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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Main Authors: Konstantin Tanida, Carsten Balczun, Andreas Hahn, Alexandra Veit, Beatrice Nickel, Sven Poppert, Patrick Leander Scheid, Ralf Matthias Hagen, Hagen Frickmann, Ulrike Loderstädt, Egbert Tannich
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Pathogens
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Online Access:https://www.mdpi.com/2076-0817/10/7/826
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spelling 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
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