Evidence map›Paper›PMID 42361202›Full record

ArticlePLoS computational biology2026

Evaluating vectors for the design of a spillover-disrupting Lassa virus transmissible vaccine.

Scott L Nuismer, Christopher H Remien, Bruno Ghersi, Jenna Nichols, James Bangura, Emmanuel Amara, Marilyn C Kanu, Osman T Kanu, Edwin G Lavalie, Mohamed Turay and 7 more

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Scott L NuismerDepartment of Biological Sciences, University of Idaho, Moscow, Idaho, United States of America.ORCID https://orcid.org/0000-0001-9817-0056
Christopher H RemienDepartment of Mathematics and Statistical Science, University of Idaho, Moscow, Idaho, United States of America.
Bruno GhersiCummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, United States of America.
Jenna NicholsGenetic Design and Engineering Center (GDEC), Bioengineering Department, Rice University, Houston, Texas, United States of America.ORCID https://orcid.org/0000-0003-0093-7170
James BanguraUniversity of Makeni, Makeni, Sierra Leone.
Emmanuel AmaraUniversity of Makeni, Makeni, Sierra Leone.
Marilyn C KanuUniversity of Makeni, Makeni, Sierra Leone.
Osman T KanuUniversity of Makeni, Makeni, Sierra Leone.
Edwin G LavalieUniversity of Makeni, Makeni, Sierra Leone.
Mohamed TurayUniversity of Makeni, Makeni, Sierra Leone.
Patrick L K SwarayMinistry of Health and Sanitation, Freetown, Sierra Leone.
Mohamed A VandiMinistry of Health and Sanitation, Freetown, Sierra Leone.
Joseph HughesMRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Heinz FeldmannLaboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, United States of America.
Kyle RosenkeLaboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, United States of America.
Michael A JarvisSchool of Biomedical Sciences, University of Plymouth, Plymouth, United Kingdom.
Andrew J DavisonMRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lassa fever is a viral zoonotic disease that sickens tens of thousands of people each year when it spills over from its rodent reservoir throughout West Africa. Despite the burden this persistent spillover places on public health, stopping it has proven to be an intractable challenge despite decades of investment and effort. A revolutionary solution is the development of a transmissible vaccine that can spread through the rodent population resulting in immune coverage sufficient to eliminate Lassa virus transmission. Here, we evaluate the feasibility of a transmissible vaccine constructed from native cytomegaloviruses (CMVs) previously isolated from the natural reservoir of Lassa virus, Mastomys natalensis. Using a combination of field sampling, large-scale CMV genome characterization, and mathematical models parameterized using Bayesian methods, we quantified transmission rates and interactions among viruses in northern Sierra Leone. The results demonstrate that two of the three previously isolated CMVs co-infect freely and have R0 values consistent with autonomous elimination of Lassa virus from its rodent reservoir. These results set the stage for the development of a CMV vectored transmissible vaccine that could stop the spillover of Lassa virus throughout West Africa.

Indexed as

Lassa FeverLassa virusViral VaccinesAnimalsBayes TheoremComputational BiologyDisease ReservoirsHumansMurinaeMuromegalovirusSierra LeoneZoonosesViral Vaccines

Identifiers

PMID42361202
PMCPMC13322505

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.