Sepsis from the gut: the enteric habitat of bacteria that cause late-onset neonatal bloodstream infections - PubMed (original) (raw)
Observational Study
doi: 10.1093/cid/ciu084. Epub 2014 Mar 18.
I Malick Ndao, A Cody Springman, Shannon D Manning, James R Johnson, Brian D Johnston, Carey-Ann D Burnham, Erica Sodergren Weinstock, George M Weinstock, Todd N Wylie, Makedonka Mitreva, Sahar Abubucker, Yanjiao Zhou, Harold J Stevens, Carla Hall-Moore, Samuel Julian, Nurmohammad Shaikh, Barbara B Warner, Phillip I Tarr
Affiliations
- PMID: 24647013
- PMCID: PMC3982840
- DOI: 10.1093/cid/ciu084
Observational Study
Sepsis from the gut: the enteric habitat of bacteria that cause late-onset neonatal bloodstream infections
Mike A Carl et al. Clin Infect Dis. 2014 May.
Abstract
Background: Late-onset sepsis is a major problem in neonatology, but the habitat of the pathogens before bloodstream invasion occurs is not well established.
Methods: We examined prospectively collected stools from premature infants with sepsis to find pathogens that subsequently invaded their bloodstreams, and sought the same organisms in stools of infants without sepsis. Culture-based techniques were used to isolate stool bacteria that provisionally matched the bloodstream organisms, which were then genome sequenced to confirm or refute commonality.
Results: Of 11 children with late-onset neonatal bloodstream infections, 7 produced at least 1 stool that contained group B Streptococcus (GBS), Serratia marcescens, or Escherichia coli before their sepsis episode with provisionally matching organisms. Of 96 overlap comparison subjects without sepsis temporally associated with these cases, 4 were colonized with provisionally matching GBS or S. marcescens. Of 175 comparisons of stools from randomly selected infants without sepsis, 1 contained a GBS (this infant had also served as an overlap comparison subject and both specimens contained provisionally matching GBS). Genome sequencing confirmed common origin of provisionally matching fecal and blood isolates. The invasive E. coli were present in all presepticemic stools since birth, but gut colonization with GBS and S. marcescens occurred closer to time of bloodstream infection.
Conclusions: The neonatal gut harbors sepsis-causing pathogens, but such organisms are not inevitable members of the normal microbiota. Surveillance microbiology, decolonization, and augmented hygiene might prevent dissemination of invasive bacteria between and within premature infants.
Keywords: Escherichia coli; Serratia marcescens; group B streptococci; septicemia; whole-genome sequencing.
Figures
Figure 1.
Study flow chart. Abbreviations: GBS, group B Streptococcus; MRSA, methicillin-resistant Staphylococcus aureus.
Figure 2.
Precolonized case and overlap comparison group stool culture results. Case 1 annotations apply to all cases. Boxes in bottom rows represent 10 days before sepsis (including day of sepsis if stool was produced before blood culture was obtained). Box with number is day of sepsis; number denotes day of life the episode of sepsis occurred. Boxes above bottom row represent all overlap comparison group specimens relative to day of sepsis in corresponding case, including those collected on the day after sepsis (cases 3 and 6). Inset describes key to positive, negative, and nontested specimens. Abbreviation: GBS, group B Streptococcus.
Similar articles
- Serratia marcescens colonization in preterm neonates during their neonatal intensive care unit stay.
Moles L, Gómez M, Moroder E, Jiménez E, Escuder D, Bustos G, Melgar A, Villa J, Del Campo R, Chaves F, Rodríguez JM. Moles L, et al. Antimicrob Resist Infect Control. 2019 Aug 9;8:135. doi: 10.1186/s13756-019-0584-5. eCollection 2019. Antimicrob Resist Infect Control. 2019. PMID: 31413826 Free PMC article. - Hypervirulent Streptococcus agalactiae septicemia in twin ex-premature infants transmitted by breast milk: report of source detection and isolate characterization using commonly available molecular diagnostic methods.
Ager EPC, Steele ED, Nielsen LE, Nestander MA, Mende K, Spencer SE. Ager EPC, et al. Ann Clin Microbiol Antimicrob. 2020 Nov 26;19(1):55. doi: 10.1186/s12941-020-00396-6. Ann Clin Microbiol Antimicrob. 2020. PMID: 33243275 Free PMC article. - Early onset neonatal sepsis: the burden of group B Streptococcal and E. coli disease continues.
Stoll BJ, Hansen NI, Sánchez PJ, Faix RG, Poindexter BB, Van Meurs KP, Bizzarro MJ, Goldberg RN, Frantz ID 3rd, Hale EC, Shankaran S, Kennedy K, Carlo WA, Watterberg KL, Bell EF, Walsh MC, Schibler K, Laptook AR, Shane AL, Schrag SJ, Das A, Higgins RD; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Stoll BJ, et al. Pediatrics. 2011 May;127(5):817-26. doi: 10.1542/peds.2010-2217. Epub 2011 Apr 25. Pediatrics. 2011. PMID: 21518717 Free PMC article. - Gut bacteria and late-onset neonatal bloodstream infections in preterm infants.
Tarr PI, Warner BB. Tarr PI, et al. Semin Fetal Neonatal Med. 2016 Dec;21(6):388-393. doi: 10.1016/j.siny.2016.06.002. Epub 2016 Jun 23. Semin Fetal Neonatal Med. 2016. PMID: 27345372 Review. - Serratia marcescens infections in neonatal departments: description of an outbreak and review of the literature.
van Ogtrop ML, van Zoeren-Grobben D, Verbakel-Salomons EM, van Boven CP. van Ogtrop ML, et al. J Hosp Infect. 1997 Jun;36(2):95-103. doi: 10.1016/s0195-6701(97)90115-8. J Hosp Infect. 1997. PMID: 9211156 Review.
Cited by
- CD71 + erythroid cells promote intestinal symbiotic microbial communities in pregnancy and neonatal period.
Koleva P, He J, Dunsmore G, Bozorgmehr N, Lu J, Huynh M, Tollenaar S, Huang V, Walter J, Way SS, Elahi S. Koleva P, et al. Microbiome. 2024 Jul 30;12(1):142. doi: 10.1186/s40168-024-01859-0. Microbiome. 2024. PMID: 39080725 Free PMC article. - The intestinal microbiome and surgical disease.
Krezalek MA, Skowron KB, Guyton KL, Shakhsheer B, Hyoju S, Alverdy JC. Krezalek MA, et al. Curr Probl Surg. 2016 Jun;53(6):257-93. doi: 10.1067/j.cpsurg.2016.06.001. Epub 2016 Jun 14. Curr Probl Surg. 2016. PMID: 27497246 Free PMC article. Review. No abstract available. - Persistent metagenomic signatures of early-life hospitalization and antibiotic treatment in the infant gut microbiota and resistome.
Gasparrini AJ, Wang B, Sun X, Kennedy EA, Hernandez-Leyva A, Ndao IM, Tarr PI, Warner BB, Dantas G. Gasparrini AJ, et al. Nat Microbiol. 2019 Dec;4(12):2285-2297. doi: 10.1038/s41564-019-0550-2. Epub 2019 Sep 9. Nat Microbiol. 2019. PMID: 31501537 Free PMC article. - Volatile Organic Compound Assessment as a Screening Tool for Early Detection of Gastrointestinal Diseases.
Dalis C, Mesfin FM, Manohar K, Liu J, Shelley WC, Brokaw JP, Markel TA. Dalis C, et al. Microorganisms. 2023 Jul 17;11(7):1822. doi: 10.3390/microorganisms11071822. Microorganisms. 2023. PMID: 37512994 Free PMC article. Review. - Enhanced Postnatal Acquisition of Hypervirulent Group B Streptococcus.
Ratner AJ. Ratner AJ. Clin Infect Dis. 2019 Oct 30;69(10):1749-1751. doi: 10.1093/cid/ciz035. Clin Infect Dis. 2019. PMID: 30945730 Free PMC article. No abstract available.
References
- Polin RA, Denson S, Brady MT; Committee on Fetus and Newborn, Committee on Infectious Diseases. Strategies for prevention of health care-associated infections in the NICU. Pediatrics. 2012;129:e1085–93. - PubMed
- Polin RA; Committee on Fetus and Newborn. Management of neonates with suspected or proven early-onset bacterial sepsis. Pediatrics. 2012;129:1006–15. - PubMed
- Stoll BJ, Hansen N, Fanaroff AA, et al. Late-onset sepsis in very low birth weight neonates: the experience of the NICHD Neonatal Research Network. Pediatrics. 2002;110:285–91. - PubMed
Publication types
MeSH terms
Grants and funding
- U19 AI090872/AI/NIAID NIH HHS/United States
- I01 CX000192/CX/CSRD VA/United States
- U54 HG003079/HG/NHGRI NIH HHS/United States
- UH3AI083265/AI/NIAID NIH HHS/United States
- P30 DK052574/DK/NIDDK NIH HHS/United States
- I01 CX000920/CX/CSRD VA/United States
- P30DK052574/DK/NIDDK NIH HHS/United States
- AI10903/AI/NIAID NIH HHS/United States
- UH3 AI083265/AI/NIAID NIH HHS/United States
- U54 HG004968/HG/NHGRI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical