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Insertion sequence IS200 fingerprinting of Salmonella typhi: an assessment of epidemiological applicability

Published online by Cambridge University Press:  15 May 2009

E. J. Threlfall
Affiliation:
Laboratory of Enteric Pathogens, Central Public Health Laboratory, 61 Colindale Avenue, London NW9 5HT, UK
E. Torre
Affiliation:
Departament Patología i Produccions Animals, Facultat de Veterinaria, Universitat Autónoma de Barcelona, 08193 Bellaterra, Barcelona, Spain
L. R. Ward
Affiliation:
Laboratory of Enteric Pathogens, Central Public Health Laboratory, 61 Colindale Avenue, London NW9 5HT, UK
A. Dávalos-Pérez
Affiliation:
Department of Clinical Research, Hospital Vozandes, Quito, Ecuador
B. Rowe
Affiliation:
Laboratory of Enteric Pathogens, Central Public Health Laboratory, 61 Colindale Avenue, London NW9 5HT, UK
I. Gibert
Affiliation:
Departament de Genética i Microbiología, Universitad Autónoma de Barcelona 08193 Bellaterra, Barcelona, Spain
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When Pst I–generated digests of genomic DNA from each of the type strains of 49 of the Vi phage types of Salmonella typhi were probed with a PCR–amplified IS200 gene probe, all strains were found to possess at least 11 IS200 elements carried on fragments in the range 24.2–1.2 kb. Fourteen fingerprints were identified but two patterns designated IS200Sty1 and IS200Sty2 predominated. In one strain, a plasmid–mediated IS200 element was identified. When IS200 fingerprinting was applied to epidemiologically–unrelated strains of S. typhi isolated in Ecuador, 3 patterns were identified in 10 strains belonging to 9 different phage types. It is concluded that Vi phage typing remains the method of choice for the primary differentiation of S. typhi but that IS200 fingerprinting may be of limited use in laboratories which do not have access to phage typing.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1994

References

REFERENCES

Lam, S, Roth, JR. IS200: a Salmonella–specific insertion sequence. Cell 1993; 34: 951–61.CrossRefGoogle Scholar
Gibert, I, Barbe, J, Casadesus, J. Distribution of insertion sequence IS200 in Salmonella and Shigella. J Gen Microbiol 1990; 136: 2555–60.CrossRefGoogle ScholarPubMed
Gibert, I, Carroll, K, Hillyard, DR, et al. IS200 is not a member of the IS600 family of insertion sequences. Nuc Acids Res 1991; 19: 1343.CrossRefGoogle Scholar
Casedesús, J, Roth, JR. Absence of insertions among spontaneous mutants of Salmonella typhimurium. Mol Gen Genet 1989; 216: 204–9.Google Scholar
Stanley, J, Jones, CS, Threlfall, EJ. Evolutionary lines among Salmonella enteritidis phage types are identified by insertion sequence IS200 distribution. FEMS Microbiol Lett 1991; 82: 8390.CrossRefGoogle Scholar
Stanley, J, Chowdry, N, Powell, N, Threlfall, EJ. Chromosomal genotypes (evolutionary lines) of Salmonella berta. FEMS Microbiol Lett 1992a; 95: 247–52.CrossRefGoogle Scholar
Ezquerra, E, Burnens, AP, Frith, K, et al. Molecular genotype analysis of Salmonella bovismorbificans. Mol Cell Probes 1993; 7: 4554.CrossRefGoogle ScholarPubMed
Stanley, J, Burnens, A, Powell, N, Chowdry, N, Jones, C. The insertion sequence IS200 fingerprints chromosomal genotypes and epidemiological relationships in Salmonella heidelberg. J Gen Microbiol 1992b; 138: 2329–36.CrossRefGoogle ScholarPubMed
Stanley, J, Goldsworthy, M, Threlfall, EJ. Molecular phylogenetic typing of pandemic isolates of Salmonella enteritidis. FEMS Microbiol Lett 1992; 90: 153–60.CrossRefGoogle Scholar
Torre, E, Threlfall, EJ, Hampton, MD, et al. Characterization of Salmonella virchow phage types by plasmid profile and IS200 distribution. J Appl Bact 1993; 75: 435–40.CrossRefGoogle ScholarPubMed
Stanley, J, Baquar, N, Threlfall, EJ. Genotypes and phylogenetic relationships of Salmonella typhimurium are defined by molecular fingerprinting of IS200 and 16S rrn loci. J Gen Microbiol 1993; 139: 133–40.CrossRefGoogle ScholarPubMed
Craigie, J, Felix, A. Typing of typhoid bacilli with Vi bacteriophage: suggestions for its standardisation. Lancet 1947; i: 823–7.CrossRefGoogle Scholar
Ørskov, F, Ørskov, I. Summary of a workshop on the clone concept in epidemiology, taxonomy, and evolution of the Enterobacteriaceae and other bacteria. J Inf Dis 1983; 148: 345–57.CrossRefGoogle ScholarPubMed
Threlfall, EJ, Torre, E, Ward, LR, et al. Insertion sequence IS200 can differentiate drug–resistant and drug–sensitive Salmonella typhi of Vi–phage types E1 and M1. J Med Microbiol 1993; 39: 454–8.CrossRefGoogle ScholarPubMed
Ausubel, FM, Brent, R, Kingston, RE et al. , Preparation of genomic DNA from bacteria. Current protocols in molecular biology, vol 1. USA: John Wiley & Sons, 1987. Suppl 9, Unit 2.4.1–2.4.2.Google Scholar
Soria, G, Gibert, I, Barbe, J. Construccíon y aplicaciones de uns sonda de DNA específicia para Salmonella spp. In: V Congreso de la SEMIC. 1992. Abstr. p. 53. Sociedad Española de Enfermedades Infececciosas y Microbiologí clínica. Barcelona.Google Scholar
Kado, CI, Liu, S-T. Rapid procedure for detection of large and small plasmids. J Bact 1981; 145: 1365–72.CrossRefGoogle ScholarPubMed