An assessment of the airborne longevity of group A Streptococcus.

aerosol airborne droplet group A streptococcus transmission

Journal

Microbiology (Reading, England)
ISSN: 1465-2080
Titre abrégé: Microbiology (Reading)
Pays: England
ID NLM: 9430468

Informations de publication

Date de publication:
Jan 2024
Historique:
medline: 5 1 2024
pubmed: 5 1 2024
entrez: 5 1 2024
Statut: ppublish

Résumé

Group A streptococcus (GAS) infections result in more than 500 000 deaths annually. Despite mounting evidence for airborne transmission of GAS, little is known about its stability in aerosol. Measurements of GAS airborne stability were carried out using the Controlled Electrodynamic Levitation and Extraction of Bioaerosols onto a Substrate (CELEBS) instrument. CELEBS measurements with two different isolates of GAS suggest that it is aerostable, with approximately 70 % of bacteria remaining viable after 20 min of levitation at 50 % relative humidity (RH), with lower survival as RH was reduced. GAS airborne viability loss was driven primarily by desiccation and efflorescence (i.e. salt crystallization), with high pH also potentially playing a role, given reduced survival in bicarbonate containing droplet compositions. At low enough RH for efflorescence to occur, a greater proportion of organic components in the droplet appeared to protect the bacteria from efflorescence. These first insights into the aerosol stability of GAS indicate that airborne transmission of these respiratory tract bacteria may occur, and that both the composition of the droplet containing the bacteria, and the RH of the air affect the duration of bacterial survival in this environment. Future studies will explore a broader range of droplet and air compositions and include a larger selection of GAS strains.

Identifiants

pubmed: 38180461
doi: 10.1099/mic.0.001421
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Henry P Oswin (HP)

School of Chemistry, University of Bristol, Cantock's Close, Bristol, UK.

Evie Blake (E)

School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.

Allen E Haddrell (AE)

School of Chemistry, University of Bristol, Cantock's Close, Bristol, UK.

Adam Finn (A)

School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Paediatric Immunology and Infectious Diseases, Bristol Royal Hospital for Children, Bristol, UK.

Shiranee Sriskandan (S)

NIHR Health Protection Research Unit in Healthcare-associated Infection and Antimicrobial Resistance, Imperial College London, London, UK.
Centre for Bacterial Resistance Biology, Imperial College London, London, UK.

Jonathan P Reid (JP)

School of Chemistry, University of Bristol, Cantock's Close, Bristol, UK.

Alice Halliday (A)

School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.

Anu Goenka (A)

School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Paediatric Immunology and Infectious Diseases, Bristol Royal Hospital for Children, Bristol, UK.

Classifications MeSH