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Characterization of Neisseria meningitidis isolates by ribosomal RNA gene restriction patterns and restriction endonuclease digestion of chromosomal DNA

Published online by Cambridge University Press:  15 May 2009

J. Z. Jordens
Affiliation:
Department of Medical Microbiology, University of Aberdeen Medical School, Foresterhill, Aberdeen AB9 2ZD, UK
T. H. Pennington
Affiliation:
Department of Medical Microbiology, University of Aberdeen Medical School, Foresterhill, Aberdeen AB9 2ZD, UK
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The use of ribosomal RNA (rRNA) gene restriction patterns to study the molecular epidemiology of Neisseria meningitidis was investigated. Ninety-four isolates of Neisseria meningitidis were characterized by their rRNA gene restriction patterns with 16 + 23 S rRNA from Escherichia coli as a probe. Thirteen rRNA gene restriction patterns were recognized; each of these patterns represented between 1 and 30 isolates. Isolates with the outbreak-associated phenotype B15P1.16 (sulphonamide resistant) all gave a single rRNA gene restriction pattern but this pattern also contained isolates with other phenotypes. Further discrimination between isolates was achieved by comparison of banding patterns resulting from restriction endonuclease digestion of chromosomal DNA with Bgl II. This gave a banding pattern consisting of about ten bands which was simple to interpret. Using this technique 94 isolates were classified in 54 patterns containing between 1 and 14 isolates. Restriction endonuclease analysis with Bgl II characterized outbreak-associated isolates with the phenotype B15P1.16 and enabled strains not typable by conventional methods to be identified as probable outbreak-associated isolates. The techniques should prove useful for epidemiological studies.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1991

References

REFERENCES

1.Duerden, BI, editor. Meningocoecal infection. J Med Microbiol 1988; 26: 161–87.CrossRefGoogle Scholar
2.Cartwright, KAV, Stuart, JM, Noah, ND. An outbreak of meningocoecal disease in Gloucestershire. Lancet 1986; 2: 558–61.CrossRefGoogle ScholarPubMed
3.Crowe, BA, Wall, RA, Kusecek, B, Neumann, B, Olyhoek, T, Abdillahi, H et al. Clonal and variable properties of Neisseria meningitidis isolated from cases and carriers during and after an epidemic in The Gambia, West Africa. J Infect Dis 1989; 159: 686700.CrossRefGoogle ScholarPubMed
4.Moore, PS, Reeves, MW, Schwartz, B, Gellin, BG, Broome, CV. Intercontinental spread of an epidemic group A Neisseria meningitidis strain. Lancet 1989; 2: 260–3.CrossRefGoogle Scholar
5.Achtman, M. Molecular epidemiology of epidemic bacterial meningitis. Rev Med Microbiol 1990; 12: 2938.Google Scholar
6.Owen, RJ. Chromosomal DNA fingerprinting – a new method of species and strain identification applicable to microbial pathogens. J Med Microbiol 1989; 30: 8999.CrossRefGoogle ScholarPubMed
7.Grimont, F, Grimont, PAD. Ribosomal ribonucleic acid gene restriction patterns as potential taxonomic tools. Ann Inst Pasteur Microbiol 1986; 137B: 165–75.CrossRefGoogle ScholarPubMed
8.Thomson-Carter, FM, Carter, PE, Pennington, TH. Differentiation of Staphylococcal species and strains by ribosomal ribonucleic acid gene restriction patterns. J Gen Microbiol 1989: 135: 2093–7.Google Scholar
9.Irino, K, Grimont, F, Casin, I, Grimont, PAD, the Brazilian Purpuric Fever Study Group. rRNA gene restriction patterns of Haemophilus influenzae biogroup aegyptius strains associated with Brazilian purpuric fever. J Clin Microbiol 1988; 26: 1535–8.CrossRefGoogle Scholar
10.Lipuma, JL, Stull, TL, Dasen, SE, Pidcock, KA, Kave, D, Korzeniowski, OM. DNA Polymorphisms among Escherichia coli isolated from bacteriuric women. J Infect Dis 1989; 159: 526–32.CrossRefGoogle ScholarPubMed
11.Owen, RJ, Hernandez, J, Bolton, F. DNA restriction digest and ribosomal RNA gene patterns of Campylobacter jejuni: a comparison with bio-, sero-, and bacteriophage-types of United Kingdom outbreak strains. Epidemiol Infect 1990; 105: 265–75.CrossRefGoogle ScholarPubMed
12.Bjorvatn, B, Lund, V, Kristiansen, B-E, Kornes, L, Spanne, O, Lindqvist, B. Applications of restriction endonuclease fingerprinting of chromosomal DNA of Neisseria meningitidis. J Clin Microbiol 1984; 19: 763–5.CrossRefGoogle ScholarPubMed
13.Kristiansen, B-E, Sorensen, B, Bjorvatn, B, Falk, ES, Fosse, E, Bryn, K et al. An outbreak of group B meningococcal disease: tracing the causative strain of Neisseria meningitidis by DNA fingerprinting. J Clin Microbiol 1986; 23: 764–7.CrossRefGoogle Scholar
14.Pitcher, DG, Saunders, NA, Owen, RJ. Rapid extraction of bacterial genomic DNA with guanidium thiocyanate. Letts Appl Microbiol 1989; 8: 151–6.CrossRefGoogle Scholar
15.Jordens, JZ, Hall, LMC. Chromosomally-encoded gentamicin resistance in ‘epidemic’ methicillin-resistant Staphylococeus aureus: detection with a synthetic oligonucleotide probe. J Antimicrob Chemother 1989; 23: 327–34.CrossRefGoogle Scholar
16.Maniatis, T, Fritsch, EF, Sambrook, J. Molecular cloning. A laboratory manual. New York: Cold Spring Harbor Laboratory, Cold Spring Harbor 1982.Google Scholar
17.Haimanot, RT, Caugant, DA, Fekadu, D, Bjune, G, Belete, B, Froholm, LO et al. Characteristics of serogroup A Neisseria meningitidis responsible for an epidemic in Ethiopia, 1988–89. Scand J Infect Dis 1990; 22: 171–4.CrossRefGoogle ScholarPubMed
18.Mendelman, PM, Caugant, DA, Kalaitzoglou, G, Wedege, E, Chaffin, DO, Campos, J et al. Genetic diversity of penicillin G-resistant Neisseria meningitidis from Spain. Infect Immun 1989; 57: 1025–9.CrossRefGoogle ScholarPubMed
19.Caugant, DA, Bovre, K, Gaustad, P, Bryn, K, Holten, E, Hoiby, EA. et al. Multilocus genotypes determined by enzyme electrophoresis of Neisseria meningitidis isolated from patients with systemic disease and from healthy carriers. J Gen Microbiol 1986; 132: 641–52.Google Scholar
20.Selander, RK, Caugant, DA, Ochman, H, Musser, JM, Gilmour, MN, Whittam, TS. Methods of multilocus enzyme electrophoresis for bacterial population genetics and systematics. Appl Environ Microbiol 1986; 51: 873–84.CrossRefGoogle ScholarPubMed
21.Olyhoek, T, Crowe, BA, Achtman, M. Clonal population structure of Neisseria meningitidis serogroup A isolated from epidemics and pandemics between 1915 and 1983. Rev Infect Dis 1987; 9: 665–92.CrossRefGoogle ScholarPubMed
22.Tinsley, CR, Heckels, JE. Variation in the expression of pili and outer membrane protein by Neisseria meningitidis during the course of meningococcal infection. J Gen Microbiol 1986: 132: 2483–90.Google ScholarPubMed
23.Etienne, J, Renaud, F, Bes, M, Brun, Y, Greenland, TB, Freney, J, Fleurette, J. Instability of characteristics amongst coagulase-negative staphylococci causing endocarditis. J Med Microbiol 1990; 32: 115–22.CrossRefGoogle ScholarPubMed
24.Ogle, JW, Janda, JM, Woods, DE, Vasil, ML. Characterisation and use of a DNA probe as an epidemiological marker for Pseudomonas aeruginosa. J Infect Dis 1987; 155: 119–26.CrossRefGoogle ScholarPubMed
25.Stull, TL, Lipuma, JJ, Edlind, TD. A broad-spectrum probe for molecular epidemiology of bacteria: ribosomal RNA. J Infect Dis 1988; 157: 280–6.CrossRefGoogle ScholarPubMed
26.Bruce, KD, Jordens, JZ. Characterisation of non capsulate Haemophilus influenzae by wholecell polypeptide profiles, restriction endonuclease analysis, and rRNA gene restriction patterns. J Clin Microbiol 1991; 29: 291–6.CrossRefGoogle Scholar
27.Jordens, JZ, Hall, LMC. Characterisation of methicillin-resistant Staphylococcus aureus isolates by restriction endonuclease digestion of chromosomal DNA. J Med Microbiol 1988: 27: 117–23.CrossRefGoogle ScholarPubMed
28.Blackwell, CC, Weir, DM, James, VS et al. Secretor status, smoking and carriage of Neisseria meningitidis. Epidemiol Infect 1990; 104: 203–9.CrossRefGoogle ScholarPubMed