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Volume 6
Journal of Infectious Diseases and Therapy
ISSN: 2332-0877
Infection Congress 2018
March 01-02, 2018
March 01-02, 2018 Berlin, Germany
5
th
International Congress on
INFECTIOUS DISEASES
Identification of genes in biofilm of slow and fast growing mycobacteria by using microarray and
other molecular tools including electron microscopy
V K Sharma
National Jalma Institute of Leprosy & Other Mycobacterial Diseases, India
E
lectron microscopy used to investigate the detailed structure and configuration of the mycobacteria which may lead to an
understanding the role of infections and in transmitting the diseases.ManyMycobacteria candevelop biofilm, amulticellular
structure largely combining bacteria and their extracellular polymeric substances (EPS). The formation of biofilm results in an
alternative existence in which microbes ensure their survival in adverse environments. Bacterial biofilms are often associated
with infections especially with medical implants such as catheters and other medical devices. In the natural world more than
99% of bacteria exist as biofilms and according to NIH report more than 75% of all human infections are associated with
biofilms formation. Biofilms are slimy, glue-like substance that excreted by bacteria and aggregate on living surface. Biofilms
are formed to protect the bacteria from host defenses, antibiotics and from harsh environmental conditions. Biofilms are
found almost everywhere in nature, including soil, water pipes, and even inside the human body. Attachment of mycobacteria
involved in biofilm formation in the liquid air interface is a complex process, with many variables such as pH, nutrient levels,
iron, oxygen, ionic strength and temperature, affecting the outcome. We had taken four mycobacterial species for study of
mycobacterial biofilm. The isolates were sub-cultured and characterized biochemically and molecularly. The large quantity of
biofilm was produced by M. smegmatis at temperature 37oC and 42oC as compared to 30oC. M. fortuitum developed more
amount of biofilm at 30oC as compared to 37oC and 42oC. M. avium developed strong amount of biofilm at 30oC and 42oC
as compared to 370C. M tuberculosis (H37Rv) developed strong biofilm at 37oC and no biofilm at 300C and 420C in MB 7H9
media and Sauton’s media. The selected non tuberculosis mycobacteria and H37Rv developed strong biofilm in the presence
of OADC enrichment in MB7H9 as well as Sauton’s medium. Antibiotic susceptibility of biofilms at ultra-structural level was
also studied in fast growing clinical isolates M. smegmatis in presence of streptomycin, isoniazid rifampicin, ethambutol and
pyrazinamide. Electron microscopy revealed that control (no drug) biofilms consisted primarily of bacterial clusters a mid
fibrillar elements. Isoniazid showed strong inhibited biofilm in fast grower and sensitive isolates. However, pyrazinamide and
isoniazid inhibited biofilm of M. tuberculosis (H37Rv) and in MDR isolates ethionamide and moxifloxacin inhibited biofilm in
slow grower and fast grower mycobacteria. However, many mycobacterial species are known to form biofilms, little is known
about either the genetic requirements, patterns of gene expression. In micro array hybridization, we have found that six genes
were expressed in M. avium. In M. tuberculosis, MDR isolates seven genes were expressed and two genes Rv0359 and Rv3526
were homologous as earlier reported in P. aeruginosa and M. avium which might be responsible for biofilm formation
.
vksjalma@gmail.comJ Infect Dis Ther 2018, Volume 6
DOI: 10.4172/2332-0877-C1-039