References
[1] C. Milani et al., “Exploring Vertical Transmission of Bifidobacteria from Mother to Child,” Appl Environ Microb, vol. 81, no. 20, pp. 7078–7087, 2015, doi: 10.1128/aem.02037-15.
[2] P. Ferretti et al., “Mother-to-Infant Microbial Transmission from Different Body Sites Shapes the Developing Infant Gut Microbiome,” Cell Host Microbe, vol. 24, no. 1, pp. 133-145.e5, 2018, doi: 10.1016/j.chom.2018.06.005.
[3] J. Roswall et al., “Developmental trajectory of the healthy human gut microbiota during the first 5 years of life,” Cell Host Microbe, vol. 29, no. 5, pp. 765-776.e3, 2021, doi: 10.1016/j.chom.2021.02.021.
[4] K. Korpela et al., “Selective maternal seeding and environment shape the human gut microbiome,” Genome Res, vol. 28, no. 4, pp. 561–568, 2018, doi: 10.1101/gr.233940.117.
[5] C. Milani et al., “The First Microbial Colonizers of the Human Gut: Composition, Activities, and Health Implications of the Infant Gut Microbiota,” Microbiol Mol Biol R, vol. 81, no. 4, pp. e00036-17, 2017, doi: 10.1128/mmbr.00036-17.
[6] M. G. Dominguez-Bello et al., “Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns,” Proc National Acad Sci, vol. 107, no. 26, pp. 11971–11975, 2010, doi: 10.1073/pnas.1002601107.
[7] Y. Shao et al., “Stunted microbiota and opportunistic pathogen colonization in caesarean-section birth,” Nature, vol. 574, no. 7776, pp. 117–121, 2019, doi: 10.1038/s41586-019-1560-1.
[8] S. Fukuda et al., “Bifidobacteria can protect from enteropathogenic infection through production of acetate,” Nature, vol. 469, no. 7331, pp. 543–547, 2011, doi: 10.1038/nature09646.
[9] I. O’Neill, Z. Schofield, and L. J. Hall, “Exploring the role of the microbiota member Bifidobacterium in modulating immune-linked diseases,” Emerg Top Life Sci, vol. 1, no. 4, pp. 333–349, 2017, doi: 10.1042/etls20170058.
[10] B. M. Henrick et al., “Bifidobacteria-mediated immune system imprinting early in life,” Cell, 2021, doi: 10.1016/j.cell.2021.05.030.
[11] B. M. Henrick et al., “Colonization by B. infantis EVC001 modulates enteric inflammation in exclusively breastfed infants,” Pediatr Res, vol. 86, no. 6, pp. 749–757, 2019, doi: 10.1038/s41390-019-0533-2.
[12] J. E. Spreckels and A. Zhernakova, “Milk and bugs educate infant immune systems,” Immunity, vol. 54, no. 8, pp. 1633–1635, 2021, doi: 10.1016/j.immuni.2021.07.013.
[13] S. A. Frese et al., “Persistence of Supplemented Bifidobacterium longum subsp. infantis EVC001 in Breastfed Infants,” Msphere, vol. 2, no. 6, pp. e00501-17, 2017, doi: 10.1128/msphere.00501-17.
[14] C. M. Dieterich, J. P. Felice, E. O’Sullivan, and K. M. Rasmussen, “Breastfeeding and Health Outcomes for the Mother-Infant Dyad,” Pediatr Clin N Am, vol. 60, no. 1, pp. 31–48, 2013, doi: 10.1016/j.pcl.2012.09.010.
[15] M. F. MacDorman and E. Declercq, “Trends and state variations in out‐of‐hospital births in the United States, 2004‐2017,” Birth, vol. 46, no. 2, pp. 279–288, 2019, doi: 10.1111/birt.12411.
[16] N. I. for H. and C. Excellence, “Intrapartum care for healthy women and babies,” n.d. https://www.nice.org.uk/guidance/cg190/chapter/Recommendations#place-of-birth
[17] J. L. Combellick et al., “Differences in the fecal microbiota of neonates born at home or in the hospital,” Sci Rep-uk, vol. 8, no. 1, p. 15660, 2018, doi: 10.1038/s41598-018-33995-7.
[18] M. Selma-Royo et al., “Perinatal environment shapes microbiota colonization and infant growth: impact on host response and intestinal function,” Microbiome, vol. 8, no. 1, p. 167, 2020, doi: 10.1186/s40168-020-00940-8.
[19] L. Wampach et al., “Birth mode is associated with earliest strain-conferred gut microbiome functions and immunostimulatory potential,” Nat Commun, vol. 9, no. 1, p. 5091, 2018, doi: 10.1038/s41467-018-07631-x.
[20] J. Stokholm et al., “Cesarean section changes neonatal gut colonization,” J Allergy Clin Immun, vol. 138, no. 3, pp. 881-889.e2, 2016, doi: 10.1016/j.jaci.2016.01.028.
[21] F. Bäckhed et al., “Dynamics and Stabilization of the Human Gut Microbiome during the First Year of Life,” Cell Host Microbe, vol. 17, no. 5, pp. 690–703, 2015, doi: 10.1016/j.chom.2015.04.004.
[22] N. A. Bokulich et al., “Antibiotics, birth mode, and diet shape microbiome maturation during early life,” Sci Transl Med, vol. 8, no. 343, pp. 343ra82-343ra82, 2016, doi: 10.1126/scitranslmed.aad7121.
[23] T. Vatanen et al., “The human gut microbiome in early-onset type 1 diabetes from the TEDDY study,” Nature, vol. 562, no. 7728, pp. 589–594, 2018, doi: 10.1038/s41586-018-0620-2.
[24] R. M. Lebeaux et al., “The infant gut resistome is associated with E. coli and early-life exposures,” Bmc Microbiol, vol. 21, no. 1, p. 201, 2021, doi: 10.1186/s12866-021-02129-x.
[25] A. J. Gasparrini et al., “Persistent metagenomic signatures of early-life hospitalization and antibiotic treatment in the infant gut microbiota and resistome,” Nat Microbiol, vol. 4, no. 12, pp. 2285–2297, 2019, doi: 10.1038/s41564-019-0550-2.
[26] C. J. Hill et al., “Evolution of gut microbiota composition from birth to 24 weeks in the INFANTMET Cohort,” Microbiome, vol. 5, no. 1, p. 4, 2017, doi: 10.1186/s40168-016-0213-y.
[27] F. Fouhy et al., “Perinatal factors affect the gut microbiota up to four years after birth,” Nat Commun, vol. 10, no. 1, p. 1517, 2019, doi: 10.1038/s41467-019-09252-4.
[28] M.-C. Arrieta et al., “Early infancy microbial and metabolic alterations affect risk of childhood asthma,” Sci Transl Med, vol. 7, no. 307, pp. 307ra152-307ra152, 2015, doi: 10.1126/scitranslmed.aab2271.
[29] K. E. Fujimura et al., “Neonatal gut microbiota associates with childhood multisensitized atopy and T cell differentiation,” Nat Med, vol. 22, no. 10, pp. 1187–1191, 2016, doi: 10.1038/nm.4176.
[30] C. S. Algert, A. McElduff, J. M. Morris, and C. L. Roberts, “Perinatal risk factors for early onset of Type 1 diabetes in a 2000–2005 birth cohort,” Diabetic Med, vol. 26, no. 12, pp. 1193–1197, 2009, doi: 10.1111/j.1464-5491.2009.02878.x.
[31] S. Y. Huh et al., “Delivery by caesarean section and risk of obesity in preschool age children: a prospective cohort study,” Arch Dis Child, vol. 97, no. 7, p. 610, 2012, doi: 10.1136/archdischild-2011-301141.
[32] J. Blustein et al., “Association of caesarean delivery with child adiposity from age 6 weeks to 15 years,” Int J Obesity, vol. 37, no. 7, pp. 900–906, 2013, doi: 10.1038/ijo.2013.49.
[33] E. Decker, M. Hornef, and S. Stockinger, “Cesarean delivery is associated with celiac disease but not inflammatory bowel disease in children,” Gut Microbes, vol. 2, no. 2, pp. 91–98, 2011, doi: 10.4161/gmic.2.2.15414.
[34] K. Mårild, O. Stephansson, S. Montgomery, J. A. Murray, and J. F. Ludvigsson, “Pregnancy Outcome and Risk of Celiac Disease in Offspring: A Nationwide Case-Control Study,” Gastroenterology, vol. 142, no. 1, pp. 39-45.e3, 2012, doi: 10.1053/j.gastro.2011.09.047.
[35] A. Ransjö‐Arvidson, A. Matthiesen, G. Lilja, E. Nissen, A. Widström, and K. Uvnäs‐Moberg, “Maternal Analgesia During Labor Disturbs Newborn Behavior: Effects on Breastfeeding, Temperature, and Crying,” Birth, vol. 28, no. 1, pp. 5–12, 2001, doi: 10.1046/j.1523-536x.2001.00005.x.
[36] J. N. Lind, C. G. Perrine, and R. Li, “Relationship between Use of Labor Pain Medications and Delayed Onset of Lactation,” J Hum Lact, vol. 30, no. 2, pp. 167–173, 2013, doi: 10.1177/0890334413520189.
[37] Y. Beilin et al., “Effect of Labor Epidural Analgesia with and without Fentanyl on Infant Breast-feeding,” Anesthesiology, vol. 103, no. 6, pp. 1211–1217, 2005, doi: 10.1097/00000542-200512000-00016.
[38] A. I. Lee, R. J. McCarthy, P. Toledo, M. J. Jones, N. White, and C. A. Wong, “Epidural Labor Analgesia—Fentanyl Dose and Breastfeeding Success,” Anesthesiology, vol. 127, no. 4, pp. 614–624, 2017, doi: 10.1097/aln.0000000000001793.
[39] M.-A. Davey and J. King, “Caesarean section following induction of labour in uncomplicated first births- a population-based cross-sectional analysis of 42,950 births,” Bmc Pregnancy Childb, vol. 16, no. 1, p. 92, 2016, doi: 10.1186/s12884-016-0869-0.
[40] L. Jansen, M. Gibson, B. C. Bowles, and J. Leach, “First Do No Harm: Interventions During Childbirth,” J Périnat Educ, vol. 22, no. 2, pp. 83–92, 2013, doi: 10.1891/1058-1243.22.2.83.
[41] M. B. Azad et al., “Impact of maternal intrapartum antibiotics, method of birth and breastfeeding on gut microbiota during the first year of life: a prospective cohort study,” Bjog Int J Obstetrics Gynaecol, vol. 123, no. 6, pp. 983–993, 2016, doi: 10.1111/1471-0528.13601.
[42] K. Conroy, A. F. Koenig, Y.-H. Yu, A. Courtney, H. J. Lee, and E. R. Norwitz, “Infectious morbidity after cesarean delivery: 10 strategies to reduce risk.,” Rev Obstetrics Gynecol, vol. 5, no. 2, pp. 69–77, 2012.
[43] C. J. Stewart et al., “Temporal development of the gut microbiome in early childhood from the TEDDY study,” Nature, vol. 562, no. 7728, pp. 583–588, 2018, doi: 10.1038/s41586-018-0617-x.
[44] R. E. Moore and S. D. Townsend, “Temporal development of the infant gut microbiome,” Open Biol, vol. 9, no. 9, p. 190128, 2019, doi: 10.1098/rsob.190128.
[45] M. O. Coker et al., “Infant Feeding Alters the Longitudinal Impact of Birth Mode on the Development of the Gut Microbiota in the First Year of Life,” Front Microbiol, vol. 12, p. 642197, 2021, doi: 10.3389/fmicb.2021.642197.
[46] T. Ding and P. D. Schloss, “Dynamics and associations of microbial community types across the human body,” Nature, vol. 509, no. 7500, pp. 357–360, 2014, doi: 10.1038/nature13178.
[47] M. G. Dominguez-Bello et al., “Partial restoration of the microbiota of cesarean-born infants via vaginal microbial transfer,” Nat Med, vol. 22, no. 3, pp. 250–253, 2016, doi: 10.1038/nm.4039.
[48] M.-C. Arrieta, L. T. Stiemsma, N. Amenyogbe, E. M. Brown, and B. Finlay, “The Intestinal Microbiome in Early Life: Health and Disease,” Front Immunol, vol. 5, p. 427, 2014, doi: 10.3389/fimmu.2014.00427.
[49] S. J. Song et al., “Naturalization of the microbiota developmental trajectory of Cesarean-born neonates after vaginal seeding,” Med, vol. 2, no. 8, pp. 951-964.e5, 2021, doi: 10.1016/j.medj.2021.05.003.
[50] M. Yassour et al., “Strain-Level Analysis of Mother-to-Child Bacterial Transmission during the First Few Months of Life,” Cell Host Microbe, vol. 24, no. 1, pp. 146-154.e4, 2018, doi: 10.1016/j.chom.2018.06.007.
[51] C. M. Mitchell et al., “Delivery Mode Affects Stability of Early Infant Gut Microbiota,” Cell Reports Medicine, vol. 1, no. 9, p. 100156, 2020, doi: 10.1016/j.xcrm.2020.100156.
[52] K. Korpela et al., “Maternal Fecal Microbiota Transplantation in Cesarean-Born Infants Rapidly Restores Normal Gut Microbial Development: A Proof-of-Concept Study,” Cell, vol. 183, no. 2, pp. 324-334.e5, 2020, doi: 10.1016/j.cell.2020.08.047.
[53] M. B. Azad et al., “Infant gut microbiota and the hygiene hypothesis of allergic disease: impact of household pets and siblings on microbiota composition and diversity,” Allergy Asthma Clin Immunol Official J Can Soc Allergy Clin Immunol, vol. 9, no. 1, pp. 15–15, 2013, doi: 10.1186/1710-1492-9-15.
[54] M. Nermes, A. Endo, J. Aarnio, S. Salminen, and E. Isolauri, “Furry pets modulate gut microbiota composition in infants at risk for allergic disease,” J Allergy Clin Immun, vol. 136, no. 6, pp. 1688-1690.e1, 2015, doi: 10.1016/j.jaci.2015.07.029.
[55] M. I. Roslund et al., “Biodiversity intervention enhances immune regulation and health-associated commensal microbiota among daycare children,” Sci Adv, vol. 6, no. 42, p. eaba2578, 2020, doi: 10.1126/sciadv.aba2578.