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Rapid Molecular Detection and Differentiation of Influenza Viruses A and B
Published on: January 30, 2017
Molecular and clinical diagnosis of group A streptococcal pharyngitis in children
Susanna Felsenstein1, Diala Faddoul2, Richard Sposto3
1Division of Infectious Diseases, Department of Pediatrics, Children's Hospital Los Angeles and Keck School of Medicine of University of Southern California, Los Angeles, California, USA sfelsenstein@chla.usc.edu.
Insights
A new illumigene assay significantly improves the detection of Group A Streptococcus (GAS) pharyngitis in children compared to rapid antigen detection tests and culture. This sensitive diagnostic tool aids in timely treatment to prevent complications.
Area of Science:
- Pediatric Infectious Diseases
- Clinical Microbiology
- Molecular Diagnostics
Background:
- Group A Streptococcus (GAS) pharyngitis is a common childhood illness requiring accurate diagnosis for effective treatment and prevention of sequelae.
- Current diagnostic methods like rapid antigen detection tests (RADTs) and throat cultures have limitations in sensitivity and speed.
- There is a need for improved diagnostic tools to accurately identify GAS pharyngitis in pediatric patients.
Purpose of the Study:
- To evaluate the performance of a loop-mediated isothermal amplification (LAMP) assay, the illumigene assay, for diagnosing GAS pharyngitis in children.
- To compare the sensitivity and specificity of the illumigene assay against RADT and standard culture methods.
- To assess the clinical utility of the illumigene assay in identifying GAS pharyngitis, particularly in children meeting specific clinical criteria.
Main Methods:
- A loop-mediated isothermal amplification (LAMP) assay (illumigene) was compared with RADT and throat culture on 361 pediatric throat swab samples.
- Discrepant results were resolved using an alternative molecular assay.
- Clinical presentations and scores (McIsaac) were correlated with test results in GAS-positive patients.
Main Results:
- The illumigene assay detected 70 out of 71 GAS-positive samples, demonstrating significantly higher sensitivity than RADT (35/71) and culture (55/71).
- The assay increased the identification of GAS-positive cases among eligible children, with a specificity comparable to culture.
- The illumigene assay showed higher detection rates in children with higher McIsaac scores (≥4) compared to RADT and culture.
Conclusions:
- The illumigene assay is a highly sensitive and specific molecular diagnostic tool for Group A Streptococcus pharyngitis in children.
- Its rapid results and superior performance make it a valuable alternative to traditional methods for laboratory diagnosis.
- This assay can improve the timely and accurate diagnosis of GAS pharyngitis, facilitating appropriate antimicrobial therapy and preventing post-infectious complications.
Abstract:
Group A Streptococcus (GAS) pharyngitis is a very common condition causing significant morbidity in children. Accurate diagnosis followed by appropriate antimicrobial therapy is recommended to prevent postinfectious sequelae. Diagnosis of GAS pharyngitis by a rapid antigen detection test (RADT) or culture in the absence of discriminating clinical findings remains challenging. Validation of new sensitive rapid diagnostic tests is therefore a priority. The performance of a loop-mediated isothermal amplification (LAMP) assay (illumigene assay) for the diagnosis of GAS pharyngitis was compared with that of a RADT and standard culture in 361 pediatric throat swab samples. Discrepant results were resolved using an alternate molecular assay. Test results were correlated with clinical presentations in patients positive by either method. The closest estimate of the true prevalence of GAS pharyngitis was 19.7% (71/361 samples). The illumigene assay alone detected 70/71 GAS-positive samples; RADT and culture detected 35/71 and 55/71 samples, respectively. RADT followed by culture confirmation of RADT-negative specimens detected 58/71 cases. The illumigene assay increased identification among children eligible for testing by American College of Physicians (ACP)/American Academy of Family Physicians (AAFP) criteria from 31 to 39 positive cases, five of which were false positives. Analysis of clinical data in GAS-positive patients indicated that a significantly greater proportion of children with McIsaac scores of ≥ 4 tested positive by the illumigene assay versus RADT and culture. Overall, the illumigene assay was much more sensitive and was similarly specific for GAS detection, compared to culture alone, RADT alone, or the ACP/AAFP RADT/culture algorithm. Combining high sensitivity with rapidly available results, the illumigene GAS assay is an appropriate alternative to culture for the laboratory diagnosis of GAS pharyngitis in patients for whom testing is clinically indicated.
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