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Development and application of LAMP assays for the detection of enteric adenoviruses in feces

Loop-mediated isothermal amplification (LAMP) is an alternative to PCR that is faster and requires fewer resources. Here, we describe two LAMP assays for the detection of human adenoviruses in the feces of children with acute intestinal infections. We designed сolorimetric LAMP (c-LAMP) and real-tim...

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Autores principales: Shuryaeva, Anna K., Malova, Tatyana V., Tolokonceva, Anna A., Karceka, Sofia A., Gordukova, Maria A., Davydova, Ekaterina E., Shipulin, German A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430467/
https://www.ncbi.nlm.nih.gov/pubmed/35862966
http://dx.doi.org/10.1128/spectrum.00516-22
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author Shuryaeva, Anna K.
Malova, Tatyana V.
Tolokonceva, Anna A.
Karceka, Sofia A.
Gordukova, Maria A.
Davydova, Ekaterina E.
Shipulin, German A.
author_facet Shuryaeva, Anna K.
Malova, Tatyana V.
Tolokonceva, Anna A.
Karceka, Sofia A.
Gordukova, Maria A.
Davydova, Ekaterina E.
Shipulin, German A.
author_sort Shuryaeva, Anna K.
collection PubMed
description Loop-mediated isothermal amplification (LAMP) is an alternative to PCR that is faster and requires fewer resources. Here, we describe two LAMP assays for the detection of human adenoviruses in the feces of children with acute intestinal infections. We designed сolorimetric LAMP (c-LAMP) and real-time LAMP (f-LAMP) with fluorescent probes to detect the DNA of the adenovirus F human adenovirus 40/41 (hAdV40/41) hexon gene. The detection limit of both developed methods was 10(3) copies/mL, which is comparable to the sensitivity of PCR. The specificities of both c-LAMP and f-LAMP were high, with no false-positive results for clinical samples that do not contain adenovirus F, when testing other viruses and microorganisms. Comparative tests of PCR and LAMP on clinical samples from patients with acute gastroenteritis were carried out. For all samples with a PCR threshold cycle (C(T)) of up to 36, the PCR and LAMP results completely coincided; however, at low viral loads, the diagnostic sensitivity of LAMP, especially c-LAMP with colorimetric detection, was inferior to that of PCR. The combination of LAMP with modern methods of nucleic acid extraction, both in manual and automatic modes, can reduce the time for a complete study, including extraction of nucleic acid material and amplification, to 60 min. IMPORTANCE In April 2022, several cases of acute hepatitis of unknown origin were reported in children from 12 countries. In many cases, enteric adenovirus or SARS-CoV-2 and adenovirus coinfection were detected. It is known that human adenoviruses can cause different infections of varying severity, from asymptomatic to severe cases with lethal outcomes. There is a need to increase the diagnostic capabilities of clinical laboratories to identify such an underestimated pathogen as adenovirus. Although PCR remains the gold standard for pathogen detection, this method requires specialized equipment and has a long turnaround time to process samples. Previously, LAMP assays for the detection of human adenovirus have been based on measuring the turbidity, the fluorescence of intercalated dyes, or electrophoretic separation. Herein, we present LAMP-based assays with colorimetric or fluorescent detection and perform a detailed assessment of their sensitivity, specificity, and diagnostic performance.
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spelling pubmed-94304672022-09-01 Development and application of LAMP assays for the detection of enteric adenoviruses in feces Shuryaeva, Anna K. Malova, Tatyana V. Tolokonceva, Anna A. Karceka, Sofia A. Gordukova, Maria A. Davydova, Ekaterina E. Shipulin, German A. Microbiol Spectr Research Article Loop-mediated isothermal amplification (LAMP) is an alternative to PCR that is faster and requires fewer resources. Here, we describe two LAMP assays for the detection of human adenoviruses in the feces of children with acute intestinal infections. We designed сolorimetric LAMP (c-LAMP) and real-time LAMP (f-LAMP) with fluorescent probes to detect the DNA of the adenovirus F human adenovirus 40/41 (hAdV40/41) hexon gene. The detection limit of both developed methods was 10(3) copies/mL, which is comparable to the sensitivity of PCR. The specificities of both c-LAMP and f-LAMP were high, with no false-positive results for clinical samples that do not contain adenovirus F, when testing other viruses and microorganisms. Comparative tests of PCR and LAMP on clinical samples from patients with acute gastroenteritis were carried out. For all samples with a PCR threshold cycle (C(T)) of up to 36, the PCR and LAMP results completely coincided; however, at low viral loads, the diagnostic sensitivity of LAMP, especially c-LAMP with colorimetric detection, was inferior to that of PCR. The combination of LAMP with modern methods of nucleic acid extraction, both in manual and automatic modes, can reduce the time for a complete study, including extraction of nucleic acid material and amplification, to 60 min. IMPORTANCE In April 2022, several cases of acute hepatitis of unknown origin were reported in children from 12 countries. In many cases, enteric adenovirus or SARS-CoV-2 and adenovirus coinfection were detected. It is known that human adenoviruses can cause different infections of varying severity, from asymptomatic to severe cases with lethal outcomes. There is a need to increase the diagnostic capabilities of clinical laboratories to identify such an underestimated pathogen as adenovirus. Although PCR remains the gold standard for pathogen detection, this method requires specialized equipment and has a long turnaround time to process samples. Previously, LAMP assays for the detection of human adenovirus have been based on measuring the turbidity, the fluorescence of intercalated dyes, or electrophoretic separation. Herein, we present LAMP-based assays with colorimetric or fluorescent detection and perform a detailed assessment of their sensitivity, specificity, and diagnostic performance. American Society for Microbiology 2022-07-11 /pmc/articles/PMC9430467/ /pubmed/35862966 http://dx.doi.org/10.1128/spectrum.00516-22 Text en Copyright © 2022 Shuryaeva et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Shuryaeva, Anna K.
Malova, Tatyana V.
Tolokonceva, Anna A.
Karceka, Sofia A.
Gordukova, Maria A.
Davydova, Ekaterina E.
Shipulin, German A.
Development and application of LAMP assays for the detection of enteric adenoviruses in feces
title Development and application of LAMP assays for the detection of enteric adenoviruses in feces
title_full Development and application of LAMP assays for the detection of enteric adenoviruses in feces
title_fullStr Development and application of LAMP assays for the detection of enteric adenoviruses in feces
title_full_unstemmed Development and application of LAMP assays for the detection of enteric adenoviruses in feces
title_short Development and application of LAMP assays for the detection of enteric adenoviruses in feces
title_sort development and application of lamp assays for the detection of enteric adenoviruses in feces
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430467/
https://www.ncbi.nlm.nih.gov/pubmed/35862966
http://dx.doi.org/10.1128/spectrum.00516-22
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