Skip to main content
Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 1990 Nov;34(11):2269–2272. doi: 10.1128/aac.34.11.2269

Neisseria lactamica and Neisseria polysaccharea as possible sources of meningococcal beta-lactam resistance by genetic transformation.

J A Saez-Nieto 1, R Lujan 1, J V Martinez-Suarez 1, S Berron 1, J A Vazquez 1, M Viñas 1, J Campos 1
PMCID: PMC172037  PMID: 2127349

Abstract

We studied the susceptibilities of relatively penicillin G-resistant and -susceptible strains of Neisseria meningitidis, as well as Neisseria lactamica and Neisseria polysaccharea, to penicillin, ampicillin, and several cephalosporins. The MICs of penicillin, ampicillin, cephalothin, and cefuroxime for moderately resistant meningococci have increased two- to sixfold in relation to MICs for susceptible strains. For these strains of meningococci, N. lactamica, and N. polysaccharea, penicillin, ampicillin, cephalothin, and cefuroxime MICs for 50 and 90% of strains were similar. By genetic transformation of a penicillin-susceptible strain of N. meningitidis to low-level penicillin resistance with DNA from penicillin-resistant strains of N. meningitidis, N. lactamica, N. polysaccharea, and N. gonorrhoeae, isogenic strains with the same pattern of resistance to beta-lactams were obtained, suggesting that these commensal Neisseria spp. could be the source of meningococcal resistance genes.

Full text

PDF
2269

Selected References

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

  1. Biswas G. D., Sox T., Blackman E., Sparling P. F. Factors affecting genetic transformation of Neisseria gonorrhoeae. J Bacteriol. 1977 Feb;129(2):983–992. doi: 10.1128/jb.129.2.983-992.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Boquete M. T., Marcos C., Sáez-Nieto J. A. Characterization of Neisseria polysacchareae sp. nov. (Riou, 1983) in previously identified noncapsular strains of Neisseria meningitidis. J Clin Microbiol. 1986 May;23(5):973–975. doi: 10.1128/jcm.23.5.973-975.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Botha P. Penicillin-resistant Neisseria meningitidis in southern Africa. Lancet. 1988 Jan 2;1(8575-6):54–54. doi: 10.1016/s0140-6736(88)91029-x. [DOI] [PubMed] [Google Scholar]
  4. Campos J., Mendelman P. M., Sako M. U., Chaffin D. O., Smith A. L., Sáez-Nieto J. A. Detection of relatively penicillin G-resistant Neisseria meningitidis by disk susceptibility testing. Antimicrob Agents Chemother. 1987 Oct;31(10):1478–1482. doi: 10.1128/aac.31.10.1478. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cherubin C. E., Eng R. H., Norrby R., Modai J., Humbert G., Overturf G. Penetration of newer cephalosporins into cerebrospinal fluid. Rev Infect Dis. 1989 Jul-Aug;11(4):526–548. doi: 10.1093/clinids/11.4.526. [DOI] [PubMed] [Google Scholar]
  6. Dougherty T. J., Asmus A., Tomasz A. Specificity of DNA uptake in genetic transformation of gonococci. Biochem Biophys Res Commun. 1979 Jan 15;86(1):97–104. doi: 10.1016/0006-291x(79)90386-3. [DOI] [PubMed] [Google Scholar]
  7. Fontanals D., Pineda V., Pons I., Rojo J. C. Penicillin-resistant beta-lactamase producing Neisseria meningitidis in Spain. Eur J Clin Microbiol Infect Dis. 1989 Jan;8(1):90–91. doi: 10.1007/BF01964130. [DOI] [PubMed] [Google Scholar]
  8. Pérez Trallero E., Garcia Arenzana J. M., Ayestaran I., Muñoz Baroja I. Comparative activity in vitro of 16 antimicrobial agents against penicillin-susceptible meningococci and meningococci with diminished susceptibility to penicillin. Antimicrob Agents Chemother. 1989 Sep;33(9):1622–1623. doi: 10.1128/aac.33.9.1622. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Saez-Nieto J. A., Dominguez J. R., Monton J. L., Cristobal P., Fenoll A., Vazquez J., Casal J., Taracena B. Carriage of Neisseria meningitidis and Neisseria lactamica in a school population during an epidemic period in Spain. J Hyg (Lond) 1985 Jun;94(3):279–288. doi: 10.1017/s0022172400061507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Sparling P. F., Sarubbi F. A., Jr, Blackman E. Inheritance of low-level resistance to penicillin, tetracycline, and chloramphenicol in Neisseria gonorrhoeae. J Bacteriol. 1975 Nov;124(2):740–749. doi: 10.1128/jb.124.2.740-749.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Spratt B. G., Zhang Q. Y., Jones D. M., Hutchison A., Brannigan J. A., Dowson C. G. Recruitment of a penicillin-binding protein gene from Neisseria flavescens during the emergence of penicillin resistance in Neisseria meningitidis. Proc Natl Acad Sci U S A. 1989 Nov;86(22):8988–8992. doi: 10.1073/pnas.86.22.8988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Sutcliffe E. M., Jones D. M., el-Sheikh S., Percival A. Penicillin-insensitive meningococci in the UK. Lancet. 1988 Mar 19;1(8586):657–658. doi: 10.1016/s0140-6736(88)91469-9. [DOI] [PubMed] [Google Scholar]
  13. Sáez-Nieto J. A., Fontanals D., Garcia de Jalon J., Martinez de Artola V., Peña P., Morera M. A., Verdaguer R., Sanfeliu I., Belio-Blasco C., Perez-Saenz J. L. Isolation of Neisseria meningitidis strains with increase of penicillin minimal inhibitory concentrations. Epidemiol Infect. 1987 Oct;99(2):463–469. doi: 10.1017/s0950268800067960. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Antimicrobial Agents and Chemotherapy are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES