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Characterization of cerebrospinal fluid (CSF) microbiota at the time of initial surgical intervention for children with hydrocephalus.
Pandey, Shailly; Whitlock, Kathryn B; Test, Matthew R; Hodor, Paul; Pope, Christopher E; Limbrick, David D; McDonald, Patrick J; Hauptman, Jason S; Hoffman, Lucas R; Simon, Tamara D.
Afiliación
  • Pandey S; University of Washington School of Medicine, Seattle, Washington, United States of America.
  • Whitlock KB; New Harmony Statistical Consulting, Clinton, Washington, United States of America.
  • Test MR; Department of Pediatrics, University of Washington, Seattle, Washington, United States of America.
  • Hodor P; Seattle Children's Research Institute, Seattle, Washington, United States of America.
  • Pope CE; Department of Pediatrics, University of Washington, Seattle, Washington, United States of America.
  • Limbrick DD; Department of Neurosurgery, Washington University in St. Louis, St. Louis, Missouri, United States of America.
  • McDonald PJ; St. Louis Children's Hospital, St. Louis, Missouri, United States of America.
  • Hauptman JS; Section of Neurosurgery, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Hoffman LR; Winnipeg Children's Hospital, Winnipeg, Manitoba, Canada.
  • Simon TD; Seattle Children's Research Institute, Seattle, Washington, United States of America.
PLoS One ; 18(6): e0280682, 2023.
Article en En | MEDLINE | ID: mdl-37342995
ABSTRACT

OBJECTIVE:

To characterize the microbiota of the cerebrospinal fluid (CSF) from children with hydrocephalus at the time of initial surgical intervention. STUDY

DESIGN:

CSF was obtained at initial surgical intervention. One aliquot was stored in skim milk-tryptone-glucose-glycerol (STGG) medium and the second was unprocessed; both were then stored at -70°C. Bacterial growth for CSF samples stored in STGG were subsequently characterized using aerobic and anaerobic culture on blood agar and MALDI-TOF sequencing. All unprocessed CSF samples underwent 16S quantitative polymerase chain reaction (qPCR) sequencing, and a subset underwent standard clinical microbiological culture. CSF with culture growth (either after storage in STGG or standard clinical) were further analyzed using whole-genome amplification sequencing (WGAS).

RESULTS:

11/66 (17%) samples stored in STGG and 1/36 (3%) that underwent standard clinical microbiological culture demonstrated bacterial growth. Of the organisms present, 8 were common skin flora and 4 were potential pathogens; only 1 was also qPCR positive. WGAS findings and STGG culture findings were concordant for only 1 sample, identifying Staphylococcus epidermidis. No significant difference in time to second surgical intervention was observed between the STGG culture-positive and negative groups. CONCLUSION(S) Using high sensitivity methods, we detected the presence of bacteria in a subset of CSF samples at the time of first surgery. Therefore, the true presence of bacteria in CSF of children with hydrocephalus cannot be ruled out, though our findings may suggest these bacteria are contaminants or false positives of the detection methods. Regardless of origin, the detection of microbiota in the CSF of these children may not have any clinical significance.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Bacterias / Hidrocefalia Tipo de estudio: Prognostic_studies Límite: Child / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Bacterias / Hidrocefalia Tipo de estudio: Prognostic_studies Límite: Child / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos