Abstract
Clostridium perfringens is an anerobic microorganism that forms heat-resistant endospores in the gastrointestinal tract but does not sporulate in most routine culture media. In rich media it grows rapidly and ferments sugars to produce H2 and CO2, the evolution of which helps to maintain an anerobic environment. The organism is aerotolerant; it is capable of surviving for extended periods of time in the presence of O2. C. perfringens is of considerable clinical significance as the causative agent of human clostridial myonecrosis (gas gangrene), food poisoning, necrotic enteritis, and a variety of gastrointestinal diseases in domestic animals. The majority of these syndromes are mediated via the production of extracellular protein toxins (Hatheway, 1990).
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References
Abraham, L.J. 1986. Molecular genetics of antibiotic resistance determinants from Clostridium perfringens. Ph.D. thesis, Murdoch University, Perth, Australia.
Abraham, L.J. and J.I. Rood. 1985a. Molecular analysis of transferable tetracycline resistance plasmids from Clostridium perfringens. J. Bacteriol. 161:636–640.
Abraham, L.J. and J.I. Rood. 1985b. Cloning and analysis of the Clostridium perfringens tetracycline resistance plasmid, pCW3. Plasmid 13:155–162.
Abraham, L.J. and J.I. Rood. 1987. Identification of Tn4451 and Tn4452: Two chloramphenicol resistance transposons from Clostridium perfringens. J. Bacteriol. 169:1579–1584.
Abraham, L.J. and J.I. Rood. 1988. The Clostridium perfringens chloramphenicol resistance transposon Tn4452 excises precisely in Escherichia coli. Plasmid 19:164–168.
Abraham, L.J., D.I. Berryman and J.I. Rood. 1988. Hybridization analysis of the class P tetracycline resistance determinant from the Clostridium perfringens R-plasmid, pCW3. Plasmid 19:113–120.
Abraham, L.J., A.J. Wales, and J.I. Rood. 1985. Worldwide distribution of the conjugative Clostridium perfringens tetracycline resistance plasmid, pCW3. Plasmid 14:37–46.
Allen, S.P. and H.P. Blaschek. 1988. Electro-poration-induced transformation of intact cells of Clostridium perfringens. Appl. Environ. Microbiol. 54:2322–2324.
Bannam, T.L. and Rood, J.I. (1991). The relationship between the Clostridium perfringens catQ gene product and chloramphenicol acetyl-transferases from other bacteria. Antimicrob. Agents Chemother. 35:471–476.
Berryman, D.I. and J.I. Rood. 1989. Cloning and hybridization analysis of ermP, an MLS resistance determinant from Clostridium perfringens. Antimicrob. Agents Chemother. 33:1346–1353.
Blaschek, H.P. and M. Solberg. 1981. Isolation of a plasmid responsible for caseinase activity in Clostridium perfringens ATCC 3626B.J. Bacteriol. 147:262–266.
Blaschek, HP. and M.A. Klacik. 1984. Role of DNase in recovery of plasmid DNA from Clostridium perfringens. Appl. Environ. Microbiol. 48:178–181.
Bréfort, G., M. Magot, H. Ionesco, and M. Sebald. 1977. Characterization and transferability of Clostridium perfringens plasmids. Plasmid 1:52–66.
Brehm, J., G. Salmond, and N. Minton. 1987. Sequence of the adenine methylase gene of the Streptococcus faecalis plasmid pAMβ1. Nucleic Acids Res. 15:3177.
Dornbusch, K., C.E. Nord, and A. Dahlbäck. 1975. Antibiotic susceptibility of Clostridium species isolated from human infections. Scand. J. Infect. Dis. 7:127–134.
Dubnau, D. and M. Monod. 1986. The regulation and evolution of MLS resistance. Banbury Rep. 24:369–387.
Dutta, G.N. and L.A. Devriese. 1980. Susceptibility of Clostridium perfringens of animal origin to fifteen antimicrobial agents.J. Vet. Pharmacol. Ther. 3:227–236.
Dutta, G.N. and L.A. Devriese. 1981. Macrolide-lincosamide-streptogramin resistance patterns in Clostridium perfringens from animals. Antimicrob. Agents Chemother. 19:274–278.
Galas, D.J. and M. Chandler. 1989. Bacterial insertion sequences. In: Mobile DNA, D.E. Berg and M.M. Howe, ed., pp. 109–162. Washington, D.C.: American Society for Microbiology.
Gamier, T. and S.T. Cole. 1988. Complete nucleotide sequence and genetic organization of the bacteriocinogenic plasmid, pIP404, from Clostridium perfringens. Plasmid 19:134–150.
Hächler, H., B. Berger-Bächi, and F. H. Kayser. 1987a. Genetic characterization of a Clostridium difficile erythromycin-clindamycin resistance determinant that is transferable to Staphylococcus aureus. Antimicrob. Agents Chemother. 31:1039–1045.
Hächler, H., F.H. Kayser, and B. Berger-Bächi. 1987b. Homology of a transferable tetracycline resistance determinant of Clostridium difficile with Streptococcus (Enterococcus) faecalis trans-poson Tn916. Antimicrob. Agents and Chemother. 31:1033–1038.
Hatheway, C.L. 1990. Toxigenic Clostridia. Clin. Microbiol. Rev. 3:66–98.
Heefner, D.L., C.H. Squires, R.J. Evans, B.J. Kopp, and M.J. Yarus. 1984. Transformation of Clostridium perfringens. J. Bacteriol. 159:460–464.
Horaud, T., C. Le Bouguenec, and K. Pepper. 1985. Molecular genetics of resistance to macrolides, lincosamides and streptogramin B (MLS) in streptococci.J. Antimicrob. Chemother. 16 (Suppl. A): 111–135.
Ionesco, H. 1980. Transfert de la resistance a la tetracycline chez Clostridium difficile. Ann. Microbiol. (Paris) 131A:171–179.
Ionesco, H., G. Bieth, C. Dauget, and D. Bouanchaud. 1974. Isolement et identification de deux plasmides d’une souche bactériocinogène. Ann. Microbiol. (Paris) 127B:283–294.
Kim, A. Y and Blaschek, H. P. (1989). Construction of an Escherichia coli-Clostridium perfringens shuttle vector and plasmid transformation of Clostridium perfringens. Appl. Environ. Microbiol. 55:360–365.
Kordel, M. and G. Schallehn. 1984. Plasmid detection in a macrolide-lincosamide resistant strain of Clostridium perfringens. Fed. Eur. Microbiol. Soc. Lett. 24:153–157.
Levy, S.B., L.M. McMurray, V. Burdett, P. Courvalin, W. Hillen, M.C. Roberts, and D.E. Taylor. 1989. Nomenclature for tetracycline resistance determinants. Antimicrob. Agents Chemother. 33:1373–1374.
Magot, M. 1984. Physical characterization of the Clostridium perfringens tetracycline-chloramphenicol resistance plasmid pIP401. Ann. Microbiol. (Inst. Pasteur) 135B:269–282.
Mahony, D.E., J.A. Mader, and J.R. Dubel. 1988. Transformation of Clostridium perfringens L-forms with plasmid DNA. Appl. Environ. Microbiol. 54:264–267.
Mahony, D.E., M.F. Stringer, S.P. Borriello, and J.A. Mader. 1987. Plasmid analysis as a means of strain differentiation in Clostridium perfringens. J. Clin. Microbiol. 25:1333–1335.
Mahony, D.E., G.A. Clark, M.F. Stringer, M.C. MacDonald, D.R. Duchesne, and J.A. Mader. 1986. Rapid extraction of plasmids from Clostridium perfringens. Appl. Environ. Microbiol. 51:521–523.
Martin, B., G. Alloing, V. Méjean, and J.-P. Claverys. 1987. Constitutive expression of erythromycin resistance mediated by the ermAM determinant of plasmid pAMβ1 results from deletion of 5′ leader peptide sequences. Plasmid 18:250–253.
Miyoshi, Y. 1984. Transferability of tetracycline resistance to Clostridium perfringens isolated from human feces. Chemotherapy 30:170–174.
Miyoshi, Y. and A. Higa. 1984. Interrelationship between drug resistance and bacteriocinogeny of C. perfringens. Microbiol. Immunol. 28:281–289.
Oultram, J.D. and M. Young. 1985. Conjugal transfer of plasmid pAM β1 from Streptococcus lactis and Bacillus subtilis to Clostridium acetobutylicum. Fed. Eur. Microbiol. Soc. Lett. 27:129–134.
Phillips-Jones, M.K., L.A. Iwanejko, and M.S. Longden. 1989. Analysis of plasmid profiling as a method for rapid differentiation of food-associated Clostridium perfringens. J. Appl. Bacteriol. 67:243–254.
Roberts, I., W.M. Holmes, and P.B. Hylemon. 1986. Modified plasmid isolation method for Clostridium perfringens and Clostridium absonum. Appl. Environ. Microbiol. 52:197–199.
Roberts, I., W.M. Holmes, and P.B. Hylemon. 1988. Development of a new shuttle plasmid system for Escherichia coli and Clostridium perfringens. Appl. Environ. Microbiol. 54:268–270.
Rokos, E.A., J.I. Rood, and C.L. Duncan. 1978. Multiple plasmids in different toxigenic types of Clostridium perfringens. Fed. Eur. Microbiol. Soc. Lett. 4:323–326.
Rood, J.I. 1983. Transferable tetracycline resistance in Clostridium perfringens strains of porcine origin. Can. J. Microbiol. 29:1241–1246.
Rood J.I., V.N. Scott, and C.L. Duncan. 1978b. Identification of a transferable tetracycline resistance plasmid (pCW3) from Clostridium perfringens. Plasmid 1:563–570.
Rood, J.I., J.R. Buddie, A.J. Wales, and R. Sidhu. 1985. The occurrence of antibiotic resistance in Clostridium perfringens from pigs. Aus. Vet. J. 62:276–279.
Rood, J.I., E.A. Maher, E.B. Somers, E. Campos, and C.L. Duncan. 1978a. Isolation and characterization of multiply antibiotic-resistant Clostridium perfringens strains from porcine feces. Antimicrob. Agents Chemother. 13:871–880.
Rood, J.I., S. Jefferson, T.L. Bannam, J.M. Wilkie, P. Mullany, and B.W. Wren. 1989. Hybridization analysis of three chloramphenicol resistance determinants from Clostridium perfringens and Clostridium difficile. Antimicrob. Agents Chemother. 33:1569–1574.
Scott, P.T. and J.I. Rood. 1989. Electroporation-mediated transformation of lysostaphin-treated Clostridium perfringens. Gene 82:327–333.
Sebald, M. and G. Bréfort. 1975. Transfert du plasmide Tétracycline-Chloramphenicol chez Clostridium perfringens. C. R. Acad. Sci. Paris Ser. D. 281:317–319
Sebald, M., D. Bouanchaud, and G. Bieth. 1975. Nature plasmidique de la resistance à plusieurs antibiotiques chez C. perfringens type A, souche 659. C. R. Acad. Sci. Paris Ser. D 280:2401–2404.
Sherrat, D. 1989. Tn3 and related transposable elements: site-specific recombination and transposition. In: Mobile DNA, D.E. Berg and M.M. Howe, eds., pp. 163–184. Washington, D.C.: American Society for Microbiology.
Smart J.L., M.L. Truman, and M.F. Stringer. 1983. A note on the antibiotic susceptibilities of Clostridium perfringens serotypes isolated from meat.J. Appl. Bacteriol. 54:135–139.
Smart, J.L., T.A. Roberts, M.F. Stringer, and N. Shah. 1979. The incidence and serotypes of Clostridium perfringens on beef, pork and lamb carcasses.J. Appl. Bacteriol. 46:377–383.
Smith, H.W. 1959. The effect of continuous administration of diets containing tetracyclines and penicillins on the number of drug-resistant and drug-sensitive Clostridium welchii in the faeces of pigs and chickens.J. Pathol. Bacteriol. 77:79–92.
Squires, C.H., D.L. Heefner, R.J. Evans, B.J. Kopp, and M.J. Yarus. 1984. Shuttle plasmids for Escherichia coli and Clostridium perfringens. J. Bacteriol. 159:465–471.
Steffen, C. and H. Matzura. 1989. Nucleotide sequence analysis and expression studies of a chloramphenicol-acetyltransferase-coding gene from Clostridium perfringens. Gene 75:349–354.
Wren, B.W., P. Mullany, C. Clayton, and S. Taba-qchali. 1988. Molecular cloning and genetic analysis of a chloramphenicol acetyltransferase determinant from Clostridium difficile. Antimicrob. Agents Chemother. 32:1213–1217.
Wren, B.W., P. Mullany, C. Clayton, and S. Tabaqchali. 1989. Nucleotide sequence of a chloramphenicol acetyltransferase gene from Clostridium difficile. Nucleic Acids Res. 17:4877.
Young, M., N.P. Minton, and W.L. Staudenbauer. 1989. Recent advances in the genetics of the Clostridia. Fed. of Eur. Microbiol. Soc. Rev. 63:301–326.
Zaidenzaig, Y., J.E. Fitton, L.C. Packman, and W.V. Shaw. 1979. Characterization and comparison of chloramphenicol acetyltransferase variants. Eur. J. Biochem. 100:609–618.
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Rood, J.I. (1993). Antibiotic Resistance Determinants of Clostridium perfringens . In: Sebald, M. (eds) Genetics and Molecular Biology of Anaerobic Bacteria. Brock/Springer Series in Contemporary Bioscience. Springer, New York, NY. https://doi.org/10.1007/978-1-4615-7087-5_9
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