An antigen detection assay for diagnosing filariasis

In this study we examined the diagnostic potential of monoclonal antibodies (MAb) reactive to antigens of adult Brugia malayi, their microfilariae and antigen of Dirofilaria immitis. The MAb of clone 17E10, which were of IgM isotype, reacted to the inner cuticles and internal content of both male an...

Full description

Saved in:
Bibliographic Details
Main Authors: Wongkamchai S., Choochote W., Jitpuckdee A., Suvannadabba S., Loymak S., Sakolvaree Y., Tapchaisri P., Chaicumpa W.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-2942615197&partnerID=40&md5=5993414220ee04458dca87e203f450a1
http://cmuir.cmu.ac.th/handle/6653943832/2678
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
Language: English
id th-cmuir.6653943832-2678
record_format dspace
spelling th-cmuir.6653943832-26782014-08-30T02:25:15Z An antigen detection assay for diagnosing filariasis Wongkamchai S. Choochote W. Jitpuckdee A. Suvannadabba S. Loymak S. Sakolvaree Y. Tapchaisri P. Chaicumpa W. In this study we examined the diagnostic potential of monoclonal antibodies (MAb) reactive to antigens of adult Brugia malayi, their microfilariae and antigen of Dirofilaria immitis. The MAb of clone 17E10, which were of IgM isotype, reacted to the inner cuticles and internal content of both male and female worms and also to the sheath and internal content of microfilariae in utero. However, these MAb did not react to the sheath of blood circulating microfilariae. The MAb 17E10 produced a smear pattern between 37 to > 200 kDa in the Western blot analysis against a SDS-PAGE separated extract of B. malayi. The epitopes were non-protein in nature as indicated by their resistance to proteinase-K treatment. The MAb 17E10 were applied in a sandwich ELISA to detect filarial antigen in the buffy coat and plasma of patients. We tested patients with different clinical manifestations of brugian filariasis, i.e. microfilaremia (M), lymphangitis (L) and elephantiasis (E), as well as non-symptomatic inhabitants of a filariasis endemic area (NE), and compared them to samples from non-symptomatic inhabitants of disease non-endemic areas (NNE). It was found that 22 of 31 (70.9%) of M, 7 of 13 (53.8%) of L, 2 of 14 (14.2%) of E, 10 of 100 (10.0%) of NE and none (0%) of the NNE were positive for antigenaemia. The assay was also positive in 14 of 15 (93.3%) blood samples from B. malayi microfilaremic cats and in 7 of 7 (100%) blood samples of Dirofilaria immitis microfilaremic dogs. The so-developed test has a high potential for routine diagnosis of active filariasis, for epidemiological studies in both humans and reservoir animals and for monitoring treatment efficacy. 2014-08-30T02:25:15Z 2014-08-30T02:25:15Z 2003 Article 0125877X 15198342 APJIE http://www.scopus.com/inward/record.url?eid=2-s2.0-2942615197&partnerID=40&md5=5993414220ee04458dca87e203f450a1 http://cmuir.cmu.ac.th/handle/6653943832/2678 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description In this study we examined the diagnostic potential of monoclonal antibodies (MAb) reactive to antigens of adult Brugia malayi, their microfilariae and antigen of Dirofilaria immitis. The MAb of clone 17E10, which were of IgM isotype, reacted to the inner cuticles and internal content of both male and female worms and also to the sheath and internal content of microfilariae in utero. However, these MAb did not react to the sheath of blood circulating microfilariae. The MAb 17E10 produced a smear pattern between 37 to > 200 kDa in the Western blot analysis against a SDS-PAGE separated extract of B. malayi. The epitopes were non-protein in nature as indicated by their resistance to proteinase-K treatment. The MAb 17E10 were applied in a sandwich ELISA to detect filarial antigen in the buffy coat and plasma of patients. We tested patients with different clinical manifestations of brugian filariasis, i.e. microfilaremia (M), lymphangitis (L) and elephantiasis (E), as well as non-symptomatic inhabitants of a filariasis endemic area (NE), and compared them to samples from non-symptomatic inhabitants of disease non-endemic areas (NNE). It was found that 22 of 31 (70.9%) of M, 7 of 13 (53.8%) of L, 2 of 14 (14.2%) of E, 10 of 100 (10.0%) of NE and none (0%) of the NNE were positive for antigenaemia. The assay was also positive in 14 of 15 (93.3%) blood samples from B. malayi microfilaremic cats and in 7 of 7 (100%) blood samples of Dirofilaria immitis microfilaremic dogs. The so-developed test has a high potential for routine diagnosis of active filariasis, for epidemiological studies in both humans and reservoir animals and for monitoring treatment efficacy.
format Article
author Wongkamchai S.
Choochote W.
Jitpuckdee A.
Suvannadabba S.
Loymak S.
Sakolvaree Y.
Tapchaisri P.
Chaicumpa W.
spellingShingle Wongkamchai S.
Choochote W.
Jitpuckdee A.
Suvannadabba S.
Loymak S.
Sakolvaree Y.
Tapchaisri P.
Chaicumpa W.
An antigen detection assay for diagnosing filariasis
author_facet Wongkamchai S.
Choochote W.
Jitpuckdee A.
Suvannadabba S.
Loymak S.
Sakolvaree Y.
Tapchaisri P.
Chaicumpa W.
author_sort Wongkamchai S.
title An antigen detection assay for diagnosing filariasis
title_short An antigen detection assay for diagnosing filariasis
title_full An antigen detection assay for diagnosing filariasis
title_fullStr An antigen detection assay for diagnosing filariasis
title_full_unstemmed An antigen detection assay for diagnosing filariasis
title_sort antigen detection assay for diagnosing filariasis
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-2942615197&partnerID=40&md5=5993414220ee04458dca87e203f450a1
http://cmuir.cmu.ac.th/handle/6653943832/2678
_version_ 1681419904148832256