Literature DB >> 34845351

Nasogastric enteral feeding tubes modulate preterm colonization in early life.

J Jara Pérez1,2, B Moreno-Sanz3,4, I Castro Navarro1, C Alba Rubio1,2, B Chinea Jiménez3, E Escribano Palomino3, L Fernández Álvarez2, J M Rodríguez1, B Orgaz Martín5, M Sáenz de Pipaón3,6.   

Abstract

BACKGROUND: Preterm infants are generally fed through nasogastric enteral feeding tubes (NEFTs). The aim of this work was to evaluate the role of NEFTs in the initial colonization of the preterm gut and its evolution within the first 2 weeks after birth.
METHODS: For this purpose, fecal and NEFT-derived samples from 30 preterm infants hospitalized in a neonatal intensive care unit (NICU) were collected from birth to the second week of life. Samples were cultivated in ten culture media, including three for the isolation of antibiotic-resistant microorganisms.
RESULTS: Isolates (561) were identified by 16S ribosomal RNA gene sequencing. Although the first NEFTs inserted into the neonates after birth were rarely colonized, analysis of NEFTs and fecal samples over time revealed a significant increase in bacterial abundance, diversity, and detection frequency. Results showed a parallel colonization between time-matched NEFTs and fecal samples, suggesting an ongoing bidirectional transfer of bacteria from the neonatal gut to the NEFTs and vice versa.
CONCLUSIONS: In short-term hospitalization, length is by far the determinant factor for the early colonization of preterm infants. As NEFT populations reflect the bacterial populations that are colonizing the preterm in a precise moment, their knowledge could be useful to prevent the dissemination of antibiotic-resistant strains. IMPACT: The hospital environment modulates preterm colonization immediately after birth. The colonization of preterm feces and NEFTs occurs in parallel. There is an ongoing bidirectional transfer of microorganisms from the neonatal gut to the NEFTs and vice versa. Bacterial communities inside NEFTs could act as reservoirs of antibiotic resistance genes. NEFT populations reflect the bacteria that are colonizing the preterm at a precise moment.
© 2021. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc.

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Year:  2021        PMID: 34845351     DOI: 10.1038/s41390-021-01852-5

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.953


  51 in total

1.  Nosocomial colonization of premature babies with Klebsiella oxytoca: probable role of enteral feeding procedure in transmission and control of the outbreak with the use of gloves.

Authors:  P Berthelot; F Grattard; H Patural; A Ros; H Jelassi-Saoudin; B Pozzetto; G Teyssier; F Lucht
Journal:  Infect Control Hosp Epidemiol       Date:  2001-03       Impact factor: 3.254

2.  Development of co-ordination of sucking, swallowing and breathing: ultrasound study of term and preterm infants.

Authors:  F Bu'Lock; M W Woolridge; J D Baum
Journal:  Dev Med Child Neurol       Date:  1990-08       Impact factor: 5.449

3.  Nasogastric feeding tubes from a neonatal department yield high concentrations of potentially pathogenic bacteria- even 1 d after insertion.

Authors:  Sandra Meinich Petersen; Gorm Greisen; Karen Angeliki Krogfelt
Journal:  Pediatr Res       Date:  2016-04-11       Impact factor: 3.756

4.  Establishment and development of intestinal microbiota in preterm neonates.

Authors:  Silvia Arboleya; Ana Binetti; Nuria Salazar; Nuria Fernández; Gonzalo Solís; Ana Hernández-Barranco; Abelardo Margolles; Clara G de Los Reyes-Gavilán; Miguel Gueimonde
Journal:  FEMS Microbiol Ecol       Date:  2011-12-15       Impact factor: 4.194

5.  Epidemiologic Features and Clinical Course of Patients Infected With SARS-CoV-2 in Singapore.

Authors:  Barnaby Edward Young; Sean Wei Xiang Ong; Shirin Kalimuddin; Jenny G Low; Seow Yen Tan; Jiashen Loh; Oon-Tek Ng; Kalisvar Marimuthu; Li Wei Ang; Tze Minn Mak; Sok Kiang Lau; Danielle E Anderson; Kian Sing Chan; Thean Yen Tan; Tong Yong Ng; Lin Cui; Zubaidah Said; Lalitha Kurupatham; Mark I-Cheng Chen; Monica Chan; Shawn Vasoo; Lin-Fa Wang; Boon Huan Tan; Raymond Tzer Pin Lin; Vernon Jian Ming Lee; Yee-Sin Leo; David Chien Lye
Journal:  JAMA       Date:  2020-04-21       Impact factor: 56.272

6.  Development of the intestinal bacterial composition in hospitalized preterm infants in comparison with breast-fed, full-term infants.

Authors:  Andreas Schwiertz; Bärbel Gruhl; Manuela Löbnitz; Peter Michel; Michael Radke; Michael Blaut
Journal:  Pediatr Res       Date:  2003-06-04       Impact factor: 3.756

7.  Serratia marcescens Outbreak in a Neonatal Intensive Care Unit: New Insights from Next-Generation Sequencing Applications.

Authors:  Christine Martineau; Xuejing Li; Cindy Lalancette; Thérèse Perreault; Eric Fournier; Julien Tremblay; Milagros Gonzales; Étienne Yergeau; Caroline Quach
Journal:  J Clin Microbiol       Date:  2018-08-27       Impact factor: 5.948

8.  Trends and determinants of gastric bacterial colonization of preterm neonates in a NICU setting.

Authors:  Ketki Patel; Kavitha Konduru; Alok K Patra; Dinesh S Chandel; Pinaki Panigrahi
Journal:  PLoS One       Date:  2015-07-01       Impact factor: 3.240

Review 9.  Impact of repeated procedural pain-related stress in infants born very preterm.

Authors:  Jillian Vinall; Ruth E Grunau
Journal:  Pediatr Res       Date:  2014-02-05       Impact factor: 3.756

Review 10.  The Preterm Gut Microbiota: An Inconspicuous Challenge in Nutritional Neonatal Care.

Authors:  Jannie G E Henderickx; Romy D Zwittink; Richard A van Lingen; Jan Knol; Clara Belzer
Journal:  Front Cell Infect Microbiol       Date:  2019-04-02       Impact factor: 5.293

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