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Deciphering Microbiota of Acute Upper Respiratory Infections: A Comparative Analysis of PCR and mNGS Methods for Lower Respiratory Trafficking Potential

HIGHLIGHTS: What are the main findings? Although there was a high concordance between methodologies, a hybridization-capture-based mNGS workflow was able to detect 29 additional upper respiratory microorganisms versus PCR. The identified microorganisms were rapidly characterized into three phenotypi...

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Detalles Bibliográficos
Autores principales: Almas, Sadia, Carpenter, Rob E., Singh, Anuradha, Rowan, Chase, Tamrakar, Vaibhav K., Sharma, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952210/
https://www.ncbi.nlm.nih.gov/pubmed/36825940
http://dx.doi.org/10.3390/arm91010006
Descripción
Sumario:HIGHLIGHTS: What are the main findings? Although there was a high concordance between methodologies, a hybridization-capture-based mNGS workflow was able to detect 29 additional upper respiratory microorganisms versus PCR. The identified microorganisms were rapidly characterized into three phenotypic groups for infectivity and trafficking potential. What is the implication of the main finding? A hybridization-capture-based mNGS workflow can provide a comprehensive yet clinically relevant microbiology profile of acute upper respiratory infection. Deciphering upper respiratory microbiota with phenotypic grouping has potential to provide respiratory medicine a tool to better manage immunocompromised, immunocompetent with comorbidity and complex respiratory cases. ABSTRACT: Although it is clinically important for acute respiratory tract (co)infections to have a rapid and accurate diagnosis, it is critical that respiratory medicine understands the advantages of current laboratory methods. In this study, we tested nasopharyngeal samples (n = 29) with a commercially available PCR assay and compared the results with those of a hybridization-capture-based mNGS workflow. Detection criteria for positive PCR samples was Ct < 35 and for mNGS samples it was >40% target coverage, median depth of 1X and RPKM > 10. A high degree of concordance (98.33% PPA and 100% NPA) was recorded. However, mNGS yielded positively 29 additional microorganisms (23 bacteria, 4 viruses, and 2 fungi) beyond PCR. We then characterized the microorganisms of each method into three phenotypic categories using the IDbyDNA Explify(®) Platform (Illumina(®) Inc, San Diego, CA, USA) for consideration of infectivity and trafficking potential to the lower respiratory region. The findings are significant for providing a comprehensive yet clinically relevant microbiology profile of acute upper respiratory infection, especially important in immunocompromised or immunocompetent with comorbidity respiratory cases or where traditional syndromic approaches fail to identify pathogenicity. Accordingly, this technology can be used to supplement current syndrome-based tests, and data can quickly and effectively be phenotypically characterized for trafficking potential, clinical (co)infection, and comorbid consideration—with promise to reduce morbidity and mortality.