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Erschienen in: Current Infectious Disease Reports 5/2010

01.09.2010

Clostridial Myonecrosis: New Insights in Pathogenesis and Management

verfasst von: Amy E. Bryant, Dennis L. Stevens

Erschienen in: Current Infectious Disease Reports | Ausgabe 5/2010

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Abstract

Clostridial myonecrosis remains an important cause of human morbidity and mortality worldwide. Although traumatic gas gangrene can be readily diagnosed from clinical findings and widely available technologies, spontaneous gas gangrene is more insidious, and gynecologic infections due to Clostridium sordellii progress so rapidly that death often precedes diagnosis. In each case, extensive tissue destruction and the subsequent systemic manifestations are mediated directly and indirectly by potent bacterial exotoxins. The management triumvirate of timely diagnosis, thorough surgical removal of necrotic tissue, and treatment with antibiotics that inhibit toxin synthesis remains the gold standard of care. Yet, despite these measures, mortality remains 30% to 100% and survivors often must cope with life-altering amputations. Recent insights regarding the genetic regulation of toxin production, the molecular mechanisms of toxin-induced host cell dysfunction, and the roles of newly described toxins in pathogenesis suggest that novel prevention, diagnostic, and treatment modalities may be on the horizon for these devastating infections.
Literatur
1.
Zurück zum Zitat Aldape MJ, Bryant AE, Stevens DL: Clostridium sordellii infection: epidemiology, clinical findings, and current perspectives on diagnosis and treatment. Clin Infect Dis 2006, 43:1436–1446.CrossRefPubMed Aldape MJ, Bryant AE, Stevens DL: Clostridium sordellii infection: epidemiology, clinical findings, and current perspectives on diagnosis and treatment. Clin Infect Dis 2006, 43:1436–1446.CrossRefPubMed
2.
Zurück zum Zitat Centers for Disease Control and Prevention: Update: Clostridium novyi and unexplained illness among injecting-drug users—Scotland, Ireland, and England, April–June 2000. MMWR Morb Mortal Wkly Rep 2000, 49:543–545. Centers for Disease Control and Prevention: Update: Clostridium novyi and unexplained illness among injecting-drug users—Scotland, Ireland, and England, April–June 2000. MMWR Morb Mortal Wkly Rep 2000, 49:543–545.
3.
Zurück zum Zitat Centers for Disease Control and Prevention: Soft tissue infections among injection drug users—San Francisco, California, 1996–2000. MMWR Morb Mortal Wkly Rep 2001, 50:381–384. Centers for Disease Control and Prevention: Soft tissue infections among injection drug users—San Francisco, California, 1996–2000. MMWR Morb Mortal Wkly Rep 2001, 50:381–384.
4.
Zurück zum Zitat Bangsberg DR, Rosen JI, Aragon T, et al.: Clostridial myonecrosis cluster among injection drug users: a molecular epidemiology investigation. Arch Intern Med 2002, 162:517–522.CrossRefPubMed Bangsberg DR, Rosen JI, Aragon T, et al.: Clostridial myonecrosis cluster among injection drug users: a molecular epidemiology investigation. Arch Intern Med 2002, 162:517–522.CrossRefPubMed
5.
Zurück zum Zitat Brazier JS, Gal M, Hall V, Morris T: Outbreak of Clostridium histolyticum infections in injecting drug users in England and Scotland. Euro Surveill 2004, 9:15–16.PubMed Brazier JS, Gal M, Hall V, Morris T: Outbreak of Clostridium histolyticum infections in injecting drug users in England and Scotland. Euro Surveill 2004, 9:15–16.PubMed
6.
Zurück zum Zitat Kimura AC, Higa JI, Levin RM, et al.: Outbreak of necrotizing fasciitis due to Clostridium sordellii among black-tar heroin users. Clin Infect Dis 2004, 38:e87–e91.CrossRefPubMed Kimura AC, Higa JI, Levin RM, et al.: Outbreak of necrotizing fasciitis due to Clostridium sordellii among black-tar heroin users. Clin Infect Dis 2004, 38:e87–e91.CrossRefPubMed
7.
Zurück zum Zitat •• McNee JW, Dunn JS: The method of spread of gas gangrene into living muscle. Br Med J 1917, 1:727–729. Although this work is more than 90 years old, the histologic observations made by the authors have stood the test of time, and the proposed mechanisms of pathogenesis have been confirmed only recently. CrossRef •• McNee JW, Dunn JS: The method of spread of gas gangrene into living muscle. Br Med J 1917, 1:727–729. Although this work is more than 90 years old, the histologic observations made by the authors have stood the test of time, and the proposed mechanisms of pathogenesis have been confirmed only recently. CrossRef
8.
Zurück zum Zitat Stevens DL: Clostridial myonecrosis and other clostridial diseases. In Cecil Textbook of Medicine, edn 21. Edited by Goldman L, Bennett JC. Philadelphia: WB Saunders; 2000:1668–1673. Stevens DL: Clostridial myonecrosis and other clostridial diseases. In Cecil Textbook of Medicine, edn 21. Edited by Goldman L, Bennett JC. Philadelphia: WB Saunders; 2000:1668–1673.
9.
Zurück zum Zitat Stevens DL, Musher DM, Watson DA, et al.: Spontaneous, nontraumatic gangrene due to Clostridium septicum. Rev Infect Dis 1990, 12:286–296.PubMed Stevens DL, Musher DM, Watson DA, et al.: Spontaneous, nontraumatic gangrene due to Clostridium septicum. Rev Infect Dis 1990, 12:286–296.PubMed
10.
Zurück zum Zitat Johnson S, Driks MR, Tweten RK, et al.: Clinical courses of seven survivors of Clostridium septicum infection and their immunologic responses to α toxin. Clin Infect Dis 1994, 19:761–764.PubMed Johnson S, Driks MR, Tweten RK, et al.: Clinical courses of seven survivors of Clostridium septicum infection and their immunologic responses to α toxin. Clin Infect Dis 1994, 19:761–764.PubMed
12.
Zurück zum Zitat •• Ramirez N, Abel-Santos E: Requirements for germination of Clostridium sordellii spores in vitro. J Bacteriol 2010, 192:418–425. These authors used kinetic methods to elucidate the microenvironmental factors necessary for germination of C. sordellii spores. In addition, using available information on the germinant conditions of the pregnant vs postpartum uterus, the authors predicted that following birth or abortion, all signals for germination would be present. CrossRefPubMed •• Ramirez N, Abel-Santos E: Requirements for germination of Clostridium sordellii spores in vitro. J Bacteriol 2010, 192:418–425. These authors used kinetic methods to elucidate the microenvironmental factors necessary for germination of C. sordellii spores. In addition, using available information on the germinant conditions of the pregnant vs postpartum uterus, the authors predicted that following birth or abortion, all signals for germination would be present. CrossRefPubMed
13.
Zurück zum Zitat Stevens DL, Bryant AE, Berger A, von Eichel-Streiber C: Clostridium. In American Society of Microbiology’s Manual of Clinical Microbiology, edn 10. Washington, DC: ASM Press; 2010. Stevens DL, Bryant AE, Berger A, von Eichel-Streiber C: Clostridium. In American Society of Microbiology’s Manual of Clinical Microbiology, edn 10. Washington, DC: ASM Press; 2010.
14.
Zurück zum Zitat Khanna N: Clindamycin-resistant Clostridium perfringens cellulitis. J Tissue Viability 2008, 17:95–97.CrossRefPubMed Khanna N: Clindamycin-resistant Clostridium perfringens cellulitis. J Tissue Viability 2008, 17:95–97.CrossRefPubMed
15.
Zurück zum Zitat • Holzel CS, Harms KS, Schwaiger K, Bauer J: Resistance to linezolid in a porcine Clostridium perfringens strain carrying a mutation in the rplD gene encoding the ribosomal protein L4. Antimicrob Agents Chemother 2010, 54:1351–1353. These authors describe and characterize the molecular mechanism conferring linezolid resistance in a veterinary isolate of C. perfringens. The work re-emphasizes the interconnectedness between veterinary practice and the emergence of strains resistant to human reserve antibiotics. CrossRefPubMed • Holzel CS, Harms KS, Schwaiger K, Bauer J: Resistance to linezolid in a porcine Clostridium perfringens strain carrying a mutation in the rplD gene encoding the ribosomal protein L4. Antimicrob Agents Chemother 2010, 54:1351–1353. These authors describe and characterize the molecular mechanism conferring linezolid resistance in a veterinary isolate of C. perfringens. The work re-emphasizes the interconnectedness between veterinary practice and the emergence of strains resistant to human reserve antibiotics. CrossRefPubMed
16.
Zurück zum Zitat Flores-Diaz M, Alape-Giron A, Clark G, et al.: A cellular deficiency of gangliosides causes hypersensitivity to Clostridium perfringens phospholipase C. J Biol Chem 2005, 280:26680–26689.CrossRefPubMed Flores-Diaz M, Alape-Giron A, Clark G, et al.: A cellular deficiency of gangliosides causes hypersensitivity to Clostridium perfringens phospholipase C. J Biol Chem 2005, 280:26680–26689.CrossRefPubMed
17.
Zurück zum Zitat Awad MM, Bryant AE, Stevens DL, Rood JI: Virulence studies on chromosomal α-toxin and θ toxin mutants constructed by allelic exchange provide genetic evidence for the essential role of α-toxin in Clostridium perfringens-mediated gas gangrene. Mol Microbiol 1995, 15:191–202.CrossRefPubMed Awad MM, Bryant AE, Stevens DL, Rood JI: Virulence studies on chromosomal α-toxin and θ toxin mutants constructed by allelic exchange provide genetic evidence for the essential role of α-toxin in Clostridium perfringens-mediated gas gangrene. Mol Microbiol 1995, 15:191–202.CrossRefPubMed
18.
Zurück zum Zitat Stevens DL, Titball RW, Jepson M, et al.: Immunization with the C-domain of alpha-toxin prevents lethal infection, localizes tissue injury, and promotes host response to challenge with Clostridium perfringens. J Infect Dis 2004, 190:767–773.CrossRefPubMed Stevens DL, Titball RW, Jepson M, et al.: Immunization with the C-domain of alpha-toxin prevents lethal infection, localizes tissue injury, and promotes host response to challenge with Clostridium perfringens. J Infect Dis 2004, 190:767–773.CrossRefPubMed
19.
Zurück zum Zitat Williamson ED, Titball RW: A genetically engineered vaccine against alpha-toxin of Clostridium perfringens protects against experimental gas gangrene. Vaccine 1993, 11:1253–1258.CrossRefPubMed Williamson ED, Titball RW: A genetically engineered vaccine against alpha-toxin of Clostridium perfringens protects against experimental gas gangrene. Vaccine 1993, 11:1253–1258.CrossRefPubMed
20.
Zurück zum Zitat Shepard LA, Heuck AP, Hamman BD, et al.: Identification of a membrane-spanning domain of the thiol-activated pore-forming toxin Clostridium perfringens perfringolysin O: an alpha-helical to beta-sheet transition identified by fluorescence spectroscopy. Biochem 1998, 37:14563–14574.CrossRef Shepard LA, Heuck AP, Hamman BD, et al.: Identification of a membrane-spanning domain of the thiol-activated pore-forming toxin Clostridium perfringens perfringolysin O: an alpha-helical to beta-sheet transition identified by fluorescence spectroscopy. Biochem 1998, 37:14563–14574.CrossRef
21.
Zurück zum Zitat Bryant AE, Bergstrom R, Zimmerman GA, et al.: Clostridium perfringens invasiveness is enhanced by effects of theta toxin upon PMNL structure and function: the roles of leukocytotoxicity and expression of CD11/CD18 adherence glycoprotein. FEMS Immunol Med Microbiol 1993, 7:321–336.CrossRefPubMed Bryant AE, Bergstrom R, Zimmerman GA, et al.: Clostridium perfringens invasiveness is enhanced by effects of theta toxin upon PMNL structure and function: the roles of leukocytotoxicity and expression of CD11/CD18 adherence glycoprotein. FEMS Immunol Med Microbiol 1993, 7:321–336.CrossRefPubMed
22.
Zurück zum Zitat Stevens DL, Tweten RK, Awad MM, et al.: Clostridial gas gangrene: Evidence that alpha and theta toxins differentially modulate the immune response and induce acute tissue necrosis. J Infect Dis 1997, 176:189–195.CrossRefPubMed Stevens DL, Tweten RK, Awad MM, et al.: Clostridial gas gangrene: Evidence that alpha and theta toxins differentially modulate the immune response and induce acute tissue necrosis. J Infect Dis 1997, 176:189–195.CrossRefPubMed
23.
Zurück zum Zitat Knapp O, Maier E, Mkaddem SB, et al.: Clostridium septicum alpha-toxin forms pores and induces rapid cell necrosis. Toxicon 2010, 55:61–72.CrossRefPubMed Knapp O, Maier E, Mkaddem SB, et al.: Clostridium septicum alpha-toxin forms pores and induces rapid cell necrosis. Toxicon 2010, 55:61–72.CrossRefPubMed
24.
Zurück zum Zitat Ballard J, Bryant A, Stevens D, Tweten RK: Purification and characterization of the lethal toxin (alpha-toxin) of Clostridium septicum. Infect Immun 1992, 60:784–790.PubMed Ballard J, Bryant A, Stevens D, Tweten RK: Purification and characterization of the lethal toxin (alpha-toxin) of Clostridium septicum. Infect Immun 1992, 60:784–790.PubMed
25.
Zurück zum Zitat Voth DE, Martinez OV, Ballard JD: Variations in lethal toxin and cholesterol-dependent cytolysin production correspond to differences in cytotoxicity among strains of Clostridium sordellii. FEMS Microbiol Lett 2006, 259:295–302.CrossRefPubMed Voth DE, Martinez OV, Ballard JD: Variations in lethal toxin and cholesterol-dependent cytolysin production correspond to differences in cytotoxicity among strains of Clostridium sordellii. FEMS Microbiol Lett 2006, 259:295–302.CrossRefPubMed
26.
Zurück zum Zitat Aldape MJ, Bryant AE, Ma Y, Stevens DL: The leukemoid reaction in Clostridium sordellii infection: neuraminidase induction of promyelocytic cell proliferation. J Infect Dis 2007, 195:1838–1845.CrossRefPubMed Aldape MJ, Bryant AE, Ma Y, Stevens DL: The leukemoid reaction in Clostridium sordellii infection: neuraminidase induction of promyelocytic cell proliferation. J Infect Dis 2007, 195:1838–1845.CrossRefPubMed
27.
Zurück zum Zitat Aldape MJ, Bryant AE, Katahira EJ, et al.: Innate immune recognition of, and response to, Clostridium sordellii. Anaerobe 2010, 16:125–130.CrossRefPubMed Aldape MJ, Bryant AE, Katahira EJ, et al.: Innate immune recognition of, and response to, Clostridium sordellii. Anaerobe 2010, 16:125–130.CrossRefPubMed
28.
Zurück zum Zitat Stevens DL, Rood JI: Histotoxic Clostridia. In Gram Positive Pathogens. Edited by Fischetti VA, Novick RP, Ferretti J, et al. Washington DC: ASM Press; 1999:563–572. Stevens DL, Rood JI: Histotoxic Clostridia. In Gram Positive Pathogens. Edited by Fischetti VA, Novick RP, Ferretti J, et al. Washington DC: ASM Press; 1999:563–572.
29.
Zurück zum Zitat Shimizu T, Yaguchi H, Ohtani K, et al.: Clostridial VirR/VirS regulon involves a regulatory RNA molecule for expression of toxins. Mol Microbiol 2002, 43:257–265.CrossRefPubMed Shimizu T, Yaguchi H, Ohtani K, et al.: Clostridial VirR/VirS regulon involves a regulatory RNA molecule for expression of toxins. Mol Microbiol 2002, 43:257–265.CrossRefPubMed
30.
Zurück zum Zitat • Okumura K, Ohtani K, Hayashi H, Shimizu T: Characterization of genes regulated directly by the VirR/VirS system in Clostridium perfringens. J Bacteriol 2008, 190:7719–7727. Searching the C. perfringens genome for genes controlled by VirR, these authors identify and characterize two novel genes coding for regulatory RNA molecules involved in virulence factor production. CrossRefPubMed • Okumura K, Ohtani K, Hayashi H, Shimizu T: Characterization of genes regulated directly by the VirR/VirS system in Clostridium perfringens. J Bacteriol 2008, 190:7719–7727. Searching the C. perfringens genome for genes controlled by VirR, these authors identify and characterize two novel genes coding for regulatory RNA molecules involved in virulence factor production. CrossRefPubMed
31.
Zurück zum Zitat • Ohtani K, Hirakawa H, Tashiro K, et al.: Identification of a two-component VirR/VirS regulon in Clostridium perfringens. Anaerobe 2010, 16:258–264. Using various genetic approaches, including qRT-PCR, these authors demonstrate that 147 different genes (including complete operons) in multiple functional categories are under the control of the VirR/S/VR-RNA system. They suggest that this is a global regulatory system that provides the organism with the tools for survival and propagation in the human host. CrossRefPubMed • Ohtani K, Hirakawa H, Tashiro K, et al.: Identification of a two-component VirR/VirS regulon in Clostridium perfringens. Anaerobe 2010, 16:258–264. Using various genetic approaches, including qRT-PCR, these authors demonstrate that 147 different genes (including complete operons) in multiple functional categories are under the control of the VirR/S/VR-RNA system. They suggest that this is a global regulatory system that provides the organism with the tools for survival and propagation in the human host. CrossRefPubMed
32.
Zurück zum Zitat • Frandi A, Mengoni A, Brilli M: Comparative genomics of VirR regulons in Clostridium perfringens strains. BMC Microbiol 2010, 10:65. These authors demonstrate that the number and types of genes controled by the VirR/S system vary widely among different strains of C. perfringens. CrossRefPubMed • Frandi A, Mengoni A, Brilli M: Comparative genomics of VirR regulons in Clostridium perfringens strains. BMC Microbiol 2010, 10:65. These authors demonstrate that the number and types of genes controled by the VirR/S system vary widely among different strains of C. perfringens. CrossRefPubMed
33.
Zurück zum Zitat •• Ohtani K, Yuan Y, Hassan S, et al.: Virulence gene regulation by the agr system in Clostridium perfringens. J Bacteriol 2009, 191:3919–3927. This work is the first description of a S. aureus agr-like toxin regulatory system in C. perfringens. Production of θ toxin, but not α toxin or collagenase, was strictly dependent on this system and involved a soluble component analogous to the quorum-sensing autoinducing peptide of S. aureus. CrossRefPubMed •• Ohtani K, Yuan Y, Hassan S, et al.: Virulence gene regulation by the agr system in Clostridium perfringens. J Bacteriol 2009, 191:3919–3927. This work is the first description of a S. aureus agr-like toxin regulatory system in C. perfringens. Production of θ toxin, but not α toxin or collagenase, was strictly dependent on this system and involved a soluble component analogous to the quorum-sensing autoinducing peptide of S. aureus. CrossRefPubMed
34.
Zurück zum Zitat • Vidal JE, Chen J, Li J, McClane BA: Use of an EZ-Tn5-based random mutagenesis system to identify a novel toxin regulatory locus in Clostridium perfringens strain 13. PLoS One 2009, 4:e6232. Using a random mutagenesis approach with a novel transposon construct, these authors also identified agr system component homologues in C. perfringens. CrossRefPubMed • Vidal JE, Chen J, Li J, McClane BA: Use of an EZ-Tn5-based random mutagenesis system to identify a novel toxin regulatory locus in Clostridium perfringens strain 13. PLoS One 2009, 4:e6232. Using a random mutagenesis approach with a novel transposon construct, these authors also identified agr system component homologues in C. perfringens. CrossRefPubMed
35.
Zurück zum Zitat Stevens DL, Bryant AE: Clostridial gas gangrene: clinical correlations, microbial virulence factors, and molecular mechanisms of pathogenesis. In Microbial Toxins: Molecular and Cellular Biology. Edited by Proft T. Norfolk,UK: Horizon Bioscience; 2005:313–335. Stevens DL, Bryant AE: Clostridial gas gangrene: clinical correlations, microbial virulence factors, and molecular mechanisms of pathogenesis. In Microbial Toxins: Molecular and Cellular Biology. Edited by Proft T. Norfolk,UK: Horizon Bioscience; 2005:313–335.
36.
Zurück zum Zitat Bryant AE, Chen RYZ, Nagata Y, et al.: Clostridial gas gangrene I: cellular and molecular mechanisms of microvascular dysfunction induced by exotoxins of C. perfringens. J Infect Dis 2000, 182:799–807.CrossRefPubMed Bryant AE, Chen RYZ, Nagata Y, et al.: Clostridial gas gangrene I: cellular and molecular mechanisms of microvascular dysfunction induced by exotoxins of C. perfringens. J Infect Dis 2000, 182:799–807.CrossRefPubMed
37.
Zurück zum Zitat Bryant AE, Chen RYZ, Nagata Y, et al.: Clostridial gas gangrene II: phospholipase C-induced activation of platelet gpIIb/IIIa mediates vascular occlusion and myonecrosis in C. perfringens gas gangrene. J Infect Dis 2000, 182:808–815.CrossRefPubMed Bryant AE, Chen RYZ, Nagata Y, et al.: Clostridial gas gangrene II: phospholipase C-induced activation of platelet gpIIb/IIIa mediates vascular occlusion and myonecrosis in C. perfringens gas gangrene. J Infect Dis 2000, 182:808–815.CrossRefPubMed
38.
Zurück zum Zitat Bryant AE, Bayer CR, Chen RY, et al.: Vascular dysfunction and ischemic destruction of tissue in Streptococcus pyogenes infection: the role of streptolysin O-induced platelet/neutrophil complexes. J Infect Dis 2005, 192:1014–1022.CrossRefPubMed Bryant AE, Bayer CR, Chen RY, et al.: Vascular dysfunction and ischemic destruction of tissue in Streptococcus pyogenes infection: the role of streptolysin O-induced platelet/neutrophil complexes. J Infect Dis 2005, 192:1014–1022.CrossRefPubMed
39.
Zurück zum Zitat Bryant AE, Bayer CR, Aldape MJ, et al.: Clostridium perfringens phospholipase C-induced platelet/leukocyte interactions impede neutrophil diapedesis. J Med Microbiol 2006, 55(Pt 5):495–504.CrossRefPubMed Bryant AE, Bayer CR, Aldape MJ, et al.: Clostridium perfringens phospholipase C-induced platelet/leukocyte interactions impede neutrophil diapedesis. J Med Microbiol 2006, 55(Pt 5):495–504.CrossRefPubMed
40.
Zurück zum Zitat Stevens DL, Bisno AL, Chambers HF, et al.: Practice guidelines for the diagnosis and management of skin and soft-tissue infections. Clin Infect Dis 2005, 41:1373–1406.CrossRefPubMed Stevens DL, Bisno AL, Chambers HF, et al.: Practice guidelines for the diagnosis and management of skin and soft-tissue infections. Clin Infect Dis 2005, 41:1373–1406.CrossRefPubMed
41.
Zurück zum Zitat Stevens DL, Maier KA, Laine BM, Mitten JE: Comparison of clindamycin, rifampin, tetracycline, metronidazole, and penicillin for efficacy in prevention of experimental gas gangrene due to Clostridium perfringens. J Infect Dis 1987, 155:220–228.PubMed Stevens DL, Maier KA, Laine BM, Mitten JE: Comparison of clindamycin, rifampin, tetracycline, metronidazole, and penicillin for efficacy in prevention of experimental gas gangrene due to Clostridium perfringens. J Infect Dis 1987, 155:220–228.PubMed
42.
Zurück zum Zitat Stevens DL, Laine BM, Mitten JE: Comparison of single and combination antimicrobial agents for prevention of experimental gas gangrene caused by Clostridium perfringens. Antimicrob Agents Chemother 1987, 31:312–316.PubMed Stevens DL, Laine BM, Mitten JE: Comparison of single and combination antimicrobial agents for prevention of experimental gas gangrene caused by Clostridium perfringens. Antimicrob Agents Chemother 1987, 31:312–316.PubMed
43.
Zurück zum Zitat Stevens DL, Maier KA, Mitten JE: Effect of antibiotics on toxin production and viability of Clostridium perfringens. Antimicrob Agents Chemother 1987, 31:213–218.PubMed Stevens DL, Maier KA, Mitten JE: Effect of antibiotics on toxin production and viability of Clostridium perfringens. Antimicrob Agents Chemother 1987, 31:213–218.PubMed
44.
Zurück zum Zitat Stevens DL, Bryant AE, Hackett SP: Antibiotic effects on bacterial viability, toxin production, and host response. Clin Infect Dis 1995, 20(Suppl 2):S154–S157.PubMed Stevens DL, Bryant AE, Hackett SP: Antibiotic effects on bacterial viability, toxin production, and host response. Clin Infect Dis 1995, 20(Suppl 2):S154–S157.PubMed
45.
Zurück zum Zitat Nakano T, Hiramatsu K, Kishi K, et al.: Clindamycin modulates inflammatory-cytokine induction in lipopolysaccharide-stimulated mouse peritoneal macrophages. Antimicrob Agents Chemother 2003, 47:363–367.CrossRefPubMed Nakano T, Hiramatsu K, Kishi K, et al.: Clindamycin modulates inflammatory-cytokine induction in lipopolysaccharide-stimulated mouse peritoneal macrophages. Antimicrob Agents Chemother 2003, 47:363–367.CrossRefPubMed
46.
Zurück zum Zitat Hirata N, Hiramatsu K, Kishi K, et al.: Pretreatment of mice with clindamycin improves survival of endotoxic shock by modulating the release of inflammatory cytokines. Antimicrob Agents Chemother 2001, 45:2638–2642.CrossRefPubMed Hirata N, Hiramatsu K, Kishi K, et al.: Pretreatment of mice with clindamycin improves survival of endotoxic shock by modulating the release of inflammatory cytokines. Antimicrob Agents Chemother 2001, 45:2638–2642.CrossRefPubMed
47.
Zurück zum Zitat •• Oda M, Kihara A, Yoshioka H, et al.: Effect of erythromycin on biological activities induced by Clostridium perfringens alpha-toxin. J Pharmacol Exp Ther 2008, 327:934–940. This work clearly demonstrated that administration of erythromycin to experimental animals dramatically prevented cytokine production (tumor necrosis factor-α, interleukin [IL]-1, IL-6) and death in animals challenged with C. perfringens α toxin. This work substantiates the notion that some antibiotics (ie, macrolides and lincosamides) can directly and beneficially modulate the host immune response. CrossRefPubMed •• Oda M, Kihara A, Yoshioka H, et al.: Effect of erythromycin on biological activities induced by Clostridium perfringens alpha-toxin. J Pharmacol Exp Ther 2008, 327:934–940. This work clearly demonstrated that administration of erythromycin to experimental animals dramatically prevented cytokine production (tumor necrosis factor-α, interleukin [IL]-1, IL-6) and death in animals challenged with C. perfringens α toxin. This work substantiates the notion that some antibiotics (ie, macrolides and lincosamides) can directly and beneficially modulate the host immune response. CrossRefPubMed
Metadaten
Titel
Clostridial Myonecrosis: New Insights in Pathogenesis and Management
verfasst von
Amy E. Bryant
Dennis L. Stevens
Publikationsdatum
01.09.2010
Verlag
Current Science Inc.
Erschienen in
Current Infectious Disease Reports / Ausgabe 5/2010
Print ISSN: 1523-3847
Elektronische ISSN: 1534-3146
DOI
https://doi.org/10.1007/s11908-010-0127-y

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