Evidence map›Paper›PMID 25783448›Full record

ReviewNature reviews. Genetics2015

Evolutionary insights into host-pathogen interactions from mammalian sequence data.

Manuela Sironi, Rachele Cagliani, Diego Forni, Mario Clerici

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature reviews. Genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 173 papers.

0numbers the graph read from it
0cells of the map it votes in
173citing papers in PubMed
42.3field-weighted citation impact, top 1% 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

173 citing papers in PubMed, 306 citations in OpenAlex.

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  7. Allopatric coevolution: Migratory predators may facilitate mimicry between geographically nonoverlapping species.Proceedings of the National Academy of Sciences of the United States of America · 2026
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113 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Manuela SironiBioinformatics, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, Italy.
Rachele CaglianiBioinformatics, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, Italy.
Diego ForniBioinformatics, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, Italy.
Mario Clerici1] Department of Physiopathology and Transplantation, University of Milan, 20090 Milan, Italy. [2] Don C. Gnocchi Foundation ONLUS, IRCCS, 20148 Milan, Italy.
IRCCS Eugenio Medea · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infections are one of the major selective pressures acting on humans, and host-pathogen interactions contribute to shaping the genetic diversity of both organisms. Evolutionary genomic studies take advantage of experiments that natural selection has been performing over millennia. In particular, inter-species comparative genomic analyses can highlight the genetic determinants of infection susceptibility or severity. Recent examples show how evolution-guided approaches can provide new insights into host-pathogen interactions, ultimately clarifying the basis of host range and explaining the emergence of different diseases. We describe the latest developments in comparative immunology and evolutionary genetics, showing their relevance for understanding the molecular determinants of infection susceptibility in mammals.

Indexed as

Biological EvolutionGenomicsSequence Analysis, DNAAmino Acid SequenceAnimalsBase SequenceGenetic VariationHost-Pathogen InteractionsHumansMammalsMolecular Sequence DataSequence Homology, Amino AcidSequence Homology, Nucleic Acid

Identifiers

PMID25783448
PMCPMC7096838
OpenAlexW1983304589

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.