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Abstract

Previous studies have shown vast differences in the skin and oral microbiomes of newborns based on delivery method [Caesarean section (C-section) vs vaginal]. Exposure to or absence of certain bacteria during delivery can impact the neonate’s future susceptibility to infections, allergies or autoimmunity by altering immune functions. Few studies have focused on the impact of maternal obesity on the variations of newborn skin and oral microbiomes. Obese pregnant women typically have a higher vaginal microbiome diversity, and their pregnancies are at higher risk for adverse outcomes and complications.

We hypothesized that the skin and oral microbiomes of newborns born to obese mothers would include more diverse, potentially pathogenic bacteria and that the skin and oral microbiome in C-section delivered newborns would be less diverse than vaginally delivered newborns.

We aim to begin to establish maternal obesity and mode of delivery as factors contributing to increased risk for negative newborn outcomes through impacts on newborn bacterial dysbiosis.

A skin swab was collected immediately following delivery of 39 newborns from 13 healthy weight body mass index (BMI 18.50–24.99), 11 overweight (BMI 25.0–29.99) and 15 obese (BMI ≥30.00) pregnant participants. An oral swab was collected immediately following delivery for 38 of these newborns from 13 healthy weight, 10 overweight and 15 obese pregnant participants. Bacterial genera were identified via 16S rRNA amplicon sequencing.

The newborn skin microbiome was comprised of typical skin bacteria (i.e. ). Newborns of obese participants had a higher relative abundance of in their skin microbiome compared to newborns of healthy weight participants (=0.007). Neonates born via C-section had a higher relative abundance of in their oral microbiome compared to neonates delivered vaginally (=0.046).

We identified differences in the newborn skin and oral microbiomes based on pre-pregnancy BMI and method of delivery. These differences could be linked to an increased risk of allergies, autoimmune disease and infections. Future longitudinal studies will be crucial in determining the long-term impact of these specific genera on newborn outcomes. Understanding these connections could lead to targeted interventions that reduce the risk of adverse outcomes and improve overall health trajectory.

Funding
This study was supported by the:
  • National Center for Advancing Translational Sciences (Award UL1TR003015)
    • Principle Award Recipient: BrittanyR. Howell
  • This is an open-access article distributed under the terms of the Creative Commons Attribution License.
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/content/journal/jmm/10.1099/jmm.0.002000
2025-04-10
2025-04-27
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References

  1. Funkhouser LJ, Bordenstein SR. Mom knows best: the universality of maternal microbial transmission. PLoS Biol 2013; 11:e1001631 [View Article] [PubMed]
    [Google Scholar]
  2. Stout MJ, Conlon B, Landeau M, Lee I, Bower C et al. Identification of intracellular bacteria in the basal plate of the human placenta in term and preterm gestations. Am J Obstet Gynecol 2013; 208:226 [View Article] [PubMed]
    [Google Scholar]
  3. Gomez de Agüero M, Ganal-Vonarburg SC, Fuhrer T, Rupp S, Uchimura Y et al. The maternal microbiota drives early postnatal innate immune development. Science 2016; 351:1296–1302 [View Article]
    [Google Scholar]
  4. Dhariwala MO, Scharschmidt TC. Baby’s skin bacteria: first impressions are long-lasting. Trends Immunol 2021; 42:1088–1099 [View Article] [PubMed]
    [Google Scholar]
  5. Al Nabhani Z, Eberl G. Imprinting of the immune system by the microbiota early in life. Mucosal Immunol 2020; 13:183–189 [View Article] [PubMed]
    [Google Scholar]
  6. Renz‐Polster H, David MR, Buist AS, Vollmer WM, O’Connor EA et al. Caesarean section delivery and the risk of allergic disorders in childhood. Clin Exp Allergy 2005; 35:1466–1472 [View Article]
    [Google Scholar]
  7. Sevelsted A, Stokholm J, Bønnelykke K, Bisgaard H. Cesarean section and chronic immune disorders. Pediatrics 2015; 135:e92–8 [View Article] [PubMed]
    [Google Scholar]
  8. Kalbermatter C, Fernandez Trigo N, Christensen S, Ganal-Vonarburg SC. Maternal microbiota, early life colonization and breast milk drive immune development in the newborn. Front Immunol 2021; 12:683022 [View Article] [PubMed]
    [Google Scholar]
  9. Kim J, Ayabe A. Obesity in pregnancy. In In StatPearls. Treasure Island (FL): StatPearls Publishing 2024 http://www.ncbi.nlm.nih.gov/books/NBK572113/ [PubMed]
    [Google Scholar]
  10. Villamor E, Norman M, Johansson S, Cnattingius S. Maternal obesity and risk of early-onset neonatal bacterial sepsis: nationwide cohort and sibling-controlled studies. Clin Infect Dis 2021; 73:e2656–e2664 [View Article] [PubMed]
    [Google Scholar]
  11. Gutvirtz G, Wainstock T, Landau D, Sheiner E. Maternal obesity and offspring long-term infectious morbidity. J Clin Med 2019; 8:1466 [View Article] [PubMed]
    [Google Scholar]
  12. Nelson-Filho P, Borba IG, Mesquita KSF de, Silva RAB, Queiroz AM de et al. Dynamics of microbial colonization of the oral cavity in newborns. Braz Dent J 2013; 24:415–419 [View Article] [PubMed]
    [Google Scholar]
  13. Rotimi VO, Duerden BI. The development of the bacterial flora in normal neonates. J Med Microbiol 1981; 14:51–62 [View Article] [PubMed]
    [Google Scholar]
  14. Dominguez-Bello MG, Costello EK, Contreras M, Magris M, Hidalgo G et al. Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns. Proc Natl Acad Sci USA 2010; 107:11971–11975 [View Article]
    [Google Scholar]
  15. Hočevar K, Maver A, Vidmar Šimic M, Hodžić A, Haslberger A et al. Vaginal microbiome signature is associated with spontaneous preterm delivery. Front Med 2019; 6:201 [View Article] [PubMed]
    [Google Scholar]
  16. Si J, You HJ, Yu J, Sung J, Ko G. Prevotella as a hub for vaginal microbiota under the influence of host genetics and their association with obesity. Cell Host & Microbe 2017; 21:97–105 [View Article]
    [Google Scholar]
  17. Prince AL, Chu DM, Seferovic MD, Antony KM, Ma J et al. The perinatal microbiome and pregnancy: moving beyond the vaginal microbiome. Cold Spring Harb Perspect Med 2015; 5:a023051 [View Article] [PubMed]
    [Google Scholar]
  18. Garg A, Ellis LB, Love RL, Grewal K, Bowden S et al. Vaginal microbiome in obesity and its impact on reproduction. Best Pract Res Clin Obstet Gynaecol 2023; 90:102365 [View Article]
    [Google Scholar]
  19. Ingram K, Ngalame Eko E, Nunziato J, Ahrens M, Howell B. Impact of obesity on the perinatal vaginal environment and bacterial microbiome: effects on birth outcomes. J Med Microbiol 2024; 73:001874 [View Article] [PubMed]
    [Google Scholar]
  20. Lenth R. emmeans: Estimated Marginal Means, Aka Least-Squares Means. R Package 2023 https://CRAN.R-project.org/package=emmeans
    [Google Scholar]
  21. Wickham H. Ggplot2: Elegant Graphics for Data Analysis Springer-Verlag New York; 2016
    [Google Scholar]
  22. Wickham H, Vaughn D, Girlich M. tidyr: tidy messy data. R Package 2023 https://CRAN.R-project.org/package=tidyr
    [Google Scholar]
  23. Blaser MJ, Falkow S. What are the consequences of the disappearing human microbiota?. Nat Rev Microbiol 2009; 7:887–894 [View Article] [PubMed]
    [Google Scholar]
  24. Grice EA, Segre JA. The skin microbiome. Nat Rev Microbiol 2011; 9:244–253 [View Article] [PubMed]
    [Google Scholar]
  25. Zheng Y, Wang Q, Ma L, Chen Y, Gao Y et al. Alterations in the skin microbiome are associated with disease severity and treatment in the perioral zone of the skin of infants with atopic dermatitis. Eur J Clin Microbiol Infect Dis 2019; 38:1677–1685 [View Article]
    [Google Scholar]
  26. Amaya RA, Edwards MS. Agrobacterium radiobacter bacteremia in pediatric patients: case report and review. Pediatr Infect Dis J 2003; 22:183–186 [View Article] [PubMed]
    [Google Scholar]
  27. Wanger A, Chavez V, Huang RSP, Wahed A, Actor JK et al. Chapter 6 - Overview of bacteria. In Wanger A, Chavez V, Huang RSP, Wahed A, Actor JK et al. eds Microbiology and Molecular Diagnosis in Pathology Elsevier; 2017 pp 75–117 https://doi.org/10.1016/B978-0-12-805351-5.00006-5
    [Google Scholar]
  28. Brown K, Church D, Lynch T, Gregson D. Bloodstream infections due to Peptoniphilus spp.: report of 15 cases. Clin Microbiol Infect 2014; 20:O857–60 [View Article] [PubMed]
    [Google Scholar]
  29. Riskumäki M, Tessas I, Ottman N, Suomalainen A, Werner P et al. Interplay between skin microbiota and immunity in atopic individuals. Allergy 2021; 76:1280–1284 [View Article] [PubMed]
    [Google Scholar]
  30. Veloo ACM, Erhard M, Welker M, Welling GW, Degener JE. Identification of gram-positive anaerobic cocci by MALDI-TOF mass spectrometry. Syst Appl Microbiol 2011; 34:58–62 [View Article] [PubMed]
    [Google Scholar]
  31. Fettweis JM, Serrano MG, Brooks JP, Edwards DJ, Girerd PH et al. The vaginal microbiome and preterm birth. Nat Med 2019; 25:1012–1021 [View Article] [PubMed]
    [Google Scholar]
  32. Crost EH, Coletto E, Bell A, Juge N. Ruminococcus gnavus: friend or foe for human health. FEMS Microbiol Rev 2023; 47:fuad014 [View Article] [PubMed]
    [Google Scholar]
  33. Wexler HM. Bacteroides: the good, the bad, and the nitty-gritty. Clin Microbiol Rev 2007; 20:593–621 [View Article] [PubMed]
    [Google Scholar]
  34. Vael C, Verhulst SL, Nelen V, Goossens H, Desager KN. Intestinal microflora and body mass index during the first three years of life: an observational study. Gut Pathog 2011; 3:8 [View Article] [PubMed]
    [Google Scholar]
  35. Chua H-H, Chou H-C, Tung Y-L, Chiang B-L, Liao C-C et al. Intestinal dysbiosis featuring abundance of Ruminococcus gnavus associates with allergic diseases in infants. Gastroenterology 2018; 154:154–167 [View Article] [PubMed]
    [Google Scholar]
  36. Nishino K, Nishida A, Inoue R, Kawada Y, Ohno M et al. Analysis of endoscopic brush samples identified mucosa-associated dysbiosis in inflammatory bowel disease. J Gastroenterol 2018; 53:95–106 [View Article] [PubMed]
    [Google Scholar]
  37. Urszula K, Joanna E, Marek E, Beata M, Magdalena SB. Colonization of the lower urogenital tract with Ureaplasma parvum can cause asymptomatic infection of the upper reproductive system in women: a preliminary study. Arch Gynecol Obstet 2014; 289:1129–1134 [View Article]
    [Google Scholar]
  38. Kokkayil P, Dhawan B. Ureaplasma: current perspectives. Indian J Med Microbiol 2015; 33:205–214 [View Article] [PubMed]
    [Google Scholar]
  39. Rittenschober-Boehm J, Fuiko R, Farr A, Willinger B, Berger A et al. Intrauterine detection of Ureaplasma Species after vaginal colonization in pregnancy and neonatal outcome. Neonatology 2024; 121:187–194 [View Article] [PubMed]
    [Google Scholar]
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