An inexpensive point-of-care immunochromatographic test for Talaromyces marneffei infection based on the yeast phase specific monoclonal antibody 4D1 and Galanthus nivalis agglutinin.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
05 2021
Historique:
received: 06 08 2020
accepted: 22 12 2020
entrez: 4 5 2021
pubmed: 5 5 2021
medline: 15 9 2021
Statut: epublish

Résumé

Talaromyces marneffei is a thermally dimorphic fungus that causes opportunistic systemic mycoses in patients with AIDS or other immunodeficiency syndromes. The purpose of this study was to develop an immunochromatographic strip test (ICT) based on a solid phase sandwich format immunoassay for the detection of T. marneffei antigens in clinical urine specimens. The T. marneffei yeast phase specific monoclonal antibody 4D1 (MAb4D1) conjugated with colloidal gold nanoparticle was used as a specific signal reporter. Galanthus nivalis Agglutinin (GNA) was adsorbed onto nitrocellulose membrane to serve as the test line. Similarly, a control line was created above the test line by immobilization of rabbit anti-mouse IgG. The immobilized GNA served as capturing molecule and as non-immune mediated anti-terminal mannose of T. marneffei antigenic mannoprotein. The MAb4D1-GNA based ICT showed specific binding activity with yeast phase antigen of T. marneffei, and it did not react with other common pathogenic fungal antigens. The limit of detection of this ICT for T. marneffei antigen spiked in normal urine was approximately 0.6 μg/ml. The diagnostic performance of the ICT was validated using 341 urine samples from patents with culture- confirmed T. marneffei infection and from a control group of healthy individuals and patients with other infections in an endemic area. The ICT exhibited 89.47% sensitivity, 100% specificity, and 97.65% accuracy. Our results demonstrate that the urine-based GNA-MAb4D1 based ICT produces a visual result within 30 minutes and that the test is highly specific for the diagnosis of T. marneffei infection. The findings validate the deployment of the ICT for clinical use.

Identifiants

pubmed: 33945531
doi: 10.1371/journal.pntd.0009058
pii: PNTD-D-20-01410
pmc: PMC8096094
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antigens, Fungal 0
Antigens, Surface 0
Gold Colloid 0
Mannose-Binding Lectin 0
Mannose-Binding Lectins 0
Plant Lectins 0
snowdrop lectin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0009058

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Kritsada Pruksaphon (K)

Graduate Program in Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

Akarin Intaramat (A)

Translational Research Unit, Laboratory of Immunology and Laboratory of Biotechnology, Chulabhorn Research Institute, Bangkok, Thailand.

Pavinee Simsiriwong (P)

Translational Research Unit, Laboratory of Immunology and Laboratory of Biotechnology, Chulabhorn Research Institute, Bangkok, Thailand.

Skorn Mongkolsuk (S)

Translational Research Unit, Laboratory of Immunology and Laboratory of Biotechnology, Chulabhorn Research Institute, Bangkok, Thailand.

Kavi Ratanabanangkoon (K)

Department of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.

Joshua D Nosanchuk (JD)

Department of Medicine (Infectious Diseases), Albert Einstein College of Medicine, Bronx, New York, United States of America.

Anna Kaltsas (A)

Department of Medicine, Division of Infectious Diseases, Memorial Sloan Kettering Cancer Center, United States of America.
Department of Medicine, Weill Cornell Medical College, Cornell University, New York, United States of America.

Sirida Youngchim (S)

Department of Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

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Classifications MeSH