Ten selected Oscillibacter elongated rods appear in eight groupings: six singles and two touching pairs.
Genus representative reconstruction Editorially reviewed

Type-species-anchored Oscillibacter elongated straight-to-gently-curved rods, shown as ten bodies in six single and two paired groupings. This genus-level scientific reconstruction is representative, non-universal, non-diagnostic, and not a micrograph.

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Oscillibactertaxon · genus
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Oscillibacter is a genus of Gram-negative, strictly anaerobic, motile bacteria within the family Oscillospiraceae (phylum Firmicutes).

The type species, Oscillibacter valericigenes, was first isolated from the alimentary canal of a Japanese corbicula clam and named for its characteristic oscillating motility and its production of valerate (pentanoic acid), a five-carbon short-chain fatty acid that distinguishes it from the more commonly discussed Butyrate and propionate producers (,[1]Iino et al. 2007 — Oscillibacter valericigenes gen. nov., sp. nov.Takao Iino, Koji Mori, Kenji Tanaka et al. · 2007Open reference 1 taxonomic-description).

Oscillibacter is ecologically important as a sentinel of heavy metal exposure. Its depletion under cadmium and lead stress has been documented in multiple animal models, positioning it alongside Lachnospiraceae (Family) and Roseburia as an early casualty of metal-driven Dysbiosis.

Evidence map12 cited passagesInspect provenance +
01
Introduction

Oscillibacter is a genus of Gram-negative, strictly anaerobic, motile bacteria within the family Oscillospiraceae (phylum Firmicutes). The type species, Oscillibacter valericigenes, was first isolated from the alimentary canal of a Japanese corbicula clam and named for its characteristic oscillating motility and its production of valerate (pentanoic acid), a

02
Metal Dependencies

This iron dependency makes Oscillibacter vulnerable to toxic metal displacement. Lead exposure (100-500 ppm, 8 weeks) in Balb/C mice significantly decreased Oscillibacter alongside Lachnospiraceae and Ruminococcaceae, with concurrent increases in oxidative stress defense pathways (, animal-model).

03
Metal Dependencies

Cadmium exposure in wild long-tailed dwarf hamsters significantly decreased Oscillibacter, identifying it as one of 14 potential pathogens/commensals affected by Cd perturbation (, animal-model).

04
Ecological Role

Diet-responsive: On a low-carbohydrate, high-fat (non-ketogenic) diet, Oscillibacter was enriched alongside Escherichia/Shigella, and this LCD-associated community worsened colitis outcomes in mice—contrasting with the ketogenic diet, which enriched beneficial Akkermansia and Roseburia instead (, animal-model).

05
Ecological Role

Metformin response: Oscillibacter increased in both healthy and T2D subjects after metformin treatment (, prospective-cohort).

06
Ecological Role

Cancer ecology: In CRC tumor tissue, Oscillibacter abundance correlated with steroid biosynthesis and terpenoid pathways (, cross-sectional). After FMT in CRC mice, Oscillibacter was negatively correlated with anti-cancer cytokines, suggesting its reduction may be beneficial in the tumor microenvironment (, animal-model).

07
Depleted in:

Cadmium exposure: Significantly decreased in wild hamsters exposed to CdCl2, identified among the most affected commensals (, animal-model).

08
Depleted in:

Lead exposure: Decreased alongside Lachnospiraceae and Ruminococcaceae in lead-exposed mice (, animal-model).

09
Enriched in:

Low-carb diet (non-ketogenic): Enriched on LCD but associated with worse colitis outcomes (, animal-model).

10
Enriched in:

Metformin treatment: Increased in both healthy and T2D subjects after metformin (, prospective-cohort).

11
Complex associations:

Colorectal cancer: Tumor tissue associations with steroid/terpenoid metabolism; negatively correlated with anti-cancer cytokines after FMT (, cross-sectional;, animal-model).

12
Key Studies

| Study | Finding | Evidence Level | |-------|---------|---------------| | | Described the type species from the alimentary canal of a Japanese corbicula clam | Taxonomic description | | | Significantly depleted by cadmium in wild hamsters | Animal model | | | Depleted by lead alongside Lachnospiraceae | Animal model | | | Negatively correlated with anti-can

Contents1. Metal Dependencies2. Key Enzymes and Virulence Factors3. Ecological Role4. Conditions Associated5. Key Studies6. Cross-References

Metal Dependencies#

Oscillibacter depends on iron for its anaerobic metabolism. Iron-sulfur cluster proteins are essential for its electron transport chain and fermentation pathways.

This iron dependency makes Oscillibacter vulnerable to toxic metal displacement. Lead exposure (100-500 ppm, 8 weeks) in Balb/C mice significantly decreased Oscillibacter alongside Lachnospiraceae and Ruminococcaceae, with concurrent increases in Oxidative Stress defense pathways (,[2]Gut dysbiosis in animals due to environmental chemical exposuresRosenfeld CS · 2017Open reference 2 animal-model).

Cadmium exposure in wild long-tailed dwarf hamsters significantly decreased Oscillibacter, identifying it as one of 14 potential pathogens/commensals affected by cadmium (Cd) perturbation (,[3]Cadmium Exposure Induces Changes in Gut Microbial Composition and Metabolic Function in Long-Tailed Dwarf Hamsters, Cricetulus longicaudatusMengfan Tao, Kanglin Cao, Xinsheng Pu et al. · 2024Open reference 3 animal-model).

Key Enzymes and Virulence Factors#

Oscillibacter is not pathogenic. Its key metabolic enzymes reflect a saccharolytic fermentation strategy. Valerate synthesis enzymes: The genus's defining metabolic feature is production of valerate from carbohydrate fermentation.

Valerate has immunomodulatory properties and may influence epithelial differentiation, though it is less studied than butyrate.

Butyrate production: Some Oscillibacter species also produce butyrate, contributing to the overall SCFA pool. Bile acid metabolism: Oscillibacter has been implicated in secondary bile acid transformation, linking it to lipid metabolism and cholesterol homeostasis.

Ecological Role#

In the healthy gut, Oscillibacter is a moderately abundant member of the Firmicutes community that contributes to the SCFA pool and bile acid metabolism. Its ecological significance becomes apparent under stress.

Metal exposure indicator: The reproducible depletion of Oscillibacter under both cadmium and lead exposure makes it a candidate biomarker for environmental metal stress on the Gut Microbiome.

Diet-responsive: On a low-carbohydrate, high-fat (non-ketogenic) diet, Oscillibacter was enriched alongside Escherichia/Shigella, and this LCD-associated community worsened colitis outcomes in mice—contrasting with the ketogenic diet, which enriched beneficial Akkermansia and Roseburia instead (,[4]Ketogenic Diet Alleviates Colitis by Reduction of Colonic Group 3 Innate Lymphoid Cells Through Altering Gut MicrobiomeKong C, Yan X, Liu Y et al. · 2021Open reference 4 animal-model).

Metformin response: Oscillibacter increased in both healthy and T2D subjects after metformin treatment (,[5]Elbere 2020 — Baseline Gut Microbiome Composition Predicts Metformin Therapy Short-Term Efficacy in Newly Diagnosed Type 2 Diabetes PatientsIlze Elbere, Ivars Silamikelis, Ilze Izabella Dindune et al. · 2020Open reference 5 prospective-cohort).

Cancer ecology: In CRC tumor tissue, Oscillibacter abundance correlated with steroid biosynthesis and terpenoid pathways (,[6]Metabolomics and 16S rRNA Sequencing of Human Colorectal Cancers and Adjacent MucosaLoke MF, Chua EG, Gan HM et al. · 2018Open reference 6 cross-sectional).

After FMT in CRC mice, Oscillibacter was negatively correlated with anti-cancer cytokines, suggesting its reduction may be beneficial in the tumor microenvironment (,[7]Fecal Microbiota Transplantation Inhibits Colorectal Cancer Progression: Reversing Intestinal Microbial Dysbiosis to Enhance Anti-Cancer Immune ResponsesHao Yu, Xing-Xiu Li, Xing Han et al. · 2023Open reference 7 animal-model).

Conditions Associated#

Depleted in:#

Cadmium exposure: Significantly decreased in wild hamsters exposed to CdCl2, identified among the most affected commensals (,[3]Cadmium Exposure Induces Changes in Gut Microbial Composition and Metabolic Function in Long-Tailed Dwarf Hamsters, Cricetulus longicaudatusMengfan Tao, Kanglin Cao, Xinsheng Pu et al. · 2024Open reference 3 animal-model).

Lead exposure: Decreased alongside Lachnospiraceae and Ruminococcaceae in lead-exposed mice (,[2]Gut dysbiosis in animals due to environmental chemical exposuresRosenfeld CS · 2017Open reference 2 animal-model).

Enriched in:#

Low-carb diet (non-ketogenic): Enriched on LCD but associated with worse colitis outcomes (,[4]Ketogenic Diet Alleviates Colitis by Reduction of Colonic Group 3 Innate Lymphoid Cells Through Altering Gut MicrobiomeKong C, Yan X, Liu Y et al. · 2021Open reference 4 animal-model). Metformin treatment: Increased in both healthy and T2D subjects after metformin (,[5]Elbere 2020 — Baseline Gut Microbiome Composition Predicts Metformin Therapy Short-Term Efficacy in Newly Diagnosed Type 2 Diabetes PatientsIlze Elbere, Ivars Silamikelis, Ilze Izabella Dindune et al. · 2020Open reference 5 prospective-cohort).

Complex associations:#

  • Colorectal cancer: Tumor tissue associations with steroid/terpenoid metabolism; negatively correlated with anti-cancer cytokines after FMT (,[6]Metabolomics and 16S rRNA Sequencing of Human Colorectal Cancers and Adjacent MucosaLoke MF, Chua EG, Gan HM et al. · 2018Open reference 6 cross-sectional;,[7]Fecal Microbiota Transplantation Inhibits Colorectal Cancer Progression: Reversing Intestinal Microbial Dysbiosis to Enhance Anti-Cancer Immune ResponsesHao Yu, Xing-Xiu Li, Xing Han et al. · 2023Open reference 7 animal-model).

Key Studies#

StudyFindingEvidence Level
[1]Iino et al. 2007 — Oscillibacter valericigenes gen. nov., sp. nov.Takao Iino, Koji Mori, Kenji Tanaka et al. · 2007Open reference 1Described the type species from the alimentary canal of a Japanese corbicula clamTaxonomic description
[3]Cadmium Exposure Induces Changes in Gut Microbial Composition and Metabolic Function in Long-Tailed Dwarf Hamsters, Cricetulus longicaudatusMengfan Tao, Kanglin Cao, Xinsheng Pu et al. · 2024Open reference 3Significantly depleted by cadmium in wild hamstersAnimal model
[2]Gut dysbiosis in animals due to environmental chemical exposuresRosenfeld CS · 2017Open reference 2Depleted by lead alongside LachnospiraceaeAnimal model
[7]Fecal Microbiota Transplantation Inhibits Colorectal Cancer Progression: Reversing Intestinal Microbial Dysbiosis to Enhance Anti-Cancer Immune ResponsesHao Yu, Xing-Xiu Li, Xing Han et al. · 2023Open reference 7Negatively correlated with anti-cancer cytokines post-FMTAnimal model
[4]Ketogenic Diet Alleviates Colitis by Reduction of Colonic Group 3 Innate Lymphoid Cells Through Altering Gut MicrobiomeKong C, Yan X, Liu Y et al. · 2021Open reference 4Enriched on LCD; worse colitis vs KDAnimal model
[5]Elbere 2020 — Baseline Gut Microbiome Composition Predicts Metformin Therapy Short-Term Efficacy in Newly Diagnosed Type 2 Diabetes PatientsIlze Elbere, Ivars Silamikelis, Ilze Izabella Dindune et al. · 2020Open reference 5Increased by metformin in healthy and T2DProspective cohort

Cross-References#

Generated evidence record

References 14

Numbered by first appearance in the article, then reconciled with its declared source list.

  1. 1

    Takao Iino, Koji Mori, Kenji Tanaka et al. (2007). Iino et al. 2007 — Oscillibacter valericigenes gen. nov., sp. nov.. International Journal of Systematic and Evolutionary Microbiology.

  2. 2

    Rosenfeld CS (2017). Gut dysbiosis in animals due to environmental chemical exposures. Frontiers in Cellular and Infection Microbiology.

  3. 3

    Mengfan Tao, Kanglin Cao, Xinsheng Pu et al. (2024). Cadmium Exposure Induces Changes in Gut Microbial Composition and Metabolic Function in Long-Tailed Dwarf Hamsters, Cricetulus longicaudatus. Ecology and Evolution.

  4. 4

    Kong C, Yan X, Liu Y et al. (2021). Ketogenic Diet Alleviates Colitis by Reduction of Colonic Group 3 Innate Lymphoid Cells Through Altering Gut Microbiome. Signal Transduction and Targeted Therapy.

  5. 5

    Ilze Elbere, Ivars Silamikelis, Ilze Izabella Dindune et al. (2020). Elbere 2020 — Baseline Gut Microbiome Composition Predicts Metformin Therapy Short-Term Efficacy in Newly Diagnosed Type 2 Diabetes Patients. PLoS ONE.

  6. 6

    Loke MF, Chua EG, Gan HM et al. (2018). Metabolomics and 16S rRNA Sequencing of Human Colorectal Cancers and Adjacent Mucosa. PLOS ONE.

  7. 7

    Hao Yu, Xing-Xiu Li, Xing Han et al. (2023). Fecal Microbiota Transplantation Inhibits Colorectal Cancer Progression: Reversing Intestinal Microbial Dysbiosis to Enhance Anti-Cancer Immune Responses. Frontiers in Microbiology.

  8. 8

    Patrick A. de Jonge, Koen Wortelboer, Torsten P. M. Scheithauer et al. (2022). Gut Virome Profiling Identifies a Widespread Bacteriophage Family Associated with Metabolic Syndrome. Nature Communications.

  9. 9

    Gong W, Jin G, Bao Y et al. (2025). Characteristics and potential diagnostic value of gut microbiota in ovarian tumor patients. Scientific Reports.

  10. 10

    Quanxin Su, Yanxi Long, Yayin Luo et al. (2023). Su 2023 — Specific Gut Microbiota May Increase the Risk of Erectile Dysfunction (Two-Sample MR). Frontiers in Endocrinology.

  11. 11

    Chen et al. (2024). Chen 2024 — Causal Gut Microbiota in Male Erectile Dysfunction (MR). Frontiers in Microbiology.

  12. 12

    Zhang et al. (2023). Zhang 2023 — Causal Gut Microbiota and Erectile Dysfunction (Mendelian Randomization). Frontiers in Microbiology.

  13. 13

    Lyu J, et al. (2024). Lyu 2024 — Care Mode and Gut Microbiota in CP Children. Frontiers in Pediatrics.

  14. 14

    Congfu Huang, Chunuo Chu, Yuanping Peng et al. (2022). Huang 2022 — Correlations Between Gastrointestinal and Oral Microbiota in Children With Cerebral Palsy and Epilepsy. Frontiers in Pediatrics.

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