Home > Research > Publications & Outputs > Neonatal Paenibacilliosis

Links

Text available via DOI:

View graph of relations

Neonatal Paenibacilliosis: Paenibacillus infection as a Novel Cause of Sepsis in Term Neonates with High Risk of Sequelae in Uganda

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published
  • Jessica E Ericson
  • Kathy Burgoine
  • Elias Kumbakumba
  • Moses Ochora
  • Christine Hehnly
  • Francis Bajunirwe
  • Joel Bazira
  • Cornelia Hagmann
  • Abhaya V Kulkarni
  • M Senthil Kumar
  • Joshua Magombe
  • Edith Mbabazi-Kabachelor
  • Sarah U Morton
  • Mercedeh Movassagh
  • John Mugamba
  • Ronald Mulondo
  • Davis Natukwatsa
  • Brian Nsubuga Kaaya
  • Peter Olupot-Olupot
  • Justin Onen
  • Kathryn Sheldon
  • Jasmine Smith
  • Paddy Ssentongo
  • Peter Ssenyonga
  • Benjamin Warf
  • Emmanuel Wegoye
  • Lijun Zhang
  • Julius Kiwanuka
  • Joseph N Paulson
  • James R Broach
  • Steven J Schiff
Close
<mark>Journal publication date</mark>11/09/2023
<mark>Journal</mark>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
Issue number5
Volume77
Number of pages8
Pages (from-to)768-775
Publication StatusPublished
Early online date5/06/23
<mark>Original language</mark>English

Abstract

Background
Paenibacillus thiaminolyticus may be an underdiagnosed cause of neonatal sepsis. Methods We prospectively enrolled a cohort of 800 full-term neonates presenting with a clinical diagnosis of sepsis at 2 Ugandan hospitals. Quantitative polymerase chain reaction specific to P. thiaminolyticus and to the Paenibacillus genus were performed on the blood and cerebrospinal fluid (CSF) of 631 neonates who had both specimen types available. Neonates with Paenibacillus genus or species detected in either specimen type were considered to potentially have paenibacilliosis, (37/631, 6%). We described antenatal, perinatal, and neonatal characteristics, presenting signs, and 12-month developmental outcomes for neonates with paenibacilliosis versus clinical sepsis due to other causes. Results Median age at presentation was 3 days (interquartile range 1, 7). Fever (92%), irritability (84%), and clinical signs of seizures (51%) were common. Eleven (30%) had an adverse outcome: 5 (14%) neonates died during the first year of life; 5 of 32 (16%) survivors developed postinfectious hydrocephalus (PIH) and 1 (3%) additional survivor had neurodevelopmental impairment without hydrocephalus. Conclusions Paenibacillus species was identified in 6% of neonates with signs of sepsis who presented to 2 Ugandan referral hospitals; 70% were P. thiaminolyticus. Improved diagnostics for neonatal sepsis are urgently needed. Optimal antibiotic treatment for this infection is unknown but ampicillin and vancomycin will be ineffective in many cases. These results highlight the need to consider local pathogen prevalence and the possibility of unusual pathogens when determining antibiotic choice for neonatal sepsis.