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Journal of Clinical Microbiology, July 2000, p. 2701-2705, Vol. 38, No. 7
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Evaluation of a Commercially Available Recombinant-Protein Enzyme-Linked Immunosorbent Assay for Detection of Antibodies Produced in Scrub Typhus Rickettsial Infections

Meagan V. Land,1 Wei-Mei Ching,2 Gregory A. Dasch,2 Zhiwen Zhang,2 Daryl J. Kelly,3 Stephen R. Graves,4 and Peter L. Devine1,*

PanBio Pty. Ltd., Windsor, Queensland,1 and Australian Rickettsial Reference Laboratory, Geelong Hospital, Geelong, Victoria,4 Australia; Viral and Rickettsial Diseases Program, Naval Medical Research Institute, Bethesda, Maryland2; and Department of Rickettsial Diseases, Walter Reed Army Institute of Research, Washington, D.C.3

Received 31 January 2000/Returned for modification 3 April 2000/Accepted 9 May 2000

The 56-kDa major outer membrane protein antigen of Orientia tsutsugamuchi is the immunodominant antigen in human scrub typhus (ST) infections. An enzyme-linked immunosorbent assay (ELISA) using a recombinant 56-kDa protein (r56) to detect specific immunoglobulin M (IgM) produced in ST infections was developed, and its performance was evaluated using sera from patients with active ST (n = 59), spotted fever (SF) (n = 31), and murine typhus (MT) (n = 6) and from those without rickettsial infection (n = 52). The r56 ELISA was compared to an ELISA using native whole cell lysate of O. tsutsugamushi Karp or O. tsutsugamushi Gilliam as antigens. The performance of the assays using r56 was similar to that of those using native antigens. Using indirect immunoperoxidase (IIP) as the reference test, sensitivities were 86, 88, and 88% while specificities were 84, 90, and 87% in the three assays. Furthermore, cross-reactivity in confirmed cases of SF and MT was low (5.4, 2.7, and 2.7% respectively). The additional use of IgG in the r56 ELISA gave improved performance (sensitivity, 80%; specificity, 96%; cross-reactivity in SF and MT, 2.7%). The detection of high levels of IgG in some IgM-negative patients illustrates the importance of including a test for IgG in the detection of secondary or reactivated infections, since many of these patients were from regions in Thailand where these infections are endemic.


* Corresponding author. Mailing address: PanBio Pty. Ltd., 116 Lutwyche Rd., Windsor, Qld 4030, Australia. Phone: 61-7-33571177. Fax: 61-7-33571222. E-mail: peter_devine{at}panbio.com.au.


Journal of Clinical Microbiology, July 2000, p. 2701-2705, Vol. 38, No. 7
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Wang, Y.-C., Jian, T.-Y., Tarn, L.-J., Hung, Y.-W., Chao, H.-Y., Ji, D.-D., Liu, H.-W. (2003). Development of a Recombinant Protein-Based Enzyme-Linked Immunosorbent Assay and Its Applications in Field Surveillance of Rodent Mice for Presence of Immunoglobulin G against Orientia tsutsugamushi. CVI 10: 451-458 [Abstract] [Full Text]  
  • Ching, W.-M., Rowland, D., Zhang, Z., Bourgeois, A. L., Kelly, D., Dasch, G. A., Devine, P. L. (2001). Early Diagnosis of Scrub Typhus with a Rapid Flow Assay Using Recombinant Major Outer Membrane Protein Antigen (r56) of Orientia tsutsugamushi. CVI 8: 409-414 [Abstract] [Full Text]