TABLE 3.
Critical knowledge gaps in tuberculosis (TB) epidemiology and the potential use of environmental sampling for Mycobacterium tuberculosis
Epidemiological areas related to TB | Potential use of environmental sampling and ideas for further investigation |
---|---|
Where does TB transmission occur? | Characterising M. tuberculosis abundance in various congregate settings, including public transit, schools, churches, restaurants, bars and workplaces |
How much interindividual heterogeneity is there in community transmission? | Compare abundance of M. tuberculosis genotypes across settings |
How does dose of exposure influence risk of TB progression? | Compare abundance of M. tuberculosis in household with risk of progression among household contacts |
How long are individuals infectious prior to detection? | Whole genome sequencing of environmental samples and comparing dates of detection in the environment with date of diagnosis |
How does an individual’s infectiousness change over time? | Assess rates of environmental contamination with specific isolates, identified by whole genome sequencing, over time |
Was an intervention successful at reducing transmission? | Assess changes in M. tuberculosis abundance in congregate settings (e.g. hospitals, prisons, mines, schools] over time |
Was an individual infectious when a potential exposure occurred? | Conduct environmental sampling at sites of potential exposure (e.g. hospital rooms] |