TY - JOUR
T1 - Efficacy of Omadacycline-Containing Regimen in a Mouse Model of Pulmonary Mycobacteroides abscessus Disease
AU - Rimal, Binayak
AU - Nicklas, Danielle A.
AU - Panthi, Chandra M.
AU - Lippincott, Christopher K.
AU - Belz, Daniel C.
AU - Ignatius, Elisa H.
AU - Deck, Daniel H.
AU - Serio, Alisa W.
AU - Lamichhane, Gyanu
N1 - Publisher Copyright:
© 2023 Rimal et al.
PY - 2023/4
Y1 - 2023/4
N2 - Mycobacteroides abscessus is an opportunistic pathogen in people with structural lung conditions such as bronchiectasis, chronic obstructive pulmonary disease, and cystic fibrosis. Pulmonary M. abscessus infection causes progressive symptomatic and functional decline as well as diminished lung function and is often incurable with existing antibiotics. We investigated the efficacy of a new tetracycline, omadacycline, in combination with existing antibiotics recommended to treat this indication, in a mouse model of M. abscessus lung disease. Amikacin, azithromycin, bedaquiline, biapenem, cefoxitin, clofazimine, imipenem, linezolid, and rifabutin were selected as companions to omadacycline. M. abscessus burden in the lungs of mice over a 4-week treatment duration was considered the endpoint. Omadacycline in combination with linezolid, imipenem, cefoxitin, biapenem, or rifabutin exhibited early bactericidal activity compared to any single drug. Using three M. abscessus isolates, we also determined the in vitro frequency of spontaneous resistance against omadacycline to be between 1.9 × 10210 and 6.2 × 10210 and the frequency of persistence against omadacycline to be between 5.3 × 1026 and 1.3 × 1025. Based on these findings, the combination of omadacycline and select drugs that are included in the recent treatment guidelines may exhibit improved potency to treat M. abscessus lung disease.
AB - Mycobacteroides abscessus is an opportunistic pathogen in people with structural lung conditions such as bronchiectasis, chronic obstructive pulmonary disease, and cystic fibrosis. Pulmonary M. abscessus infection causes progressive symptomatic and functional decline as well as diminished lung function and is often incurable with existing antibiotics. We investigated the efficacy of a new tetracycline, omadacycline, in combination with existing antibiotics recommended to treat this indication, in a mouse model of M. abscessus lung disease. Amikacin, azithromycin, bedaquiline, biapenem, cefoxitin, clofazimine, imipenem, linezolid, and rifabutin were selected as companions to omadacycline. M. abscessus burden in the lungs of mice over a 4-week treatment duration was considered the endpoint. Omadacycline in combination with linezolid, imipenem, cefoxitin, biapenem, or rifabutin exhibited early bactericidal activity compared to any single drug. Using three M. abscessus isolates, we also determined the in vitro frequency of spontaneous resistance against omadacycline to be between 1.9 × 10210 and 6.2 × 10210 and the frequency of persistence against omadacycline to be between 5.3 × 1026 and 1.3 × 1025. Based on these findings, the combination of omadacycline and select drugs that are included in the recent treatment guidelines may exhibit improved potency to treat M. abscessus lung disease.
KW - Mycobacteriumabscessus
KW - Mycobacteroides abscessus
KW - amikacin
KW - azithromycin
KW - bedaquiline
KW - biapenem
KW - cefoxitin
KW - clofazimine
KW - imipenem
KW - linezolid
KW - omadacycline
KW - rifabutin
UR - http://www.scopus.com/inward/record.url?scp=85153411916&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85153411916&partnerID=8YFLogxK
U2 - 10.1128/msphere.00665-22
DO - 10.1128/msphere.00665-22
M3 - Article
C2 - 36912629
AN - SCOPUS:85153411916
SN - 2379-5042
VL - 8
JO - mSphere
JF - mSphere
IS - 2
ER -