Evidence map›Paper›PMID 33544453›Full record

ArticleMicrobiologyOpen2021

No man's land: Species-specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures.

Fatemeh Jalali, Felix Ellett, Pooja Balani, Margaret J Duncan, Floyd E Dewhirst, Gary G Borisy, Daniel Irimia

Open access · goldAbstract read
In one paragraph

Article in MicrobiologyOpen, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 13 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

7 authors at 1 institution in 1 country.

Fatemeh JalaliDivision of Surgery, BioMEMS Resource Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Felix EllettDivision of Surgery, BioMEMS Resource Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.ORCID 0000-0003-4941-4346
Pooja BalaniDepartment of Microbiology, The Forsyth Institute, Cambridge, MA, USA.
Margaret J DuncanDepartment of Microbiology, The Forsyth Institute, Cambridge, MA, USA.
Floyd E DewhirstDepartment of Microbiology, The Forsyth Institute, Cambridge, MA, USA.ORCID 0000-0003-4427-7928
Gary G BorisyDepartment of Microbiology, The Forsyth Institute, Cambridge, MA, USA.ORCID 0000-0002-0266-8018
Daniel IrimiaDivision of Surgery, BioMEMS Resource Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.ORCID 0000-0001-7347-2082
Harvard University · US

Funding

Bio-MicroElectroMechanical Systems Resource CenterP41EB002503 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI TONER, MEHMET · 2004 to 2018
$17.4M
Spatial Organization of the Oral MicrobiomeR01DE022586 · NIDCR · MARINE BIOLOGICAL LABORATORY · PI Jessica Leigh Mark Welch · 2013 to 2026
$8.7M
Cultivation, Nature, Ecology and Pathogenicity of the Uncultivable Oral MicrobiomR01DE024468 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI ALM, ERIC JOHN, DEWHIRST, FLOYD E · 2014 to 2018
$7.3M
Mechanisms of Resolvin E1 in Periodontal RegenerationR01DE025020 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI GUASTALDI, FERNANDO, VAN DYKE, THOMAS ELLIOTT · 2015 to 2023
$4.9M
Neutrophil Decision Making in Confined Environments in Health and DiseaseR01GM092804 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI IRIMIA, DANIEL · 2010 to 2022
$4.3M
Novel Mechanisms in Resolution to Harness Inflammation for ReconstructionR01DE019938 · NIDCR · BRIGHAM AND WOMEN'S HOSPITAL · PI IRIMIA, DANIEL, SERHAN, CHARLES NICHOLAS · 2009 to 2012
$2.7M
NIBIB NIH HHS P41 EB002503NIDCR NIH HHS R01 DE019938NIDCR NIH HHS R01 DE022586NIDCR NIH HHS R01 DE024468NIDCR NIH HHS R01 DE025020NIGMS NIH HHS R01 GM092804
6 · The paper itself

Abstract

To survive within complex environmental niches, including the human host, bacteria have evolved intricate interspecies communities driven by competition for limited nutrients, cooperation via complementary metabolic proficiencies, and establishment of homeostatic relationships with the host immune system. The study of such complex, interdependent relationships is often hampered by the challenges of culturing many bacterial strains in research settings and the limited set of tools available for studying the dynamic behavior of multiple bacterial species at the microscale. Here, we utilize a microfluidic-based co-culture system and time-lapse imaging to characterize dynamic interactions between Streptococcus species, Staphylococcus aureus, and Actinomyces species. Co-culture of Streptococcus cristatus or S. salivarius in nanoliter compartments with Actinomyces graevenitzii revealed localized exclusion of Streptococcus and Staphylococcus from media immediately surrounding A. graevenitzii microcolonies. This community structure did not occur with S. mitis or S. oralis strains or in co-cultures containing other Actinomycetaceae species such as S. odontolyticus or A. naeslundii. Moreover, fewer neutrophils were attracted to compartments containing both A. graevenitzii and Staphylococcus aureus than to an equal number of either species alone, suggesting a possible survival benefit together during immune responses.

Indexed as

ActinomycesAntibiosisBiofilmsCoculture TechniquesHost Microbial InteractionsHumansImmunity, InnateMicrobiotaMicrofluidicsMouthNeutrophilsStaphylococcus aureusStreptococcusActinomyces graevenitziicell-microbe interactionsmicrobial interactions and pathogenesissignallingStaphylococcus

Identifiers

PMID33544453
PMCPMC7882712
OpenAlexW3127571602

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.