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Utilization of 18s ribosomal RNA LAMP for detecting Plasmodium falciparum in microscopy and rapid diagnostic test negative patients

In this study, Plasmodium falciparum was detected in patients that were declared negative for malaria microscopy and rapid diagnostic test kit (mRDT), using Plasmodium 18s rRNA loop-mediated isothermal amplification (LAMP) technique. The main aim of this study was to assess the usefulness of LAMP as...

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Autores principales: Aninagyei, Enoch, Boakye, Adjoa Agyemang, Tettey, Clement Okraku, Ntiri, Kofi Adjei, Ofori, Samuel Ohene, Tetteh, Comfort Dede, Aphour, Thelma Teley, Rufai, Tanko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9536604/
https://www.ncbi.nlm.nih.gov/pubmed/36201568
http://dx.doi.org/10.1371/journal.pone.0275052
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author Aninagyei, Enoch
Boakye, Adjoa Agyemang
Tettey, Clement Okraku
Ntiri, Kofi Adjei
Ofori, Samuel Ohene
Tetteh, Comfort Dede
Aphour, Thelma Teley
Rufai, Tanko
author_facet Aninagyei, Enoch
Boakye, Adjoa Agyemang
Tettey, Clement Okraku
Ntiri, Kofi Adjei
Ofori, Samuel Ohene
Tetteh, Comfort Dede
Aphour, Thelma Teley
Rufai, Tanko
author_sort Aninagyei, Enoch
collection PubMed
description In this study, Plasmodium falciparum was detected in patients that were declared negative for malaria microscopy and rapid diagnostic test kit (mRDT), using Plasmodium 18s rRNA loop-mediated isothermal amplification (LAMP) technique. The main aim of this study was to assess the usefulness of LAMP assay for detecting pre-clinical malaria, when microscopy and mRDT were less sensitive. DNA was obtained from 100 μL of whole blood using the boil and spin method. Subsequently, the Plasmodium 18s rRNA LAMP assay was performed to amplify the specific Plasmodium 18s rRNA gene. Microscopy and mRDT negative samples [697/2223 (31.2%)] were used for this study. Compared to frequencies obtained for the other demographic variables, most of the patients were < 6 years (37.7%), females (59.0%), peri-urban dwellers (39.0%) and patients that sought outpatient department services (39.3%). Overall, the prevalence of Plasmodium 18s rRNA was 17.5%. when stratified by study variables, Plasmodium 18s rRNA LAMP positivity was higher in patients over 30 years [58/122 (54.2%)], males [69/122 (56.5%)], rural dwellers [69/122 (56.5%)] and patients that sought OPD services [68/122 (55.7%)]. The risk of being infected with Plasmodium when routine tests were negative was higher in 15–30-year group (OR = 3.03, 95% CI: 1.6–5.8, p = 0.0007), patients > 30 years (OR = 15.2, 95% CI: 8.3–27.7, p<0.001), males (OR = 2.1, 95% CI: 1.4–3.2, p = 0.0002) and rural dwellers (OR = 2.2, 95% CI:1.4–3.6, p = 0.0009). However, risk was lower in post-natal children (OR = 0.3, 95% CI: 0.18–0.51, p<0.001). Majority (81.5%) of the infected patients presented with headache, herpes labialis, diarrhea and vomiting. We demonstrated the lack of sensitivities of microscopy and mRDT for one-time diagnosis of malaria. Therefore, it is essential to utilize a sensitive technique such as Plasmodium 18s rRNA LAMP to increase the detection rate of Plasmodium infection.
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spelling pubmed-95366042022-10-07 Utilization of 18s ribosomal RNA LAMP for detecting Plasmodium falciparum in microscopy and rapid diagnostic test negative patients Aninagyei, Enoch Boakye, Adjoa Agyemang Tettey, Clement Okraku Ntiri, Kofi Adjei Ofori, Samuel Ohene Tetteh, Comfort Dede Aphour, Thelma Teley Rufai, Tanko PLoS One Research Article In this study, Plasmodium falciparum was detected in patients that were declared negative for malaria microscopy and rapid diagnostic test kit (mRDT), using Plasmodium 18s rRNA loop-mediated isothermal amplification (LAMP) technique. The main aim of this study was to assess the usefulness of LAMP assay for detecting pre-clinical malaria, when microscopy and mRDT were less sensitive. DNA was obtained from 100 μL of whole blood using the boil and spin method. Subsequently, the Plasmodium 18s rRNA LAMP assay was performed to amplify the specific Plasmodium 18s rRNA gene. Microscopy and mRDT negative samples [697/2223 (31.2%)] were used for this study. Compared to frequencies obtained for the other demographic variables, most of the patients were < 6 years (37.7%), females (59.0%), peri-urban dwellers (39.0%) and patients that sought outpatient department services (39.3%). Overall, the prevalence of Plasmodium 18s rRNA was 17.5%. when stratified by study variables, Plasmodium 18s rRNA LAMP positivity was higher in patients over 30 years [58/122 (54.2%)], males [69/122 (56.5%)], rural dwellers [69/122 (56.5%)] and patients that sought OPD services [68/122 (55.7%)]. The risk of being infected with Plasmodium when routine tests were negative was higher in 15–30-year group (OR = 3.03, 95% CI: 1.6–5.8, p = 0.0007), patients > 30 years (OR = 15.2, 95% CI: 8.3–27.7, p<0.001), males (OR = 2.1, 95% CI: 1.4–3.2, p = 0.0002) and rural dwellers (OR = 2.2, 95% CI:1.4–3.6, p = 0.0009). However, risk was lower in post-natal children (OR = 0.3, 95% CI: 0.18–0.51, p<0.001). Majority (81.5%) of the infected patients presented with headache, herpes labialis, diarrhea and vomiting. We demonstrated the lack of sensitivities of microscopy and mRDT for one-time diagnosis of malaria. Therefore, it is essential to utilize a sensitive technique such as Plasmodium 18s rRNA LAMP to increase the detection rate of Plasmodium infection. Public Library of Science 2022-10-06 /pmc/articles/PMC9536604/ /pubmed/36201568 http://dx.doi.org/10.1371/journal.pone.0275052 Text en © 2022 Aninagyei et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Aninagyei, Enoch
Boakye, Adjoa Agyemang
Tettey, Clement Okraku
Ntiri, Kofi Adjei
Ofori, Samuel Ohene
Tetteh, Comfort Dede
Aphour, Thelma Teley
Rufai, Tanko
Utilization of 18s ribosomal RNA LAMP for detecting Plasmodium falciparum in microscopy and rapid diagnostic test negative patients
title Utilization of 18s ribosomal RNA LAMP for detecting Plasmodium falciparum in microscopy and rapid diagnostic test negative patients
title_full Utilization of 18s ribosomal RNA LAMP for detecting Plasmodium falciparum in microscopy and rapid diagnostic test negative patients
title_fullStr Utilization of 18s ribosomal RNA LAMP for detecting Plasmodium falciparum in microscopy and rapid diagnostic test negative patients
title_full_unstemmed Utilization of 18s ribosomal RNA LAMP for detecting Plasmodium falciparum in microscopy and rapid diagnostic test negative patients
title_short Utilization of 18s ribosomal RNA LAMP for detecting Plasmodium falciparum in microscopy and rapid diagnostic test negative patients
title_sort utilization of 18s ribosomal rna lamp for detecting plasmodium falciparum in microscopy and rapid diagnostic test negative patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9536604/
https://www.ncbi.nlm.nih.gov/pubmed/36201568
http://dx.doi.org/10.1371/journal.pone.0275052
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