Detection of <I>Chlamydia trachomatis</I> by Using FITC-labeled Monoclonal Antibodies (Micro Trak<SUP>TM</SUP> Method)
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- NISHIURA Tsuneo
- Department of Urology, Gifu University School of Medicine
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- KATOH Naoki
- Department of Urology, Gifu University School of Medicine
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- NAKAO Toru
- Department of Pediatrics, Sapporo Medical College
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- KUMAMOTO Yoshiaki
- Department of Urology, Sapporo Medical College
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- HASHIZUME Sou
- Department of Microbiology and Pathology, Chiba University School of Nursing
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- KITAGAWA Ryuuichi
- Department of Urology, Juntendo University School of Medicine
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- HAYASHI Yasuyuki
- Department of Clinical Pathology, Juntendo University School of Medicine
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- NAKAMURA Masao
- Department of Laboratory Medicine, St. Marianna University School of Medicine
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- OSADA Takao
- Department of Urology, St. Marianna University School of Medicine
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- KOJIMA Hirotaka
- Department of Urology, Japan Red Cross Medical Center
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- AKAO Yoriyuki
- Central Virus Diagnostic Laboratory, National Institute of Health
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- HAGIWARA Toshikatsu
- Department of Veterinary Science, National Institute of Health
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- FUJIMORI Ippei
- Department of Internal Medicine, Kawasaki Municipal Hospital
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- TAKASE Zenjiro
- Department of Obstetrics and Gynecology, Kawasaki Medical School
Bibliographic Information
- Other Title
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- FITC標識モノクローナル抗体 (Micro Trak<SUP>TM</SUP>法) による<I>Chlamydia trachomatis</I>の検出
- FITC標識モノクローナル抗体(Micro TrakTM法)によるChlamydia trachomatisの検出
- FITC ヒョウシキ モノクローナル コウタイ Micro TrakTMホウ
- Detection of Chlamydia trachomatis by Using FITC-labeled Monoclonal Antibodies (Micro TrakTM Method)
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Description
The usefulness of FITC-labeled monoclonal antibodies (Micro TrakTM Culture Confirmation Testand Direct Specimen Test) for the detection of Chlamydia trachomatis from clinical specimens wasstudied. For examination of the specificity of Micro TrakTM method 15 reference strains (serovar A-Kand L1-L3) of C. trachomatis and one of Chlamydia psittaci were used. The reagents of Micro TrakTMmethod reacted strongly to all 15 strains of C. trachomatis but not to a strain of C. psittaci at all. A total of1034 clinical cases were tested for Micro TrakTM method. Culture Confirmation Test brought on thesame results for detection of chlamydial inclusions as Giemsa or iodine staining after cell culture ofspecimens. Number of inclusions detected from specimens by Culture Confirmation Test tended to morethan those by Giemsa or iodine staining method, and the inclusions stained with Micro TrakTM methodwere easier to be found out. Therefore, it would be concluded that Micro TrakTM Culture Confirmation Test is superior in detection of chlamydial inclusions to Giemsa or iodine staining which are now ususallyutilized. In Direct Specimen Test negative-coincidence ratio (number of negative-Direct Specimen Testcases in negative-culture cases/number of negative-culture cases) was 89.0%. This would show thatreactions of Micro TrakTM method in direct smears were almost specific to C. trachomatis organisms. Onthe other hand, positive-coincidence ratio (number of positive-Direct Specimen Test cases in positiveculturecases/number of positive-culture cases) was 69.7%. It is suggested that positive ratio isunequivocally influenced by the method for collection of specimens and for making direct smears, andthe experience of observation with fluorescence microscopy. Therefore, the carefulachievement andskillfulness of suitable method for detection of chlamydial organisms must bring better results. It mightbe suggested that Micro TrakTM Direct Specimen Test is a really rapid and easy-to-perform method fordetection of C. trachomatis and to be performed as a substitute method for cell culture method in clinicallaboratories.
Journal
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- Kansenshogaku Zasshi
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Kansenshogaku Zasshi 58 (12), 1305-1314, 1984
The Japanese Association for Infectious Diseases
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Details 詳細情報について
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- CRID
- 1390001205048257536
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- NII Article ID
- 130004328937
- 40000566267
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- NII Book ID
- AN00047715
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- ISSN
- 1884569X
- 03875911
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- NDL BIB ID
- 3024018
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- PubMed
- 6442725
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- Data Source
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- JaLC
- NDL Search
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed