Evidence map›Paper›PMID 25416769›Full record

ArticleApplied and environmental microbiology2015

Population genetic analysis of Streptomyces albidoflavus reveals habitat barriers to homologous recombination in the diversification of streptomycetes.

Kun Cheng, Xiaoying Rong, Adrián A Pinto-Tomás, Marcela Fernández-Villalobos, Catalina Murillo-Cruz, Ying Huang

Open access · bronzeAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.7field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  4. Unveiling the bioactive potential of Actinomycetota from the Tagus River estuary.International microbiology : the official journal of the Spanish Society for Microbiology · 2024
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  12. Article
  13. Chemical Ecology ofMicroorganisms · 2020
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Leveraging ecological theory to guide natural product discovery.Journal of industrial microbiology & biotechnology · 2016
    Review
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.

Kun ChengState Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China University of Chinese Academy of Sciences, Beijing, China.
Xiaoying RongState Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Adrián A Pinto-TomásCenter for Research in Cell and Molecular Biology, University of Costa Rica, San José, Costa Rica Center for Research in Microscopic Structures, University of Costa Rica, San José, Costa Rica.
Marcela Fernández-VillalobosCenter for Research in Cell and Molecular Biology, University of Costa Rica, San José, Costa Rica Center for Research in Microscopic Structures, University of Costa Rica, San José, Costa Rica.
Catalina Murillo-CruzCenter for Research in Cell and Molecular Biology, University of Costa Rica, San José, Costa Rica Center for Research in Microscopic Structures, University of Costa Rica, San José, Costa Rica.
Ying HuangState Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China huangy@im.ac.cn.
Microbiology Institute of Shaanxi · CNUniversidad de Costa Rica · CR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Examining the population structure and the influence of recombination and ecology on microbial populations makes great sense for understanding microbial evolution and speciation. Streptomycetes are a diverse group of bacteria that are widely distributed in nature and a rich source of useful bioactive compounds; however, they are rarely subjected to population genetic investigations. In this study, we applied a five-gene-based multilocus sequence analysis (MLSA) scheme to 41 strains of Streptomyces albidoflavus derived from diverse sources, mainly insects, sea, and soil. Frequent recombination was detected in S. albidoflavus, supported by multiple lines of evidence from the pairwise homoplasy index (Φw) test, phylogenetic discordance, the Shimodaira-Hasegawa (SH) test, and network analysis, underpinning the predominance of homologous recombination within Streptomyces species. A strong habitat signal was also observed in both phylogenetic and Structure 2.3.3 analyses, indicating the importance of ecological difference in shaping the population structure. Moreover, all three habitat-associated groups, particularly the entomic group, demonstrated significantly reduced levels of gene flow with one another, generally revealing habitat barriers to recombination. Therefore, a combined effect of homologous recombination and ecology is inferred for S. albidoflavus, where dynamic evolution is at least partly balanced by the extent that differential distributions of strains among habitats limit genetic exchange. Our study stresses the significance of ecology in microbial speciation and reveals the coexistence of homologous recombination and ecological divergence in the evolution of streptomycetes.

Indexed as

EcosystemGenetic VariationHomologous RecombinationAnimalsDNA, BacterialGene FlowGenetics, PopulationInsectaMolecular Sequence DataMultilocus Sequence TypingSeawaterSoil MicrobiologyStreptomycesDNA, Bacterial

Identifiers

PMID25416769
PMCPMC4292468
OpenAlexW2151172579

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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.