Transmission potential of Streptococcus pyogenes during a controlled human infection trial of pharyngitis

Author:

Enkel Stephanie L.12ORCID,Wong Bernadette1,Hla Thel K.123,Pickering Janessa14,Barnett Timothy C.14,Thomas Hannah M. M.1,Lansbury Nina5,Carapetis Jonathan R.126,Osowicki Joshua789ORCID,Steer Andrew7810,Manning Laurens123,Bowen Asha C.126

Affiliation:

1. Wesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, University of Western Australia, Nedlands, Western Australia, Australia

2. Medical School, University of Western Australia, Crawley, Western Australia, Australia

3. Department of Infectious Diseases, Fiona Stanley Hospital, Murdoch, Western Australia, Australia

4. Marshall Centre for Infectious Diseases Research and Training, School of Biomedical Sciences, University of Western Australia, Nedlands, Western Australia, Australia

5. School of Public Health, University of Queensland, Brisbane, Queensland, Australia

6. Department of Infectious Diseases, Perth Children’s Hospital, Nedlands, Western Australia, Australia

7. Tropical Diseases Research Group, Murdoch Children’s Research Institute, Melbourne, Victoria, Australia

8. Department of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia

9. Infectious Diseases Unit, Department of General Medicine, Royal Children’s Hospital Melbourne, Parkville, Victoria, Australia

10. Department of General Medicine, Royal Children’s Hospital, Melbourne, Victoria, Australia

Abstract

ABSTRACT Controlled human infection (CHI) models can provide insights into transmission of pathogens such as Streptococcus pyogenes (Strep A). As part of the Controlled Human Infection with Penicillin for Streptococcus pyogenes (CHIPS) trial, we explored the potential for transmission among participants deliberately infected with the Strep A emm75 strain. Three approaches to understanding transmission were employed: the use of agar settle plates to capture possible droplet or airborne spread of Strep A; measurement of distance droplets could spread during conversation; and environmental swabbing of high-touch items to detect Strep A on surfaces. Of the 60 (27%) CHIPS trial participants across five cohorts, 16 were enrolled in this sub-study; availability of study staff was the primary reason for selection. In total, 189 plates and 260 swabs were collected. Strep A was grown on one settle plate from a participant on the second day, using plates placed 30 cm away. This participant received the placebo dose of penicillin and had met the primary endpoint of pharyngitis. Whole-genome sequencing identified this to be the challenge strain. Strep A was not detected on any swabs. In this small sample of CHI participants, we did not find evidence of Strep A transmission by the airborne route or fomites, and just one instance of droplet spread while acutely symptomatic with streptococcal pharyngitis. Although these experiments provide evidence of minimal transmission within controlled clinical settings, greater efforts are required to explore Strep A transmission in naturalistic settings. IMPORTANCE Streptococcus pyogenes remains a significant driver of morbidity and mortality, particularly in under-resourced settings. Understanding the transmission modalities of this pathogen is essential to ensuring the success of prevention methods. This proposed paper presents a nascent attempt to determine the transmission potential of Streptococcus pyogenes nested within a larger controlled human infection model.

Publisher

American Society for Microbiology

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