TY - JOUR
T1 - Mycobacterium tuberculosis progresses through two phases of latent infection in humans
AU - Colangeli, Roberto
AU - Gupta, Aditi
AU - Vinhas, Solange Alves
AU - Chippada Venkata, Uma Deepthi
AU - Kim, Soyeon
AU - Grady, Courtney
AU - Jones-López, Edward C.
AU - Soteropoulos, Patricia
AU - Palaci, Moisés
AU - Marques-Rodrigues, Patrícia
AU - Salgame, Padmini
AU - Ellner, Jerrold J.
AU - Dietze, Reynaldo
AU - Alland, David
PY - 2020/9/25
Y1 - 2020/9/25
N2 - Little is known about the physiology of latent Mycobacterium tuberculosis infection. We studied the mutational rates of 24 index tuberculosis (TB) cases and their latently infected household contacts who developed active TB up to 5.25 years later, as an indication of bacterial physiological state and possible generation times during latent TB infection in humans. Here we report that the rate of new mutations in the M. tuberculosis genome decline dramatically after two years of latent infection (two-sided p < 0.001, assuming an 18 h generation time equal to log phase M. tuberculosis, with latency period modeled as a continuous variable). Alternatively, assuming a fixed mutation rate, the generation time increases over the latency duration. Mutations indicative of oxidative stress do not increase with increasing latency duration suggesting a lack of host or bacterial derived mutational stress. These results suggest that M. tuberculosis enters a quiescent state during latency, decreasing the risk for mutational drug resistance and increasing generation time, but potentially increasing bacterial tolerance to drugs that target actively growing bacteria.
AB - Little is known about the physiology of latent Mycobacterium tuberculosis infection. We studied the mutational rates of 24 index tuberculosis (TB) cases and their latently infected household contacts who developed active TB up to 5.25 years later, as an indication of bacterial physiological state and possible generation times during latent TB infection in humans. Here we report that the rate of new mutations in the M. tuberculosis genome decline dramatically after two years of latent infection (two-sided p < 0.001, assuming an 18 h generation time equal to log phase M. tuberculosis, with latency period modeled as a continuous variable). Alternatively, assuming a fixed mutation rate, the generation time increases over the latency duration. Mutations indicative of oxidative stress do not increase with increasing latency duration suggesting a lack of host or bacterial derived mutational stress. These results suggest that M. tuberculosis enters a quiescent state during latency, decreasing the risk for mutational drug resistance and increasing generation time, but potentially increasing bacterial tolerance to drugs that target actively growing bacteria.
UR - http://www.scopus.com/inward/record.url?scp=85091497341&partnerID=8YFLogxK
UR - https://www.nature.com/articles/s41467-020-18699-9
U2 - 10.1038/s41467-020-18699-9
DO - 10.1038/s41467-020-18699-9
M3 - Article
C2 - 32978384
AN - SCOPUS:85091497341
SN - 2041-1723
VL - 11
SP - 4870
EP - 4879
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 4870
ER -