Investigating Transfusion-related Sepsis Using Culture-Independent Metagenomic Sequencing. (29th September 2019)

• Record Type: Journal Article
• Authors: Crawford, Emily; Kamm, Jack; Miller, Steve; Li, Lucy M; Caldera, Saharai; Lyden, Amy; Yokoe, Deborah; Nichols, Amy; Tran, Nam K; Barnard, Sarah E; Conner, Peter M; Nambiar, Ashok; Zinter, Matt S; Moayeri, Morvarid; Serpa, Paula Hayakawa; Prince, Brian C; Quan, Jenai; Sit, Rene; Tan, Michelle; Phelps, Maira; Derisi, Joseph L; Tato, Cristina M; Langelier, Charles
• Is Part Of: Clinical infectious diseases. Volume 71:Number 5(2020)
• Page Start: 1179
• Page End: 1185
• Publication Date: 2019-09-29
• Subjects: healthcare infections -- platelet transfusion -- septic transfusion -- metagenomic sequencing -- mNGS; Communicable diseases -- Periodicals; 616.905
• DOI: 10.1093/cid/ciz960
• Languages: English
• ISSNs: 1058-4838

Abstract

Abstract: Background: Transfusion-related sepsis remains an important hospital infection control challenge. Investigation of septic transfusion events is often restricted by the limitations of bacterial culture in terms of time requirements and low yield in the setting of prior antibiotic administration. Methods: In 3 gram-negative septic transfusion cases, we performed metagenomic next-generation sequencing (mNGS) of direct clinical blood specimens in addition to standard culture-based approaches utilized for infection control investigations. Pathogen detection leveraged IDSeq, a new open-access microbial bioinformatics portal. Phylogenetic analysis was performed to assess microbial genetic relatedness and understand transmission events. Results: mNGS of direct clinical blood specimens afforded precision detection of pathogens responsible for each case of transfusion-related sepsis and enabled discovery of a novel Acinetobacter species in a platelet product that had become contaminated despite photochemical pathogen reduction. In each case, longitudinal assessment of pathogen burden elucidated the temporal sequence of events associated with each transfusion-transmitted infection. We found that informative data could be obtained from culture-independent mNGS of residual platelet products and leftover blood specimens that were either unsuitable or unavailable for culture or that failed to grow due to prior antibiotic administration. We additionally developed methods to enhance accuracy for detecting transfusion-associated pathogens that share taxonomic similarity to contaminants commonly found in mNGS library preparations. Conclusions: Culture-independent mNGS of blood products afforded rapid and precise assessment of pathogen identity, abundance, and genetic relatedness. Together, these challenging cases demonstrated the potential for metagenomics to advance existing methods for investigating transfusion-transmitted infections. Abstract : Transfusion-transmitted infections cause significant morbidity and are challenging to prevent and diagnose. We found that culture-independent metagenomic sequencing of blood products afforded rapid and precise assessment of pathogen identity, abundance, and genetic relatedness, enhancing traditional hospital infection control strategies.