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Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1994 Feb;32(2):377–383. doi: 10.1128/jcm.32.2.377-383.1994

Correlation between antibiotic resistance, phage-like particle presence, and virulence in Rhodococcus equi human isolates.

P Nordmann 1, M Keller 1, F Espinasse 1, E Ronco 1
PMCID: PMC263039  PMID: 8150945

Abstract

Rhodococcus equi is a gram-positive coccobacillus that appears to be emerging as a pulmonary pathogen in AIDS patients. In four human clinical isolates, two antibiotic resistance phenotypes were found to coexist: one beta-lactam resistant and the other beta-lactam susceptible. In vitro, beta-lactam-resistant mutants were obtained at a frequency of 1 x 10(-5) to 5 x 10(-5) from beta-lactam-susceptible strains on cephalothin-containing plates. Neither beta-lactamase nor plasmid DNA was detected in beta-lactam-resistant or -susceptible strains. The penicillin-binding protein patterns for the two types of strains were identical. Electron microscopy revealed that the beta-lactam-resistant strains possessed cell-surface-associated appendages and produced phage-like particles. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of total cell protein showed at least three additional bands of 42, 39, and 30 kDa found only in the beta-lactam-resistant strains. Testing for virulence in Swiss mice revealed that (i) phage-like-particle-producing strains had lower 50% lethal doses when injected intravenously in euthymic and nude mice than the non-phage-like-particle-producing strains did and (ii) intravenous inoculation of a sublethal dose (5 x 10(6) CFU) in nude mice led to chronic infection by the phage-like-particle-producing bacteria only. Finally, in vitro growth curves indicated that the phage-like-particle-producing strains possessed an ecological selection advantage. These results suggest that, among R. equi human isolates, the antibiotic resistance phenotype is associated with virulence and may be phage mediated.

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Selected References

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  1. Barondess J. J., Beckwith J. A bacterial virulence determinant encoded by lysogenic coliphage lambda. Nature. 1990 Aug 30;346(6287):871–874. doi: 10.1038/346871a0. [DOI] [PubMed] [Google Scholar]
  2. Classification and nomenclature of viruses. Fourth report of the International Committee on Taxonomy of Viruses. Intervirology. 1982;17(1-3):1–199. doi: 10.1159/000149278. [DOI] [PubMed] [Google Scholar]
  3. Desomer J., Vereecke D., Crespi M., Van Montagu M. The plasmid-encoded chloramphenicol-resistance protein of Rhodococcus fascians is homologous to the transmembrane tetracycline efflux proteins. Mol Microbiol. 1992 Aug;6(16):2377–2385. doi: 10.1111/j.1365-2958.1992.tb01412.x. [DOI] [PubMed] [Google Scholar]
  4. Edlin G., Lin L., Bitner R. Reproductive fitness of P1, P2, and Mu lysogens of Escherichia coli. J Virol. 1977 Feb;21(2):560–564. doi: 10.1128/jvi.21.2.560-564.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Edlin G., Lin L., Kudrna R. Lambda lysogens of E. coli reproduce more rapidly than non-lysogens. Nature. 1975 Jun 26;255(5511):735–737. doi: 10.1038/255735a0. [DOI] [PubMed] [Google Scholar]
  6. Emmons W., Reichwein B., Winslow D. L. Rhodococcus equi infection in the patient with AIDS: literature review and report of an unusual case. Rev Infect Dis. 1991 Jan-Feb;13(1):91–96. doi: 10.1093/clinids/13.1.91. [DOI] [PubMed] [Google Scholar]
  7. Goodfellow M. The taxonomic status of Rhodococcus equi. Vet Microbiol. 1987 Aug;14(3):205–209. doi: 10.1016/0378-1135(87)90106-4. [DOI] [PubMed] [Google Scholar]
  8. Gotoh K., Mitsuyama M., Imaizumi S., Kawamura I., Yano I. Mycolic acid-containing glycolipid as a possible virulence factor of Rhodococcus equi for mice. Microbiol Immunol. 1991;35(3):175–185. doi: 10.1111/j.1348-0421.1991.tb01546.x. [DOI] [PubMed] [Google Scholar]
  9. Harvey R. L., Sunstrum J. C. Rhodococcus equi infection in patients with and without human immunodeficiency virus infection. Rev Infect Dis. 1991 Jan-Feb;13(1):139–145. doi: 10.1093/clinids/13.1.139. [DOI] [PubMed] [Google Scholar]
  10. Hiddema R., Curran M. D., Ferreira N. P., Coetzee J. N., Lecatsas G. Characterization of phages derived from strains of Rhodococcus australis and R. equii. Intervirology. 1985;23(2):109–111. doi: 10.1159/000149592. [DOI] [PubMed] [Google Scholar]
  11. Hietala S. K., Ardans A. A. Interaction of Rhodococcus equi with phagocytic cells from R. equi-exposed and non-exposed foals. Vet Microbiol. 1987 Aug;14(3):307–320. doi: 10.1016/0378-1135(87)90118-0. [DOI] [PubMed] [Google Scholar]
  12. Kanaly S. T., Hines S. A., Palmer G. H. Failure of pulmonary clearance of Rhodococcus equi infection in CD4+ T-lymphocyte-deficient transgenic mice. Infect Immun. 1993 Nov;61(11):4929–4932. doi: 10.1128/iai.61.11.4929-4932.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  14. Lin L., Bitner R., Edlin G. Increased reproductive fitness of Escherichia coli lambda lysogens. J Virol. 1977 Feb;21(2):554–559. doi: 10.1128/jvi.21.2.554-559.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Nordmann P., Kerestedjian J. J., Ronco E. Therapy of Rhodococcus equi disseminated infections in nude mice. Antimicrob Agents Chemother. 1992 Jun;36(6):1244–1248. doi: 10.1128/aac.36.6.1244. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Nordmann P., Nicolas M. H., Gutmann L. Penicillin-binding proteins of Rhodococcus equi: potential role in resistance to imipenem. Antimicrob Agents Chemother. 1993 Jul;37(7):1406–1409. doi: 10.1128/aac.37.7.1406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Nordmann P., Ronco E. In-vitro antimicrobial susceptibility of Rhodococcus equi. J Antimicrob Chemother. 1992 Apr;29(4):383–393. doi: 10.1093/jac/29.4.383. [DOI] [PubMed] [Google Scholar]
  18. Nordmann P., Ronco E., Nauciel C. Role of T-lymphocyte subsets in Rhodococcus equi infection. Infect Immun. 1992 Jul;60(7):2748–2752. doi: 10.1128/iai.60.7.2748-2752.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nordmann P., Rouveix E., Guenounou M., Nicolas M. H. Pulmonary abscess due to a rifampin and fluoroquinolone resistant Rhodococcus equi strain in a HIV infected patient. Eur J Clin Microbiol Infect Dis. 1992 Jun;11(6):557–558. doi: 10.1007/BF01960815. [DOI] [PubMed] [Google Scholar]
  20. Prescott J. F. Rhodococcus equi: an animal and human pathogen. Clin Microbiol Rev. 1991 Jan;4(1):20–34. doi: 10.1128/cmr.4.1.20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Samies J. H., Hathaway B. N., Echols R. M., Veazey J. M., Jr, Pilon V. A. Lung abscess due to Corynebacterium equi. Report of the first case in a patient with acquired immune deficiency syndrome. Am J Med. 1986 Apr;80(4):685–688. doi: 10.1016/0002-9343(86)90825-9. [DOI] [PubMed] [Google Scholar]
  22. Seeberg A. H., Tolxdorff-Neutzling R. M., Wiedemann B. Chromosomal beta-lactamases of Enterobacter cloacae are responsible for resistance to third-generation cephalosporins. Antimicrob Agents Chemother. 1983 Jun;23(6):918–925. doi: 10.1128/aac.23.6.918. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Takai S., Iie M., Watanabe Y., Tsubaki S., Sekizaki T. Virulence-associated 15- to 17-kilodalton antigens in Rhodococcus equi: temperature-dependent expression and location of the antigens. Infect Immun. 1992 Jul;60(7):2995–2997. doi: 10.1128/iai.60.7.2995-2997.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Takai S., Koike K., Ohbushi S., Izumi C., Tsubaki S. Identification of 15- to 17-kilodalton antigens associated with virulent Rhodococcus equi. J Clin Microbiol. 1991 Mar;29(3):439–443. doi: 10.1128/jcm.29.3.439-443.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Takai S., Michizoe T., Matsumura K., Nagai M., Sato H., Tsubaki S. Correlation of in vitro properties of Rhodococcus (Corynebacterium) equi with virulence for mice. Microbiol Immunol. 1985;29(12):1175–1184. doi: 10.1111/j.1348-0421.1985.tb00907.x. [DOI] [PubMed] [Google Scholar]
  26. Takai S., Sekizaki T., Ozawa T., Sugawara T., Watanabe Y., Tsubaki S. Association between a large plasmid and 15- to 17-kilodalton antigens in virulent Rhodococcus equi. Infect Immun. 1991 Nov;59(11):4056–4060. doi: 10.1128/iai.59.11.4056-4060.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Tkachuk-Saad O., Prescott J. Rhodococcus equi plasmids: isolation and partial characterization. J Clin Microbiol. 1991 Dec;29(12):2696–2700. doi: 10.1128/jcm.29.12.2696-2700.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Trias J., Jarlier V., Benz R. Porins in the cell wall of mycobacteria. Science. 1992 Nov 27;258(5087):1479–1481. doi: 10.1126/science.1279810. [DOI] [PubMed] [Google Scholar]
  29. Van Etta L. L., Filice G. A., Ferguson R. M., Gerding D. N. Corynebacterium equi: a review of 12 cases of human infection. Rev Infect Dis. 1983 Nov-Dec;5(6):1012–1018. doi: 10.1093/clinids/5.6.1012. [DOI] [PubMed] [Google Scholar]
  30. Wurtz M., Kistler J., Hohn T. Surface structure of in vitro assembled bacteriophage lambda polyheads. J Mol Biol. 1976 Feb 15;101(1):39–56. doi: 10.1016/0022-2836(76)90065-6. [DOI] [PubMed] [Google Scholar]
  31. Yanagawa R., Honda E. Presence of pili in species of human and animal parasites and pathogens of the genuscorynebacterium. Infect Immun. 1976 Apr;13(4):1293–1295. doi: 10.1128/iai.13.4.1293-1295.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]

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