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. 1977 Oct;53(5):299–303. doi: 10.1136/sti.53.5.299

Nutritional requirements and penicillin susceptibilities of gonococci from pharyngeal and anogenital sites.

B W Catlin, P J Pace
PMCID: PMC1045426  PMID: 412557

Abstract

Neisseria gonorrhoeae was isolated from 5.9% of oropharyngeal specimens obtained from patients attending a clinic for sexually transmitted diseases. Oropharyngeal isolates from 69 patients and anogenital isolated from 97 other patients attending the same clinic were compared. Many of the gonococci could be differentiated by the compounds required for growth in chemically defined media or by differences in the minimum inhibitory concentration (MIC) of penicillin G. Strains with requirements for either proline (Pro-) or arginine (Arg-) or for none of the compounds that are used for differentiation (zero phenotype) were more common in the oropharynx (91.3% of patients) than in anogenital sites (73.2% of patients). On the other hand, gonococci with multiple requirements that include arginine, hypoxanthine, and uracil (AHU strains) were present in oropharyngeal specimens from only three patients (4.4%), but were isolated from anogenital specimens from 18 patients (18.6%). A high susceptibility to penicillin characterised the AHU strains from all sites, as others have reported. The penicillin MIC ranged from 0.003-0.72 microgram/ml for strains with Pro-, Arg-, and zero phenotypes. However, a penicillin MIC greater than or equal to 0.42 microgram/ml was found for 17.6% of oropharyngeal isolates of these types, but for only 4.1% of Pro-, Arg-, and zero isolates from anogenital sites. None of these moderately resistant strains produced beta-lactamase. Our findings indicate that gonococci differ in their ability to colonise the oropharynx successfully.

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Selected References

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

  1. Bro-Jorgensen A., Jensen T. Gonococcal pharyngeal infections. Report of 110 cases. Br J Vener Dis. 1973 Dec;49(6):491–499. doi: 10.1136/sti.49.6.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brooks G. F., Israel K. S., Petersen B. H. Bactericidal and opsonic activity against Neisseria gonorrhoeae in sera from patients with disseminated gonococcal infection. J Infect Dis. 1976 Nov;134(5):450–462. doi: 10.1093/infdis/134.5.450. [DOI] [PubMed] [Google Scholar]
  3. Carifo K., Catlin B. W. Neisseria gonorrhoeae auxotyping: differentiation of clinical isolates based on growth responses on chemically defined media. Appl Microbiol. 1973 Sep;26(3):223–230. doi: 10.1128/am.26.3.223-230.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. 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]
  5. Eisenstein B. I., Lee T. J., Sparling P. F. Penicillin sensitivity and serum resistance are independent attributes of strains of Neisseria gonorrhoeae causing disseminated gonococcal infection. Infect Immun. 1977 Mar;15(3):834–841. doi: 10.1128/iai.15.3.834-841.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fiumara N. J., Wise H. M., Jr, Many M. Gonorrheal pharyngitis. N Engl J Med. 1967 Jun 1;276(22):1248–1250. doi: 10.1056/NEJM196706012762208. [DOI] [PubMed] [Google Scholar]
  7. Givan K. F., Keyl A. The isolation of Neisseria species from unusual sites. Can Med Assoc J. 1974 Nov 16;111(10):1077–1079. [PMC free article] [PubMed] [Google Scholar]
  8. Hallqvist L., Lindgren S. Gonorrhoea of the throat at a venereological clinic. Incidence and Results of Treatment. Br J Vener Dis. 1975 Dec;51(6):395–397. doi: 10.1136/sti.51.6.395. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Karney W. W., Pedersen A. H., Nelson M., Adams H., Pfeifer R. T., Holmes K. K. Spectinomycin versus tetracycline for the treatment of gonorrhea. N Engl J Med. 1977 Apr 21;296(16):889–894. doi: 10.1056/NEJM197704212961601. [DOI] [PubMed] [Google Scholar]
  10. Knapp J. S., Holmes K. K. Disseminated gonococcal infections caused by Neisseria gonorrhoeae with unique nutritional requirements. J Infect Dis. 1975 Aug;132(2):204–208. doi: 10.1093/infdis/132.2.204. [DOI] [PubMed] [Google Scholar]
  11. McCormack W. M. Treatment of gonorrhea -- is penicillin passé. N Engl J Med. 1977 Apr 21;296(16):934–936. doi: 10.1056/NEJM197704212961610. [DOI] [PubMed] [Google Scholar]
  12. Morello J. A., Lerner S. A., Bohnhoff M. Characteristics of atypical Neisseria gonorrhoeae from disseminated and localized infections. Infect Immun. 1976 May;13(5):1510–1516. doi: 10.1128/iai.13.5.1510-1516.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Odegaard K., Gundersen T. Gonococcal pharyngeal infection. Br J Vener Dis. 1973 Aug;49(4):350–352. doi: 10.1136/sti.49.4.350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Percival A., Rowlands J., Corkill J. E., Alergant C. D., Arya O. P., Rees E., Annels E. H. Penicillinase-producing Gonococci in Liverpool. Lancet. 1976 Dec 25;2(8000):1379–1382. doi: 10.1016/s0140-6736(76)91919-x. [DOI] [PubMed] [Google Scholar]
  15. Schoolnik G. K., Buchanan T. M., Holmes K. K. Gonococci causing disseminated gonococcal infection are resistant to the bactericidal action of normal human sera. J Clin Invest. 1976 Nov;58(5):1163–1173. doi: 10.1172/JCI108569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Wiesner P. J., Tronca E., Bonin P., Pedersen A. H., Holmes K. K. Clinical spectrum of pharyngeal gonococcal infection. N Engl J Med. 1973 Jan 25;288(4):181–185. doi: 10.1056/NEJM197301252880404. [DOI] [PubMed] [Google Scholar]

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