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Development and evaluation of a nanopore 16S rRNA gene sequencing service for same day targeted treatment of bacterial respiratory infection in the intensive care unit.
Baldan, Rossella; Cliff, Penelope R; Burns, Sarah; Medina, Adela; Smith, Graeme C; Batra, Rahul; Cerda, Alberto; Wilson, Rebekah; Merrill, Tammy; Lewis, Shona J; Patel, Amita; Jeyaratnam, Dakshika; Wyncoll, Duncan L; Barrett, Nicholas; Chand, Meera A; Edgeworth, Jonathan D.
  • Baldan R; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, King's College London, St Thomas' Hospital, Westminster Bridge Road, London, UK; Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Cliff PR; Infection Sciences, Viapath, St Thomas' Hospital, London, UK.
  • Burns S; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, King's College London, St Thomas' Hospital, Westminster Bridge Road, London, UK; Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Medina A; Infection Sciences, Viapath, St Thomas' Hospital, London, UK.
  • Smith GC; Infection Sciences, Viapath, St Thomas' Hospital, London, UK.
  • Batra R; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, King's College London, St Thomas' Hospital, Westminster Bridge Road, London, UK; Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Cerda A; Infection Sciences, Viapath, St Thomas' Hospital, London, UK.
  • Wilson R; Infection Sciences, Viapath, St Thomas' Hospital, London, UK.
  • Merrill T; Infection Sciences, Viapath, St Thomas' Hospital, London, UK.
  • Lewis SJ; Infection Sciences, Viapath, St Thomas' Hospital, London, UK.
  • Patel A; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, King's College London, St Thomas' Hospital, Westminster Bridge Road, London, UK; Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Jeyaratnam D; South London Specialist Virology Centre, King's College Hospital NHS Foundation Trust, London, UK.
  • Wyncoll DL; Department of Critical Care, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Barrett N; Department of Critical Care, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Chand MA; Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK; Department of Critical Care, Guy's and St Thomas' NHS Foundation Trust, London, UK; National Infection Service, Public Health England, London, UK; Health Protection Research Unit in Respiratory Infections, Impe
  • Edgeworth JD; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, King's College London, St Thomas' Hospital, Westminster Bridge Road, London, UK; Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK; Infection Sciences, Viapath, St Thomas
J Infect ; 83(2): 167-174, 2021 08.
Article in English | MEDLINE | ID: covidwho-1271692
ABSTRACT

OBJECTIVES:

Assess the feasibility and impact of nanopore-based 16S rRNA gene sequencing (Np16S) service on antibiotic treatment for acute severe pneumonia on the intensive care unit (ICU).

METHODS:

Speciation and sequencing accuracy of Np16S on isolates with bioinformatics pipeline optimisation, followed by technical evaluation including quality checks and clinical-reporting criteria analysing stored respiratory samples using single-sample flow cells. Pilot service comparing Np16S results with all routine respiratory tests and impact on same-day antimicrobial prescribing.

RESULTS:

Np16S correctly identified 140/167 (84%) isolates after 1h sequencing and passed quality control criteria including reproducibility and limit-of-detection. Sequencing of 108 stored respiratory samples showed concordance with routine culture in 80.5% of cases and established technical and clinical reporting criteria. A 10-week same-day pilot Np16S service analysed 45 samples from 37 patients with suspected community (n=15) or hospital acquired (n=30) pneumonia. Np16S showed concordance compared with all routine culture or molecular tests for 27 (82%) of 33 positive samples. It identified the causative pathogen in 32/33 (97%) samples and contributed to antimicrobial treatment changes for 30 patients (67%).

CONCLUSIONS:

This study demonstrates feasibility of providing a routine same-day nanopore sequencing service that makes a significant contribution to early antibiotic prescribing for bacterial pneumonia in the ICU.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Nanopores Type of study: Experimental Studies / Observational study / Prognostic study Limits: Humans Language: English Journal: J Infect Year: 2021 Document Type: Article Affiliation country: J.jinf.2021.06.014

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Nanopores Type of study: Experimental Studies / Observational study / Prognostic study Limits: Humans Language: English Journal: J Infect Year: 2021 Document Type: Article Affiliation country: J.jinf.2021.06.014