bovis (ATCC 19210), M. bovis BCG (ATCC 35734), M. africanum (ATCC 25420), M. microti strain Pasteur (donated by Dr. Françoise Portaels), M. flavescens (ATCC 14474), M. fortuitum (ATCC 6841), M. szulgai (ATCC 35799), M. peregrinum (ATCC 14467), M. phlei (ATCC 11758), M. scrofulaceum (ATCC 19981), M. avium (ATCC 25291), M. smegmatis (ATCC 14468), M. nonchromogenicum (ATCC 19530), M. simiae (TMC 1595), M. intracellulare (ATCC 13950), M. gastri (ATCC 15754), M. kansasii (ATCC 12478), M. dierhoferi
(ATCC 19340), M. gordonae (ATCC 14470), M. marinum (ATCC 927), M. terrae (ATCC 15755), M. chelonae-chelonae (ATCC 35752), M. vaccae (ATCC 15483), M. triviale (ATCC 23292). All mycobacterial strains were cultured for 5 to 15 days in Alpelisib research buy Middlebrook 7H9 medium (Difco, New Jersey, USA) containing 0.05% Tween 80. Growth media YM155 purchase EVP4593 were supplemented with oleic acid-albumin-dextrose-catalase (OADC) (Becton Dickinson, BBL; Sparks, MD) or ADC as needed. Genomic DNA isolated phenol-chloroform extraction, as described elsewhere [31]. PCR assays were carried out on a GeneAmp PCR System 9600 thermal cycler (Perkin-Elmer Life Sciences Inc., Boston, MA, USA) using 0.4 mM of direct (5′-CGCTACCCACTCCCG-3′) and reverse primers (5′-CTTGTTGTTCGCACCAC-3′)
to amplify a 346-bp fragment of Rv0679c. Thermocycling conditions consisted of an initial denaturation at 94°C for 5 min, followed by 25 cycles according to the following conditions: 56°C for 30 s, 72°C for 40 s and 95°C for 40 s. A final 5 min extension step was performed at 72°C. Amplification products were separated in SYBR-stained 1% (w/v) agarose gels (Invitrogen). For RT-PCR assays, RNA was isolated based on Katoch’s methodology [32], assessing transcription of the rpoB housekeeping gene as positive transcription control [33]. Detection of Rv0679c by Western blot and immunoelectron microscopy (IEM) Expression of the Rv0679c gene was assessed by Western blot analysis of M. tuberculosis H37Rv sonicates using sera raised in goats obtained. Briefly, two goats (A-29 and B-86) nonreactive to M. tuberculosis H37Rv sonicate were inoculated with 5 mg of either polymerized
Florfenicol forms of peptide 28528 (43CGTTTPATATTTTATSGPTAAPGC62) or peptide 28530 (145CGTYKNGDPTIDNLGAGNRINKEGC165), both in polymeric form and emulsified with Freund’s incomplete adjuvant. These two peptides were chosen because the BepiPred 1.0b server http://www.cbs.dtu.dk/services/BepiPred/ predicted them as B cell epitopes. Subcellular localization was determined in a CM 10 transmission electron microscope (Philips, Suresne, Hauts-de-Seine, France), using thin slices (400 nm) of LR-White resin embedded mycobacteria. Goat anti-peptide sera were used as primary antibody and anti-goat IgG coupled to 10-nm colloidal gold particles as secondary antibody. Slices were stained with 6% uranyl acetate to enhance image contrast.