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Persistence of human enteric viruses in artificial and human saliva
Sharon C Kosgei1, Olivia N Birch1, Justin C Greaves1
1Department of Environmental and Occupational Health, School of Public Health, Indiana University-Bloomington.
Insights
Human saliva reduces enteric virus stability, but fecal particles and oral bacteria like Streptococcus mutans can alter Adenovirus 41 (AdV41) and Coxsackievirus B3 (CVB3) persistence, impacting oral transmission risks.
Area of Science:
- Virology
- Microbiology
- Public Health
Background:
- Enteric viruses, including Adenovirus 41 (AdV41) and Coxsackievirus B3 (CVB3), cause significant gastrointestinal infections, especially in children and immunocompromised individuals.
- While fecal-oral transmission is common, saliva's role as a potential reservoir and route for oral transmission is increasingly recognized.
- Limited research exists on enteric virus persistence in human saliva compared to studies on aqueous environments.
Purpose of the Study:
- To investigate the persistence of AdV41 and CVB3 in human and artificial saliva.
- To examine the influence of fecal particles and specific oral bacteria on viral stability in saliva.
- To understand the complex interactions affecting oral viral persistence and transmission dynamics.
Main Methods:
- AdV41 and CVB3 persistence was assessed in human and artificial saliva.
- Experiments included varying conditions with fecal particles and the oral bacterium Streptococcus mutans.
- Viral titers were measured over time to determine stability and recovery rates.
Main Results:
- Human saliva significantly decreased viral stability compared to artificial saliva, with notable titer reductions within 24-48 hours.
- Fecal particles prolonged CVB3 persistence but reduced AdV41 stability, indicating virus-specific interactions.
- Streptococcus mutans significantly enhanced CVB3 stability, increasing recovery from 0.7% to 23.2% after 24 hours (p=0.001).
Conclusions:
- Human saliva generally reduces enteric virus stability, but oral environmental factors create complex persistence dynamics.
- Fecal particles and oral bacteria can significantly alter AdV41 and CVB3 persistence in saliva.
- Findings highlight the need for further research into oral viral persistence to inform public health strategies against transmission.
Abstract:
Enteric viruses, such as Adenovirus 41 (AdV41) and Coxsackievirus B3 (CVB3), are significant contributors to gastrointestinal infections, particularly among young children and immunocompromised individuals. While fecal-oral transmission is the primary route of infection, emerging evidence indicates that saliva may also function as a reservoir for these viruses, posing a potential risk for oral transmission. Previous studies have primarily focused on the decay of viruses in aqueous matrices, like wastewater and freshwater, but the persistence of these viruses in human saliva remains underexplored. This study aimed to investigate the persistence of AdV41 and CVB3 in both human and artificial saliva under various conditions, including the presence of fecal particles and specific oral bacteria. Our findings demonstrated that human saliva significantly reduced viral stability compared to artificial saliva, with marked reductions in viral titers observed within 24-48 hours. Particularly, the presence of fecal particles in both saliva types extended CVB3 viral persistence, suggesting a protective effect due to particle adsorption. However, AdV41 demonstrated an opposite trend when in the presence of fecal particles, suggesting virus-specific differences in how particulate matter influences stability. Additionally, specific oral bacteria, such as Streptococcus mutans, significantly enhanced CVB3 stability, with a mean viral recovery of 23.2% of the viral titer after 24 hours in the presence of the bacteria compared to 0.7% in their absence (p = 0.001). This study shows complex interactions between viruses, oral bacteria, and fecal particles within the oral environment, emphasizing the need for further research on oral viral persistence and transmission dynamics. Understanding these mechanisms behind viral persistence in saliva can inform public health strategies aimed at mitigating the risk of transmission.
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