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A confocal microscopic study on biofilm formed by Pseudomonas spp. isolated from lower respiratory tract infection from HIV and non-HIV populations

  • 1Email author,
  • 2,
  • 1,
  • 3,
  • 4,
  • 4,
  • 4,
  • 5,
  • 6 and
  • 4
BMC Infectious Diseases201212 (Suppl 1) :P56

  • Published:


  • Confocal Laser Scan Microscope
  • Acridine
  • Acridine Orange
  • Lower Respiratory Tract Infection
  • Developmental Step


Pseudomonas is one of the predominant microorganisms of chronic lung infections. Bacteria growing in biofilm often develop multicellular, three-dimensional structures known as micro colonies. Pseudomonas colonizes the lungs by forming biofilm micro colonies throughout the lung. In this study, using Pseudomonas spp. artificial biofilm was grown on flow cell chamber and images were taken using Confocal Laser Scanning Microscope (CLSM), to establish an experimental model for artificial biofilm in vitro.


Out of 71 isolates analysed, 45 were HIV and 24 non-HIV isolates. 19 (26.76%) produced biofilm. 6/45 (13.33%) HIV isolates and 13/24 (54.17%) non-HIV isolates were biofilm producers. 4 strains were taken to study the in vitro biofilm formation using flow cell chamber and their 3D structure and architects were studied using CLSM. Biofilm formation was monitored at different time intervals (3, 72 and 144 h). For each time interval, one channel was stained with acridine orange dye and the images obtained were quantitatively analyzed by COMSTAT.


A time lapse study of various time intervals (3, 72 and 144 hrs) were taken to study the biofilm formed by the Pseudomonas aeruginosa. We therefore used a computer program COMSTAT for quick and easy analysis of the biofilm image data which calculates a number of variables characterizing the three-dimensional structures.


Biofilm have been established as a main cause of infections due to the increased chemo resistance compared with bacteria in suspensions. Hence it is necessary to characterize the developmental steps leading to the formation of the P. aeruginosa biofilm.

Authors’ Affiliations

Dept of Microbiology (Faculty of Medicine), Dr. ALM PGIBMS, University of Madras, Taramani, Chennai-113, India
LIFE/P.G and Research Department of Advanced Zoology and Biotechnology, Loyola College, Chennai, India
Condensed Matter, Physics Division, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603 102, India
Meenakshi Medical College and Research Institute, Kanchipuram, Tamil Nadu, India
Government Hospital of Thoracic Medicine, Tambaram Sanatorium, Tambaram, Chennai, India
Department of Immunohaemotology, Dr. M.G.R Medical University, Guindy, Chennai, India


© Anitha et al; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.