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Novel Tools for Lassa Virus Surveillance in Peri-domestic Rodents.

Authors :
Smither AR
Koninga J
Kanneh FB
Foday M
Boisen ML
Bond NG
Momoh M
Sandi JD
Kanneh L
Alhasan F
Kanneh IM
Yillah MS
Grant DS
Bush DJ
Nelson DKS
Cruz KM
Klitting R
Pauthner M
Andersen KG
Shaffer JG
Cross RW
Schieffelin JS
Garry RF
Source :
MedRxiv : the preprint server for health sciences [medRxiv] 2023 Mar 20. Date of Electronic Publication: 2023 Mar 20.
Publication Year :
2023

Abstract

Background: Lassa fever (LF) is a rodent-borne disease endemic to West Africa. In the absence of licensed therapeutics or vaccines, rodent exclusion from living spaces remains the primary method of preventing LF. Zoonotic surveillance of Lassa virus (LASV), the etiologic agent of LF, can assess the burden of LASV in a region and guide public health measures against LF.<br />Methods: In this study, we adapted commercially available LASV human diagnostics to assess the prevalence of LASV in peri-domestic rodents in Eastern Sierra Leone. Small mammal trapping was conducted in Kenema district, Sierra Leone between November 2018-July 2019. LASV antigen was detected using a commercially available LASV NP antigen rapid diagnostic test. LASV IgG antibodies against LASV nucleoprotein (NP) and glycoprotein (GP) were tested by adapting a commercially available semi-quantitative enzyme linked immunosorbent assay (ELISA) for detection of mouse-related and rat-related species IgG.<br />Findings: Of the 373 tested specimens, 74 (20%) tested positive for LASV antigen. 40 (11%) specimens tested positive for LASV NP IgG, while an additional 12 (3%) specimens only tested positive for LASV GP IgG. Simultaneous antigen presence and IgG antibody presence was linked in Mastomys sp . specimens ( p < 0.01), but not Rattus sp . specimens ( p = 1). Despite the link between antigen presence and IgG antibody presence in Mastomys sp ., the strength of antigen response did not correlate with the strength of IgG response to either GP IgG or NP IgG.<br />Interpretation: The tools developed in this study can aid in the generation of valuable public health data for rapid field assessment of LASV burden during outbreak investigations and general LASV surveillance.<br />Funding: Funding for this work was supported by the National Institute of Allergy and Infectious Diseases National Institute of Health, Department of Health and Human Services under the following grants: International Collaboration in Infectious Disease Research on Lassa fever and Ebola - ICIDR - U19 AI115589, Consortium for Viral Systems Biology - CViSB - 5U19AI135995, West African Emerging Infectious Disease Research Center - WARN-ID - U01AI151812, West African Center for Emerging Infectious Diseases: U01AI151801.<br />Competing Interests: Conflicts of Interest MLB, DSG, KGA, JGS, JSS, RWC, and RFG are members of The Viral Hemorrhagic Fever Consortium (www.vhfc.org). The VHFC is a partnership of academic and industry scientists who are developing diagnostic tests, therapeutic agents, and vaccines for Lassa fever, Ebola, and other severe diseases. Tulane University and its various academic and industry partners have filed US and foreign patent applications on behalf of the consortium for several of these technologies. Technical information may also be kept as trade secrets. If commercial products are developed, consortium members may receive royalties or profits. This does not alter our adherence to all policies of the NIH and Scientific Reports on sharing data and materials. Financial and non-financial competing interests that the editors consider relevant to the content of the manuscript have been disclosed. RFG is a co-founder of Zalgen Labs, a biotechnology company developing countermeasures for emerging viruses. MLB, DJB, and DKSN are Zalgen employees. All other authors declare no competing interests.

Details

Language :
English
Database :
MEDLINE
Journal :
MedRxiv : the preprint server for health sciences
Accession number :
36993465
Full Text :
https://doi.org/10.1101/2023.03.17.23287380