Specificities of multi-primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in human

Objectives. The objectives of this work are the development of a multi-primer system based on the polymerase chain reaction (PCR) aimed at the simultaneous detection of six bacterial pathogens that cause human pneumonia and the determination of the parameters important for the optimization of this m...

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Main Authors: E. S. Klochikhina, V. E. Shershov, V. E. Kuznetsova, S. A. Lapa, A. V. Chudinov
Format: Article
Language:Russian
Published: MIREA - Russian Technological University 2021-07-01
Series:Тонкие химические технологии
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Online Access:https://www.finechem-mirea.ru/jour/article/view/1710
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author E. S. Klochikhina
V. E. Shershov
V. E. Kuznetsova
S. A. Lapa
A. V. Chudinov
author_facet E. S. Klochikhina
V. E. Shershov
V. E. Kuznetsova
S. A. Lapa
A. V. Chudinov
author_sort E. S. Klochikhina
collection DOAJ
description Objectives. The objectives of this work are the development of a multi-primer system based on the polymerase chain reaction (PCR) aimed at the simultaneous detection of six bacterial pathogens that cause human pneumonia and the determination of the parameters important for the optimization of this multi-primer system, including solid-phase PCR systems (biological microarrays).Methods. To determine the optimal parameters of the system, PCR methods were used in monoplex and multiplex formats.Results. Primers for Staphylococcus aureus, Pseudomonas aeruginosa, Haemophilus influenza, Legionella pneumophila, Klebsiella pneumoniae, and Streptococcus pneumoniae detection were designed, and the PCR cycling conditions were optimized. The patterns of primer design for solidphase PCR were revealed.Conclusions. The developed prototype of a system specifically identifies six clinically significant bacterial pathogens. It could be expanded for the analysis of viral and fungal pathogens and used in clinical diagnostics. A prototype of a system for pathogenic agent detection in the immobilized phase (biological microarray) was created.
format Article
id doaj-art-49fba6f0f3034ce9af72acad3ae1005f
institution Matheson Library
issn 2410-6593
2686-7575
language Russian
publishDate 2021-07-01
publisher MIREA - Russian Technological University
record_format Article
series Тонкие химические технологии
spelling doaj-art-49fba6f0f3034ce9af72acad3ae1005f2025-08-04T10:19:39ZrusMIREA - Russian Technological UniversityТонкие химические технологии2410-65932686-75752021-07-0116322523110.32362/2410-6593-2021-16-3-225-2311638Specificities of multi-primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in humanE. S. Klochikhina0V. E. Shershov1V. E. Kuznetsova2S. A. Lapa3A. V. Chudinov4Engelhardt Institute of Molecular Biology, Russian Academy of SciencesEngelhardt Institute of Molecular Biology, Russian Academy of SciencesEngelhardt Institute of Molecular Biology, Russian Academy of SciencesEngelhardt Institute of Molecular Biology, Russian Academy of SciencesEngelhardt Institute of Molecular Biology, Russian Academy of SciencesObjectives. The objectives of this work are the development of a multi-primer system based on the polymerase chain reaction (PCR) aimed at the simultaneous detection of six bacterial pathogens that cause human pneumonia and the determination of the parameters important for the optimization of this multi-primer system, including solid-phase PCR systems (biological microarrays).Methods. To determine the optimal parameters of the system, PCR methods were used in monoplex and multiplex formats.Results. Primers for Staphylococcus aureus, Pseudomonas aeruginosa, Haemophilus influenza, Legionella pneumophila, Klebsiella pneumoniae, and Streptococcus pneumoniae detection were designed, and the PCR cycling conditions were optimized. The patterns of primer design for solidphase PCR were revealed.Conclusions. The developed prototype of a system specifically identifies six clinically significant bacterial pathogens. It could be expanded for the analysis of viral and fungal pathogens and used in clinical diagnostics. A prototype of a system for pathogenic agent detection in the immobilized phase (biological microarray) was created.https://www.finechem-mirea.ru/jour/article/view/1710infectious pneumoniamultiplex pcrbiochipscovid-19
spellingShingle E. S. Klochikhina
V. E. Shershov
V. E. Kuznetsova
S. A. Lapa
A. V. Chudinov
Specificities of multi-primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in human
Тонкие химические технологии
infectious pneumonia
multiplex pcr
biochips
covid-19
title Specificities of multi-primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in human
title_full Specificities of multi-primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in human
title_fullStr Specificities of multi-primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in human
title_full_unstemmed Specificities of multi-primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in human
title_short Specificities of multi-primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in human
title_sort specificities of multi primer polymerase chain reaction optimization for the detection of infectious pneumonia agents in human
topic infectious pneumonia
multiplex pcr
biochips
covid-19
url https://www.finechem-mirea.ru/jour/article/view/1710
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AT vekuznetsova specificitiesofmultiprimerpolymerasechainreactionoptimizationforthedetectionofinfectiouspneumoniaagentsinhuman
AT salapa specificitiesofmultiprimerpolymerasechainreactionoptimizationforthedetectionofinfectiouspneumoniaagentsinhuman
AT avchudinov specificitiesofmultiprimerpolymerasechainreactionoptimizationforthedetectionofinfectiouspneumoniaagentsinhuman