Comparison of Three In-House Real PCR Assays Targeting Kinetoplast DNA, the Small Subunit Ribosomal RNA Gene and the Glucose-6-Phosphate Isomerase Gene for the Detection of <i>Leishmania</i> spp. in Human Serum
To perform PCR from serum for the diagnosis of visceral leishmaniasis is convenient and much less invasive than the examination of deeper compartments such as bone marrow. We compared three <i>Leishmania</i>-specific real-time PCRs with three different molecular targets (kinetoplast DNA,...
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doaj-3280294f73754129b2ae8c9c0765057a2021-07-23T13:59:28ZengMDPI AGPathogens2076-08172021-06-011082682610.3390/pathogens10070826Comparison of Three In-House Real PCR Assays Targeting Kinetoplast DNA, the Small Subunit Ribosomal RNA Gene and the Glucose-6-Phosphate Isomerase Gene for the Detection of <i>Leishmania</i> spp. in Human SerumKonstantin Tanida0Carsten Balczun1Andreas Hahn2Alexandra Veit3Beatrice Nickel4Sven Poppert5Patrick Leander Scheid6Ralf Matthias Hagen7Hagen Frickmann8Ulrike Loderstädt9Egbert Tannich10Department of Microbiology and Hospital Hygiene, Bundeswehr Hospital Hamburg, 20359 Hamburg, GermanyDepartment XXI, Microbiology and Hospital Hygiene, Section B, Bundeswehr Central Hospital Koblenz, 56070 Koblenz, GermanyDepartment of Medical Microbiology, Virology and Hygiene, University Medicine Rostock, 18057 Rostock, GermanyBernhard Nocht Institute for Tropical Medicine Hamburg, National Reference Centre for Tropical Pathogens, 20359 Hamburg, GermanySwiss Tropical and Public Health Institute, 4051 Basel, SwitzerlandSwiss Tropical and Public Health Institute, 4051 Basel, SwitzerlandDepartment XXI, Microbiology and Hospital Hygiene, Section B, Bundeswehr Central Hospital Koblenz, 56070 Koblenz, GermanyDepartment XXI, Microbiology and Hospital Hygiene, Section B, Bundeswehr Central Hospital Koblenz, 56070 Koblenz, GermanyDepartment of Microbiology and Hospital Hygiene, Bundeswehr Hospital Hamburg, 20359 Hamburg, GermanyDepartment of Hospital Hygiene & Infectious Diseases, University Medicine Göttingen, 37075 Göttingen, GermanyBernhard Nocht Institute for Tropical Medicine Hamburg, National Reference Centre for Tropical Pathogens, 20359 Hamburg, GermanyTo perform PCR from serum for the diagnosis of visceral leishmaniasis is convenient and much less invasive than the examination of deeper compartments such as bone marrow. We compared three <i>Leishmania</i>-specific real-time PCRs with three different molecular targets (kinetoplast DNA, the small subunit-ribosomal RNA-(ssrRNA-)gene, the glucose-6-phosphate isomerase-(<i>gpi</i>-)gene) regarding their sensitivity and specificity in human serum. Residual sera from previous diagnostic assessments at the German National Reference Center for Tropical Pathogens Bernhard Nocht Institute for Tropical Medicine Hamburg and the Swiss Tropical and Public Health Institute were used. The sensitivities of kinetoplast DNA-PCR, ssrRNA-gene PCR, and <i>gpi</i>-PCR were 93.3%, 73.3%, and 33.3%, respectively, with 15 initial serum samples from visceral leishmaniasis patients, as well as 9.1%, 9.1%, and 0.0%, respectively, with 11 follow-up serum samples taken at various time points following anti-leishmanial therapy. Specificity was 100.0% in all assays as recorded with 1.137 serum samples from deployed soldiers and migrants without clinical suspicion of visceral leishmaniasis. Kinetoplast-DNA PCR from serum was confirmed as a sensitive and specific approach for the diagnosis of visceral leishmaniasis. The results also indicate the suitability of serum PCR for diagnostic follow-up after therapy, in particular regarding therapeutic failure in case of persisting positive PCR results.https://www.mdpi.com/2076-0817/10/7/826leishmaniavisceralKala Azarreal-time PCRtest comparisonin-house |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Konstantin Tanida Carsten Balczun Andreas Hahn Alexandra Veit Beatrice Nickel Sven Poppert Patrick Leander Scheid Ralf Matthias Hagen Hagen Frickmann Ulrike Loderstädt Egbert Tannich |
spellingShingle |
Konstantin Tanida Carsten Balczun Andreas Hahn Alexandra Veit Beatrice Nickel Sven Poppert Patrick Leander Scheid Ralf Matthias Hagen Hagen Frickmann Ulrike Loderstädt Egbert Tannich Comparison of Three In-House Real PCR Assays Targeting Kinetoplast DNA, the Small Subunit Ribosomal RNA Gene and the Glucose-6-Phosphate Isomerase Gene for the Detection of <i>Leishmania</i> spp. in Human Serum Pathogens leishmania visceral Kala Azar real-time PCR test comparison in-house |
author_facet |
Konstantin Tanida Carsten Balczun Andreas Hahn Alexandra Veit Beatrice Nickel Sven Poppert Patrick Leander Scheid Ralf Matthias Hagen Hagen Frickmann Ulrike Loderstädt Egbert Tannich |
author_sort |
Konstantin Tanida |
title |
Comparison of Three In-House Real PCR Assays Targeting Kinetoplast DNA, the Small Subunit Ribosomal RNA Gene and the Glucose-6-Phosphate Isomerase Gene for the Detection of <i>Leishmania</i> spp. in Human Serum |
title_short |
Comparison of Three In-House Real PCR Assays Targeting Kinetoplast DNA, the Small Subunit Ribosomal RNA Gene and the Glucose-6-Phosphate Isomerase Gene for the Detection of <i>Leishmania</i> spp. in Human Serum |
title_full |
Comparison of Three In-House Real PCR Assays Targeting Kinetoplast DNA, the Small Subunit Ribosomal RNA Gene and the Glucose-6-Phosphate Isomerase Gene for the Detection of <i>Leishmania</i> spp. in Human Serum |
title_fullStr |
Comparison of Three In-House Real PCR Assays Targeting Kinetoplast DNA, the Small Subunit Ribosomal RNA Gene and the Glucose-6-Phosphate Isomerase Gene for the Detection of <i>Leishmania</i> spp. in Human Serum |
title_full_unstemmed |
Comparison of Three In-House Real PCR Assays Targeting Kinetoplast DNA, the Small Subunit Ribosomal RNA Gene and the Glucose-6-Phosphate Isomerase Gene for the Detection of <i>Leishmania</i> spp. in Human Serum |
title_sort |
comparison of three in-house real pcr assays targeting kinetoplast dna, the small subunit ribosomal rna gene and the glucose-6-phosphate isomerase gene for the detection of <i>leishmania</i> spp. in human serum |
publisher |
MDPI AG |
series |
Pathogens |
issn |
2076-0817 |
publishDate |
2021-06-01 |
description |
To perform PCR from serum for the diagnosis of visceral leishmaniasis is convenient and much less invasive than the examination of deeper compartments such as bone marrow. We compared three <i>Leishmania</i>-specific real-time PCRs with three different molecular targets (kinetoplast DNA, the small subunit-ribosomal RNA-(ssrRNA-)gene, the glucose-6-phosphate isomerase-(<i>gpi</i>-)gene) regarding their sensitivity and specificity in human serum. Residual sera from previous diagnostic assessments at the German National Reference Center for Tropical Pathogens Bernhard Nocht Institute for Tropical Medicine Hamburg and the Swiss Tropical and Public Health Institute were used. The sensitivities of kinetoplast DNA-PCR, ssrRNA-gene PCR, and <i>gpi</i>-PCR were 93.3%, 73.3%, and 33.3%, respectively, with 15 initial serum samples from visceral leishmaniasis patients, as well as 9.1%, 9.1%, and 0.0%, respectively, with 11 follow-up serum samples taken at various time points following anti-leishmanial therapy. Specificity was 100.0% in all assays as recorded with 1.137 serum samples from deployed soldiers and migrants without clinical suspicion of visceral leishmaniasis. Kinetoplast-DNA PCR from serum was confirmed as a sensitive and specific approach for the diagnosis of visceral leishmaniasis. The results also indicate the suitability of serum PCR for diagnostic follow-up after therapy, in particular regarding therapeutic failure in case of persisting positive PCR results. |
topic |
leishmania visceral Kala Azar real-time PCR test comparison in-house |
url |
https://www.mdpi.com/2076-0817/10/7/826 |
work_keys_str_mv |
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