Isolation and identification of legionellosis agents from fishponds, swimming pools and cooling towers in Khuzestan province, Iran

Mojtaba Moosavian; Amir Dashti

Jundishapur Journal of Microbiology

Ahvaz Jundishapur University of Medical Sciences

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Isolation and identification of legionellosis agents from fishponds, swimming pools and cooling towers in Khuzestan province, Iran

Author(s):

Mojtaba Moosavian^1,*,

Amir Dashti²

1Department of Medical Microbiology, School of Medicine, Infectious and Tropical Diseases Research Center, Ahvaz Jundishapur University of Medical Sciences, moosavian_m@yahoo.com, Ahvaz, Iran

2Department of Medical Microbiology, School of Medicine, Infectious and Tropical Diseases Research Center, Ahvaz Jundishapur University of Medical Sciences, Iran

Jundishapur Journal of Microbiology:Vol. 4, issue 4

Article type:Research Article

How to Cite:Mojtaba MoosavianAmir DashtiIsolation and identification of legionellosis agents from fishponds, swimming pools and cooling towers in Khuzestan province, Iran.Jundishapur J Microbiol.4(4):null-null.

Abstract

Introduction and objective: Legionella are the causative agents of pneumonia in human and it is reported that up to 90% cases of legionnaires` disease are due to Legionella pneumophila. These organisms are ubiquitous distributed in natural and man made water sources. They are spread to human by inhalation or aspiration of contaminated aerosols of these sources. We studied some of man made water sources in view of the presence of Legionella, by two methods of culture and PCR.

Materials and methods: One hundred and fifty water samples collected from different man made water sources were examined. After acidic treatment of samples, water pellet was inoculated onto buffered charcoal yeast extract agar (BCYE) and BMPA (BCYE supplemented with three antibiotics) media. Isolated colonies were identified by morphological and biochemical tests. DNA was extracted from the bacteria and was used for PCR technique. DNA pattern of Legionella were identified after electrophoresis of PCR products.

Results: Survey of water samples collected from different sources resulted in isolation of Legionella pneumophila (7.3%) by culture, and identification of them (15.3%) by PCR. The highest isolates of L. pneumophila were from fish ponds in rates of 6.6% by culture and 13.3% by PCR method. Sensitivity and specificity of PCR in this survey were 100% and 95%, respectively.

Conclusion: This study showed that legionnaires` disease agents were widely spread in our examined water sources and compared with culture; PCR method has suitable sensitivity and specificity for rapid detection of these organisms in environmental water sources.

Significance and impact of the study: The results of this study will increase physicians and microbiologists awareness about spreading of Legionella and this will be useful for control of legionellosis agents.

Keywords

Legionella

Legionnaires` disease

Fishponds

Swimming pools

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