Group A Strep – How can we Help

The recent reports of invasive Group A Streptococcal infections in children have drawn attention to this relatively common pathogen. MWE has a range of products that can help with diagnosis.

The recent reports of invasive Group A Streptococcal infections in children have drawn attention to this relatively common pathogen. Perhaps best known as a cause of pharyngitis, Streptococcus pyogenes is ubiquitous in the population, with many people being colonized without symptoms. It is, however, an opportunist pathogen, and if untreated can cause more serious, potentially life-threatening illness such as scarlet fever, rheumatic fever, and necrotizing fasciitis. 

Streptococcus pyogenes is readily diagnosed by microbiological methods, whether conventional culture, rapid direct tests, or most molecular platforms. Swabs are taken from the patient’s throat or from skin lesions. It is important to use only transport swabs which are M40-A2 compliant1. Streptococcus pyogenes is one of the 10 bacterial species included in the M40-A2 panel of test organisms, against which compliant products have been tested. 

MWE’s Transwab® with Plain Amies (MW170), and Charcoal Amies (MW171), and Sigma Transwab® with Liquid Amies (MW176S) are routinely tested for the effective recovery of Streptococcus pyogenes. In addition, a recent study demonstrated that the organism is successfully identified when tested on the Cepheid GeneXpert® XVI system utilising Xpert ® Xpress Strep A (XPRSTREPA CE 10).2  Our products meet M40-A2 compliance. 

We would be happy to help and support laboratories and kit manufacturers where needed. Our products have been used globally on various platforms and we have the clinical evidence to back that. If you need further information, please get in touch.  

  1. Clinical and Laboratory Standards Institute (CLSI). Quality Control of Microbiological Transport Systems; Approved Standard- Second Edition. CLSI document M40-A2 
  2. Laughlin, J., 2019,  Molecular efficacy of two commercially available liquid transport collection devices for downstream testing on the GeneXpert® platform and the Roche FLOW® system, European Meeting on Molecular Diagnostics, 11th Meeting, Noordwijk, Netherlands 

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Related Clinical studies

SIGMA VCM meet and exceed CLSI M40-A2 requirements

A study done by Cardiff University showed that Ʃ-VCM transport medium met and exceeded the basic requirements for transport of bacteria set
out by the Clinical and Laboratory Standards Institute Standard M40-A2. Viability of Ureaplasma species in Ʃ-VCM transport medium was stable for 4 days at room temperature. Viability could be extended to at least 264 hours if kept at 4˚C.

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