Evidence map›Paper›PMID 39677573›Full record

ArticleEvolution letters2024

Quantifying the strength of viral fitness trade-offs between hosts: a meta-analysis of pleiotropic fitness effects.

Xuechun 'May' Wang, Julia Muller, Mya McDowell, David A Rasmussen

Abstract read
In one paragraph

Article in Evolution letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

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  6. bioRxiv : the preprint server for biology · 2024
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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

4 authors.

Xuechun 'May' WangDepartment of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, United States.
Julia MullerGillings School of Global Public Health, University of North Carolina Chapel Hill, Chapel Hill, NC, United States.
Mya McDowellDepartment of Biological Sciences, North Carolina State University, Raleigh, NC, United States.
David A RasmussenDepartment of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, United States.ORCID https://orcid.org/0000-0001-9457-7561

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The range of hosts a given virus can infect is widely presumed to be limited by fitness trade-offs between alternative hosts. These fitness trade-offs may arise naturally due to antagonistic pleiotropy if mutations that increase fitness in one host tend to decrease fitness in alternate hosts. Yet there is also growing recognition that positive pleiotropy may be more common than previously appreciated. With positive pleiotropy, mutations have concordant fitness effects such that a beneficial mutation can simultaneously increase fitness in different hosts, providing a genetic mechanism by which selection can overcome fitness trade-offs. How readily evolution can overcome fitness trade-offs therefore depends on the overall distribution of mutational fitness effects between hosts, including the relative frequency of antagonistic versus positive pleiotropy. We therefore conducted a systematic meta-analysis of the pleiotropic fitness effects of viral mutations reported in different hosts. Our analysis indicates that while both antagonistic and positive pleiotropy are common, fitness effects are overall positively correlated between hosts and unconditionally beneficial mutations are not uncommon. Moreover, the relative frequency of antagonistic versus positive pleiotropy may simply reflect the underlying frequency of beneficial and deleterious mutations in individual hosts. Given a mutation is beneficial in one host, the probability that it is deleterious in another host is roughly equal to the probability that any mutation is deleterious, suggesting there is no natural tendency toward antagonistic pleiotropy. The widespread prevalence of positive pleiotropy suggests that many fitness trade-offs may be readily overcome by evolution given the right selection pressures.

Indexed as

distribution of fitness effectsfitness trade-offshost rangemutationpleiotropyviral evolution

Identifiers

PMID39677573
PMCPMC11637551

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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.