Development of a DNA Microarray Method for Detection and Identification of All 15 Distinct O-Antigen Forms of Legionella pneumophila

Author:

Cao Boyang1234,Yao Fangfang1234,Liu Xiangqian1234,Feng Lu1234,Wang Lei12345

Affiliation:

1. Key Laboratory of Molecular Microbiology and Technology of the Ministry of Education, TEDA College, Nankai University, TEDA, Tianjin, People's Republic of China

2. TEDA School of Biological Sciences and Biotechnology, Nankai University, TEDA, Tianjin, People's Republic of China

3. Tianjin Research Center for Functional Genomics and Biochips, TEDA College, Nankai University, TEDA, Tianjin, People's Republic of China

4. Tianjin Key Laboratory of Microbial Functional Genomics, TEDA College, Nankai University, TEDA, Tianjin, People's Republic of China

5. Tianjin Biochip Corporation, TEDA, Tianjin, People's Republic of China

Abstract

ABSTRACT Legionella is ubiquitous in many environments. At least 50 species and 70 serogroups of the Gram-negative bacterium have been identified. Of the 50 species, 20 are pathogenic, and Legionella pneumophila is responsible for the great majority (approximately 90%) of the Legionnaires' disease cases that occur. Furthermore, of the 15 L. pneumophila serogroups identified, O1 alone causes more than 84% of the Legionnaires' disease cases that occur worldwide. Rapid and reliable assays for the detection and identification of L. pneumophila in water, environmental, and clinical samples are in great demand. L. pneumophila bacteria are traditionally identified by their O antigens by immunological methods. We have recently developed an O serogroup-specific DNA microarray for the detection of all 15 distinct O-antigen forms of L. pneumophila , including serogroups O1 to O15. A total of 35 strains were used to verify the specificity of the microarray, including 15 L. pneumophila O-antigen standard reference strains and seven L. pneumophila clinical isolates as target strains, seven reference strains of other non- pneumophila Legionella species as closely related strains, and six non- Legionella bacterial species as nonrelated strains. The detection sensitivity was 1 ng of genomic DNA or 0.4 CFU/ml in water samples with filter enrichment and plate culturing. This study demonstrated that the microarray allows specific, sensitive, and reproducible detection of L. pneumophila serogroups. To the best of our knowledge, this is the first report of a microarray serotyping method for all 15 distinct O-antigen forms of L. pneumophila .

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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