Cited by 1,011Gut microbiota and healthInfant Nutrition and HealthMaternal and Perinatal Health Interventions

The DOI matches its Crossref record; 55 of the 55 references it cites were found in a registry or an index.

Decreased gut microbiota diversity, delayed Bacteroidetes colonisation and reduced Th1 responses in infants delivered by Caesarean section

Open access

Jakobsson, Hedvig E, Abrahamsson, Thomas R, Jenmalm, Maria C, Harris, Keith, Quince, Christopher, Jernberg, Cecilia, Björkstén, Bengt, Engstrand, Lars, Andersson, Anders F·2014·Gut

DOI 10.1136/gutjnl-2012-303249

Open this paper in CoChat — free account

Abstract

OBJECTIVE: The early intestinal microbiota exerts important stimuli for immune development, and a reduced microbial exposure as well as caesarean section (CS) has been associated with the development of allergic disease. Here we address how microbiota development in infants is affected by mode of delivery, and relate differences in colonisation patterns to the maturation of a balanced Th1/Th2 immune response. DESIGN: The postnatal intestinal colonisation pattern was investigated in 24 infants, born vaginally (15) or by CS (nine). The intestinal microbiota were characterised using pyrosequencing of 16S rRNA genes at 1 week and 1, 3, 6, 12 and 24 months after birth. Venous blood levels of Th1- and Th2-associated chemokines were measured at 6, 12 and 24 months. RESULTS: Infants born through CS had lower total microbiota diversity during the first 2 years of life. CS delivered infants also had a lower abundance and diversity of the Bacteroidetes phylum and were less often colonised with the Bacteroidetes phylum. Infants born through CS had significantly lower levels of the Th1-associated chemokines CXCL10 and CXCL11 in blood. CONCLUSIONS: CS was associated with a lower total microbial diversity, delayed colonisation of the Bacteroidetes phylum and reduced Th1 responses during the first 2 years of life.

Integrity signals

Registry

Crossref · 10.1136/gutjnl-2012-303249

Cites

55 of 55 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

The text we found for this paper looks like another document, so its claims and self-check weren’t run. The registry and citation checks still apply.

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The text we found for this paper looks like another document, so the self-check wasn’t run.

Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies.
Klindworth, A., Pruesse, E., Schweer, T., Peplies, J., Quast, C., Horn, M., & Glöckner, F. O. (2013) · Nucleic Acids Research · doi:10.1093/nar/gks808 · Cited by 8,850
Diversity of the Human Intestinal Microbial Flora
Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913
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
Human gut microbiome viewed across age and geography
Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815
The measurement of diversity in different types of biological collections
Pielou, E. C. (1966) · Journal of Theoretical Biology · doi:10.1016/0022-5193(66)90013-0 · Cited by 6,021
Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns
Dominguez-Bello, M. G., Costello, E. K., Contreras, M., Magris, M., Hidalgo, G., Fierer, N., & Knight, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002601107 · Cited by 4,774
Nonparametric estimation of the number of classes in a population
Chao, A. (1984) · Scandinavian Journal of Statistics · Cited by 4,263
Ecological and Evolutionary Forces Shaping Microbial Diversity in the Human Intestine
Ley, R. E., Peterson, D. A., & Gordon, J. I. (2006) · Cell · doi:10.1016/j.cell.2006.02.017 · Cited by 3,358
An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System
Mazmanian, S. K., Liu, C. H., Tzianabos, A. O., & Kasper, D. L. (2005) · Cell · doi:10.1016/j.cell.2005.05.007 · Cited by 2,910
Transitions in bacterial communities along the 2000 km salinity gradient of the Baltic Sea
Herlemann, D. P. R., Labrenz, M., Jürgens, K., Bertilsson, S., Waniek, J. J., & Andersson, A. F. (2011) · The ISME Journal · doi:10.1038/ismej.2011.41 · Cited by 2,885

Show all 55 references

Sorted by citations

Items 901–1,000 of 1,000

Promotion of a healthy gut microbiome in elective caesarean section arrivals (PROMESA) by supplementing breastfed newborns with an infant probiotic.
Briley, A. L., & Tribe, R. M. (2018) · http://isrctn.com/ · doi:10.1186/isrctn11690200
Associations between C-section and hand grip strength: an observational analysis and genome-wide environmental interaction studyPreprint
Chu, X., Liu, L., Ye, J., Wen, Y., Li, P., Cheng, B., Cheng, S., Zhang, L., Qi, X., Ma, M., et al. (2020) · doi:10.22541/au.160340474.48291773/v1
Faculty Opinions recommendation of Stunted microbiota and opportunistic pathogen colonization in caesarean-section birth.
Hall, L. J. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736621062.793574623
Peer Review #1 of "Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management (v0.2)"
(2018) · PeerJ · doi:10.7287/peerj.5826v0.2/reviews/1
Peer Review #1 of "Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management (v0.3)"
(2018) · PeerJ · doi:10.7287/peerj.5826v0.3/reviews/1
Faculty Opinions recommendation of Strain-Level Analysis of Mother-to-Child Bacterial Transmission during the First Few Months of Life.
Hall, L. J. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733629219.793574622
Evaluation of the genetic influence on the infant gut microbiome through 16S rRNA sequence data analysis of triplets
Palmeira, O. F. J. (2022) · doi:10.11606/d.95.2022.tde-26052022-165736
COVID19 PANDEMIC EVOLUTION THROUGH GOMPERTZ’S EQUATION
Rotgé, H. G. R., & Riveros-Rosas, D. (2022) · South Florida Publishing eBooks · doi:10.47172/sfp2020.ed.0000036
Development of Gastrointestinal Function
(2020) · American Academy of PediatricsItasca, IL eBooks · doi:10.1542/9781610023610-2
Immunological paradox for maintaining normal flora: it is all by design, not by chance
Mehtani, D., & Puri, N. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-96128-8.00002-x
Early Life Environmental Risk Factors and Gut Microbiota in Juvenile Idiopathic Arthritis : - More than a gut feeling
Kindgren, E. (2022) · Linköping University medical dissertations · doi:10.3384/9789179294724
Anaerobic Bacteria
Brook, I., Albenberg, L. G., Zong, W., & Long, S. S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-75608-2.00187-7
Desenvolvimento de pão fermentado com Saccharomyces cerevisiae UFMG A-905 e avaliação de seus efeitos em um modelo animal de asma
CARVALHO, A. P. F. D. (2019) · doi:10.11606/d.17.2019.tde-07102022-155342
Cesarean section and the risk of allergic rhinitis in children: A systematic review and meta-analysisPreprint
Liu, Z., Zhou, Y., Chen, J., Liu, X., Xie, L. H., Zhang, J., Su, H., Yang, Y., Tian, M., Dong, Y., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-2279376/v1
Associação entre nascidos por cesárea e desenvolvimento de doenças alérgicas em crianças e adolescentes
Barcelos, G. B., Gomes, D. R., de Oliveira, D. S., & Mattos, M. P. (2022) · Revista de Ciências Médicas e Biológicas · doi:10.9771/cmbio.v21i2.42445
The Human Gut Microbiome in Health, Disease, and Therapeutics
Pati, N. B., Panda, S., & Jahnsen, F. L. (2022) · Springer eBooks · doi:10.1007/978-981-19-3979-2_11
Risk of Overweight and Obesity in Children under 6 Years Old Following Cesarean Delivery: A Systematic Review and Meta-analysis of Cohort StudiesPreprint
Zhou, C., Tang, L., Retnakaran, R. R., Krewski, D. R., Wen, S. W., Zhou, L., & Xie, R. (2023) · Research Square · doi:10.21203/rs.3.rs-2682417/v1
Fixing the Damage: The Evolution of Probiotics from Fermented Food to Biotherapeutic Products
de Freitas, P. N. N., Silva, C. R., Constantin, P. P., Pileggi, S. A. V., Vicari, M. R., & Pileggi, M. (2023) · Springer eBooks · doi:10.1007/978-3-031-24942-6_12
Education Based-Application And Prenatal Yoga Reduces Cesarean Section
Dewianti, N. M., Widiantari, K., Witari, N. N. D., & Chania, M. P. (2023) · Jurnal MID-Z (Midwivery Zigot) Jurnal Ilmiah Kebidanan · doi:10.56013/jurnalmidz.v6i1.2120
Variant identification in human periodontal ligament stem cells associated to proto-oncogenes: A review
sharma, M., Srivastav, V., & Bhat, M. (2023) · Microbial Biosystems · doi:10.21608/mb.2023.211416.1071
The survey of factors associated with the development of immune tolerance in children with cow’s milk allergy; a cross-sectional study in Gorgan, Iran
Ebrahimi, M., Ghelichi-Ghojogh, M., Ghezeljeh, E., Kazemi, K., Charkazi, A., & Aghapour, S. A. (2023) · Journal of Preventive Epidemiology · doi:10.34172/jpe.2023.35202
Current Status and Efficacy of Fecal Microbiota Transplantation for Patients Suffering from Irritable Bowel Syndrome
Arbab, M. H. (2023) · Wiley eBooks · doi:10.1002/9781119904786.ch20
Development of Gastrointestinal Function
(2020) · American Academy of PediatricsItasca, IL eBooks · doi:10.1542/9781610024181-2
Efficacy of Specially Formulated Combination Three Probiotic Strains with Vitamin D3 and Zn in Children with Atopic Dermatitis
Filipović, I., Ostojić, O., Veković, V., Mihajlovic, S., Caminati, M., & Živković, Z. (2023) · American Journal of Pediatrics · doi:10.11648/j.ajp.20230904.11
Hyperglycemia in pregnancy : diagnostics and duration of labor
Nevander, S. (2023) · Linköping University medical dissertations · doi:10.3384/9789180753302
MODERN DATA ON THE INTESTINAL MICROBIOME AND THE STAGES OF ITS FORMATION
Богданова, Н. М. (2023) · Children s medicine of the North-West · doi:10.56871/cmn-w.2023.62.43.002
THE PREDICTIVE ROLE OF OBESITY FOR MATERNAL AND CHILD HEALTH IN THE FIRST YEAR OF LIFE
Иванов, Д. О., Прокопьева, Н. Э., & Петренко, Ю. В. (2023) · Children s medicine of the North-West · doi:10.56871/cmn-w.2023.40.28.001 · Cited by 1
Factors affecting the quality of mother-infant first contact after vaginal delivery
Salamończyk, M. W., & Błachnio, M. (2022) · Pielegniarstwo XXI wieku / Nursing in the 21st Century · doi:10.2478/pielxxiw-2022-0037
Does Neonatal Microbiome Research Encompass the Placental Transfer Pathway?
Choi, Y. (2023) · Neonatal Medicine · doi:10.5385/nm.2023.30.4.96
First year of life: the Golden Age of gut microbiota
Mazzone, M., Marcantonio, M. C. D., Mincione, G., & Muraro, R. (2023) · Italian Journal of Anatomy and Embryology · doi:10.36253/ijae-14682
Probiotics as Curators of a Healthy Gut Microbiota
Mills, S., Murphy, A., Dinan, T. G., Cryan, J. F., Stanton, C., & Ross, R. P. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99971-7.00006-0
Birth by caesarean section and semen quality in adulthood: a Danish population-based cohort study
Huang, K., Gaml‐Sørensen, A., Brix, N., Ernst, A., Arendt, L. H., Bonde, J. P., Hougaard, K. S., Toft, G. V., Tøttenborg, S. S., & Ramlau‐Hansen, C. H. (2024) · Reproductive Health · doi:10.1186/s12978-024-01761-w
Maternal-Neonate Microbiome: Considerations for Future Studies
Merhavy, Z. I. (2024) · Epidemiology and Public Health · doi:10.52768/epidemiology/1033
Maternal-Neonate Microbiome: Considerations for Future Studies
(2024) · Epidemiology and Public Health · doi:10.52768/eph/1033
Comparison of gut microbiomes between neonates born by cesarean section and vaginal delivery: prospective observational studyPreprint
Laosooksathit, W., Pahirah, N., Narkwichean, A., Taweechotipatr, M., Wannaiampikul, S., & Duang-Udom, C. (2024) · doi:10.22541/au.171487981.10974685/v1
Part 1: Heterogeneity within bariatric surgery Part 2: Abdominal pain: the dark side of bariatric surgery
van Olst, N. (2024) · doi:10.5463/thesis.624
Maternal-Neonate Microbiome: Considerations for Future Studies
Merhavy, Z. I. (2024) · Epidemiology and Public Health · doi:10.52768/epidemiolpublichealth/1033
Non-traditional methods of microbiota disorders correction in children born by cesarean section
Barinova, B. V. V., Bushtyreva, I. O., Иванов, Д. О., Kuznetsova, N. B., & Artouz, E. E. (2024) · Pediatrician (St Petersburg) · doi:10.17816/ped15179-89
Evaluation of Probiotic Use in Children With and Without Allergic Diseases
Yaytokgil, Ş. B., & Vezir, E. (2024) · Dicle Medical Journal / Dicle Tip Dergisi · doi:10.5798/dicletip.1552572
Case study
Reehana, N., Imran, M. M., Thajuddin, N., & Dharumadurai, D. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-22348-8.00013-1
Burden of Cesarian Delivery and its Impact on Preschool Children in Bangladesh: Survey in Rajshahi District
Hossain, M. A., Karim, M. R., & Hossain, M. G. (2024) · Springer eBooks · doi:10.1007/978-981-97-7890-4_7
Gut Microbiota Mechanism of Fetal-Originated Disease
Wang, H., Lu, X., & Ma, C. (2024) · Springer eBooks · doi:10.1007/978-981-97-5730-5_6
Longitudinal Relations Between Early Life Stress, Gut Microbiota, and Executive Functioning from Pregnancy to Childhood
Eckermann, H. A. (2025) · Radboud University Press eBooks · doi:10.54195/9789465150147
Development of Gastrointestinal Function
(2025) · American Academy of PediatricsItasca, IL eBooks · doi:10.1542/9781610027700-ch2
Health outcomes up to 5 years in children born as a second child after a previous caesarean section in a first pregnancy: a Swedish population-based register study between 1999 and 2015
Dencker, A., Li, H., Thelin, I. L., Smith, V. A., Nilsson, C., Lundgren, I., Ladfors, L., & Elfvin, A. (2025) · BMJ Paediatrics Open · doi:10.1136/bmjpo-2024-003026
A humán bélmikrobiom szerepe és változásai myeloma multiplexben
Korózs, D., & Szabó, B. G. (2025) · Hematológia–Transzfuziológia · doi:10.1556/2068.2025.00208
Immunomodulating Agents
Furst, L. E., Hill, H. R., & Lapine, T. R. (2025) · Elsevier eBooks · doi:10.1016/b978-0-323-82763-8.00258-2
Influence of Cesarean Section on the Establishment and Diversity of the Infant Gut Microbiome
Boudar, Z., Janahi, S. E., Yacoubi, F. A. E., Akhattab, A., Amzel, S., Chahboune, S., Maher, W., Allali, I., Rfaki, A., Dini, N., et al. (2025) · Lecture notes in networks and systems · doi:10.1007/978-3-031-91337-2_6
Babies born by caesarean develop slower in first year than those born naturally – new findings
Andersson, O., & Zaigham, M. (2020) · doi:10.64628/ab.xpur75han
Role of the Microbiota in Immune Development
Zhao, Q. S., & Elson, C. O. (2016) · Elsevier eBooks · doi:10.1016/b978-0-128-24465-4.00539-1
The variation of gut microbiota in captive Sichuan golden snub-nosed monkeys (Rhinopithecus roxellana) from infancy to adulthood
Chen, R., Liu, X.-Y., Wang, S., Guo, L. P., Li, M., Xu, X., Lv, R., Hong, L., Wang, G., Deng, C., et al. (2025) · Frontiers in Veterinary Science · doi:10.3389/fvets.2025.1683047
The Impact of Antimicrobial Therapy on the Development of Microbiota in Infants
Priputnevich, T. V., Denisov, P., Zhigalova, K. N., Muravieva, V. V., Шабанова, Н. Е., Gordeev, A. B., Zubkov, V. V., Bembeeva, B. O., Леонидовна, И. Е., Nikolaeva, A. V., et al. (2025) · Antibiotics · doi:10.3390/antibiotics14121245
Links Between Gut Microbiota of Uruguayan Infants, Breastmilk Composition, and Maternal Factors During Exclusive BreastfeedingPreprint
Herrera, M., Mathó, C., Pereira-Pagola, J., Pomi, J., Bilbao, L., Farías, C., Puyol, A., Rodríguez-Camejo, C., Sotelo-Silveira, J. R., & Hernández, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.16.691825
Additional file 5 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Parra-Llorca, A., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278689
Additional file 2 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Llorca, A. P., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278680
Additional file 12 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Parra-Llorca, A., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278671
Additional file 1 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Llorca, A. P., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278677
Additional file 10 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Llorca, A. P., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278665
Additional file 7 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Llorca, A. P., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278695
Additional file 9 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Parra-Llorca, A., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278701
Additional file 1 of Opportunities and limits of combining microbiome and genome data for complex trait prediction
Miguel Pérez-enciso, A., Zingaretti, L. M., Ramayo‐Caldas, Y., & de los Campos, G. (2021) · Figshare · doi:10.6084/m9.figshare.15128421
Additional file 1 of PRObiotics and SYNbiotics to improve gut health and growth in infants in western Kenya (PROSYNK Trial): study protocol for a 4-arm, open-label, randomised, controlled trial
Otiti, M. I., Kariuki, S., Wang, D., Hall, L. J., ter Kuile, F. O., & Allen, S. J. (2022) · Figshare · doi:10.6084/m9.figshare.19663716
Additional file 1 of Birth by caesarean section and semen quality in adulthood: a Danish population-based cohort study
Huang, K., Gaml‐Sørensen, A., Brix, N., Ernst, A., Arendt, L. H., Bonde, J. P. E., Hougaard, K. S., Toft, G. V., Tøttenborg, S. S., & Ramlau-Hansen, C. H. (2024) · Figshare · doi:10.6084/m9.figshare.25374719
Additional file 4 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Parra-Llorca, A., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278686
Additional file 1 of Early life exposure of infants to benzylpenicillin and gentamicin is associated with a persistent amplification of the gut resistome
Patangia, D. V., Grimaud, G. M., O’Shea, C.-A., Ryan, C. A., Dempsey, E., Stanton, C., & Ross, R. P. (2024) · Figshare · doi:10.6084/m9.figshare.26676569
Additional file 1 of A synbiotic intervention modulates meta-omics signatures of gut redox potential and acidity in elective caesarean born infants
Lay, C., Chu, C. W., Purbojati, R. W., Acerbi, E., Drautz‐Moses, D. I., de Sessions, P. F., Jie, S., Ho, E. X. P., Kok, Y. J., Bi, X., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14850770
Additional file 3 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Parra-Llorca, A., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278683
Additional file 8 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Llorca, A. P., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278698
Additional file 6 of Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function
Selma-Royo, M., Calatayud Arroyo, M., García‐Mantrana, I., Llorca, A. P., Escuriet, R., Martínez‐Costa, C., & Collado, M. C. (2020) · Figshare · doi:10.6084/m9.figshare.13278692
Lactobacillus casei Shirota and Inflammatory Biomarkers: A Literature Review
Raygoza, N. P., Monroy‐Torres, R., López-Guzmán, O., & Rodríguez-Aguilar, Y. V. (2025) · Biomedical & Pharmacology Journal · doi:10.13005/bpj/3278
Visualization of childhood allergic diseases based on VOSviewer and CiteSpace
Wang, Y., Liu, X., Cui, W., Hu, Y., Song, W., Zhu, L., Wang, Z., Ji, X., & Wang, Y. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2025.1615154
Epigenetic Modulation by Gut Microbiota Metabolites
Hammou, H. A., Moummou, H., Elhidar, N., Achbani, A., Belokda, W., Baz, S. E., Chatoui, H., Hassania Khalloufi, E. L., Ougjij, A. A., Zine, H., et al. (2026) · IGI Global eBooks · doi:10.4018/979-8-3373-1365-8.ch010
Microbial and metabolic profiles in autism spectrum disorder with atopic dermatitis in children
Dong, X., Zhang, T., Tang, B., Zeng, Q., Hu, Z., Huang, P. H., Xiong, X., Wang, X., Dong, W., & Cai, Y. (2026) · AMB Express · doi:10.1186/s13568-026-02037-1
Multi-omics analysis reveals the association of cesarean delivery with altered gut microbial profiles and a Th2-biased immune response in neonates
Lai, C., Zhang, J., Xiong, Y. H., Wang, Y., Liu, Z., Shi, M., Ye, S., & Zeng, J. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-07988-4
Impact d'un polluant environnemental, le benzo[a]pyrène, sur le microbiote intestinal en modèle murin
Ribière, C. (2015) · theses.fr (ABES) · doi:10.70675/3235c2c3z2d52z4177z81a6z661b79958ea6
Rôle du récepteur nucléaire PPARgamma dans les fonctions immuno-modulatrices de la cellule épithéliale intestinale au cours de la rectocolite hémorragique : contrôle de l’expression de l’isoforme courte de la TSLP
Mena, A. M. (2017) · theses.fr (ABES) · doi:10.70675/43188209zc3cdz4a72z9316z64f11f796f0d
Influence de variations de conditions environnementales sur l'évolution des biofilms oraux
Nguyen, D. (2018) · doi:10.70675/d9a2e208z6d75z4402zba4bza071c3798483
Term or preterm cesarean section delivery does not lead to long-term detrimental consequences in mice
Chiesa, M. (2018) · theses.fr (ABES) · doi:10.70675/6ef32b4fzb74az4b06zb8edz92268c28d542
Étude du lien entre maladie alcoolique du foie, microbiote intestinal et acides biliaires : rôles spécifiques de la pectine et du récepteur aux acides biliaires TGR5
Spatz, M. (2018) · theses.fr (ABES) · doi:10.70675/b092156fz2e11z40fbza4cbz9262830ab0c1
Increased intake of fermentable carbohydrates induces IBS-like symptoms : a complementary understanding of mechanisms involved
Kamphuis, J. B. J. (2019) · theses.fr (ABES) · doi:10.70675/e4003e6fzeffaz48a2z95a6zba874fe5eb4c
Existe-t-il un microbiote placentaire ?
Gschwind, R. (2019) · theses.fr (ABES) · doi:10.70675/17e6f238z574fz4359z923dz6aa21459d1a2
Exposition orale à l'argent colloïdal en condition de fonction barrière digestive intègre puis fragilisée : quels impacts croisés sur l'épithélium, le mucus et le microbiote intestinal?
Gillois, K. (2021) · theses.fr (ABES) · doi:10.70675/35137d8dz8c15z47a9z85bfzbf06df41a6a4
Impact du microbiote et de la réponse inflammatoire de type 2 (lgE et éosinophiles) en contexte allo-immun : l'exemple de la transplantation rénale
Colas, L. (2021) · theses.fr (ABES) · doi:10.70675/3220daf9z6b92z4464zb501za9586f76e539
Analyse fonctionnelle de bactéries du microbiote intestinal humain et évaluation de leurs propriétés bénéfiques contre l’obésité et l’inflammation intestinale
Cuffaro, B. (2021) · theses.fr (ABES) · doi:10.70675/c303a161z5e08z4284za4baz590c01ce4043
Health outcomes of children born by cesarean delivery: Survey in Rajshahi district, BangladeshPreprint
Hossain, M. A., Karim, M. R., Islam, M. S., & Tohan, M. M. (2026) · Research Square · doi:10.21203/rs.3.rs-9254493/v1
Facteurs de variation précoce du microbiote intestinal des enfants de 3 ans et relations avec l'évolution de la corpulence : données des cohortes EPIPAGE 2 et ELFE
Toubon, G. (2023) · theses.fr (ABES) · doi:10.70675/638acae3z4651z4ecfz9b2bzbbd1859ef6f8
Bactériophages et vésicules extracellulaires du microbiote intestinal : développement de nouveaux outils d’étude et rôles dans les Maladies Inflammatoires Chroniques de l’Intestin (MICI)
Sausset, R. (2022) · theses.fr (ABES) · doi:10.70675/cbe2ca53z6c38z4615zafe0z731fbdda12a4
Human lifestyle-associated factors modulate the gut resistome
Poopalarajah, R., & Jha, A. R. (2026) · mSystems · doi:10.1128/msystems.01458-25
Rôle de la dysbiose du microbiote intestinal et réponse Th17 dans les spondyloarthrites : pathogénie et causalité
Beaufrère, M. (2024) · theses.fr (ABES) · doi:10.70675/e2ad4bb8zc461z4159z99eaz2d8e71144ddf
The ‘gut feeling’: Connecting neurodegenerative diseases and gut microbiota
Niyogi, S., & Basu, S. (2026) · The Microbe · doi:10.1016/j.microb.2026.100719
Factors Associated with Nonadherence to American College of Obstetricians and Gynecologists Guidelines for Labor Arrest Disorders
Carbonell, K. V., Simpson, L., Beermann, S. E., Paul, R. A., Frolova, A. I., Kelly, J. C., Raghuraman, N., & Goodman, B. A. (2026) · American Journal of Perinatology · doi:10.1055/a-2864-0651
Impact of Early-Life Antibiotic Exposure on Gut Microbiome and Vaccine Immunogenicity in Infants: A Narrative Review
Babik, K., Bomze, Z., Szuba, M., Borek-Dzięcioł, B., & Kociszewska‐Najman, B. (2026) · Journal of Clinical Medicine · doi:10.3390/jcm15114161
Progressive microbial alterations in the human gut and lung across early life: implications for translational medicine
Zhao, Y., Gao, Y., Li, X., Georgian, E. M., Pinkerton, K. E., & Zhang, C. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1739520
Health outcomes following caesarean birth- An observational study of twins discordant for mode of delivery
Sturm, A., Wäringer, I., Wikström, A., & Hesselman, S. (2026) · European Journal of Obstetrics & Gynecology and Reproductive Biology X · doi:10.1016/j.eurox.2026.100476
Association between cesarean delivery and pediatric leukemia: A case-control study using a Japanese administrative claims database
Nakamura, Y., Terada, Y., Kaneko, N., Hippo, Y., & Michihata, N. (2026) · Cancer Epidemiology · doi:10.1016/j.canep.2026.103167
From Womb to World: Unravelling the Microbiota′s Impact on Health and Disease
Poterico, J. A., Babu, R. V., Jaramillo‐Valverde, L., Sánchez, C., Alayo, E. C., Valdivia‐Silva, J., & Guio, H. (2026) · International Journal of Microbiology · doi:10.1155/ijm/9228548
Cesarean section-induced changes in the gut microbiota facilitate metabolic disease in high-fat diet-induced obese mice
Zachariassen, L. F., Mortensen, F. U. F., Mentzel, C. M. J., Jiang, P., Atienza, P., Krych, Ł., Canibe, N., Kirk, R. K., Vegge, A., Rasmussen, M. A., et al. (2026) · Microbiome · doi:10.1186/s40168-026-02468-9
Postpartum compositional changes in bovine calf nasal and dam vaginal microbiota and concurrent immune responses following prepartum betadine lavages
Messman, R. D., Swanson, R. M., Shanmugam, S. G., & Lemley, C. O. (2026) · Journal of Animal Science · doi:10.1093/jas/skag225
Impact of labor before delivery on necrotizing enterocolitis in very low birth weight infants
Dhawan, N., Yasrebi, S. M., Hagan, J., Brasher, M. I., & Patil, M. S. (2026) · Journal of Neonatal-Perinatal Medicine · doi:10.1177/19345798261475330
The Clock Is Ticking
Mustafa, S. S., & Sokol, K. C. (2026) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2026.06.001

Authors: Jakobsson, H. E., Abrahamsson, T. R., Jenmalm, M. C., Harris, K., Quince, C., Jernberg, C., Björkstén, B., Engstrand, L., & Andersson, A. F.
Affiliations: Swedish Institute (SE)
Linköping University (SE)
University of Glasgow (GB)
Örebro University (SE)
Karolinska Institutet (SE)
Science for Life Laboratory (SE)
Corresponding author: Andersson, Anders F
ORCID: Jakobsson, Hedvig E
Abrahamsson, Thomas R
Jenmalm, Maria C
Quince, Christopher
Jernberg, Cecilia
Engstrand, Lars
Andersson, Anders F
Venue: Gut
Publisher: BMJ
Published: 2013-08-07
Volume: 63
Issue: 4
Pages: 559-566
ISSN: 0017-5749 (ISSN-L)
1468-3288
DOI: 10.1136/gutjnl-2012-303249
OpenAlex: W2167562610
Cited by: 1,011
References: 55
Citations by year: 2026: 39 · 2025: 43 · 2024: 59 · 2023: 71 · 2022: 100 · 2021: 121 · 2020: 114 · 2019: 87 · 2018: 100 · 2017: 71 · 2016: 91 · 2015: 66 · 2014: 42 · 2013: 2
FWCI: 29.99
Type: journal article
Language: en
Open access: green
urn.kb.se
Licence: other-oa
Locations: Gut (publishedVersion)
PubMed (publishedVersion)
KTH Publication Database DiVA (KTH Royal Institute of Technology) (submittedVersion, other-oa)
ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (submittedVersion)
HighWire Press Open Archive (submittedVersion)
UEA Digital Repository (University of East Anglia) (submittedVersion)
Funders: Engineering and Physical Sciences Research Council (EP/H003851/1)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Health Sciences › Nursing › Nutrition and Dietetics › Infant Nutrition and Health
Health Sciences › Medicine › Obstetrics and Gynecology › Maternal and Perinatal Health Interventions
Keywords: cesarean section, mode of delivery, infant gut microbiota, microbial diversity, Th1/Th2 immune response, chemokines, CXCL10, CXCL11, allergy risk, immune system development, early life
MeSH terms: Age Factors, Cesarean Section, DNA, Bacterial, Feces, Female, Humans, Immunity, Cellular, Infant, Infant, Newborn, Intestines, Male, RNA, Ribosomal, 16S, Th1 Cells, Bacteroidetes, Chemokine CXCL10, Chemokine CXCL11, Microbiota

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Decreased gut microbiota diversity, delayed Bacteroidetes colonisation and reduced Th1 responses in infants delivered by Caesarean section

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks