TY - JOUR
T1 - Neonatal Paenibacilliosis
T2 - Paenibacillus Infection as a Novel Cause of Sepsis in Term Neonates With High Risk of Sequelae in Uganda
AU - Ericson, Jessica E.
AU - Burgoine, Kathy
AU - Kumbakumba, Elias
AU - Ochora, Moses
AU - Hehnly, Christine
AU - Bajunirwe, Francis
AU - Bazira, Joel
AU - Fronterre, Claudio
AU - Hagmann, Cornelia
AU - Kulkarni, Abhaya V.
AU - Kumar, M. Senthil
AU - Magombe, Joshua
AU - Mbabazi-Kabachelor, Edith
AU - Morton, Sarah U.
AU - Movassagh, Mercedeh
AU - Mugamba, John
AU - Mulondo, Ronald
AU - Natukwatsa, Davis
AU - Kaaya, Brian Nsubuga
AU - Olupot-Olupot, Peter
AU - Onen, Justin
AU - Sheldon, Kathryn
AU - Smith, Jasmine
AU - Ssentongo, Paddy
AU - Ssenyonga, Peter
AU - Warf, Benjamin
AU - Wegoye, Emmanuel
AU - Zhang, Lijun
AU - Kiwanuka, Julius
AU - Paulson, Joseph N.
AU - Broach, James R.
AU - Schiff, Steven J.
N1 - Publisher Copyright:
© 2023 The Author(s).
PY - 2023/9/1
Y1 - 2023/9/1
N2 - 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.
AB - 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.
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U2 - 10.1093/cid/ciad337
DO - 10.1093/cid/ciad337
M3 - Article
C2 - 37279589
AN - SCOPUS:85163284199
SN - 1058-4838
VL - 77
SP - 768
EP - 775
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 5
ER -