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Applied and Environmental Microbiology, November 2006, p. 7311-7323, Vol. 72, No. 11
0099-2240/06/$08.00+0     doi:10.1128/AEM.01179-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

The Mosaic Nature of Intergenic 16S-23S rRNA Spacer Regions Suggests rRNA Operon Copy Number Variation in Clostridium difficile Strains{triangledown}

Nourkhoda Sadeghifard,1,{dagger} Volker Gürtler,2* Michael Beer,1 and Robert J. Seviour1

Biotechnology Research Centre, La Trobe University, Bendigo, Victoria 3552, Australia,1 Microbiology Department, Austin Hospital, Studley Road, Heidelberg, Melbourne, Victoria 3084, Australia2

Received 22 May 2006/ Accepted 7 September 2006

Clostridium difficile is a major spore-forming environmental pathogen that causes serious health problems in patients undergoing antibiotic therapy. Consequently, reliable and sensitive methods for typing individual strains are required for epidemiological and environmental studies. Ribotyping is generally considered the best method, but it fails to account for sequence diversity which might exist in intergenic 16S-23S rRNA spacer regions (ISRs) within and among strains of this organism. Therefore, this study was undertaken to compare the sequence of each individual ISR in five strains of C. difficile to explore the extent of this diversity and see whether such information might provide the basis for more sensitive and discriminatory strain typing methods. After targeted PCR amplification, cloning, and sequencing, the diversity of the ISRs was used as a measure of rRNA operon copy number. In C. difficile strains 630, ATCC 43593, A, and B, 11, 11, 7, and 8 ISR length variants, respectively, were found (containing different combinations of sequence groups [i to xiii]), suggesting 11, 11, 7, and 8 rrn copies in the respective strains. Many ISRs of the same length differed markedly in their sequences, and some of these were restricted in occurrence to a single strain. Most of these ISRs did not contain any tRNA genes, and only single copies of the tRNAAla gene were found in those that did. The presence of ISR sequence groups (i to xiii) varied between strains, with some found in one, two, three, four, or all five strains. We conclude that the intergenic 16S-23S rRNA spacer regions showed a high degree of diversity, not only among the rrn operons in different strains and different rrn copies in a single strain but also among ISRs of the same length. It appears that C. difficile ISRs vary more at the inter- and intragenic levels than those of other species as determined by empirical comparison of sequences. The precise characterization of these sequences has demonstrated a high level of mosaic sequence block rearrangements that are present or absent in multiple strain-variable rrn copies within and between five different strains of C. difficile.

* Corresponding author. Mailing address: Microbiology Department, Austin Hospital, Studley Road, Heidelberg, Melbourne, Victoria 3084, Australia. Phone: 61 3 9496 3136. Fax: 61 3 9457 2590. E-mail: volker.gurtler{at}austin.org.au.

{triangledown} Published ahead of print on 15 September 2006.

{dagger} Present address: Microbiology Department, Ilam University of Medical Sciences, Ilam, Iran.

Applied and Environmental Microbiology, November 2006, p. 7311-7323, Vol. 72, No. 11
0099-2240/06/$08.00+0     doi:10.1128/AEM.01179-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.



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