Use of Metagenomic Next-Generation Sequencing to Identify Pathogens in Pediatric Osteoarticular Infections

• Published in: Open forum infectious diseases Vol. 8; no. 7; p. ofab346
• Main Authors: Ramchandar, Nanda, Burns, Jessica, Coufal, Nicole G, Pennock, Andrew, Briggs, Benjamin, Stinnett, Rita, Bradley, John, Arnold, John, Liu, George Y, Pring, Maya, Upasani, Vidyadhar V, Rickert, Kathleen, Dimmock, David, Chiu, Charles, Farnaes, Lauge, Cannavino, Christopher
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 01.07.2021
• Subjects: Arthritis; Major; Pathogens; Pediatrics; osteomyelitis; septic arthritis; next-generation sequencing; metagenomics; mNGS
• ISSN: 2328-8957; 2328-8957
• DOI: 10.1093/ofid/ofab346

Abstract Background Osteoarticular infections (OAIs) are frequently encountered in children. Treatment may be guided by isolation of a pathogen; however, operative cultures are often negative. Metagenomic next-generation sequencing (mNGS) allows for broad and sensitive pathogen detection that is culture-independent. We sought to evaluate the diagnostic utility of mNGS in comparison to culture and usual care testing to detect pathogens in acute osteomyelitis and/or septic arthritis in children. Methods This was a single-site study to evaluate the use of mNGS in comparison to culture to detect pathogens in acute pediatric osteomyelitis and/or septic arthritis. Subjects admitted to a tertiary children’s hospital with suspected OAI were eligible for enrollment. We excluded subjects with bone or joint surgery within 30 days of admission or with chronic osteomyelitis. Operative samples were obtained at the surgeon’s discretion per standard care (fluid or tissue) and based on imaging and operative findings. We compared mNGS to culture and usual care testing (culture and polymerase chain reaction [PCR]) from the same site. Results We recruited 42 subjects over the enrollment period. mNGS of the operative samples identified a pathogen in 26 subjects compared to 19 subjects in whom culture identified a pathogen. In 4 subjects, mNGS identified a pathogen where combined usual care testing (culture and PCR) was negative. Positive predictive agreement and negative predictive agreement both were 93.0% for mNGS. Conclusions In this single-site prospective study of pediatric OAI, we demonstrated the diagnostic utility of mNGS testing in comparison to culture and usual care (culture and PCR) from operative specimens. We evaluate the utility of next-generation sequencing in comparison to operative culture to detect a pathogen in acute pediatric osteomyelitis and septic arthritis.