Detection of Leptospira-Specific Antibodies Using a Recombinant Antigen-Based Enzyme-Linked Immunosorbent Assay

Hua-Wei Chen Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Zhiwen Zhang Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Eric S. Halsey Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Carolina Guevara Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Enrique Canal Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Eric Hall Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Ryan Maves Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Drake H. Tilley Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Tadeusz J. Kochel Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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Wei-Mei Ching Naval Medical Research Center, Silver Spring, Maryland; Naval Medical Research Unit No.6, Lima, Peru; Naval Medical Center San Diego, San Diego, California

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We produced three highly purified recombinant antigens rLipL32, rLipL41, and rLigA-Rep (leptospiral immunoglobulin-like A repeat region) for the detection of Leptospira-specific antibodies in an enzyme-linked immunosorbent assay (ELISA). The performance of these recombinant antigens was evaluated using 121 human sera. Among them, 63 sera were microscopic agglutination test (MAT)-confirmed positive sera from febrile patients in Peru, 22 sera were indigenous MAT-negative febrile patient sera, and 36 sera were from patients with other febrile diseases from Southeast Asia, where leptospirosis is also endemic. Combining the results of immunoglobulin M (IgM) and IgG detection from these three antigens, the overall sensitivity is close to 90% based on the MAT. These results suggest that an ELISA using multiple recombinant antigens may be used as an alternative method for the detection of Leptospira-specific antibodies.

Author Notes

* Address correspondence to Wei-Mei Ching, Naval Medical Research Center, 503 Robert Grant Avenue, Silver Spring, MD 20910. E-mail: weimei.ching@med.navy.mil

Financial support: This research was supported by the Naval Medical Research Center (research work unit 6000.RAD1.J.A0310) and the US Department of Defense Global Emerging Infections Systems Research Program (work unit number: 847705.82000.25GB.B0016).

Authors' addresses: Hua-Wei Chen, Zhiwen Zhang, Eric Hall, Tadeusz J. Kochel, and Wei-Mei Ching, Naval Medical Research Center, Silver Spring, MD, E-mails: Hua-Wei.Chen@med.navy.mil, Zhiwen.Zhang@med.navy.mil, Eric.Hall@med.navy.mil, Tad.Kochel@med.navy.mil, and WeiMei.Ching@med.navy.mil. Eric S. Halsey, Carolina Guevara, Enrique Canal, and Drake H. Tilley, Naval Medical Research Unit No. 6, Lima, Peru, E-mails: Eric.Halsey@med.navy.mil, Carolina.Guevara@med.navy.mil, Enrique.Canal@med.navy.mil, and Drake.Tilley@med.navy.mil. Ryan Maves, Naval Medical Center San Diego, San Diego, CA, E-mail: Ryan.Maves@med.navy.mil.

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