Fecal IgA Levels Are Determined by Strain-Level Differences in Bacteroides ovatus and Are Modifiable by Gut Microbiota Manipulation

Prokka: rapid prokaryotic genome annotation

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Structure, function and diversity of the healthy human microbiome

The Human Microbiome Project Consortium (2012) · Nature · doi:10.1038/nature11234 · Cited by 11,726

A core gut microbiome in obese and lean twins

Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823

Roary: rapid large-scale prokaryote pan genome analysis

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Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria

Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554

Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species

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Duodenal Infusion of Donor Feces for Recurrent Clostridium difficile

van Nood, E., Vrieze, A., Nieuwdorp, M., Fuentes, S., Zoetendal, E. G., de Vos, W. M., Visser, C. E., Kuijper, E. J., Bartelsman, J. F. W. M., Tijssen, J. G. P., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1205037 · Cited by 3,708

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

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Intestinal inflammation targets cancer-inducing activity of the microbiota

Arthur, J. C., Perez-Chanona, E., Mühlbauer, M., Tomkovich, S., Uronis, J. M., Fan, T.-J., Campbell, B. J., Abujamel, T., Dogan, B., Rogers, A. B., et al. (2012) · Science · doi:10.1126/science.1224820 · Cited by 2,263

Inducible Foxp3 + regulatory T-cell development by a commensal bacterium of the intestinal microbiota

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From probiotic chassis to modification strategies, control and improvement of genetically engineered probiotics for inflammatory bowel disease

Huang, Y., Peng, S., Zeng, R., Yao, H., Feng, G., & Fang, J. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.127928 · Cited by 19

Dietary supplement of mushrooms promotes SCFA production and moderately associates with IgA production: A pilot clinical study

Nishimoto, Y., Kawai, J., Mori, K., Hartanto, T., Komatsu, K., Kudo, T., & Fukuda, S. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1078060 · Cited by 17

Effects of Exposure to Low Zearalenone Concentrations Close to the EU Recommended Value on Weaned Piglets’ Colon

Grosu, I. A., Bulgaru, C. V., Pistol, G. C., Cișmileanu, A. E., Marin, D. E., & Țăranu, I. (2023) · Toxins · doi:10.3390/toxins15030206 · Cited by 14

Living on the edge: Mucus-associated microbes in the colon

Joja, M., Grant, E. T., & Desai, M. S. (2025) · Mucosal Immunology · doi:10.1016/j.mucimm.2025.04.003 · Cited by 16

Strain‐level immunomodulatory variation of gut bacteria

Hajjo, H., & Geva‐Zatorsky, N. (2021) · FEBS Letters · doi:10.1002/1873-3468.14057 · Cited by 14

Enhancement of IgA production by membrane vesicles derived from Bifidobacterium longum subsp. infantis

Kurata, A., Yamasaki-Yashiki, S., Imai, T., Miyazaki, A., Watanabe, K., & Uegaki, K. (2022) · Bioscience Biotechnology and Biochemistry · doi:10.1093/bbb/zbac172 · Cited by 13

Effect of intestinal microbiota on liver disease and its related future prospection: From the perspective of intestinal barrier damage and microbial metabolites

Jiang, N., Xiao, Y., Yuan, K., & Wang, Z. (2023) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.16129 · Cited by 13

Immune communication between the intestinal microbiota and the cardiovascular system

Ren, H., Zhu, B., An, Y., Xie, F., Wang, Y., & Tan, Y. (2023) · Immunology Letters · doi:10.1016/j.imlet.2023.01.007 · Cited by 13

Compensatory intestinal immunoglobulin response after vancomycin treatment in humans

Scheithauer, T. P. M., Bakker, G. J., Winkelmeijer, M., Davids, M., Nieuwdorp, M., van Raalte, D. H., & Herrema, H. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1875109 · Cited by 14

Novel technologies to characterize and engineer the microbiome in inflammatory bowel disease

Boix-Amorós, A., Monaco, H., Sambataro, E., & Clemente, J. C. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2107866 · Cited by 13

Micro-coevolution of host genetics with gut microbiome in three Chinese ethnic groups

Cheng, M., Ge, X., Zhong, C., Fu, R., Ning, K., & Xu, S. (2021) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2021.09.002 · Cited by 12

Salivary polyreactive antibodies andHaemophilus influenzaeare associated with respiratory infection severity in young children with recurrent respiratory infections

Koenen, M. H., Piters, W. A. A. D. S., de Jonge, M. I., Langereis, J. D., Nierkens, S., Chu, M. L. J. N., van der Woude, R., de Vries, R. P., Sanders, E. A. M., Bogaert, D., et al. (2024) · European Respiratory Journal · doi:10.1183/13993003.00317-2024 · Cited by 12

Recent advances in understanding the role of extracellular vesicles from probiotics in intestinal immunity signaling

Kurata, A., & Uegaki, K. (2025) · Biochemical Society Transactions · doi:10.1042/bst20240150 · Cited by 11

Gut Microbiota and Immunoglobulin A Nephropathy: Exploration of Dietary Intervention and Treatment Strategies

Dong, Z., Zhang, R., Shen, L., Ji, H., He, H., Ji, X., & Zhao, L. (2025) · Food Science & Nutrition · doi:10.1002/fsn3.70218 · Cited by 11

Comparative Genomic Study of Streptococcus anginosus Reveals Distinct Group of Urinary Strains

Prasad, A., Ene, A., Jablonska, S., Du, J., Wolfe, A. J., & Putonti, C. (2023) · mSphere · doi:10.1128/msphere.00687-22 · Cited by 11

Dietary Supplementation with Popped Amaranth Modulates the Gut Microbiota in Low Height-for-Age Children: A Nonrandomized Pilot Trial

Calva-Cruz, O. D. J., Ovando‐Vázquez, C., León‐Rodríguez, A. D., Veana, F., Rangel, E. E., Treviño, S., & de la Rosa, A. P. B. (2023) · Foods · doi:10.3390/foods12142760 · Cited by 11

Toxin-Antitoxin Systems: A Tool for Taxonomic Analysis of Human Intestinal Microbiota

Klimina, K. M., Voroshilova, V. N., Poluektova, E. U., Veselovsky, V. A., Yunes, R. А., Kovtun, A. S., Kudryavtseva, A. V., Kasianov, A. S., & Даниленко, В. Н. (2020) · Toxins · doi:10.3390/toxins12060388 · Cited by 11

Strain-level structure of gut microbiome showed potential association with cognitive function in major depressive disorder: A pilot study

Dong, Z., Xie, Q., Yuan, Y., Shen, X., Hao, Y., Li, J., Xu, H., & Kuang, W. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.08.129 · Cited by 11

The protozoan commensal Tritrichomonas musculis is a natural adjuvant for mucosal IgA

Cao, E. Y., Burrows, K., Chiaranunt, P., Popovic, A., Zhou, X., Xie, C., Thakur, A., Britton, G. J., Spindler, M. P., Ngai, L., et al. (2024) · The Journal of Experimental Medicine · doi:10.1084/jem.20221727 · Cited by 10

Environmental concentration of the quaternary ammonium disinfectant benzalkonium chloride strongly induces resistance gene profiles in fish

Yin, X., Li, Y., Wang, S., Wang, Y., Li, Y., Achterberg, E. P., & Wang, X. (2025) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2025.137875 · Cited by 10

The endocannabinoidome–gut microbiome–brain axis as a novel therapeutic target for autism spectrum disorder

Campanale, A., Siniscalco, D., & Marzo, V. D. (2025) · Journal of Biomedical Science · doi:10.1186/s12929-025-01145-7 · Cited by 13

The Impact of IgA and the Microbiota on CNS Disease

Pu, A., Lee, D. S. W., Isho, B., Naouar, I., & Gommerman, J. L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.742173 · Cited by 10

Strain population structure varies widely across bacterial species and predicts strain colonization in unrelated individualsPreprint

Faith, J. J., Chen-Liaw, A., Aggarwala, V., Kaakoush, N. O., Borody, T. J., Mitchell, H. M., Kamm, M. A., Paramsothy, S., Snitkin, E. S., & Mogno, I. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.17.343640 · Cited by 10

Accurate estimation of intraspecific microbial gene content variation in metagenomic data with MIDAS v3 and StrainPGCPreprint

Smith, B. J., Zhao, C., Dubinkina, V. B., Jin, X., Zahavi, L., Shoer, S., Anderson, J. M., Segal, E., & Pollard, K. S. (2025) · Genome Research · doi:10.1101/gr.279543.124 · Cited by 11

Exploring the regulatory mechanism of intestinal flora based on PD-1 receptor/ligand targeted cancer immunotherapy

Gao, X., & Jiang, J. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1359029 · Cited by 10

Bioinspired Claw‐Engaged Adhesive Microparticles Armed with γGC Alleviate Ulcerative Colitis via Targeted Suppression of Macrophage Ferroptosis

Wang, R., Zhu, J., Zhou, J., Li, J., Wang, M., Wu, Y., Zhao, D., Chen, X., Chen, X. S., Wang, Y., et al. (2025) · Advanced Science · doi:10.1002/advs.202503903 · Cited by 9

Friend or foe? Contextualizing Bacteroides through the lens of niche remodeling

Fansler, R. T., Wu, Y., & Zhu, W. (2025) · Trends in Microbiology · doi:10.1016/j.tim.2025.11.005 · Cited by 9

Species- or genus-dependent immunostimulatory effects of gut-derived potential probiotics

Feng, S., Wang, S., Qu, D., Li, J., Tian, F., Yu, L., Zhang, H., Zhao, J., Chen, W., & Zhai, Q. (2022) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2022.11.001 · Cited by 10

Assessing functional properties of diet protein hydrolysate and oil from fish waste on canine immune parameters, cardiac biomarkers, and fecal microbiota

Cabrita, A. R. J., Barroso, C., Fontes-Sousa, A. P., Correia, A., Teixeira, L., Maia, M. R. G., Vilanova, M., Yergaliyev, T., Camarinha‐Silva, A., & Fonseca, A. J. M. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1449141 · Cited by 8

Fasting builds a favorable environment for effective gut microbiota modulation by microbiota-accessible carbohydrates

Satô, K., Nakashima, A., Fukuda, S., Inoue, J., & Kim, Y. (2025) · BMC Microbiology · doi:10.1186/s12866-025-04140-y · Cited by 8

All Bacteroides Are Equal but Some Are More Equal than Others For the Induction of IgA

Hand, T. W. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.02.011 · Cited by 8

Deletion of metal transporter Zip14 reduces major histocompatibility complex II expression in murine small intestinal epithelial cells

Jimenez, F. R., Ruggiero, C. H., Riva, A., Yu, F., Stafford, L. S., Cross, T. R., Larkin, J., & Cousins, R. J. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2422321121 · Cited by 7

Bacteroides ovatus Has the Potential to Be a Next-Generation Probiotic Strain

Shen, Y., Meng, L., Li, Y., & Yang, J. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10699-9 · Cited by 8

Intestinal Anti-Inflammatory Improvement with Fenugreek Seeds as A prebiotic and Synbiotic with Lactobacillus acidophilus in Rats Experimentally Infected with Escherichia coli

Noor Zuhair Bakheet, N. Z., A.J, A.-Q. M., & Falih, I. B. (2020) · The Iraqi Journal of Veterinary Medicine · doi:10.30539/ijvm.v44i2.984 · Cited by 8

Responsiveness of fecal immunoglobulin A to HPA‐axis activation limits its use for mucosal immunity assessment

Behringer, V., Müller‐Klein, N., Strübe, C., Schülke, O., Heistermann, M., & Ostner, J. (2021) · American Journal of Primatology · doi:10.1002/ajp.23329 · Cited by 7

Proceedings of 16th International Symposium on IgA Nephropathy

Tesař, V., & Barratt, J. (2021) · Kidney Diseases · doi:10.1159/000519532 · Cited by 7

Gut bacteria induce IgA expression in pituitary hormone-secreting cells during aging

Li, Y., Wang, J., Wang, R., Chang, Y., & Wang, X. (2023) · iScience · doi:10.1016/j.isci.2023.107747 · Cited by 6

B cell responses to the gut microbiota

Ng, K. W., Hobbs, A., Wichmann, C., Victora, G. D., & Donaldson, G. P. (2022) · Advances in immunology · doi:10.1016/bs.ai.2022.08.003 · Cited by 6

Comparison and characterization of the bacterial microbiota and SIgA production in different gastrointestinal segments in horses

Żak, A., Żebrowska-Różańska, P., Bajzert, J., Siwińska, N., Madej, J. P., Kaleta‐Kuratewicz, K., Bochen, P., Łaczmański, Ł., & Chełmońska‐Soyta, A. (2024) · Veterinary Research Communications · doi:10.1007/s11259-024-10489-8 · Cited by 6

Microbial-Driven Immunological Memory and Its Potential Role in Microbiome Editing for the Prevention of Colorectal Cancer

Campillo-Gimenez, L., Ríos-Covián, D., Rivera–Nieves, J., Kiyono, H., Chu, H., & Ernst, P. B. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.752304 · Cited by 6

Human Microbial Transplant Restores T Cell Cytotoxicity and Anti-Tumor Response to PD-L1 Blockade in Gnotobiotic MicePreprint

Borgerding, J. N., Shang, J., Britton, G. J., Salmon, H., Bigenwald, C., Maier, B., Rose, S. R., Mogno, I., Kamphorst, A. O., Mérad, M., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.07.242040 · Cited by 6

Strain dynamics of specific contaminant bacteria modulate the performance of ethanol biorefineriesPreprint

Lino, F. S. D. O., Misiakou, M.-A., Kang, K., Li, S. S., da Costa, B. L. V., Basso, T. O., Panagiotou, G., & Sommer, M. O. A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.07.430133 · Cited by 6

Bacteroides ovatus alleviates dysbiotic microbiota-induced intestinal graft-versus-host diseasePreprint

Jenq, R. R., Hayase, E., Hayase, T., Mukherjee, A., Stinson, S. C., Jamal, M. A., Ortega, M. R., Sanchez, C., Ahmed, S., Karmouch, J. L., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2460097/v1 · Cited by 6

Identification of strain-specific cues that regulate biofilm formation in Bacteroides thetaiotaomicron

Glowacki, R. W. P., Engelhart, M. J., Till, J. M., Kadam, A., Nemet, I., Sangwan, N., & Ahern, P. P. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.03419-24 · Cited by 5

Supplementation with whey peptide rich in β-lactolin improves trait anxiety and subjective stress in healthy adults: a randomized, double-blind, placebo-controlled study

Ayabe, T., Shinohara, M., Kita, M., Takahashi, C., Saito, J., Furuyashiki, T., Toba, K., Umeda, S., & Ano, Y. (2024) · Scientific Reports · doi:10.1038/s41598-024-73780-3 · Cited by 5

Gut microbiota metabolites, secretory immunoglobulin A and Bayley-III cognitive scores in children from the CHILD Cohort Study

Davias, A., Verghese, M., Bridgman, S. L., Tun, H. M., Field, C. J., Hicks, M., Pei, J. R., Hicks, A., Moraes, T. J., Simons, E., et al. (2025) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2025.100946 · Cited by 5

Gut microbiome-based prediction of autoimmune neuroinflammationPreprint

Steimle, A., Neumann, M., Grant, E. T., Willième, S., Sciscio, A. D., Parrish, A., Ollert, M. W., Miyauchi, E., Soga, T., Fukuda, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.14.536901 · Cited by 5

Effect of Bacteroides on Crohn’s disease

Wei, X., & Tang, D. (2024) · Zeitschrift für Gastroenterologie · doi:10.1055/a-2435-2659 · Cited by 4

Correlation Between Fecal Microbiota and Corticosteroid Responsiveness in Primary Immune Thrombocytopenia: an Exploratory Study

Liu, F., An, Z., Cui, L., Xiao, M., Wu, Y., Li, W., Zhang, B., Li, Y., Feng, J., Liu, Z., et al. (2025) · Advanced Science · doi:10.1002/advs.202410417 · Cited by 4

Novel Small-Molecule miR-124 Inducer Acts as “a Physiological Brake” of Inflammation in Ulcerative Colitis by Targeting the PIK3R2/PI3K/Akt Axis

Wang, T., Xu, Y., Li, S., Du, R., Shi, J., Jiang, C., Wang, R., & Zhu, Y. (2025) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c01398 · Cited by 4

Traditional fermented milk product from Zambia shifts the gut microbiota to healthier metabolism in a simulated SHIME® model system

Alekseeva, A. Y., Ye, K., Mentani, J., Wolkers-Rooijackers, J. C. M., Smid, E. J., & Schoustra, S. E. (2025) · Beneficial Microbes · doi:10.1163/18762891-bja00068 · Cited by 4

Changes in the gut microbiome associated with liver stiffness improvement in nonalcoholic steatohepatitis

Sharpton, S. R., Podlaha, O., Chuang, J.-C., Gindin, Y., Myers, R. P., & Loomba, R. S. (2022) · Therapeutic Advances in Gastroenterology · doi:10.1177/17562848221098243 · Cited by 5

Seminars in immunology special issue: Nutrition, microbiota and immunity The unexplored microbes in health and disease

Plitt, T., & Faith, J. J. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101735 · Cited by 3

Quantification of discrete gut bacterial strains following fecal transplantation for recurrent Clostridioides difficile infection demonstrates long-term stable engraftment in non-relapsing recipientsPreprint

Aggarwala, V., Mogno, I., Li, Z., Yang, C., Britton, G. J., Chen-Liaw, A., Mitcham, J., Bongers, G., Gevers, D., Clemente, J. C., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.10.292136 · Cited by 4

A Conceptual Review of Gut, Skin, and Oral Microbiota in Autoimmune Bullous Diseases: From Dysbiosis to Therapeutic Potential

Xu, H., Li, S., Liu, S., & Zuo, Y. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s551394 · Cited by 3

Restriction of IgA secretion in gut plasma cells is driven by a tissue-specific glycolytic program

Zoccoli-Rodriguez, V., Iwaniec, J., & Wilmore, J. R. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf310 · Cited by 3

Parabacteroides distasonis AR1098 mediates anti-hyperlipidemic effects via coordinated bile acid excretion and lipogenesis suppression in the gut-liver axis

Qu, D., Xia, Y., Wang, G., Xiong, Z., Yang, Y., Song, X., Song, Z., Zhu, T., Qian, B., & Ai, L. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.108095 · Cited by 3

Bacteroides fragilis colonization induces protective systemic IgA

Harris, J., Gubitosi, N., Zoccoli-Rodriguez, V., Borg, K. M., Delaney, M., Cruz, T. N., Gaudette, B. T., & Wilmore, J. R. (2025) · Microbiome · doi:10.1186/s40168-025-02222-7 · Cited by 3

Immunoglobulin A protease from Sutterella wadsworthensis modifies outcome of infection with Campylobacter jejuni and is associated with microbiome diversity

Majzoub, M. E., Santiago, F. S., Raich, S. S., Sirigeri, P., Simovic, I., Tedla, N. T., & Kaakoush, N. O. (2026) · Gut Microbes · doi:10.1080/19490976.2025.2611543 · Cited by 3

Gut microbiota alterations and associations with nutrients in children with celiac disease

Öztürk, Y. E., Karabudak, E., Gürkan, Ö. E., & Dalgıç, B. (2024) · Food Science & Nutrition · doi:10.1002/fsn3.4337 · Cited by 3

Mendelian randomization analysis revealed a gut microbiota-eye axis in acute anterior uveitis

Mi, Y., Chen, L., Liao, N., & Wan, M. (2025) · Eye · doi:10.1038/s41433-025-03715-3 · Cited by 4

Gut microbial features may influence antiviral IgG levels after vaccination against viral respiratory infectious diseases: the evidence from two-sample bidirectional mendelian randomization

Tu, J., Wang, Y., Ye, X., Wang, Y., Zou, Y., Jia, L., Yang, S., Yu, R., Liu, W. Y., & Huang, P. (2024) · BMC Infectious Diseases · doi:10.1186/s12879-024-09189-0 · Cited by 3

Combinatorial Click Chemistry Labeling to Study Live Human Gut-Derived Microbiota Communities

Hajjo, H., Bhardwaj, N., Gefen, T., & Geva‐Zatorsky, N. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.750624 · Cited by 3

An evolution-based framework for describing human gut bacteriaPreprint

Doran, B. A., Chen, R. Y., Giba, H., Behera, V., Barat, B., Sundararajan, A., Lin, H., Sidebottom, A. M., Pamer, E. G., & Raman, A. S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.04.569969 · Cited by 3

Exploring the epidemiology, pathogenesis, and immunotherapeutic advancements in Clostridium difficile infection

Wang, L., Lee, C., Galvez, J. V., Kelly, C. P., Lin, Q., Yao, J., Chen, X., & Cao, Y. (2024) · The Innovation Life · doi:10.59717/j.xinn-life.2024.100107 · Cited by 2

Subspecies phylogeny in the human gut revealed by co-evolutionary constraints across the bacterial kingdom

Doran, B. A., Chen, R. Y., Giba, H., Behera, V., Barat, B., Sundararajan, A., Lin, H., Sidebottom, A. M., Pamer, E. G., & Raman, A. S. (2025) · Cell Systems · doi:10.1016/j.cels.2024.12.008 · Cited by 5

Characteristics of Intestinal Barrier State and Immunoglobulin-Bound Fraction of Stool Microbiota in Advanced Melanoma Patients Undergoing Anti-PD-1 Therapy

Drymel, B., Tomela, K., Galus, Ł., Olejnik‐Schmidt, A., Mackiewicz, J., Kaczmarek, M., Mackiewicz, A. A., & SCHMIDT, M. T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26168063 · Cited by 2

The Antibody‐Microbiota Interface in Autoimmune Diseases

Puechberty, S., & Sterlin, D. (2026) · Muscle & Nerve · doi:10.1002/mus.70131 · Cited by 2

Resident microbes shape host immunity and protect against pathogen infection and inflammatory disease

Mori, D., & Goto, Y. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-026-06219-9 · Cited by 3

Isolation by distance promotes gut microbial strain divergence in wild mouse populations

Dillard, B. A., Sanders, J. G., Husain, A. P., Yule, K. M., & Moeller, A. H. (2026) · Nature Ecology & Evolution · doi:10.1038/s41559-026-03073-7 · Cited by 2

Duality of Bacteroides cross-feeding networks in health and disease

Chen, R., Zhan, Z., Zhang, S., Tang, S., Qin, H., Deng, Z., & Gao, J. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108327 · Cited by 2

Genetic Diversity - Recent Advances and Applications

Çalişkan, M., & Aydin, S. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.100913 · Cited by 2

Defining Innate Immune Responses to the Human Gut Microbiota from Phylum to StrainPreprint

Spindler, M. P., Siu, S., Mogno, I., Li, Z., Yang, C., Mehandru, S., Britton, G. J., & Faith, J. J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.13.468498 · Cited by 2

Causal relationships between gut microbiota and IgA nephropathy: evidence from Mendelian randomization and microbiome validation

Wang, X., Liu, J., Huoshen, W., Liu, J., Qiao, X., Zhang, H., & Zhou, S. (2025) · Renal Failure · doi:10.1080/0886022x.2025.2522979 · Cited by 2

Decoding the Gut Microbiota: Mechanisms of Host-Microbe Interactions and Inflammatory Pathologies

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Purified diet reduces intestinal IgA and alters the microbiota accordingly

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