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10.1186/s13073-021-00991-y

http://scihub22266oqcxt.onion/10.1186/s13073-021-00991-y
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34784976!8594956!34784976
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suck abstract from ncbi


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pmid34784976      Genome+Med 2021 ; 13 (1): 182
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  • Evaluating the potential for respiratory metagenomics to improve treatment of secondary infection and detection of nosocomial transmission on expanded COVID-19 intensive care units #MMPMID34784976
  • Charalampous T; Alcolea-Medina A; Snell LB; Williams TGS; Batra R; Alder C; Telatin A; Camporota L; Meadows CIS; Wyncoll D; Barrett NA; Hemsley CJ; Bryan L; Newsholme W; Boyd SE; Green A; Mahadeva U; Patel A; Cliff PR; Page AJ; O'Grady J; Edgeworth JD
  • Genome Med 2021[Nov]; 13 (1): 182 PMID34784976show ga
  • BACKGROUND: Clinical metagenomics (CMg) has the potential to be translated from a research tool into routine service to improve antimicrobial treatment and infection control decisions. The SARS-CoV-2 pandemic provides added impetus to realise these benefits, given the increased risk of secondary infection and nosocomial transmission of multi-drug-resistant (MDR) pathogens linked with the expansion of critical care capacity. METHODS: CMg using nanopore sequencing was evaluated in a proof-of-concept study on 43 respiratory samples from 34 intubated patients across seven intensive care units (ICUs) over a 9-week period during the first COVID-19 pandemic wave. RESULTS: An 8-h CMg workflow was 92% sensitive (95% CI, 75-99%) and 82% specific (95% CI, 57-96%) for bacterial identification based on culture-positive and culture-negative samples, respectively. CMg sequencing reported the presence or absence of beta-lactam-resistant genes carried by Enterobacterales that would modify the initial guideline-recommended antibiotics in every case. CMg was also 100% concordant with quantitative PCR for detecting Aspergillus fumigatus from 4 positive and 39 negative samples. Molecular typing using 24-h sequencing data identified an MDR-K. pneumoniae ST307 outbreak involving 4 patients and an MDR-C. striatum outbreak involving 14 patients across three ICUs. CONCLUSION: CMg testing provides accurate pathogen detection and antibiotic resistance prediction in a same-day laboratory workflow, with assembled genomes available the next day for genomic surveillance. The provision of this technology in a service setting could fundamentally change the multi-disciplinary team approach to managing ICU infections. The potential to improve the initial targeted treatment and rapidly detect unsuspected outbreaks of MDR-pathogens justifies further expedited clinical assessment of CMg.
  • |*Metagenomics[MESH]
  • |Anti-Bacterial Agents/therapeutic use[MESH]
  • |COVID-19/*pathology/virology[MESH]
  • |Coinfection/drug therapy/microbiology[MESH]
  • |Corynebacterium/genetics/isolation & purification[MESH]
  • |Cross Infection/microbiology/*transmission[MESH]
  • |DNA, Bacterial/chemistry/metabolism[MESH]
  • |Drug Resistance, Multiple, Bacterial/genetics[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Intensive Care Units[MESH]
  • |Klebsiella pneumoniae/genetics/isolation & purification[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Polymorphism, Single Nucleotide[MESH]
  • |SARS-CoV-2/isolation & purification[MESH]
  • |Sequence Analysis, DNA[MESH]


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