scholarly journals Screening and identification of immunoactive FlaB protein fragments of Treponema pallidum for the serodiagnosis of syphilis

2017 ◽  
Vol 76 (2) ◽  
Author(s):  
Manyi Tan ◽  
Man Xu ◽  
Yongjian Xiao ◽  
Yafeng Xie ◽  
Chuanhao Jiang ◽  
...  
2003 ◽  
Vol 41 (8) ◽  
pp. 3668-3674 ◽  
Author(s):  
W. C. Van Voorhis ◽  
L. K. Barrett ◽  
S. A. Lukehart ◽  
B. Schmidt ◽  
M. Schriefer ◽  
...  

2016 ◽  
Vol 84 (2) ◽  
pp. 105-111 ◽  
Author(s):  
Chuanhao Jiang ◽  
Jinhong Xiao ◽  
Yafeng Xie ◽  
Yongjian Xiao ◽  
Chuan Wang ◽  
...  

1984 ◽  
Vol 60 (6) ◽  
pp. 364-370
Author(s):  
T Sato ◽  
E Kubo ◽  
M Yokota ◽  
T Kayashima ◽  
T Tomizawa

1998 ◽  
Vol 9 (4) ◽  
pp. 196-200 ◽  
Author(s):  
H Young ◽  
A Moyes ◽  
A Mcmillan

We report an assessment of Syphilis Fast, a new latex test that uses a pool of 3 recombinant Treponema pallidum antigens (TpN15, TpN17, and TpN47) for the serodiagnosis of syphilis. Specificity was evaluated by screening 1518 unselected blood specimens in parallel with Syphilis Fast, the Captia SelectSyphG EIA and the Venereal Disease Research Laboratory (VDRL) cardiolipin antigen test while sensitivity was tested using a panel of 99 treponemal sera (treated and untreated) representing various stages of infection and 15 treponemal sera detected on screening. The specificity of Syphilis Fast on initial testing (99.8%) was significantly higher (P 0.02) than that of Captia SelectSyph-G (99.2%) and the VDRL (99.1%): the specificity of Syphilis Fast remained significantly higher (P 0.02) after repeat testing (respective values 99.9%, 99.5% and 99.4%). There was no difference in the sensitivity of Syphilis Fast and Captia SelectSyph-G on initial (93% vs 92.1%) or repeat (95.6% vs 94.7%) testing: both were significantly more sensitive (P 0.001) than the VDRL (46.5% on initial and 43.9% on repeat testing). The sensitivities of the Treponema pallidum haemagglutination test (TPHA) and FTA-abs were 98.2% and 95.6% respectively. Negative reactions in Syphilis Fast and SelectSyph-G were associated with treated infections and correlated with low TPHA titres (80). We conclude that Syphilis Fast is a highly specific, simple and fast screening test with a sensitivity comparable to native antigen treponemal tests and that it merits consideration as a front-line screening test.


1998 ◽  
Vol 36 (4) ◽  
pp. 913-917 ◽  
Author(s):  
H. Young ◽  
A. Moyes ◽  
L. Seagar ◽  
A. McMillan

Enzyme immunoassay (EIA) is an ideal method for screening large numbers of patients for syphilis. We evaluated a novel immune-capture EIA (ICE Syphilis; Murex Diagnostics) that uses three recombinantTreponema pallidum antigens (TpN15, TpN17, and TpN47) and compared the results with those obtained by the native T. pallidum antigen EIA (Captia SelectSyph-G; Centocor) that we currently use for the serodiagnosis of syphilis. Specificity was evaluated by screening 1,184 unselected serum specimens in parallel by the ICE Syphilis and SelectSyph-G assays, while sensitivity was tested with a panel of 101 serum specimens containing antitreponemal antibodies (treated and untreated) from patients with various stages of infection. The specificity of the ICE Syphilis EIA (99.8%) on screening was significantly higher (P < 0.02) than that of the SelectSyph-G EIA (99.2%). The sensitivity of the ICE Syphilis EIA was significantly higher (P < 0.01) than that of the SelectSyph-G EIA on both initial (99 versus 91.4%) and repeat (100 versus 92.4%) testing. The ICE Syphilis EIA was also significantly more sensitive (P < 0.01) than the fluorescent treponemal antibody-abs (92.4%) but not the T. pallidum hemagglutination assay (97.1%). Sera containing antitreponemal antibodies gave a much higher antibody index (absorbance of test serum/kit cutoff) by the ICE Syphilis EIA than by the SelectSyph-G EIA. This combined with the overall high sensitivity makes the ICE Syphilis EIA an ideal test for excluding or detecting treponemal infection in human immunodeficiency virus (HIV)-infected patients. The ICE Syphilis EIA was positive with sera from all 15 HIV-infected patients in the study, whereas sera from 3 HIV-infected patients were negative by the SelectSyph-G EIA. We conclude that the high sensitivity and specificity of the ICE Syphilis EIA and its suitability for automation make it an ideal screening test.


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