Use of Host Response to Refine the Diagnosis of Group A Streptococcal Pharyngitis

Author:

Yu Jinsheng1,Tycksen Eric1,Yang Wei1,Mariani Thomas J2,Bhattacharya Soumyaroop2,Falsey Ann R3,Topham David J3,Storch Gregory A4ORCID

Affiliation:

1. Department of Genetics, Genome Technology Access Center at the McDonnell Genome Institute, Washington University School of Medicine , St. Louis, Missouri 63110 , USA

2. Department of Pediatrics, Division of Neonatology and Pediatric Molecular and Personalized Medicine Program, University of Rochester School of Medicine , Rochester, New York 14642 , USA

3. Department of Medicine, University of Rochester School of Medicine , Rochester, New York 14642 , USA

4. Department of Pediatrics, Washington University School of Medicine , St. Louis, Missouri 63110 , USA

Abstract

Abstract Background Current diagnostic tests for pharyngitis do not distinguish between symptomatic group A Streptococcus (GAS) infection and asymptomatic colonization, resulting in over-diagnosis and unnecessary use of antibiotics. We assessed whether measures of host response could make this distinction. Methods We enrolled 18 children with pharyngitis having Centor scores of 4 or 5 and 21 controls without pharyngitis or other acute infections. Both groups had throat cultures, molecular tests for GAS and respiratory viruses and IgM serology for Epstein–Barr virus. Host response was evaluated with white blood cell count (WBC), C-reactive protein (CRP), procalcitonin (PCT), and sequencing of RNA from peripheral blood leukocytes. Results Of 18 cases, 11 had GAS pharyngitis, 3 had adenovirus pharyngitis and 4 had other pharyngitis. Among asymptomatic controls, 5 were positive for GAS. WBC, CRP, and PCT were higher in subjects with pharyngitis compared to asymptomatic controls including those with GAS. Transcriptional profiles from children with symptomatic GAS were clearly distinct from those of children in all other groups. The levels of two genes, CD177 and TLR5 each individually accurately distinguished between symptomatic and asymptomatic GAS. Optimal diagnostic sensitivity and specificity were achieved by the combination of CRP and PCT, and by each of the two gene markers. Conclusion In this exploratory study, we showed that traditional measures of inflammation and markers of host gene expression distinguish between symptomatic and asymptomatic GAS. These results point to future rapid molecular approaches for improving the diagnosis of GAS pharyngitis, that may help reduce unnecessary antibiotic use.

Funder

National Institute of Allergy and Infectious Diseases

National Cancer Institute

Institute of Clinical and Translational Sciences

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,General Medicine,Pediatrics, Perinatology and Child Health

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