TY - JOUR
T1 - Diagnosis of Schistosomiasis without a Microscope
T2 - Evaluating Circulating Antigen (CCA, CAA) and DNA Detection Methods on Banked Samples of a Community-Based Survey from DR Congo
AU - Hoekstra, Pytsje T.
AU - Madinga, Joule
AU - Lutumba, Pascal
AU - van Grootveld, Rebecca
AU - Brienen, Eric A.T.
AU - Corstjens, Paul L.A.M.
AU - van Dam, Govert J.
AU - Polman, Katja
AU - van Lieshout, Lisette
N1 - Funding Information:
This research was funded by the Prof. Dr. P.C. Flu Foundation (8244-30453), based in The Netherlands.
Publisher Copyright:
© 2022 by the authors.
PY - 2022/10/19
Y1 - 2022/10/19
N2 - Detection of Schistosoma eggs in stool or urine is known for its low sensitivity in diagnosing light infections. Alternative diagnostics with better sensitivity while remaining highly specific, such as real-time PCR and circulating antigen detection, are progressively used as complementary diagnostic procedures but have not yet replaced microscopy. This study evaluates these alternative methods for the detection of Schistosoma infections in the absence of microscopy. Schistosomiasis presence was determined retrospectively in 314 banked stool and urine samples, available from a previous survey on the prevalence of taeniasis in a community in the Democratic Republic of the Congo, using real-time PCR, the point-of-care circulating cathodic antigen (POC-CCA) test, as well as the up-converting particle lateral flow circulating anodic antigen (UCP-LF CAA) test. Schistosoma DNA was present in urine (3%) and stool (28%) samples, while CCA (28%) and CAA (69%) were detected in urine. Further analysis of the generated data indicated stool-based PCR and the POC-CCA test to be suitable diagnostics for screening of S. mansoni infections, even in the absence of microscopy. A substantial proportion (60%) of the 215 CAA-positive cases showed low antigen concentrations, suggesting that even PCR and POC-CCA underestimated the “true” number of schistosome positives.
AB - Detection of Schistosoma eggs in stool or urine is known for its low sensitivity in diagnosing light infections. Alternative diagnostics with better sensitivity while remaining highly specific, such as real-time PCR and circulating antigen detection, are progressively used as complementary diagnostic procedures but have not yet replaced microscopy. This study evaluates these alternative methods for the detection of Schistosoma infections in the absence of microscopy. Schistosomiasis presence was determined retrospectively in 314 banked stool and urine samples, available from a previous survey on the prevalence of taeniasis in a community in the Democratic Republic of the Congo, using real-time PCR, the point-of-care circulating cathodic antigen (POC-CCA) test, as well as the up-converting particle lateral flow circulating anodic antigen (UCP-LF CAA) test. Schistosoma DNA was present in urine (3%) and stool (28%) samples, while CCA (28%) and CAA (69%) were detected in urine. Further analysis of the generated data indicated stool-based PCR and the POC-CCA test to be suitable diagnostics for screening of S. mansoni infections, even in the absence of microscopy. A substantial proportion (60%) of the 215 CAA-positive cases showed low antigen concentrations, suggesting that even PCR and POC-CCA underestimated the “true” number of schistosome positives.
KW - CAA
KW - CCA
KW - circulating antigen
KW - community-based survey
KW - diagnostics
KW - DNA detection
KW - PCR
KW - schistosomiasis
KW - stool
KW - urine
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U2 - 10.3390/tropicalmed7100315
DO - 10.3390/tropicalmed7100315
M3 - Article
AN - SCOPUS:85140631457
SN - 2414-6366
VL - 7
SP - 1
EP - 11
JO - Tropical Medicine and Infectious Disease
JF - Tropical Medicine and Infectious Disease
IS - 10
M1 - 315
ER -