Skip to main content
Genitourinary Medicine logoLink to Genitourinary Medicine
. 1989 Jun;65(3):171–176. doi: 10.1136/sti.65.3.171

Serological classification in relation to auxotypes, plasmid contents, and susceptibilities to antimicrobials of PPNG and non-PPNG strains isolated in Greece.

G Tzanakaki 1, L Mavrommati 1, E Tzelepi 1, S Kolyva 1, E Fragouli 1
PMCID: PMC1194326  PMID: 2503435

Abstract

Thirty three penicillinase producing Neisseria gonorrhoeae (PPNG) and 152 non-PPNG strains were serologically classified in relation to their patterns of resistance to antimicrobials, nutritional requirements (auxotypes), and plasmid contents. Of the 185 strains, 65 (35%) belonged to the WI and 120 (65%) to the WII/III serogroup, the predominant serovars of which were Arost and Bropt, respectively. Associations between serotype and susceptibility to antimicrobial agents, auxotype, and plasmid content were observed. Of the 152 non-PPNG strains, 112 (74%) belonged to serogroup WI. The WI non-PPNG strains were more sensitive to penicillin, thiamphenicol, tetracycline, and cefotaxime than the WII/III non-PPNG strains. Auxotyping and serogrouping the strains showed no differentiation other than that arginine, hypoxanthine, and uracil dependent (AHU-) strains belonged to serogroup WI. The proline, citrulline, and uracil dependent (PCU-) strains belonged, as expected, to serogroup WII/III. Analysing the 33 PPNG strains showed that of 21 carrying the 4.5 megadalton (Asian type) penicillin resistance plasmid, 17 (81%) belonged to serogroup WI, with serovar Arst predominating, and only four (19%) to serogroup WII/III. Of 11 isolates carrying the 3.2 megadalton (African type) resistance plasmid, seven (64%) belonged to serogroup WI (serovar Av predominating) and four (36%) to WII/III (with serovar Bropyst predominating). One strain carried the 3.05 megadalton penicillin resistance plasmid (Toronto type), belonged to the WI serogroup, and had serovar Arost.

Full text

PDF

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ambrosino D. M., Landesman S. H., Gorham C. C., Siber G. R. Passive immunization against disease due to Haemophilus influenzae type b: concentrations of antibody to capsular polysaccharide in high-risk children. J Infect Dis. 1986 Jan;153(1):1–7. doi: 10.1093/infdis/153.1.1. [DOI] [PubMed] [Google Scholar]
  2. Brunham R. C., Plummer F., Slaney L., Rand F., DeWitt W. Correlation of auxotype and protein I type with expression of disease due to Neisseria gonorrhoeae. J Infect Dis. 1985 Aug;152(2):339–343. doi: 10.1093/infdis/152.2.339. [DOI] [PubMed] [Google Scholar]
  3. Bygdeman S. M., Mårdh P. A., Sandström E. G. Susceptibility of Neisseria gonorrhoeae to rifampicin and thiamphenicol: correlation with protein I antigenic determinants. Sex Transm Dis. 1984 Oct-Dec;11(4 Suppl):366–370. doi: 10.1097/00007435-198410001-00012. [DOI] [PubMed] [Google Scholar]
  4. Bygdeman S., Danielsson D., Sandström E. Gonococcal W serogroups in Scandinavia. A study with polyclonal and monoclonal antibodies. Acta Pathol Microbiol Immunol Scand B. 1983 Oct;91(5):293–305. [PubMed] [Google Scholar]
  5. Catlin B. W. Nutritional profiles of Neisseria gonorrhoeae, Neisseria meningitidis, and Neisseria lactamica in chemically defined media and the use of growth requirements for gonococcal typing. J Infect Dis. 1973 Aug;128(2):178–194. doi: 10.1093/infdis/128.2.178. [DOI] [PubMed] [Google Scholar]
  6. Danielsson D., Bygdeman S., Kallings I. Epidemiology of gonorrhoea: serogroup, antibiotic susceptibility and auxotype patterns of consecutive gonococcal isolates from ten different areas of Sweden. Scand J Infect Dis. 1983;15(1):33–42. doi: 10.3109/inf.1983.15.issue-1.07. [DOI] [PubMed] [Google Scholar]
  7. Dillon J. R., Bygdeman S. M., Sandström E. G. Serological ecology of Neisseria gonorrhoeae (PPNG and non-PPNG) strains: Canadian perspective. Genitourin Med. 1987 Jun;63(3):160–168. doi: 10.1136/sti.63.3.160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Dillon J. R., Carballo M., King S. D., Brathwaite A. R. Auxotypes, plasmid contents, and serovars of gonococcal strains (PPNG and non-PPNG) from Jamaica. Genitourin Med. 1987 Aug;63(4):233–238. doi: 10.1136/sti.63.4.233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dillon J. R., Pauzé M., Gould R., Sutherland R., Romanowski B. Penicillinase-producing Neisseria gonorrhoeae with pro- orn-, WI, Asia+ phenotype. Lancet. 1986 Jan 11;1(8472):103–104. doi: 10.1016/s0140-6736(86)90758-0. [DOI] [PubMed] [Google Scholar]
  10. Dillon J. R., Pauzé M. Introductory address: resistance to antimicrobial agents. What next for Neisseria gonorrhoeae? Sex Transm Dis. 1984 Oct-Dec;11(4 Suppl):353–359. [PubMed] [Google Scholar]
  11. Easmon C. S. Gonococcal resistance to antibiotics. J Antimicrob Chemother. 1985 Oct;16(4):409–412. doi: 10.1093/jac/16.4.409. [DOI] [PubMed] [Google Scholar]
  12. Handsfield H. H., Sandström E. G., Knapp J. S., Perine P. L., Whittington W. L., Sayers D. E., Holmes K. K. Epidemiology of penicillinase-producing Neisseria gonorrhoeae infections: analysis by auxotyping and serogrouping. N Engl J Med. 1982 Apr 22;306(16):950–954. doi: 10.1056/NEJM198204223061602. [DOI] [PubMed] [Google Scholar]
  13. Hendry A. T., Stewart I. O. Auxanographic grouping and typing of Neisseria gonorrhoeae. Can J Microbiol. 1979 Apr;25(4):512–521. doi: 10.1139/m79-075. [DOI] [PubMed] [Google Scholar]
  14. Knapp J. S., Tam M. R., Nowinski R. C., Holmes K. K., Sandström E. G. Serological classification of Neisseria gonorrhoeae with use of monoclonal antibodies to gonococcal outer membrane protein I. J Infect Dis. 1984 Jul;150(1):44–48. doi: 10.1093/infdis/150.1.44. [DOI] [PubMed] [Google Scholar]
  15. Odugbemi T. O., Brown S. T., Biddle J., Johnson S., Perkins G., DeWitt W., Albritton W. L. Plasmid profile, serogrouping, and auxotyping of Neisseria gonorrhoeae isolates from Africa. Br J Vener Dis. 1983 Feb;59(1):41–43. doi: 10.1136/sti.59.1.41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Odugbemi T. O., Whittington W. L., DeWitt W., Perkins G., Johnson S., Biddle J., Piziak M., Albritton W. L. Epidemiological characterisation of Neisseria gonorrhoeae isolates from the Far East. Br J Vener Dis. 1983 Oct;59(5):285–288. doi: 10.1136/sti.59.5.285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Portnoy D. A., Moseley S. L., Falkow S. Characterization of plasmids and plasmid-associated determinants of Yersinia enterocolitica pathogenesis. Infect Immun. 1981 Feb;31(2):775–782. doi: 10.1128/iai.31.2.775-782.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Ramstedt K. M., Hallhagen G. J., Bygdeman S. M., Lincoln K. A., Kallings I., Gillenius C., Sandström E. G. Serologic classification and contact-tracing in the control of microepidemics of beta-lactamase-producing Neisseria gonorrhoeae. Sex Transm Dis. 1985 Oct-Dec;12(4):209–214. doi: 10.1097/00007435-198510000-00008. [DOI] [PubMed] [Google Scholar]
  19. Riou J. Y., Guibourdenche M., Courvalin P. Antibiotic susceptibility testing of Neisseria gonorrhoeae by disk-agar diffusion. Ann Microbiol (Paris) 1981 Jul-Aug;132B(1):23–39. [PubMed] [Google Scholar]
  20. Riou J. Y., Lind I., Guibourdenche M. Antibiotic susceptibility of 83 penicillinase-producing Neisseria gonorrhoeae strains isolated in France (May 1979-April 1983). J Antimicrob Chemother. 1985 Jul;16 (Suppl A):209–212. doi: 10.1093/jac/16.suppl_a.209. [DOI] [PubMed] [Google Scholar]
  21. Sandström E. G., Knapp J. S., Reller L. B., Thompson S. E., Hook E. W., 3rd, Holmes K. K. Serogrouping of Neisseria gonorrhoeae: correlation of serogroup with disseminated gonococcal infection. Sex Transm Dis. 1984 Apr-Jun;11(2):77–80. doi: 10.1097/00007435-198404000-00005. [DOI] [PubMed] [Google Scholar]
  22. Yvert F., Frost E., Guibourdenche M., Riou J. Y., Ivanoff B. Auxotypes and serogroups of penicillinase producing and non-producing strains of Neisseria gonorrhoeae isolated in Franceville, Gabon. Genitourin Med. 1985 Apr;61(2):99–102. doi: 10.1136/sti.61.2.99. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genitourinary Medicine are provided here courtesy of BMJ Publishing Group

RESOURCES