Skip to main content
Genitourinary Medicine logoLink to Genitourinary Medicine
. 1995 Apr;71(2):126–128. doi: 10.1136/sti.71.2.126

A case cluster of possible tissue invasive gonorrhoea.

M G Brook 1, S Clark 1, A Stirland 1, M C Kelsey 1, E W Paice 1, P D Kell 1, W A Atia 1
PMCID: PMC1195469  PMID: 7744403

Abstract

OBJECTIVE--To describe a cluster of patients presenting with severe symptoms and infected with an unusual strain of Neisseria gonorrhoeae. SETTING--A north London Department of Sexual Health. PATIENTS--Five patients were linked by reported sexual contact or other epidemiological evidence as part of a cluster of gonococcal infection. Cultured N gonorrhoea were subtyped by serological (serovar) and cultural (auxotype) methods and antibiotic sensitivities measured by minimum inhibitory concentration (MIC). RESULTS--Four of the patients had severe gonorrhoea-related systemic or extragenital symptoms: disseminated gonococcal infection with oligoarthritis (1 patient), acute pelvic inflammatory disease (1 patient, who was also chlamydia positive) and tender inguinal adenopathy (2 patients). The fifth patient was asymptomatic. N gonorrhoeae was isolated in four of the patients. All four organisms had identical MICs. Three of the organisms were subtyped and found to be the same rare strain (serovar 1A1, auxotype NR). CONCLUSION--This case cluster provides evidence for strain-related virulence in an uncommon gonococcal subtype.

Full text

PDF
126

Selected References

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

  1. Akers W. A. Tender inguinal lymph nodes and gonococcal urethritis. Mil Med. 1972 Mar;137(3):107–108. [PubMed] [Google Scholar]
  2. Crawford C., Knapp J. S., Hale J., Holmes K. K. Asymptomatic gonorrhea in men: caused by gonococci with unique nutritional requirements. Science. 1977 Jun 17;196(4296):1352–1353. doi: 10.1126/science.405742. [DOI] [PubMed] [Google Scholar]
  3. Knapp J. S., Holmes K. K., Bonin P., Hook E. W., 3rd Epidemiology of gonorrhea: distribution and temporal changes in auxotype/serovar classes of Neisseria gonorrhoeae. Sex Transm Dis. 1987 Jan-Mar;14(1):26–32. [PubMed] [Google Scholar]
  4. Morello J. A., Bohnhoff M. Serovars and serum resistance of Neisseria gonorrhoeae from disseminated and uncomplicated infections. J Infect Dis. 1989 Dec;160(6):1012–1017. doi: 10.1093/infdis/160.6.1012. [DOI] [PubMed] [Google Scholar]
  5. Plummer F. A., Simonsen J. N., Chubb H., Slaney L., Kimata J., Bosire M., Ndinya-Achola J. O., Ngugi E. N. Epidemiologic evidence for the development of serovar-specific immunity after gonococcal infection. J Clin Invest. 1989 May;83(5):1472–1476. doi: 10.1172/JCI114040. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ross J. D., Wardropper A., Sprott M., Moyes A., Young H. Gonococcal infection in Edinburgh and Newcastle: serovar prevalence in relation to clinical features and sexual orientation. Genitourin Med. 1994 Feb;70(1):35–39. doi: 10.1136/sti.70.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Tapsall J. W., Phillips E. A., Shultz T. R., Way B., Withnall K. Strain characteristics and antibiotic susceptibility of isolates of Neisseria gonorrhoeae causing disseminated gonococcal infection in Australia. Members of the Australian Gonococcal Surveillance Programme. Int J STD AIDS. 1992 Jul-Aug;3(4):273–277. doi: 10.1177/095646249200300408. [DOI] [PubMed] [Google Scholar]

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

RESOURCES