Degeneration and Regeneration of Murine Skeletal Neuromuscular Junctions after Intramuscular Injection with a Sublethal Dose of Clostridium sordellii Lethal Toxin
Open Access
- 1 June 2004
- journal article
- research article
- Published by American Society for Microbiology in Infection and Immunity
- Vol. 72 (6) , 3120-3128
- https://doi.org/10.1128/iai.72.6.3120-3128.2004
Abstract
Clostridium sordellii lethal toxin (LT), a 250-kDa protein which is the bacteria's major virulence factor, belongs to a family of large clostridial cytotoxins which glucosylate small GTP-binding proteins. Here, we report the results of our ex vivo analysis of the structure and function of skeletal neuromuscular tissue obtained from mice at various times after intramuscular injection of a sublethal dose of LT (0.25 ng/g of body wt). The toxin caused, within 24 h, pronounced localized edema, inflammation, myofibril disassembly, and degeneration of skeletal muscle fibers in the injected area, and it glucosylated the muscle tissue's small GTPases. Regeneration of the damaged fibers was evident 6 to 9 days postinjury and was completed by 60 days. The expression of dystrophin, laminin, and fast and neonatal myosin in regenerating fibers, detected by immunofluorescence microscopy, confirmed that LT does not impair the high regenerative capacity of murine skeletal muscle fibers. Functional studies revealed that LT affects muscle contractility and neuromuscular transmission. However, partial recovery of nerve-evoked muscle twitches and tetanic contractions was observed by day 15 postinjection, and extensive remodeling of the neuromuscular junction's nerve terminals and clusters of muscle acetylcholine receptors was still evident 30 days postinjection. In conclusion, to the best of our knowledge, this is the first report to characterize the degeneration and regeneration of skeletal neuromuscular tissue after in vivo exposure to a large clostridial cytotoxin. In addition, our data may provide an explanation for the severe neuromuscular alterations accompanying wound infections caused by C. sordellii .Keywords
This publication has 51 references indexed in Scilit:
- Differentiation of Muscle-Derived Cells into Myofibroblasts in Injured Skeletal MuscleThe American Journal of Pathology, 2002
- Infections Associated with Use of the LifeSite Hemodialysis Access SystemClinical Infectious Diseases, 2002
- Snake venom metalloproteinases:Their role in the pathogenesis of local tissue damagePublished by Elsevier ,2001
- Genetic Analysis of Collagen Q: Roles in Acetylcholinesterase and Butyrylcholinesterase Assembly and in Synaptic Structure and FunctionThe Journal of cell biology, 1999
- Studies of the dynamics of skeletal muscle regeneration: the mouse came back!Biochemistry and Cell Biology, 1998
- A fatal postpartum Clostridium sordellii associated toxic shock syndrome.Journal of Clinical Pathology, 1997
- UDP-Glucose Deficiency in a Mutant Cell Line Protects against Glucosyltransferase Toxins from Clostridium difficile and Clostridium sordelliiPublished by Elsevier ,1996
- Skeletal muscle satellite cellsPublished by Springer Nature ,1994
- Comparison of Clostridium sordellii toxins HT and LT with toxins A and B of C. difficileJournal of Medical Microbiology, 1992
- Myosin isozyme transitions occurring during the postnatal development of the rat soleus muscleDevelopmental Biology, 1984