Genotypic characterization of Mycobacterium avium strains recovered from animals and their comparison to human strains

M Bono, T Jemmi, C Bernasconi, D Burki, A Telenti, T Bodmer
1995 Applied and Environmental Microbiology  
Mycobacterium avium was recovered from 21 birds and 10 pigs. Bird isolates carried IS901 and a few copies of IS1245 and appeared highly related by pulsed-field gel electrophoresis. Pig isolates showed features previously described in human isolates: a lack of IS901, a high copy number of IS1245, and marked polymorphism by pulsed-field gel electrophoresis. Mycobacterium avium represents an important pathogen in both humans (5, 7, 12, 19, 25) and animals (8, 16). For humans, water has been
more » ... ter has been identified as a definitive source of infection (24). However, the observed genetic diversity of M. avium strains recovered from AIDS patients (1) and the occurrence of M. avium in animals and various environmental samples suggest the existence of additional reservoirs (17). The purpose of this study was to characterize M. avium strains recovered from animal sources within a defined geographical area-the German-speaking part of Switzerland-by using a number of genotype markers, namely, the presence of insertion elements IS900 (9), IS901 (15), and the novel element IS1245 (10), and by evaluating strain relatedness by pulsed-field gel electrophoresis (PFGE). Materials investigated (n ϭ 398) included mandibular and mesenteric lymph nodes from 120 slaughtered pigs collected from two different abattoirs; 103 samples from 25 chickens and 15 eggs from eight different flocks; organs (n ϭ 21) from seven additional birds, including five exotic birds, in which acid-fast bacilli had been detected (Institute for Veterinary Bacteriology, University of Berne); and environmental samples, such as those from soil (n ϭ 8), pig and chicken litter (n ϭ 9), pondwater (n ϭ 1), and chicken feed (n ϭ 1). Samples were homogenized, decontaminated with sodium dodecyl sulfate-sodium hydroxide, and neutralized, and the sediments were resuspended in phosphate-buffered saline (20). One BACTEC 12B vial supplemented with Panta Plus (Becton Dickinson Diagnostic Instrument Systems, Sparks, Md.), one pyruvate-containing Löwenstein-Jensen slant, and one slant of Herrold's medium were inoculated. Slants were incubated at 37ЊC for 12 weeks and inspected for growth weekly. BACTEC 12B vials were processed for 12 weeks with the BACTEC-460 TB apparatus (Johnston Laboratories Inc., Sparks, Md.) according to the manufacturer's recommendations. For identification, mycobacterial isolates underwent PCR-restriction enzyme analysis of the gene coding for the 65-kDa heat shock protein of mycobacteria (21) and conventional biochemical tests (13).
doi:10.1128/aem.61.1.371-373.1995 fatcat:mghrxy4nmjf6zb5a4t62dt24pm