Evidence map›Paper›PMID 40460116›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Population sequencing for phylogenetic diversity and transmission analyses.

Talima Pearson, Tara Furstenau, Colin Wood, Vanessa Rigas, Kylie Drake, Jason Sahl, Sara Maltinsky, Bart J Currie, Mark Mayo, Carina Hall and 2 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Talima PearsonPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.ORCID 0000-0003-3696-041X
Tara FurstenauPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.ORCID 0000-0001-5233-7383
Colin WoodPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.
Vanessa RigasGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, NT 0811, Australia.
Kylie DrakePathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.
Jason SahlPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.
Sara MaltinskyPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.ORCID 0000-0001-6037-2103
Bart J CurrieGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, NT 0811, Australia.ORCID 0000-0002-8878-8837
Mark MayoGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, NT 0811, Australia.ORCID 0000-0002-9413-0142
Carina HallPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.ORCID 0000-0001-6941-3207
Paul KeimPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.ORCID 0000-0003-0089-5820
Viacheslav FofanovPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011.ORCID 0000-0001-7142-0764

Funding

SSCIMA: Integrating Analysis of Socio-economic Sub-population Dynamics to Improve Spatial Models of Infectious DiseaseU54MD012388 · NIMHD · NORTHERN ARIZONA UNIVERSITY · PI Samantha Jane Sabo · 2017 to 2026
$49.7M
Leptospira prevalence, cycling, and infection in the peridomestic environmentR01AI172924 · NIAID · NORTHERN ARIZONA UNIVERSITY · PI Talima Ross Pearson · 2023 to 2026
$2.8M
Are Minority Health Disparities in MRSA/MSSA Infections Related to Carriage and Social Relationships?R15AI156771 · NIAID · NORTHERN ARIZONA UNIVERSITY · PI PEARSON, TALIMA ROSS · 2021 to 2021
$456k
HHS | National Institutes of Health (NIH) R01AI172924HHS | National Institutes of Health (NIH) R15AI156771HHS | National Institutes of Health (NIH) U54MD012388NIAID NIH HHS R01 AI172924NIAID NIH HHS R15 AI156771NIMHD NIH HHS U54 MD012388
6 · The paper itself

Abstract

Genomic diversity in pathogen populations is foundational for evolution and adaptation. Understanding population-level diversity is also essential for tracking sources and revealing detailed pathways of transmission and spread. For bacteria, culturing, isolating, and sequencing the large number of individual colonies required to adequately sample diversity can be prohibitively time-consuming and expensive. While sequencing directly from a mixed population will show variants among reads, they cannot be linked to reveal allele combinations associated with phylogenetic inheritance patterns. Here, we describe the theory and method for using population sequencing directly from a mixed sample, along with a minimal number of individually sequenced colonies, to describe the phylogenetic diversity of a population without haplotype reconstruction. To demonstrate the utility of population sequencing in capturing phylogenetic diversity, we compared isogenic clones to population sequences of

Indexed as

Burkholderia pseudomalleiGenetic VariationPhylogenyStaphylococcus aureusHumansMelioidosisSputumdeep sequencingpathogen evolutionpathogen population diversitypathogen population sequencingpathogen transmission directionality

Identifiers

PMID40460116
PMCPMC12167970

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.