Evidence map›Paper›PMID 17603099›Full record

ArticleGenetics2007

Major histocompatibility complex heterozygosity reduces fitness in experimentally infected mice.

Petteri Ilmonen, Dustin J Penn, Kristy Damjanovich, Linda Morrison, Laleh Ghotbi, Wayne K Potts

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
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

36 citing papers in PubMed, 102 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Petteri IlmonenKonrad Lorenz Institute for Ethology, Austrian Academy of Sciences, Savoyenstrasse 1a, A-1160 Vienna, Austria. p.ilmonen@klivv.oeaw.ac.at
Dustin J Penn
Kristy Damjanovich
Linda Morrison
Laleh Ghotbi
Wayne K Potts
University of Utah · USAustrian Academy of Sciences · AT

Funding

SELECTIVE MECHANISMS MAINTAINING H-2 POLYMORPHISMSR01GM039578 · NIGMS · UNIVERSITY OF UTAH · PI POTTS, WAYNE K. · 1989 to 2007
$2.0M
NIGMS NIH HHS GM 39578NIGMS NIH HHS R01 GM039578
6 · The paper itself

Abstract

It is often suggested that heterozygosity at major histocompatibility complex (MHC) loci confers enhanced resistance to infectious diseases (heterozygote advantage, HA, hypothesis), and overdominant selection should contribute to the evolution of these highly polymorphic genes. The evidence for the HA hypothesis is mixed and mainly from laboratory studies on inbred congenic mice, leaving the importance of MHC heterozygosity for natural populations unclear. We tested the HA hypothesis by infecting mice, produced by crossbreeding congenic C57BL/10 with wild ones, with different strains of Salmonella, both in laboratory and in large population enclosures. In the laboratory, we found that MHC influenced resistance, despite interacting wild-derived background loci. Surprisingly, resistance was mostly recessive rather than dominant, unlike in most inbred mouse strains, and it was never overdominant. In the enclosures, heterozygotes did not show better resistance, survival, or reproductive success compared to homozygotes. On the contrary, infected heterozygous females produced significantly fewer pups than homozygotes. Our results show that MHC effects are not masked on an outbred genetic background, and that MHC heterozygosity provides no immunological benefits when resistance is recessive, and can actually reduce fitness. These findings challenge the HA hypothesis and emphasize the need for studies on wild, genetically diverse species.

Indexed as

Major Histocompatibility ComplexAnimalsBase SequenceDNA, MitochondrialFemaleHeterozygoteMaleMiceMice, CongenicMice, Inbred C57BLModels, GeneticModels, ImmunologicalPregnancySalmonella Infections, AnimalSpecies SpecificityDNA, Mitochondrial

Identifiers

PMID17603099
PMCPMC1950649
OpenAlexW2107144321

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.