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Journal of Clinical Microbiology, November 2003, p. 5347-5348, Vol. 41, No. 11
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.11.5347-5348.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

LETTERS TO THE EDITOR

Towards "Molecular Esperanto" or the Tower of Babel? (The Need for Harmonization of Techniques for Genotyping Clinical Isolates of Pseudomonas aeruginosa Isolated from Patients with Cystic Fibrosis)


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LETTER
 
We read with interest the letter of Armstrong et al. (D. Armstrong, S. Bell, M. Robinson, P. Bye, B. Rose, C. Harbour, C. Lee, H. Service, M. Nissen, M. Syrmis, and C. Wainwright, Letter, J. Clin. Microbiol. 41:2266-2267, 2003) describing the occurrence of a clonal type (pulsotype I) of Pseudomonas aeruginosa at five cystic fibrosis (CF) centers along the east coast of Australia. This letter strongly asserts that this clonal type has spread to CF patients, not from either the hospital or external environments, but by person-to-person transmission. This letter also describes some of the recent events that have led to advances in molecular typing techniques and thus to the identification of a dominant and hypertransmissible clonal strain of P. aeruginosa at several CF centers. What this letter also demonstrates to the CF microbiology community is that there is an urgent requirement for the standardization and harmonization of genotyping techniques, both nationally and internationally, where several methods presently exist for strain characterization (for a detailed review of P. aeruginosa typing, see reference 15).

Armstrong et al. (letter) cite several previous studies employing pulsed-field gel electrophoresis (PFGE) typing of P. aeruginosa. A methodological comparison highlighting technical variations in previous PFGE typing studies of P. aeruginosa is detailed in Table 1. Thus, Armstrong et al. were correct and diligent in comparing interlaboratory variability in deciding the relatedness of isolates from five CF centers, when more than one microbiology laboratory was involved in strain analysis.


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  		TABLE 1. Comparison of PFGE typing methodologies

Recently Jones et al. (9) have stressed the importance of microbiological surveillance through molecular fingerprinting, namely, PFGE typing, in order to ascertain the extent of cross-infection of P. aeruginosa among CF patients. PFGE is no longer a method solely restricted to epidemiological typing research studies, but is one which is now used in many clinical diagnostic laboratories to aid with routine epidemiological analysis. Laboratories which are introducing such techniques for the analysis of their P. aeruginosa subtypes should adopt protocols that will yield data for their isolates which can be compared with data from other CF centers. This strategy has been successfully applied for typing enteric bacterial pathogens through the PulseNet system (www.cdc.gov/pulsenet). The exchange of typing data obtained by employing standardized and harmonized methods, via an electronic medium, as has been developed recently by the ESF Network for Exchange of Microbial Typing Information (http://lists.nottingham.ac.uk/mailman/listinfo/enemti), would facilitate our understanding of the molecular epidemiology of P. aeruginosa in CF patient populations.

Consensus is thus needed in order to ascertain if such differences, for example, different suppliers of restriction enzymes, internal standards, pulse field parameters, etc., are significant or not. If the effects of such differences are not known, then a feasibility study involving several centers needs to be undertaken to resolve these technical anomalies, so that a robust method may be adopted by the CF microbiology community. If it felt that such a trial is unnecessary, then it will be a relatively easy task to define a consensus PFGE protocol that will gain widespread acceptance.

The real treasure to the CF microbiology community of adopting standardized and harmonized genotyping protocols such as PFGE is that it will allow us to identify transmissible types locally as well as globally and provide a basis for the examination of virulence in common genotypes. If we fail to attempt to learn a form of "molecular Esperanto" in terms of speaking a common language of harmonized and standardized methodology, we will potentially suffer, as befell the Israelites in Old Testament times with the Tower of Babel (Genesis 11), from misunderstanding. Indeed, if we cannot communicate with each other, we can hardly cooperate with each other.


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REFERENCES
 
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John E. Moore*
Colin E. Goldsmith
Northern Ireland Public Health Laboratory
Department of Bacteriology

J. Stuart Elborn
Northern Ireland Regional Adult Cystic Fibrosis Centre
Belfast City Hospital
Belfast BT9 7AD, Northern Ireland

Philip G. Murphy
Department of Microbiology
The Adelaide and Meath Hospital
Tallaght
Dublin, Ireland

Peter H. Gilligan
Clinical Microbiology-Immunology Laboratories
UNC Hospitals
Chapel Hill, NC 27514

Séamus Fanning
Faculty of Veterinary Medicine
University College Dublin
Belfield
Dublin 4, Ireland

Graham Hogg
Department of Bacteriology
The Royal Group of Hospitals
Grosvenor Road
Belfast BT12 6BA, Northern Ireland

* Phone: 44 (28) 9026 3554, Fax: 44 (28) 2589 2887, E-mail: jemoore{at}niphl.dnet.co.uk

Journal of Clinical Microbiology, November 2003, p. 5347-5348, Vol. 41, No. 11
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.11.5347-5348.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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