Evidence map›Paper›PMID 30660331›Full record

ArticleThe American journal of pathology2019

Antibiotic Perturbation of Gut Microbiota Dysregulates Osteoimmune Cross Talk in Postpubertal Skeletal Development.

Jessica D Hathaway-Schrader, Heidi M Steinkamp, Michael B Chavez, Nicole A Poulides, Joy E Kirkpatrick, Michael E Chew, Emily Huang, Alexander V Alekseyenko, Jose I Aguirre, Chad M Novince

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Dysbiosis in the Gut-Liver Axis Is Associated With Low Bone Mass During Murine Cholestasis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  4. Article
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  15. Review
  16. Analysis of the Associations Between the Human Fecal Microbiome and Bone Density, Structure, and Strength: The Osteoporotic Fractures in Men (MrOS) Cohort.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  17. Commensal gut bacterium critically regulates alveolar bone homeostasis.Laboratory investigation; a journal of technical methods and pathology · 2022
    Article
  18. Article
  19. Review
  20. Gut microbiota can affect bone quality by regulating serum estrogen levels.American journal of translational research · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Jessica D Hathaway-SchraderDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina; Endocrinology Division, Department of Pediatrics, Medical University of South Carolina College of Medicine, Charleston, South Carolina.
Heidi M SteinkampDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina; Division of Pediatric Dentistry, The Ohio State University College of Dentistry, Columbus, Ohio.
Michael B ChavezDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina; Division of Biosciences, The Ohio State University College of Dentistry, Columbus, Ohio.
Nicole A PoulidesDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina; Endocrinology Division, Department of Pediatrics, Medical University of South Carolina College of Medicine, Charleston, South Carolina.
Joy E KirkpatrickDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina.
Michael E ChewDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina.
Emily HuangDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina.
Alexander V AlekseyenkoDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina; Department of Public Health Sciences, Medical University of South Carolina College of Medicine, Charleston, South Carolina.
Jose I AguirreDepartment of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, Florida.
Chad M NovinceDepartment of Oral Health Sciences, Medical University of South Carolina College of Dental Medicine, Charleston, South Carolina; Endocrinology Division, Department of Pediatrics, Medical University of South Carolina College of Medicine, Charleston, South Carolina. Electronic address: novincec@musc.edu.
Medical University of South Carolina · USUniversity of Florida · US

Funding

T-COHR: Training in Craniofacial and Oral Health ResearchT32DE017551 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YAO, HAI · 2006 to 2025
$10.3M
Pilot and Feasibility Project ProgramP30GM103331 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WESTWATER, CAROLINE · 2012 to 2016
$5.2M
Post-Transcriptional Regulation of Periodontal DiseR01DE021423 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KIRKWOOD, KEITH L · 2011 to 2015
$2.1M
Distance-based Panomic Analytics for Microbiome DataR01LM012517 · NLM · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ALEKSEYENKO, ALEXANDER V · 2018 to 2021
$1.3M
Impact of the Microbiome on Osteoimmunology and Skeletal DevelopmentK08DE025337 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI NOVINCE, CHAD MICHAEL · 2016 to 2020
$679k
T-COHR: Summer Undergraduate Research ProgramR25DE022677 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CRAY, JAMES J. · 2012 to 2016
$263k
Validation and Development of KDM4B Inhibitors to Target Peridontal DiseaseF30DE027290 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GERASCO, JOY ELIZABETH · 2017 to 2020
$193k
NIDCR NIH HHS F30 DE027290NIDCR NIH HHS K08 DE025337NIDCR NIH HHS L40 DE025410NIDCR NIH HHS R01 DE021423NIDCR NIH HHS R25 DE022677NIDCR NIH HHS T32 DE017551NIGMS NIH HHS P30 GM103331NLM NIH HHS R01 LM012517
6 · The paper itself

Abstract

Commensal gut microbiota-host immune responses are experimentally delineated via gnotobiotic animal models or alternatively by antibiotic perturbation of gut microbiota. Osteoimmunology investigations in germ-free mice, revealing that gut microbiota immunomodulatory actions critically regulate physiologic skeletal development, highlight that antibiotic perturbation of gut microbiota may dysregulate normal osteoimmunological processes. We investigated the impact of antibiotic disruption of gut microbiota on osteoimmune response effects in postpubertal skeletal development. Sex-matched C57BL/6T mice were administered broad-spectrum antibiotics or vehicle-control from the age of 6 to 12 weeks. Antibiotic alterations in gut bacterial composition and skeletal morphology were sex dependent. Antibiotics did not influence osteoblastogenesis or endochondral bone formation, but notably enhanced osteoclastogenesis. Unchanged Tnf or Ccl3 expression in marrow and elevated tumor necrosis factor-α and chemokine (C-C motif) ligand 3 in serum indicated that the pro-osteoclastic effects of the antibiotics are driven by increased systemic inflammation. Antibiotic-induced broad changes in adaptive and innate immune cells in mesenteric lymph nodes and spleen demonstrated that the perturbation of gut microbiota drives a state of dysbiotic hyperimmune response at secondary lymphoid tissues draining local gut and systemic circulation. Antibiotics up-regulated the myeloid-derived suppressor cells, immature myeloid progenitor cells known for immunosuppressive properties in pathophysiologic inflammatory conditions. Myeloid-derived suppressor cell-mediated immunosuppression can be antigen specific. Therefore, antibiotic-induced broad suppression of major histocompatibility complex class II antigen presentation genes in bone marrow discerns that antibiotic perturbation of gut microbiota dysregulates critical osteoimmune cross talk.

Indexed as

Gastrointestinal MicrobiomeOsteogenesisSexual MaturationAnimalsAnti-Bacterial AgentsChemokine CCL3FemaleLymph NodesMaleMesenteryMiceMyeloid-Derived Suppressor CellsOsteoclastsSpleenTumor Necrosis Factor-alphaAnti-Bacterial AgentsCcl3 protein, mouseChemokine CCL3Tumor Necrosis Factor-alpha

Identifiers

PMID30660331
PMCPMC6360355
OpenAlexW2910559662

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.