ABSTRACT
Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene. Mutations in this chloride channel lead to mucus accumulation, subsequent recurrent pulmonary infections, and inflammation, which, in turn, cause chronic lung disease and respiratory failure. Recently, rates of nontuberculous mycobacterial (NTM) infections in CF patients have been increasing. Of particular relevance is infection with
Mycobacterium abscessus
, which causes a serious, life-threatening disease and constitutes one of the most antibiotic-resistant NTM species. Interestingly, an increased prevalence of NTM infections is associated with worsening lung function in CF patients who are also coinfected with
Aspergillus fumigatus
. We established a new mouse model to investigate the relationship between
A. fumigatus
and
M. abscessus
pulmonary infections. In this model, animals exposed to
A. fumigatus
and coinfected with
M. abscessus
exhibited increased lung inflammation and decreased mycobacterial burden compared with those of mice infected with
M. abscessus
alone. This increased control of
M. abscessus
infection in coinfected mice was mucus independent but dependent on both transcription factors T-box 21 (Tbx21) and retinoic acid receptor (RAR)-related orphan receptor gamma t (RORγ-t), master regulators of type 1 and type 17 immune responses, respectively. These results implicate a role for both type 1 and type 17 responses in
M. abscessus
control in
A. fumigatus
-coinfected lungs. Our results demonstrate that
A. fumigatus
, an organism found commonly in CF patients with NTM infection, can worsen pulmonary inflammation and impact
M. abscessus
control in a mouse model.
</jats:p