Development of a rapid serological assay for the diagnosis of strongyloidiasis using a novel diffraction-based biosensor technology
Autor: | Isabel McAuliffe, Brian J. Ward, Herbert B. Tanowitz, Paul T. Smith, Evgeniya Kalinichenko, Fabio Vasquez-Camargo, Thomas B. Nutman, Michael Libman, Peter L. Chiodini, Patricia P. Wilkins, Momar Ndao, Brian J. Pak |
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Jazyk: | angličtina |
Rok vydání: | 2014 |
Předmět: |
lcsh:Arctic medicine. Tropical medicine
lcsh:RC955-962 Antibodies Helminth Enzyme-Linked Immunosorbent Assay Schistosomiasis Biosensing Techniques Trichinosis Microbiology Asymptomatic Serology Strongyloides stercoralis medicine Animals Humans Serologic Tests Retrospective Studies biology lcsh:Public aspects of medicine Public Health Environmental and Occupational Health Biology and Life Sciences lcsh:RA1-1270 biology.organism_classification medicine.disease Echinococcosis Virology Infectious Diseases Strongyloidiasis Strongyloides Immunology Female Parasitology medicine.symptom Research Article |
Zdroj: | PLoS Neglected Tropical Diseases, Vol 8, Iss 8, p e3002 (2014) PLoS Neglected Tropical Diseases |
ISSN: | 1935-2735 1935-2727 |
Popis: | Background Strongyloidiasis is a persistent human parasitic infection caused by the intestinal nematode, Strongyloides stercoralis. The parasite has a world-wide distribution, particularly in tropical and subtropical regions with poor sanitary conditions. Since individuals with strongyloidiasis are typically asymptomatic, the infection can persist for decades without detection. Problems arise when individuals with unrecognized S. stercoralis infection are immunosuppressed, which can lead to hyper-infection syndrome and disseminated disease with an associated high mortality if untreated. Therefore a rapid, sensitive and easy to use method of diagnosing Strongyloides infection may improve the clinical management of this disease. Methodology/Principal Findings An immunological assay for diagnosing strongyloidiasis was developed on a novel diffraction-based optical bionsensor technology. The test employs a 31-kDa recombinant antigen called NIE derived from Strongyloides stercoralis L3-stage larvae. Assay performance was tested using retrospectively collected sera from patients with parasitologically confirmed strongyloidiasis and control sera from healthy individuals or those with other parasitoses including schistosomiasis, trichinosis, echinococcosis or amebiasis who were seronegative using the NIE ELISA assay. If we consider the control group as the true negative group, the assay readily differentiated S. stercoralis-infected patients from controls detecting 96.3% of the positive cases, and with no cross reactivity observed in the control group These results were in excellent agreement (κ = 0.98) with results obtained by an NIE-based enzyme-linked immunosorbent assay (ELISA). A further 44 sera from patients with suspected S. stercoralis infection were analyzed and showed 91% agreement with the NIE ELISA. Conclusions/Significance In summary, this test provides high sensitivity detection of serum IgG against the NIE Strongyloides antigen. The assay is easy to perform and provides results in less than 30 minutes, making this platform amenable to rapid near-patient screening with minimal technical expertise. Author Summary A rapid and sensitive serodiagnostic assay for strongyloidiasis based on a 31-kDa recombinant antigen from Strongyloides stercoralis (NIE) was developed using a novel diffraction-based optical biosensor technology. Assay performance was tested using retrospectively collected sera from patients with parasitologically confirmed strongyloidiasis (n = 54) and control sera from healthy individuals (n = 7) or those with other parasitoses including schistosomiasis, trichinosis, echinococcosis or amebiasis (n = 40). If we consider the control group as the true negative group, the assay readily differentiated S. stercoralis-infected patients from controls detecting 96.3% of the positive cases, and with no cross reactivity observed in the control group. These results were in excellent agreement (κ = 0.98) with results obtained by an NIE-based enzyme-linked immunosorbent assay (ELISA). A further 44 sera from patients with suspected S. stercoralis infection were analyzed and showed 91% agreement with the NIE ELISA. This test provides high sensitivity detection of serum IgG against the NIE Strongyloides antigen. The assay is easy to perform and provides results in less than 30 minutes, making this platform amenable to rapid near-patient screening with minimal technical expertise. |
Databáze: | OpenAIRE |
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