Evaluation of synthetic‐gene recombinant LipL32 antigen for IgM ELISA detection of Leptospira infection

Leptospirosis presents with nonspecific clinical features and requires time‐consuming laboratory tests for gold standard diagnosis. This study aims to design and characterize the recombinant LipL32 from synthetic gene and assess its performance as an antigen for detecting leptospirosis. The antigen was developed by cloning the LipL32 gene conserved portion of Leptospira interrogans serovar Icterohaemorrhagiae strain Langkawi. The immunoinformatic was used to characterize the developed rLipL32. Western blot results using anti‐histidine revealed a band of rLipL32 protein at ~40 kDa. Subsequently, it was used to examine the IgM antibody on human sera by using ELISA. The IgM‐LipL32 ELISA was evaluated using 67‐positive and 25‐negative sera and compared with a commercial ELISA. With a cut‐off value of 0.8, it showed 85.7% sensitivity, 83.3% specificity, a 48% positive prediction value (PPV), and 97% negative prediction value (NPV), indicating modest performance compared to existing commercial kits. The rLipL32 is a potential antigen for detecting IgM using ELISA; however, for use in low incidence areas, a confirmation test is crucial.

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Publication Details

Journal
Indonesian Journal of Biotechnology
Published
2025-12-31
DOI
https://doi.org/10.22146/ijbiotech.111102
Primary Topic
Leptospirosis research and findings
Type
article
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article

Evaluation of synthetic‐gene recombinant LipL32 antigen for IgM ELISA detection of Leptospira infection

Ina Kusrini, Retno Murwanti, Nastiti Wijayanti, Dyah Widiastuti et al.
Indonesian Journal of Biotechnology
Leptospirosis research and findings
article

Evaluation of synthetic‐gene recombinant LipL32 antigen for IgM ELISA detection of Leptospira infection

Ina Kusrini, Retno Murwanti, Nastiti Wijayanti, Dyah Widiastuti, Dewi Kartikawati Paramita, Aris Haryanto
article en

Abstract

Leptospirosis presents with nonspecific clinical features and requires time‐consuming laboratory tests for gold standard diagnosis. This study aims to design and characterize the recombinant LipL32 from synthetic gene and assess its performance as an antigen for detecting leptospirosis. The antigen was developed by cloning the LipL32 gene conserved portion of Leptospira interrogans serovar Icterohaemorrhagiae strain Langkawi. The immunoinformatic was used to characterize the developed rLipL32. Western blot results using anti‐histidine revealed a band of rLipL32 protein at ~40 kDa. Subsequently, it was used to examine the IgM antibody on human sera by using ELISA. The IgM‐LipL32 ELISA was evaluated using 67‐positive and 25‐negative sera and compared with a commercial ELISA. With a cut‐off value of 0.8, it showed 85.7% sensitivity, 83.3% specificity, a 48% positive prediction value (PPV), and 97% negative prediction value (NPV), indicating modest performance compared to existing commercial kits. The rLipL32 is a potential antigen for detecting IgM using ELISA; however, for use in low incidence areas, a confirmation test is crucial.

Indonesian Journal of BiotechnologyVol. 30(4)
Universitas Gadjah Mada (ID), National Nuclear Energy Agency of Indonesia (ID)
Openalex Percentile: Top 28%
Leptospirosis research and findings
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