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. 1989 Feb;33(2):235–238. doi: 10.1128/aac.33.2.235

Characterization of a streptomycin-sulfonamide resistance plasmid from Actinobacillus pleuropneumoniae.

P J Willson 1, H G Deneer 1, A Potter 1, W Albritton 1
PMCID: PMC171464  PMID: 2541656

Abstract

An Actinobacillus pleuropneumoniae strain contained a plasmid (pHD8.1) conferring resistance to streptomycin and sulfonamide. Restriction endonuclease mapping and DNA-DNA hybridization showed that pHD8.1 is related to RSF1010 from Salmonella panama, which also confers resistance to streptomycin and sulfonamide, and to pHD148 from Haemophilus ducreyi, which confers resistance only to sulfonamide.

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Selected References

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  1. Albritton W. L., Brunton J. L., Slaney L., MacLean I. Plasmid-mediated sulfonamide resistance in Haemophilus ducreyi. Antimicrob Agents Chemother. 1982 Jan;21(1):159–165. doi: 10.1128/aac.21.1.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Araki Y., Inoue M., Hashimoto H. Characterization and mobilization of nonconjugative plasmids encoding resistance to streptomycin and sulfanilamide. Microbiol Immunol. 1987;31(11):1107–1111. doi: 10.1111/j.1348-0421.1987.tb01342.x. [DOI] [PubMed] [Google Scholar]
  3. Derbyshire K. M., Hatfull G., Willetts N. Mobilization of the non-conjugative plasmid RSF1010: a genetic and DNA sequence analysis of the mobilization region. Mol Gen Genet. 1987 Jan;206(1):161–168. doi: 10.1007/BF00326552. [DOI] [PubMed] [Google Scholar]
  4. Haring V., Scholz P., Scherzinger E., Frey J., Derbyshire K., Hatfull G., Willetts N. S., Bagdasarian M. Protein RepC is involved in copy number control of the broad host range plasmid RSF1010. Proc Natl Acad Sci U S A. 1985 Sep;82(18):6090–6094. doi: 10.1073/pnas.82.18.6090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hirsh D. C., Martin L. D., Libal M. C. Plasmid-mediated antimicrobial resistance in Haemophilus pleuropneumoniae. Am J Vet Res. 1982 Feb;43(2):269–272. [PubMed] [Google Scholar]
  6. Lax A. J., Walker C. A. Plasmids related to RSF1010 from Bordetella bronchiseptica. Plasmid. 1986 May;15(3):210–216. doi: 10.1016/0147-619x(86)90039-9. [DOI] [PubMed] [Google Scholar]
  7. Meyer R. J., Lin L. S., Kim K., Brasch M. A. Broad host-range plasmid R1162: replication, incompatibility, and copy-number control. Basic Life Sci. 1985;30:173–188. doi: 10.1007/978-1-4613-2447-8_16. [DOI] [PubMed] [Google Scholar]
  8. Persson C., Nordström K. Control of replication of the broad host range plasmid RSF1010: the incompatibility determinant consists of directly repeated DNA sequences. Mol Gen Genet. 1986 Apr;203(1):189–192. doi: 10.1007/BF00330402. [DOI] [PubMed] [Google Scholar]
  9. Phillips I., Shannon K. Aminoglycoside resistance. Br Med Bull. 1984 Jan;40(1):28–35. doi: 10.1093/oxfordjournals.bmb.a071943. [DOI] [PubMed] [Google Scholar]
  10. Reed K. C., Mann D. A. Rapid transfer of DNA from agarose gels to nylon membranes. Nucleic Acids Res. 1985 Oct 25;13(20):7207–7221. doi: 10.1093/nar/13.20.7207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Rotger R., Rubio F., Nombela C. A multi-resistance plasmid isolated from commensal Neisseria species is closely related to the enterobacterial plasmid RSF1010. J Gen Microbiol. 1986 Sep;132(9):2491–2496. doi: 10.1099/00221287-132-9-2491. [DOI] [PubMed] [Google Scholar]
  12. Scholz P., Haring V., Scherzinger E., Lurz R., Bagdasarian M. M., Schuster H., Bagdasarian M. Replication determinants of the broad host-range plasmid RSF1010. Basic Life Sci. 1985;30:243–259. doi: 10.1007/978-1-4613-2447-8_20. [DOI] [PubMed] [Google Scholar]
  13. Sebunya T. N., Saunders J. R. Haemophilus pleuropneumoniae infection in swine: a review. J Am Vet Med Assoc. 1983 Jun 15;182(12):1331–1337. [PubMed] [Google Scholar]
  14. Sebunya T. N., Saunders J. R., Osborne A. D. A model aerosol exposure system for induction of porcine Haemophilus pleuropneumonia. Can J Comp Med. 1983 Jan;47(1):48–53. [PMC free article] [PubMed] [Google Scholar]
  15. Swedberg G. Organization of two sulfonamide resistance genes on plasmids of gram-negative bacteria. Antimicrob Agents Chemother. 1987 Feb;31(2):306–311. doi: 10.1128/aac.31.2.306. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Wiedemann B. Mechanisms of antibiotic resistance and their dissemination of resistance genes in the hospital environment. Infect Control. 1983 Nov-Dec;4(6):444–447. doi: 10.1017/s0195941700058434. [DOI] [PubMed] [Google Scholar]
  17. Willson P. J., Falk G., Klashinsky S. Detection of Actinobacillus pleuropneumoniae Infection in Pigs. Can Vet J. 1987 Mar;28(3):111–116. [PMC free article] [PubMed] [Google Scholar]
  18. Willson P. J., Osborne A. D. Comparison of common antibiotic therapies for haemophilus pleuropneumonia in pigs. Can Vet J. 1985 Oct;26(10):312–316. [PMC free article] [PubMed] [Google Scholar]
  19. Wilson M. R., Takov R., Friendship R. M., Martin S. W., McMillan I., Hacker R. R., Swaminathan S. Prevalence of respiratory diseases and their association with growth rate and space in randomly selected swine herds. Can J Vet Res. 1986 Apr;50(2):209–216. [PMC free article] [PubMed] [Google Scholar]
  20. van Treeck U., Schmidt F., Wiedemann B. Molecular nature of a streptomycin and sulfonamide resistance plasmid (pBP1) prevalent in clinical Escherichia coli strains and integration of an ampicillin resistance transposon (TnA). Antimicrob Agents Chemother. 1981 Mar;19(3):371–380. doi: 10.1128/aac.19.3.371. [DOI] [PMC free article] [PubMed] [Google Scholar]

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