Evaluation of antigen and antibody assays for surveillance of Lassa virus in peri-domestic rodents in southeastern Sierra Leone: a cross-sectional study

<h2>Summary</h2><h3>Background</h3> Lassa fever, caused by Lassa mammarenavirus (LASV), is a rodent-borne disease endemic to west Africa. Zoonotic surveillance of LASV provides epidemiological insights into its potential presence. We aimed to assess LASV antigen and antibody prevalence in peri-domestic rodents in southeastern Sierra Leone. <h3>Methods</h3> In this cross-sectional study, small mammal trapping was conducted in Kenema District, Sierra Leone, from Nov 8, 2018 to July 10, 2019. LASV antigen was detected with a nucleoprotein antigen rapid diagnostic test at necropsy, then compared with gold-standard quantitative RT-PCR in a subset of specimens to assess specificity and sensitivity. LASV IgG antibodies against nucleoprotein and glycoprotein were tested using a semi-quantitative ELISA in <i>Mastomys</i> and <i>Rattus</i> species. <h3>Findings</h3> Of the 373 specimens tested, 74 (20%) were positive for LASV antigen. Compared with qRT-PCR, antigen testing showed a specificity of 61·9% (95% CI 52·5–70·6) and sensitivity of 100·0% (95% CI 2·5–100·0%). 40 (11%) specimens tested positive for LASV nucleoprotein-specific IgG, whereas an additional 12 (3%) were only positive for LASV glycoprotein-specific IgG, respectively. Simultaneous antigen and IgG antibody presence was observed in some <i>Mastomys</i> sp specimens (odds ratio 0·43 [95% CI 0·24–0·73], p=0·0011). However, the relative strength of antigen response did not explain the variability in the IgG response to either glycoprotein (ρ 0·04 [95% CI –0·34 to 0·41], p=0·85) or nucleoprotein (ρ –0·23 [95% CI –0·52 to 0·11], p=0·17). <h3>Interpretation</h3> Although further evaluation is needed, the tools used in this study can aid in generating valuable public health data for LASV surveillance and in prioritising specimens for further downstream analyses. <h3>Funding</h3> National Institute of Allergy and Infectious Diseases of the National Institutes of Health.

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Journal
The Lancet Microbe
Published
2025-10-25
DOI
https://doi.org/10.1016/j.lanmic.2025.101188
Primary Topic
Viral Infections and Outbreaks Research
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article
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article

Evaluation of antigen and antibody assays for surveillance of Lassa virus in peri-domestic rodents in southeastern Sierra Leone: a cross-sectional study

Matthew L. Boisen, Matthias Pauthner, John Demby Sandi, John S. Schieffelin et al.
The Lancet Microbe
Viral Infections and Outbreaks Research
article

Evaluation of antigen and antibody assays for surveillance of Lassa virus in peri-domestic rodents in southeastern Sierra Leone: a cross-sectional study

Matthew L. Boisen, Matthias Pauthner, John Demby Sandi, John S. Schieffelin, Nell G. Bond, Momoh Foday, Robert F. Garry, Donald Samuel Grant, Kaitlin M. Cruz, Mambu Momoh, Kristian G. Andersen, Lansana Kanneh, Allison R. Smither, Robert W. Cross, Ibrahim M Kanneh, Mohamed Yillah, James Koninga, Duane J. Bush, Jeffrey G. Shaffer, Luis M. Branco, Raphaëlle Klitting, Franklyn Kanneh, Foday Alhasan, Diana K. S. Nelson
article en

Abstract

<h2>Summary</h2><h3>Background</h3> Lassa fever, caused by Lassa mammarenavirus (LASV), is a rodent-borne disease endemic to west Africa. Zoonotic surveillance of LASV provides epidemiological insights into its potential presence. We aimed to assess LASV antigen and antibody prevalence in peri-domestic rodents in southeastern Sierra Leone. <h3>Methods</h3> In this cross-sectional study, small mammal trapping was conducted in Kenema District, Sierra Leone, from Nov 8, 2018 to July 10, 2019. LASV antigen was detected with a nucleoprotein antigen rapid diagnostic test at necropsy, then compared with gold-standard quantitative RT-PCR in a subset of specimens to assess specificity and sensitivity. LASV IgG antibodies against nucleoprotein and glycoprotein were tested using a semi-quantitative ELISA in <i>Mastomys</i> and <i>Rattus</i> species. <h3>Findings</h3> Of the 373 specimens tested, 74 (20%) were positive for LASV antigen. Compared with qRT-PCR, antigen testing showed a specificity of 61·9% (95% CI 52·5–70·6) and sensitivity of 100·0% (95% CI 2·5–100·0%). 40 (11%) specimens tested positive for LASV nucleoprotein-specific IgG, whereas an additional 12 (3%) were only positive for LASV glycoprotein-specific IgG, respectively. Simultaneous antigen and IgG antibody presence was observed in some <i>Mastomys</i> sp specimens (odds ratio 0·43 [95% CI 0·24–0·73], p=0·0011). However, the relative strength of antigen response did not explain the variability in the IgG response to either glycoprotein (ρ 0·04 [95% CI –0·34 to 0·41], p=0·85) or nucleoprotein (ρ –0·23 [95% CI –0·52 to 0·11], p=0·17). <h3>Interpretation</h3> Although further evaluation is needed, the tools used in this study can aid in generating valuable public health data for LASV surveillance and in prioritising specimens for further downstream analyses. <h3>Funding</h3> National Institute of Allergy and Infectious Diseases of the National Institutes of Health.

The Lancet MicrobeVol. 6(11)
Tulane University (US), Scripps Research Institute (US), University of Sierra Leone (SL), Zalgen (United States) (US), The University of Texas Medical Branch at Galveston (US)
U.S. Department of Health and Human Services, Tulane University, National Institutes of Health, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 64%
Viral Infections and Outbreaks Research
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