Mutant atténué nitrosoguanidine-induit dans la gangrène gazeuse à Clostridium perfringens type A

1975 ◽  
Vol 21 (8) ◽  
pp. 1259-1269 ◽  
Author(s):  
Jean-Rock Lapointe ◽  
Victorien Fredette

A fully virulent classical type A strain of Clostridium perfringens was treated during its logarithmic growth phase with 100 μg/ml of N-méthyl-N′-nitro-N-nitrosoguanidine, the bacteria being exposed to the mutagen for 30 min at 37 °C in a phosphate buffer adjusted to pH 6.2; after treatment the suspension was streaked on sheep blood agar plates, and colonies that showed an alteration in the theta-hemolysis pattern were selected for isolation. The virulence of two mutants, thus altered in their thêta-hemolysis, was studied. One, designated LNG 5, was still capable of killing most of the inoculated guinea pigs in less than 24 h with all the clinical, macroscopic, and bacteriological signs of gas gangrene; however, histological sections showed that tissue damage was not as marked as with the wild strain. On the contrary, the second mutant, labelled LNG 11, was completely avirulent as far as gas gangrene was concerned; indeed, the injection of fluid cultures containing 1 × 108-109/ml viable bacteria, was not followed by any clinical, bacteriological, or histological signs of gas gangrene. However, strain LNG 11 did give rise to a firm swelling of the inoculated thigh with a corresponding acute inflammatory response of the connective tissue, although the muscle fiber was unaltered. Eventually, this local reaction was followed by necrosis of the skin accompanied by an acute or subacute inflammation with fibroblastic proliferation. These superficial lesions healed spontaneously. They could not be reproduced with crude filtrate alone or with washed bacilli. Strain LNG 11 was therefore considered to be solely an attenuated strain since, although avirulent as far as gas gangrene is concerned, it is still capable of producing low levels of toxic material. This appears to be the first time that such a strain of C. perfringens type A has been obtained by nitrosoguanidine treatment.

2015 ◽  
Vol 45 (8) ◽  
pp. 1476-1479
Author(s):  
Prhiscylla Sadanã Pires ◽  
Jose Azael Zambrano Uribe ◽  
Antônio Último de Carvalho ◽  
Rodrigo Otávio Silveira Silva ◽  
Felipe Masiero Salvarani ◽  
...  

Clostridium perfringens type A has been incriminated as the etiologic agent in jejunal hemorrhage syndrome (JHS), which is a disease that affects dairy cattle. Although this microorganism is considered an important enteropathogen the pathogenesis of JHS is still not clear, and there have been no reports of its occurrence in Brazil so far. The aim of this study was to describe the occurrence of JHS by infection with a C. perfringens type A strain carrying the beta-2 toxin gene in a zebu cow in Brazil, for the first time.


1999 ◽  
Vol 67 (9) ◽  
pp. 4902-4907 ◽  
Author(s):  
Darren M. Ellemor ◽  
Rebecca N. Baird ◽  
Milena M. Awad ◽  
Richard L. Boyd ◽  
Julian I. Rood ◽  
...  

ABSTRACT A hallmark of gas gangrene (clostridial myonecrosis) pathology is a paucity of leukocytes infiltrating the necrotic tissue. The cause of this paucity most likely relates to the observation of leukocyte aggregates at the border of the area of tissue necrosis, often within the microvasculature itself. Infecting mice with genetically manipulated strains of Clostridium perfringens type A (deficient in either alpha-toxin or theta-toxin production) resulted in significantly reduced leukocyte aggregation when alpha-toxin was absent and complete abrogation of leukocyte aggregation when theta-toxin was absent. Thus, both alpha-toxin and theta-toxin are necessary for the characteristic vascular leukostasis observed in clostridial myonecrosis.


1968 ◽  
Vol 14 (6) ◽  
pp. 705-709 ◽  
Author(s):  
A. H. W. Hauschild ◽  
F. S. Thatcher

Classical and food-poisoning strains of Clostridium perfringens type A were tested for their capacity to produce gas gangrene in guinea pigs.The virulence of food-poisoning strains producing heat-sensitive spores and showing beta hemolysis on sheep-blood agar was comparable to that of the classical strains. The most virulent strains of both groups produced fatal infection with only three to five vegetative cells. Of 13 food-poisoning, heat-sensitive strains showing no beta hemolysis, only three were lethal when a minimum of 4 × 104 to 4 × 108 cells was injected. None of the food-poisoning, heat-resistant strains produced fatal infection with cell numbers up to 4 × 108. The groups of strains showed a correlation between virulence and formation of alpha toxin in liquid culture.It is concluded that a number of heat-sensitive, beta-hemolytic strains of C. perfringens may cause gas gangrene as well as food poisoning, and that the current subdivision of C. perfringens type A strains into classical and food-poisoning groups is no longer tenable.


2003 ◽  
Vol 6 (4) ◽  
pp. 259-261
Author(s):  
Norma Heredia ◽  
Elva Ar�chiga ◽  
Ronald Labb� ◽  
Santos Garc�a

PLoS ONE ◽  
2017 ◽  
Vol 12 (9) ◽  
pp. e0185215 ◽  
Author(s):  
Xueling Zheng ◽  
Xiumin Wang ◽  
Da Teng ◽  
Ruoyu Mao ◽  
Ya Hao ◽  
...  

mSphere ◽  
2020 ◽  
Vol 5 (3) ◽  
Author(s):  
Mauricio A. Navarro ◽  
Jihong Li ◽  
Juliann Beingesser ◽  
Bruce A. McClane ◽  
Francisco A. Uzal

ABSTRACT Clostridium perfringens type A is involved in gas gangrene in humans and animals. Following a traumatic injury, rapid bacterial proliferation and exotoxin production result in severe myonecrosis. C. perfringens alpha toxin (CPA) and perfringolysin (PFO) are the main virulence factors responsible for the disease. Recent in vitro studies have identified an Agr-like quorum-sensing (QS) system in C. perfringens that regulates the production of both toxins. The system is composed of an AgrB membrane transporter and an AgrD peptide that interacts with a two-component regulatory system in response to fluctuations in the cell population density. In addition, a synthetic peptide named 6-R has been shown to interfere with this signaling mechanism, affecting the function of the Agr-like QS system in vitro. In the present study, C. perfringens type A strain ATCC 3624 and an isogenic agrB-null mutant were tested in a mouse model of gas gangrene. When mice were intramuscularly challenged with 106 CFU of wild-type ATCC 3624, severe myonecrosis and leukocyte aggregation occurred by 4 h. Similar numbers of an agrB-null mutant strain produced significantly less severe changes in the skeletal muscle of challenged mice. Complementation of the mutant to regain agrB expression restored virulence to wild-type levels. The burdens of all three C. perfringens strains in infected muscle were similar. In addition, animals injected intramuscularly with wild-type ATCC 3624 coincubated with the 6-R peptide developed less severe microscopic changes. This study provides the first in vivo evidence that the Agr-like QS system is important for C. perfringens type A-mediated gas gangrene. IMPORTANCE Clostridium perfringens type A strains produce toxins that are responsible for clostridial myonecrosis, also known as gas gangrene. Toxin production is regulated by an Agr-like quorum-sensing (QS) system that responds to changes in cell population density. In this study, we investigated the importance of this QS system in a mouse model of gas gangrene. Mice challenged with a C. perfringens strain with a nonfunctional regulatory system developed less severe changes in the injected skeletal muscle compared to animals receiving the wild-type strain. In addition, a synthetic peptide was able to decrease the effects of the QS in this disease model. These studies provide new understanding of the pathogenesis of gas gangrene and identified a potential therapeutic target to prevent the disease.


1971 ◽  
Vol 17 (1) ◽  
pp. 1-6 ◽  
Author(s):  
D. E. Mahony ◽  
M. E. Butler

Thirty-three strains of Clostridium perfringens were screened for bacteriocin production. Four bacteriocin-producing strains were detected by plating the supernatant fluids of these cultures on all available strains of C. perfringens seeded in semisolid agar and noting zones of bacterial inhibition after subsequent incubation. The spectrum of sensitive strains differed for each bacteriocin as did the degree of bacterial sensitivity to each bacteriocin.One bacteriocin and one indicator strain were chosen for further study. This bacteriocin, which was spontaneously produced during the logarithmic growth phase of the bacteriocinogenic strain, was not inducible with ultraviolet light but was sensitive to heat and trypsin. Adsorption of bacteriocin to the indicator strain was not detected and electron microscopy did not reveal any particulate substance associated with bacteriocin activity. The degree of bacterial inhibition was dependent on the titer of the bacteriocin used, and the age of the indicator culture appeared to influence its relative response to bacteriocin treatment.


2020 ◽  
Vol 29 (5) ◽  
pp. 981-989
Author(s):  
Ali Haghroosta ◽  
Hossein Goudarzi ◽  
Ebrahim Faghihloo ◽  
Zohreh Ghalavand ◽  
Mohammad Mahdi Ranjbar ◽  
...  

Abstract In silico analysis is the most important approach to understand protein structure and functions, and the most important problem for designing and producing a fusion construct is producing large amounts of functional protein. Clostridium perfringens type A and Clostridium septicum produce alpha (plc) and alpha toxins respectively. C. perfringens can cause gas gangrene and gastrointestinal diseases. C. septicum can cause traumatic and non-traumatic gas gangrene. The aim of current research was in silico analysis of a chimeric fusion protein against C. perfringens type A and C. septicum alpha toxins. Firstly, the chimeric fusion gene was designed according to nucleotide sequences of C. perfringens type A alpha (KY584046.1) and C. septicum alpha (JN793989.2) toxin genes and then its fusion protein is constructed by amino acid sequences of C. perfringens type A and C. septicum alpha toxins. Secondly, online software was used to determine prediction of secondary and tertiary structures and physicochemical characteristics of the fusion protein. Finally, the validation of the fusion protein was confirmed by Rampage and proSA program. The designed fusion protein has 777 amino acids in length. TASSER server and physicochemical parameters are showed: C-score = − 2.68 and molecular weight = 87.9 KD respectively. Rampage and proSA software revealed the fusion protein is valid. Deposited accession number for the sequence of the fusion gene in the GenBank is MK908396. The designed fusion protein is valid and functional. Thus, the fusion gene could be used for clone and expression in a proper prokaryotic cell and also as a recombinant vaccine candidate.


1998 ◽  
Vol 61 (7) ◽  
pp. 874-878 ◽  
Author(s):  
RENATA G. K. LEUSCHNER ◽  
WALTER P. HAMMES

Red smear formation during fermentation of Munster cheese was started by using three different strains of Brevibacterium linens as surface inocula. The cheeses were produced with and without supplementation of histamine and tyramine. After smearing the cheese surface for the first time with B. linens viable counts of 107 CFU/g were detected. At the end of the logarithmic growth phase cell numbers increased to 1010 CFU/g and remained constant during the whole ripening period. During a 4-week ripening period strains of B. linens reduced histamine and tyramine content by 55 to 70%. B. linens LTH 456 and LTH 3686 degraded histamine and tyramine in a phosphate buffer (pH 7) containing 0.54 M histamine and 0.58 M tyramine when incubated with agitation at 30°C. B. linens LTH 3813 did not reveal any amine degradation activity in a buffer system. The pH on the cheese surface increased from 5 to 7, whereas it increased in the center only to 5.3 after a 3-week ripening period.


Sign in / Sign up

Export Citation Format

Share Document