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1.
Pathog Dis ; 77(5)2019 07 01.
Article in English | MEDLINE | ID: mdl-31583400

ABSTRACT

Non-pigmented rapidly growing mycobacteria (NPRGM) are widely distributed in water, soil and animals. It has been observed an increasing importance of NPRGM related-infections, particularly due to the high antimicrobial resistance. NPRGM have rough and smooth colony phenotypes, and several studies have showed that rough colony variants are more virulent than smooth ones. However, other studies have failed to validate this observation. In this study, we have performed two models, invitro and in vivo, in order to assess the different pathogenicity of these two phenotypes. We used collection and clinical strains of Mycobacteriumabscessus, Mycobacterium fortuitum and Mycobacteriumchelonae. On the invitro model (macrophages), phagocytosis was higher for M. abscessus and M. fortuitum rough colony variant strains when compared to smooth colony variants. However, we did not find differences with colonial variants of M. chelonae. Survival of Galleriamellonella larvae in the experimental model was lower for M. abscessus and M. fortuitum rough colony variants when compared with larvae infected with smooth colony variants. We did not find differences in larvae infected with M. chelonae.Results of our in vivo study correlated well with the experimental model. This fact could have implications on the interpretation of the clinical significance of the NPRGM isolate colonial variants.


Subject(s)
Mycobacterium Infections, Nontuberculous/microbiology , Mycobacterium Infections, Nontuberculous/pathology , Mycobacterium abscessus/pathogenicity , Mycobacterium chelonae/pathogenicity , Mycobacterium fortuitum/pathogenicity , Phenotype , Animals , Disease Models, Animal , Larva , Lepidoptera , Macrophages/immunology , Macrophages/microbiology , Models, Theoretical , Mycobacterium abscessus/growth & development , Mycobacterium chelonae/growth & development , Mycobacterium fortuitum/growth & development , Phagocytosis , Pigments, Biological/analysis , Survival Analysis , Virulence
2.
Int J Med Microbiol ; 308(3): 413-423, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29555180

ABSTRACT

Lung disease in cystic fibrosis (CF) is characterized by the progressive colonization of the respiratory tract by different bacteria, which develop polymicrobial biofilms. In the past decades, there has been an increase in the number of CF patients infected with Non-Tuberculous Mycobacteria (NTM). Although Mycobacterium abscessus is the main NTM isolated globally, little is known about M. abscessus multispecies biofilm formation. In the present study we developed an in vitro model to study the phenotypic characteristics of biofilms formed by M. abscessus and Pseudomonas aeruginosa, a major pathogen in CF. For that purpose, dual species biofilms were grown on polycarbonate membranes with a fixed concentration of P. aeruginosa and different inoculums of M. abscessus. The biofilms were sampled at 24, 48, and 72 h and bacteria were quantified in specific media. The results revealed that the increasing initial concentration of M. abscessus in dual species biofilms had an effect on its population only at 24 and 48 h, whereas P. aeruginosa was not affected by the different concentrations used of M. abscessus. Time elapsed increased biofilm formation of both species, specially between 24 and 48 h. According to the results, the conditions to produce a mature dual species biofilm in which the relative species distribution remained stable were 72 h growth of the mixed microbial culture at a 1:1 ratio. A significant decrease in mycobacterial population in dual compared to single species biofilms was found, suggesting that P. aeruginosa has a negative influence on M. abscessus. Finally, in a proof of concept experiment, young and mature dual species biofilms were exposed to clarithromycin.


Subject(s)
Biofilms/growth & development , Cystic Fibrosis/microbiology , Mycobacterium abscessus/physiology , Nontuberculous Mycobacteria/physiology , Pseudomonas aeruginosa/physiology , Anti-Bacterial Agents , Biofilms/drug effects , Clarithromycin/pharmacology , Humans , In Vitro Techniques , Models, Biological , Mycobacterium abscessus/growth & development , Mycobacterium abscessus/ultrastructure , Nontuberculous Mycobacteria/growth & development , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/growth & development , Pseudomonas aeruginosa/ultrastructure
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