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. 1985 Aug;28(2):176–180. doi: 10.1128/aac.28.2.176

Molecular characterization of chloramphenicol-resistant Haemophilus parainfluenzae and Haemophilus ducreyi.

M C Roberts, L A Actis, J H Crosa
PMCID: PMC180214  PMID: 3879658

Abstract

We examined chloramphenicol-resistant Haemophilus parainfluenzae and Haemophilus ducreyi strains isolated in various parts of the world. The antibiotic resistance determinants were located on conjugative plasmids in H. ducreyi, but were chromosomally located in H. parainfluenzae. Both species produced chloramphenicol acetyltransferases (CATs) that were sensitive to 5,5'-dithiobis(2-nitrobenzoic acid) like the enteric type II and Haemophilus influenzae CAT enzymes, but differed from these enzymes in elution patterns and subunit molecular weight. Southern blot analysis showed the H. parainfluenzae and H. ducreyi CAT genes were molecularly related to the enteric type II class as well as the H. influenzae CAT. Heterogeneity of the physiochemical properties of the CATs was observed; however, the data suggested that all three Haemophilus spp. have a common ancestral source for the CATs.

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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. Albritton W. L., Maclean I. W., Slaney L. A., Ronald A. R., Deneer H. G. Plasmid-mediated tetracycline resistance in Haemophilus ducreyi. Antimicrob Agents Chemother. 1984 Feb;25(2):187–190. doi: 10.1128/aac.25.2.187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bolivar F., Rodriguez R. L., Greene P. J., Betlach M. C., Heyneker H. L., Boyer H. W., Crosa J. H., Falkow S. Construction and characterization of new cloning vehicles. II. A multipurpose cloning system. Gene. 1977;2(2):95–113. [PubMed] [Google Scholar]
  4. Brunton J., Meier M., Ehrman N., Maclean I., Slaney L., Albritton W. L. Molecular epidemiology of beta-lactamase-specifying plasmids of Haemophilus ducreyi. Antimicrob Agents Chemother. 1982 Jun;21(6):857–863. doi: 10.1128/aac.21.6.857. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Crosa J. H., Brenner D. J., Falkow S. Use of a single-strand specific nuclease for analysis of bacterial and plasmid deoxyribonucleic acid homo- and heteroduplexes. J Bacteriol. 1973 Sep;115(3):904–911. doi: 10.1128/jb.115.3.904-911.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Crosa J. H., Luttropp L. K., Falkow S. Molecular cloning of replication and incompatibility regions from the R-plasmid R6K. J Mol Biol. 1978 Sep 25;124(3):443–468. doi: 10.1016/0022-2836(78)90181-x. [DOI] [PubMed] [Google Scholar]
  7. De Graaff J., Elwell L. P., Falkow S. Molecular nature of two beta-lactamase-specifying plasmids isolated from Haemophilus influenzae type b. J Bacteriol. 1976 Apr;126(1):439–446. doi: 10.1128/jb.126.1.439-446.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Elwell L. P., Saunders J. R., Richmond M. H., Falkow S. Relationships among some R plasmids found in Haemophilus influenzae. J Bacteriol. 1977 Jul;131(1):356–362. doi: 10.1128/jb.131.1.356-362.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hartley D. L., Jones K. R., Tobian J. A., LeBlanc D. J., Macrina F. L. Disseminated tetracycline resistance in oral streptococci: implication of a conjugative transposon. Infect Immun. 1984 Jul;45(1):13–17. doi: 10.1128/iai.45.1.13-17.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Jahn G., Laufs R., Kaulfers P. M., Kolenda H. Molecular nature of two Haemophilus influenzae R factors containing resistances and the multiple integration of drug resistance transposons. J Bacteriol. 1979 May;138(2):584–597. doi: 10.1128/jb.138.2.584-597.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kaulfers P. M., Laufs R., Jahn G. Molecular properties of transmissible R factors of Haemophilus influenzae determing tetracycline resistance. J Gen Microbiol. 1978 Apr;105(2):243–252. doi: 10.1099/00221287-105-2-243. [DOI] [PubMed] [Google Scholar]
  12. 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]
  13. Marshall B., Roberts M., Smith A., Levy S. B. Homogeneity of transferable tetracycline-resistance determinants in Haemophilus species. J Infect Dis. 1984 Jun;149(6):1028–1029. doi: 10.1093/infdis/149.6.1028. [DOI] [PubMed] [Google Scholar]
  14. Meyers J. A., Sanchez D., Elwell L. P., Falkow S. Simple agarose gel electrophoretic method for the identification and characterization of plasmid deoxyribonucleic acid. J Bacteriol. 1976 Sep;127(3):1529–1537. doi: 10.1128/jb.127.3.1529-1537.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Packman L. C., Shaw W. V. The use of naturally occurring hybrid variants of chloramphenicol acetyltransferase to investigate subunit contacts. Biochem J. 1981 Feb 1;193(2):541–552. doi: 10.1042/bj1930541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Roberts M. C., Swenson C. D., Owens L. M., Smith A. L. Characterization of chloramphenicol-resistant Haemophilus influenzae. Antimicrob Agents Chemother. 1980 Oct;18(4):610–615. doi: 10.1128/aac.18.4.610. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Roberts M., Corney A., Shaw W. V. Molecular characterization of three chloramphenicol acetyltransferases isolated from Haemophilus influenzae. J Bacteriol. 1982 Aug;151(2):737–741. doi: 10.1128/jb.151.2.737-741.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Roberts M., Stull T. L., Smith A. L. Comparative virulence of Haemophilus influenzae with a type b or type d capsule. Infect Immun. 1981 May;32(2):518–524. doi: 10.1128/iai.32.2.518-524.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Sanson-Le Pors M. J., Casin I. M., Ortenberg M., Perol Y. Detection of chloramphenicol acetyltransferase (CAT) activity in a strain of Haemophilus ducreyi. Ann Microbiol (Paris) 1982 Sep-Oct;133(2):311–315. [PubMed] [Google Scholar]
  20. Shaw W. V., Bouanchaud D. H., Goldstein F. W. Mechanism of transferable resistance to chloramphenicol in Haemophilus parainfluenzae. Antimicrob Agents Chemother. 1978 Feb;13(2):326–330. doi: 10.1128/aac.13.2.326. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Shaw W. V. Chloramphenicol acetyltransferase: enzymology and molecular biology. CRC Crit Rev Biochem. 1983;14(1):1–46. doi: 10.3109/10409238309102789. [DOI] [PubMed] [Google Scholar]
  22. Syriopoulou V. P., Scheifele D. W., Sack C. M., Smith A. L. Effect of inoculum size on the susceptibility of Haemophilus influenzae b to beta-lactam antibiotics. Antimicrob Agents Chemother. 1979 Oct;16(4):510–513. doi: 10.1128/aac.16.4.510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Tait R. C., Rodriguez R. L., West R. W., Jr The rapid purification of T4 DNA ligase from a lambda T4 lig lysogen. J Biol Chem. 1980 Feb 10;255(3):813–815. [PubMed] [Google Scholar]
  24. Totten P. A., Handsfield H. H., Peters D., Holmes K. K., Falkow S. Characterization of ampicillin resistance plasmids from Haemophilus ducreyi. Antimicrob Agents Chemother. 1982 Apr;21(4):622–627. doi: 10.1128/aac.21.4.622. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Van A. D., Goldstein F., Acar J. F., Bouanchaud D. H. A transferable kanamycin resistance plasmid isolated from Haemophilus influenzae. Ann Microbiol (Paris) 1975 Apr;126(3):397–399. [PubMed] [Google Scholar]
  26. Wahl G. M., Stern M., Stark G. R. Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate. Proc Natl Acad Sci U S A. 1979 Aug;76(8):3683–3687. doi: 10.1073/pnas.76.8.3683. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Zaidenzaig Y., Shaw W. V. Affinity and hydrophobic chromatography of three variants of chloramphenicol acetyltransferases specified by R factors in Escherichia coli. FEBS Lett. 1976 Mar 1;62(3):266–271. doi: 10.1016/0014-5793(76)80072-5. [DOI] [PubMed] [Google Scholar]
  28. van Klingeren B., van Embden J. D., Dessens-Kroon M. Plasmid-mediated chloramphenicol resistance in Haemophilus influenzae. Antimicrob Agents Chemother. 1977 Mar;11(3):383–387. doi: 10.1128/aac.11.3.383. [DOI] [PMC free article] [PubMed] [Google Scholar]

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