Depletion of Butyrate-Producing Clostridia from the Gut Microbiota Drives an Aerobic Luminal Expansion of Salmonella

Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species

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Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota

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The Global Burden of Nontyphoidal Salmonella Gastroenteritis

Majowicz, S. E., Musto, J., Scallan, E., Angulo, F. J., Kirk, M., O’Brien, S. J., Jones, T. F., Fazil, A., & Hoekstra, R. M. (2010) · Clinical Infectious Diseases · doi:10.1086/650733 · Cited by 2,465

Diversity, metabolism and microbial ecology of butyrate-producing bacteria from the human large intestine

Louis, P., & Flint, H. J. (2009) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2009.01514.x · Cited by 2,179

Complete genome sequence of Salmonella enterica serovar Typhimurium LT2

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Crosstalk between microbiota-derived short-chain fatty acids and intestinal epithelial HIF augments tissue barrier function

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Gut inflammation provides a respiratory electron acceptor for Salmonella

Winter, S., Thiennimitr, P., Winter, M. G., Butler, B. P., Huseby, D. L., Crawford, R. W., Russell, J. M., Bevins, C. L., Adams, L. G., Tsolis, R. M., et al. (2010) · Nature · doi:10.1038/nature09415 · Cited by 1,271

Why is the partial oxygen pressure of human tissues a crucial parameter? Small molecules and hypoxia

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Simultaneous Identification of Bacterial Virulence Genes by Negative Selection

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Revealing the Bacterial Butyrate Synthesis Pathways by Analyzing (Meta)genomic Data

Vital, M., Howe, A. C., & Tiedje, J. M. (2014) · mBio · doi:10.1128/mbio.00889-14 · Cited by 1,189

Unveiling the effects of shrimp hydrolysate as a dietary ingredient in healthy adult Beagle dogs

Guilherme-Fernandes, J., Fonseca, A. J. M., Aires, T., Lima, S. A. C., Maia, M. R. G., & Cabrita, A. R. J. (2024) · Journal of Animal Science · doi:10.1093/jas/skae280 · Cited by 6

Diagnosing and engineering gut microbiomes

Barazzone, E. C., Diard, M., Hug, I., Larsson, L., & Slack, E. M. C. (2024) · EMBO Molecular Medicine · doi:10.1038/s44321-024-00149-4 · Cited by 7

Intestine epithelial–specific hypoxia-inducible factor-1α overexpression ameliorates western diet–induced MASLD

Xu, M., Taylor, M. S., Hill, B. G., Li, X., Rouchka, E. C., McClain, C. J., & Song, M. (2024) · Hepatology Communications · doi:10.1097/hc9.0000000000000572 · Cited by 9

In mouse and in vitro models, bowel preparation promotes pathogen colonization, translocation, and exacerbation of inflammation

Clayton, C. A., Porter, I., Deng, B., McCallum, G., Srinivas, A., Sie, C., He, J., Pei, A., Tertigas, D., Pepin, D. M., et al. (2025) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.102517 · Cited by 7

Butyrate and Intestinal Homeostasis: Effects on the Intestinal Microbiota and Epithelial Hypoxia

Bortoluzzi, C., Castro, F. L. D. S., & Kogut, M. H. (2022) · The microbiomes of humans, animals, plants, and the environment · doi:10.1007/978-3-030-90303-9_4 · Cited by 6

Salmonella respiration turns the tables on propionate

Walker, G. T., & Raffatellu, M. (2022) · Trends in Microbiology · doi:10.1016/j.tim.2022.01.011 · Cited by 5

Responses of Fermentation Characteristics and Microbial Communities to Vitamin B12 Supplementation in In Vitro Ruminal Cultures

Wang, K., Liu, Z., Du, C., Xiong, B., & Yang, L. (2022) · Fermentation · doi:10.3390/fermentation8080406 · Cited by 5

Resistance is futile? Mucosal immune mechanisms in the context of microbial ecology and evolution

Slack, E. M. C., & Diard, M. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00574-z · Cited by 6

Microbial management

Byndloss, M. X. (2020) · Science · doi:10.1126/science.abc5619 · Cited by 6

Disclosing the benefits of multi-strain compounds and their health impact mechanisms utilizing intestinal biomimetic technology

Liao, J., Huang, J., Li, X., Kuang, J., Li, J., Wang, W., & Li, J. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1550913 · Cited by 5

Exploring the Gut and Oral Microbiomes in Psychoactive Substance Use: A Scoping Review of Clinical Studies

Barkus, A., Baltrūnienė, V., Barkienė, L., Baušienė, J., Baltrūnas, T., Brazys, M., Rauduvytė, K., Kazlauskaitė, P., & Baušys, A. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70165 · Cited by 7

Synergistic impact of starch-tannic acid complex in regulating gut microbiota to produce propionate

Duan, S., Hu, Y., Zhang, X., Li, E., & Li, C. (2025) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2025.124077 · Cited by 5

Oral multifunctional gel beads for the targeted treatment of inflammatory bowel disease

Hu, D., Chen, D., Zhang, A., Meng, K., Chen, M., Abbas, M., Qu, W., & Xie, S. (2025) · Journal of Controlled Release · doi:10.1016/j.jconrel.2025.114240 · Cited by 5

Power and poison: The intersections of H2S and O2 metabolism

Brake, J., & Banerjee, R. V. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110810 · Cited by 6

Simulated Digestion and Metabolic Outcomes of Tremella fuciformis Polysaccharides and Their Effects on the Gut Microbiota

Ye, K., Fu, C., Du, H., Qiu, Z., Chen, S., Liu, D., Ma, G., & Xiao, H. (2025) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c07680 · Cited by 5

From gut dysbiosis to eubiosis: understanding microbiome recovery as an ecological process

Kennedy, M. S., & Chang, E. B. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2649448 · Cited by 5

Hypoxia is a key mechanism for regulating inflammation in ulcerative colitis

Postovalova, E., Makarova, O. V., Kosyreva, A. M., & Dzhalilova, D. S. (2020) · Russian Open Medical Journal · doi:10.15275/rusomj.2020.0101 · Cited by 5

Comparison of rectum fecal bacterial community of finishing bulls fed high-concentrate diets with active dry yeast and yeast culture supplementation

Gao, K., & Geng, C. (2022) · Animal Bioscience · doi:10.5713/ab.22.0215 · Cited by 5

Wash-Free and High-Contrast Imaging of Single-Nucleotide Variation in Single Cells Using Transcription-Amplified Light-Up RNA Aptamer

Xia, X., Li, F., Zhang, Y., Zhu, Y., Song, S., He, G., Zhang, J., He, Q., & Deng, R. (2023) · Analytical Chemistry · doi:10.1021/acs.analchem.3c00089 · Cited by 5

FG-4592 relieves diabetic kidney disease severity by influencing metabolic profiles via gut microbiota reconstruction in both human and mouse models

Jiang, Y., Cui, W., Zhang, Y., Wang, T., Zheng, X., Li, H., & Shang, J. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1195441 · Cited by 5

Exploring the Gut–Mitochondrial Axis: p66Shc Adapter Protein and Its Implications for Metabolic Disorders

Pinaffi‐Langley, A. C. D. C., Melia, E., & Hays, F. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25073656 · Cited by 4

Breathe and bloom: Gut hypoxia limits C. albicans growth

Mishra, A. A., & Koh, A. Y. (2024) · Cell Host & Microbe · doi:10.1016/j.chom.2024.06.006 · Cited by 5

RcsB-dependent effects on nar operon regulation during the aerobic growth of Salmonella Typhimurium

Lamberti, M., Ballesteros, M. F., López, F. E., Pescaretti, M. D. L. M., & Delgado, M. A. (2019) · Biochimie · doi:10.1016/j.biochi.2019.09.014 · Cited by 5

Chemoproteomic Approaches for Unraveling Prokaryotic Biology

Malarney, K. P., & Chang, P. V. (2023) · Israel Journal of Chemistry · doi:10.1002/ijch.202200076 · Cited by 5

Oxygen as a Virulence Determinant in Polymicrobial Infections

Selleck, E. M., & Gilmore, M. S. (2016) · mBio · doi:10.1128/mbio.01249-16 · Cited by 5

Checks and Balances—Microbiota Shifts in Immunosuppressed Mice

Fricke, W. F., & Bromberg, J. S. (2016) · Transplantation · doi:10.1097/tp.0000000000001493 · Cited by 5

A chemically-defined growth medium to support Lactobacillus – Acetobacter community analysisPreprint

Aumiller, K., Stevens, E. T., Scheffler, R. J., Güvener, Z. T., Tung, E., Grimaldo, A. B. G., Carlson, H. K., Deutschbauer, A. M., Taga, M. E., Marco, M. L., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.12.443930 · Cited by 5

Monosaccharides Drive Salmonella Gut Colonization in a Context-Dependent MannerPreprint

Schubert, C., Nguyen, B. D., Sichert, A., Näpflin, N. C., Sintsova, A., Feer, L., Näf, J., Daniel, B. B. J., Steiger, Y., von Mering, C., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.06.606610 · Cited by 5

Beyond Random Fecal Microbial Transplants

Sartor, R. B. (2024) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2024.11.002 · Cited by 4

Yeast β-glucan ameliorated Salmonella-induced gut impairment in broiler chickens by modulating gut microbiome

Bi, R., Abbas, W., Li, J., Huang, J., Hu, J., Guo, F., & Wang, Z. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.145630 · Cited by 4

HIF-1 attenuates high-fiber diet-mediated proliferation and stemness of colonic epithelium

Castro, P. R., Corrêa, R. O., Angelim, M. K. S. C., Rodovalho, V. D. R., Fernandes, M. F., Nirello, V. D., Gomes, A. B. D. S. P., Felipe, J. D. S., Pral, L. P., de Oliveira, S., et al. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2543123 · Cited by 4

Cross-kingdom dialogs in the gut: Integrating bacterial pathogens, helminths, and microbiota interactions for immune homeostasis

Hu, S., Liu, Z., Yan, W., & Guo, R. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1013494 · Cited by 6

Lactiplantibacillus plantarum Q180 supplementation restores high-fat diet-induced gut dysbiosis and intestinal barrier dysfunction in mice

Cho, M., Chu, J., No, C., Kim, Y.-W., Lee, J., Joung, H., Kwon, Y. J., Shin, C. H., Lee, J., & Ha, J. (2026) · Journal of Applied Microbiology · doi:10.1093/jambio/lxag021 · Cited by 4

Decoding the gut microbiota-immune dialogue: from bidirectional axis to therapeutic applications

Liu, Y., Chen, C., Liu, H., Wang, W., Zhou, X., Guo, M., Zhao, J., Zeng, Z., & Xu, L. (2026) · Journal of Nanobiotechnology · doi:10.1186/s12951-026-04376-4 · Cited by 4

Spatial analysis of murine microbiota and bile acid metabolism during amoxicillin treatment

Beekman, C. N., Penumutchu, S., Peterson, R., Han, G., Belenky, M., Hasan, M., Belenky, A., Beura, L. K., & Belenky, P. A. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114572 · Cited by 4

Oral amoxicillin treatment disrupts the gut microbiome and metabolome without interfering with luminal redox potential in the intestine of Wistar Han rats

Sanchez, S. B., Bahl, M. I., Hansen, E. B., Licht, T. R., & Laursen, M. F. (2025) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiaf003 · Cited by 4

Decoding the role of the arginine dihydrolase pathway in shaping human gut community assembly and health-relevant metabolites

Liu, Y., Cheng, Y., Thompson, J. C., Zhou, Z., Vivas, E. I., Warren, M. F., DuClos, J. M., Anantharaman, K., Rey, F. E., & Venturelli, O. S. (2025) · Cell Systems · doi:10.1016/j.cels.2025.101292 · Cited by 4

Gut microbiota dysbiosis and protein energy wasting in patients on hemodialysis: an observational longitudinal study

Bi, X., Liu, Y., Lu, Y., Ling, L., Lü, J., Hu, C., & Ding, W. Q. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1270690 · Cited by 4

Chemical Toolbox to Decode the Microbiota Lexicon

Qiao, Y., Hayashi, H., & Teo, S. C. (2020) · Chemistry - An Asian Journal · doi:10.1002/asia.202000541 · Cited by 4

Spore Preparation Protocol for Enrichment of Clostridia from Murine Intestine

Velazquez, E. M., Rivera-Chávez, F., & Bäumler, A. J. (2017) · BIO-PROTOCOL · doi:10.21769/bioprotoc.2296 · Cited by 4

Infection and ImmunityWelcomes the New Microbiology

Bäumler, A. J. (2017) · Infection and Immunity · doi:10.1128/iai.00255-17 · Cited by 4

Resistant potato starch fuels beneficial host-microbe interactions in the gutPreprint

Trachsel, J., Briggs, C., Gabler, N. K., Allen, H. K., & Loving, C. L. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/389007 · Cited by 4

Gut-bladder axis syndrome associated with recurrent UTIs in humansPreprint

Worby, C. J., Schreiber, H. L., Straub, T. J., van Dijk, L. R., Bronson, R. A., Olson, B. S., Pinkner, J. S., Obernuefemann, C. L. P., Muñoz, V. L., Paharik, A. E., et al. (2021) · medRxiv · doi:10.1101/2021.11.15.21266268 · Cited by 4

C. difficile may be overdiagnosed in adults and is a prevalent commensal in infantsPreprint

Ferretti, P., Wirbel, J., Maistrenko, O. M., Rossum, T. V., Alves, R., Fullam, A., Akanni, W. A., Schudoma, C., Schwarz, A. M., Thielemann, R., et al. (2023) · doi:10.7554/elife.90111 · Cited by 4

C. difficile may be overdiagnosed in adults and is a prevalent commensal in infantsPreprint

Ferretti, P., Wirbel, J., Maistrenko, O. M., Rossum, T. V., Alves, R., Fullam, A., Akanni, W. A., Schudoma, C., Schwarz, A. M., Thielemann, R., et al. (2023) · doi:10.7554/elife.90111.1 · Cited by 4

Byproducts of inflammatory radical metabolism provide transient nutrient niches for microbes in the inflamed gutPreprint

Spiga, L., Winter, M. G., Muramatsu, M. K., Rojas, V. K., Chanin, R. B., Zhu, W., Hughes, E. R., Taylor, S., Faber, F., Porwollik, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.08.570695 · Cited by 3

The hidden piece in inflammatory bowel diseases: The significance of intestinal mucus in mediating the bacteria-cells crosstalk

Guagliano, G., Boeri, L., Merli, M., Yan, H., Vangosa, F. B., Visai, L., Visentin, S., Petrini, P., & Sardelli, L. (2025) · Materials Today Bio · doi:10.1016/j.mtbio.2025.101937 · Cited by 4

Mechanisms of bacterial host-to-host transmission

Zafar, M. A., Hernandez, G. E., & Walker, K. A. (2025) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00259-24 · Cited by 3

A social-architecture perspective on gut microbiota dynamics and host physiology

Ni, Z., Zhou, W. J., & Gao, Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1642080 · Cited by 4

Cytochrome bd-II oxidase CyxA promotes the pathogenicity of Klebsiella pneumoniae by resisting oxidative stress

Xiao, X., Song, G., Lu, H., Zheng, W., Meng, P., Peng, W., Yang, J., Wang, M., Zhu, J., Wang, J., et al. (2025) · Virulence · doi:10.1080/21505594.2025.2590244 · Cited by 3

The role of the gut microbiome in multidrug-resistant organism colonization and infection

Merrick, B., Cooper, R., Davido, B., & Goldenberg, S. D. (2026) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2026.01.009 · Cited by 3

Preoperative exercise induces anti-tumor Kupffer cells to prevent surgical stress-promoted colorectal cancer liver metastasis

Zhang, Y., Zhang, Y., Shen, C., Li, J., Wang, H., Hamad, A. B., Cao, C., Moheb, M. E., Wang, Y., Xia, Y., et al. (2026) · Cell Reports Medicine · doi:10.1016/j.xcrm.2026.102589 · Cited by 3

The gut microbiota in Salmonella Typhi infection and translocation: Mechanisms of colonization resistance, pathogen subversion, and prospects for microecological intervention

Ma, C., Zou, Z., Zhao, W., Rao, Y., Liu, B., Sun, M., & Chen, D. (2026) · Microbial Pathogenesis · doi:10.1016/j.micpath.2026.108381 · Cited by 5

Microbiota-derived short-chain fatty acids mediate Candida albicans gastrointestinal colonization resistance

Mishra, A. A., Palmer, S. N., Zarek, C. M., Coughlin, L. A., Poulides, N. A., Dakour, J., Chiu, R. S.-Y., Sabaeifard, P., Li, W., Morrill, A. C., et al. (2026) · Cell Host & Microbe · doi:10.1016/j.chom.2026.05.007 · Cited by 4

Butyrate Affects Bacterial Virulence: A New Perspective on Preventing Enteric Bacterial Pathogen Invasion

Liu, X., Tang, H., Huang, X., & Xu, M. (2023) · Future Microbiology · doi:10.2217/fmb-2023-0148 · Cited by 3

Microbiota of the Gut: Antibiotic-Induced Dysbiosis and the Adverse Effects on Human Health

Morozov, I. Y. (2018) · Academic Journal of Gastroenterology & Hepatology · doi:10.33552/ajgh.2018.01.000504 · Cited by 3

Impact of Intensive Care Unit Nutrition on the Microbiome and Patient Outcomes

Serbanescu, M. A., Silva, M. D., & Zaky, A. (2023) · Anesthesiology Clinics · doi:10.1016/j.anclin.2022.10.007 · Cited by 4

Outrunning Salmonella – the role of endogenous Enterobacteriaceae in variable colonization resistance

Hapfelmeier, S. (2019) · Lab Animal · doi:10.1038/s41684-019-0327-5 · Cited by 3

When Cultures Meet: The Landscape of “Social” Interactions between the Host and Its Indigenous Microbes

Geva‐Zatorsky, N., Elinav, E., & Pettersson, S. (2019) · BioEssays · doi:10.1002/bies.201900002 · Cited by 3

Intraluminal fluorescence lifetime imaging (FLIm) as a diagnostic tool for gastrointestinal disease

Garcia, A. A., Cevallos, S. A., Lee, J., Li, C., Bec, J., Bäumler, A. J., & Marcu, L. (2021) · Optics in the Life Sciences · doi:10.1364/boda.2021.dm3a.4 · Cited by 3

Importance of intestinal microbiota in foodborne diseases

Parlak, L., & Dikmen, D. (2020) · Turkish Bulletin of Hygiene and Experimental Biology · doi:10.5505/turkhijyen.2019.54926 · Cited by 2

Individual differences in members of Actinobacteria, Bacteroidetes, and Firmicutes is associated with resistance or vulnerability to addiction-like behaviors in heterogeneous stock ratsPreprint

Simpson, S., de Guglielmo, G., Brennan, M., Maturin, L., Peters, G., Jia, H., Wellmeyer, E., Andrews, S., Woods, L. C. S., Palmer, A. A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.23.453592 · Cited by 2

Microbiota-derived aspartate drives pathogenic Enterobacteriaceae expansion in the inflamed gutPreprint

Yoo, W., Zieba, J. K., Shealy, N. G., Torres, T. P., Thomas, J., Shelton, C. D., Foegeding, N. J., Olsan, E. E., & Byndloss, M. X. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.14.480453 · Cited by 3

Exposing New Taxonomic Variation with Inflammation – A Murine Model-Specific Genome Database for Gut Microbiome ResearchersPreprint

Leleiwi, I., Rodríguez-Ramos, J. A., Shaffer, M., Sabag-Daigle, A., Kokkinias, K., Flynn, R. M., Daly, R. A., Kop, L. F. M., Solden, L., Ahmer, B. M. M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.24.513540 · Cited by 3

Prenatal maternal stress effects in wild Assamese macaques (Macaca assamensis)

Anzà, S. (2022) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9510 · Cited by 3

Enterocloster clostridioformis induces host intestinal epithelial responses that protect against Salmonella infectionPreprint

Beresford-Jones, B. S., Suyama, S., Clare, S., Soderholm, A. T., Xia, W., Sardar, P., Harcourt, K., Lawley, T. D., & Pedicord, V. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.20.549886 · Cited by 3

A new synbiotic supplementation ameliorates ulcerative colitis via modulating microbial homeostasis, protecting intestinal barrier integrity, and maintaining immunity homeostasis in mice

Kang, Y., Li, L., Guo, J., Yue, C., & Yang, Y. (2025) · Food Science and Human Wellness · doi:10.26599/fshw.2024.9250446 · Cited by 3

O2-dependent incapacitation of the Salmonella pathogenicity island 1 repressor HilE

Walter, S., Schatz, V., Petzold, J., Schmidt, C., Hoffmann, S., Jantsch, J., & Gerlach, R. G. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1434254 · Cited by 2

Agent-based model of the human colon to investigate mechanisms of pathogen colonization resistance

Fletcher, S. J., Ching, C., Suprenant, M. P., Desai, D., & Zaman, M. H. (2025) · Biophysical Journal · doi:10.1016/j.bpj.2025.03.022 · Cited by 2

New method for early detection of gut health issues in broilers

van Hees, K., van Velzen, R., Thijssen, J., Hofmans, L., Dijkman, R., Ducatelle, R., & Molenaar, R. J. (2025) · Avian Pathology · doi:10.1080/03079457.2025.2521354 · Cited by 2

Lactic Acid Fermentation Inactivates Salmonella Typhimurium in Contaminated Cattle Manure at Moderate and Low Temperatures

Halm, H., Woelke, S., Lehnert, I., Schilling, T., Meißner, T., Schröder, C., Hoelzle, L. E., & Scheinemann, H. (2025) · Applied Microbiology · doi:10.3390/applmicrobiol5030088 · Cited by 2

The improved growth performance of Cyprinus carpio by dietary yeast culture depends on improvement of intestinal structure and digestive enzyme activities rather than changes of intestinal microbiota composition

Tao, S., Wang, J., Xue, Z., Bai, Y., Wang, Y., Zhou, W., Liang, T., & Yang, Y. (2025) · Aquaculture Reports · doi:10.1016/j.aqrep.2025.103053 · Cited by 2

Exploring the gut microbiota-Parkinson’s disease link: preliminary insights from metagenomics and Mendelian randomization

Liu, J., Wang, L., Su, L., Chen, J., & Su, R. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1654418 · Cited by 2

The Oral Microbiota, Its Evolution, and Aspects of Support for Oral Health

Плескова, С. Н., & Bezrukov, N. A. (2025) · Molecular Oral Microbiology · doi:10.1111/omi.70011 · Cited by 4

Polarity effects, resistance, and probiotic enhancement of intoxication of Salmonella enterica fraB mutants in murine models

Sabag-Daigle, A., Boulanger, E. F., Baniasad, M., Kim, Y., Moore, M., Hogue, B., Schwieters, A., Gopalan, V., Wysocki, V. H., & Ahmer, B. M. M. (2025) · PLoS ONE · doi:10.1371/journal.pone.0339602 · Cited by 2

Yam Polysaccharide Ameliorates High-Fat and Fructose Diet-Induced Gestational Diabetes Mellitus in Mice via Gut Microbiota Remodeling

Zhao, S. N., Deng, Z. N., Xing, B., Hu, X. N., Xu, W. N., Hong, M. N., & Jiang, P. N. (2025) · Clinical and Experimental Obstetrics & Gynecology · doi:10.31083/ceog45098 · Cited by 2

From dysbiosis to prediction: a novel gut microbiota–derived index for spontaneous bacterial peritonitis in HBV-related cirrhosis

周哲雯, Sun, X. L., Cheng, D., & Xing, H. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1753063 · Cited by 2

The AMP–antibiotic–microbiota triad in IBD: a mechanistic framework for dysregulated antimicrobial defense

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Tissue-specific metabolism of Naringin and its modulation of the UA metabolism and gut microbiota in hyperuricemia mice

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