infectious Human Pneumonia Pathogens
title_full_unstemmed Development of Multiplex RT-PCR with Immobilized Primers for Identification of Infectious Human Pneumonia Pathogens
title_short Development of Multiplex RT-PCR with Immobilized Primers for Identification of Infectious Human Pneumonia Pathogens
title_sort development of multiplex rt-pcr with immobilized primers for identification of infectious human pneumonia pathogens
topic Genomics. Transcryptomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682033/
https://www.ncbi.nlm.nih.gov/pubmed/34955557
http://dx.doi.org/10.1134/S0026893321040063
work_keys_str_mv AT lapasa developmentofmultiplexrtpcrwithimmobilizedprimersforidentificationofinfectioushumanpneumoniapathogens
AT miftakhovra developmentofmultiplexrtpcrwithimmobilizedprimersforidentificationofinfectioushumanpneumoniapathogens
AT klochikhinaes developmentofmultiplexrtpcrwithimmobilizedprimersforidentificationofinfectioushumanpneumoniapathogens
AT ammuryui developmentofmultiplexrtpcrwithimmobilizedprimersforidentificationofinfectioushumanpneumoniapathogens
AT blagodatskikhsa developmentofmultiplexrtpcrwithimmobilizedprimersforidentificationofinfectioushumanpneumoniapathogens
AT shershovve developmentofmultiplexrtpcrwithimmobilizedprimersforidentificationofinfectioushumanpneumoniapathogens
AT zasedatelevas developmentofmultiplexrtpcrwithimmobilizedprimersforidentificationofinfectioushumanpneumoniapathogens
AT chudinovav developmentofmultiplexrtpcrwithimmobilizedprimersforidentificationofinfectioushumanpneumoniapathogens