Tissue Distribution of Doxycycline in Animal Models of Tuberculosis.
Martin GengenbacherMatthew D ZimmermanJansy P SarathyFirat KayaHan WangMarizel MinaClaire CarterMd Amir HossenHongwei SuCarolina TrujilloSabine EhrtDirk SchnappingerVeronique Anne DartoisPublished in: Antimicrobial agents and chemotherapy (2020)
Doxycycline, an FDA-approved tetracycline, is used in tuberculosis in vivo models for the temporal control of mycobacterial gene expression. In these models, animals are infected with recombinant Mycobacterium tuberculosis carrying genes of interest under transcriptional control of the doxycycline-responsive TetR-tetO unit. To minimize fluctuations of plasma levels, doxycycline is usually administered in the diet. However, tissue penetration studies to identify the minimum doxycycline content in food achieving complete repression of TetR-controlled genes in tuberculosis (TB)-infected organs and lesions have not been conducted. Here, we first determined the tetracycline concentrations required to achieve silencing of M. tuberculosis target genes in vitro Next, we measured doxycycline concentrations in plasma, major organs, and lung lesions in TB-infected mice and rabbits and compared these values to silencing concentrations measured in vitro We found that 2,000 ppm doxycycline supplemented in mouse and rabbit feed is sufficient to reach target concentrations in TB lesions. In rabbit chow, the calcium content had to be reduced 5-fold to minimize chelation of doxycycline and deliver adequate oral bioavailability. Clearance kinetics from major organs and lung lesions revealed that doxycycline levels fall below concentrations that repress tet promoters within 7 to 14 days after doxycycline is removed from the diet. In summary, we have shown that 2,000 ppm doxycycline supplemented in standard mouse diet and in low-calcium rabbit diet delivers concentrations adequate to achieve full repression of tet promoters in infected tissues of mice and rabbits.
Keyphrases
- mycobacterium tuberculosis
- gene expression
- pulmonary tuberculosis
- weight loss
- physical activity
- hiv aids
- transcription factor
- hepatitis c virus
- emergency department
- oxidative stress
- cancer therapy
- single cell
- high fat diet induced
- human immunodeficiency virus
- bioinformatics analysis
- hiv infected
- heat stress
- genome wide identification