All posts by Postępy Mikrobiologii

MECHANIZMY WIRULENCJI STREPTOCOCCUS PYOGENES

Patogenicity mechanisms of Streptococcus pyogenes
K. Szczypa, J. Wilemska, W. Hryniewicz, I. Sitkiewicz

1. Wstęp. 2. Charakterystyka zakażeń powodowanych przez S. pyogenes. 3. Czynniki wirulencji S. pyogenes. 3.1. Adhezyny. 3.2. Czynniki sprzyjające rozprzestrzenianiu się infekcji w organizmie gospodarza. 3.3. Toksyny. 4. Regulacja ekspresji czynników wirulencji. 5. Podsumowanie

1. Introduction. 2. Infections caused by S. pyogenes. 3. Virulence factors of S. pyogenes. 3.1. Adhesins. 3.2. Factors of infections in host organism. 3.3. Toxins. 4. Regulation of virulence factors expression. 5. Summary

Abstract: The group A Streptococcus (Streptococcus pyogenes, GAS) is responsible for over 600 million infections and over half million deaths a year. GAS is a major human pathogen which causes diseases ranging from mild superficial infections of the throat or skin, up to severe systemic and invasive diseases such as necrotizing fasciitis and streptococcal toxic shock syndrome. Nowadays, post-infection sequelae such as glomerulonephritis and rheumatic fever are also alarming medical problems worldwide. Molecular analyses of streptococcal virulence carried by multiple centers worldwide, suggest the presence of a complex mechanism that coordinates pathogenesis. It involves a broad range of unique protein virulence factors, as M protein, superantigens, proteases and DNases, affecting tissues and the host’s immune system. Detailed analyses of individual virulence factors as well as regulatory systems that coordinate expression of virulence factors are the first steps on the way to develop innovative strategies for diagnostics and treatment. This review aims to highlight the epidemiology of S. pyogenes and summarize the current state of knowledge about the mechanisms of its virulence.

CLOSTRIDIUM PERFRINGENS JAKO CZYNNIK ETIOLOGICZNY BIEGUNKI POANTYBIOTYKOWEJ

Clostridium perfringens as the etiological agent of antibiotic associated diarrhoea
J. Kądzielska, P. Obuch-Woszczatyński, H. Pituch, G. Młynarczyk

1. Wstęp. 2. Enterotoksyna Clostridium perfringens (CPE). 2.1. Budowa enterotoksyny. 2.2. Molekularne podstawy toksynotwórczości szczepów C. perfringens typu A. 2.3. Mechanizm działania enterotoksyny C. perfringens (CPE). 3. Sporulacja C. perfringens. 4. Biegunka poantybiotykowa o etiologii C. perfringens. 5. Diagnostyka biegunki o etiologii C. perfringens typu A. 6. Nowe czynniki zjadliwości C. perfringens typu A. 7. Podsumowanie

Abstract: Clostridium perfringens strains are classified into one of five types (A-E) based on their ability to produce four major toxins: α, β, ε, ι. C. perfringens strains belonging to biotype A may cause gas gangrene and different gastrointestinal infections such as antibioticassociated diarrhoea (AAD), sporadic diarrhoea (SD), necrotizing enterocolitis and food poisoning. The major role in the pathogenesisof C. perfringens diarrhoea plays the enterotoxin (CPE). Presented review describes structure, mechanism of action and molecular background of C. perfringens enterotoxin (CPE). Mechanism of C. perfringens type A sporulation and its importance in causing case of diarrhoea is described. In addition literature reports of cases of AAD and sporadic diarrhoea, risk groups and available diagnostic methods are discussed. Special attention is paid to new virulence factors produced by C. perfringens such as beta2 toxin (β2), isolated from AAD cases, and its possible inffuence on clinical picture of the disease.

1. Introduction. 2. Clostridium perfringens enterotoxin (CPE). 2.1. Structure of enterotoxin. 2.2. Molecular background of toxicity of C. perfringens type A strains. 2.3. Mechanism of action of C. perfringens enterotoxin (CPE). 3. Sporulation of C. perfringens. 4. Antibioticassociated diarrhoea caused by C. perfringens. 5. Diagnosis of diarrhoea caused by C. perfringens type A. 6. New virulence factors of C. perfringens type A. 7. Summary

MIKROBIOM CZŁOWIEKA – ZDROWIE I CHOROBA

Human microbiome – health and disease
M. Binek

1. Wstęp. 2. Techniki wykorzystywane do badań mikrobiomu. 3. Poznanie mikrobiomu człowieka w projekcie NIH. 4. Inne korzyści wynikające z realizacji projektu. 5. Jelitowy mikrobiom człowieka. 6. Skład i funkcja mikrobiomu na podstawie badań metagenomowych. 7. Mikrobiota a zachowanie homeostazy. 8. Mikrobiom a indukcja odpowiedzi poszczepiennej. 9. Podsumowanie

Abstract: Commensal microorganisms are known to colonize and form complex communities (microbiome) at various sites within the mammalian body. Because the human microbiome has the potential to affect so many aspects of human health, it has recently become the focus of a series of international human microbiome projects. Such studies are expected to lead to understanding of the impact of microbiota on human health and disease. Recent advances in sequencing technology have opened an entirely new arena in the research of diverse human microbiomes (the ecological community of commensal, symbiotic, and pathogenic microorganisms). In 2007 the National Institutes of Health launched the Human Microbiome Project to study the human microbiom broadly by examining at least four body sites i.e. gastrointestinal tract, the mouth, the vagina, and the skin. The primary goal of this project is to characterize the human microbiome and determine changes in the microbiome correlated to specific disease states. High-throughput sequencing is used to produce microbiome sequence data of samples from normal and diseased donors. Progress to date includes more than 1000 commensal bacteria genomes that have been completed and deposited in GenBank. In recent years, special attention has been paid to the ability of microbiota to modulate the expression of host genes. This is phenomenon forms part of the „cross-talk process” that takes place between the host and its indigenous microbiota. Studies on human intestinal microbiota suggest that host epithelials cell can express specific glycoconjugates in response to the presence of bacteria. Therefore, the gut microflora is responsible for modifying potential sites for attachment. This could be a selective advantage when competing with other bacteria for a niche with limited resources. The mucosal immune system has developed specialized regulatory, anti-inflammatory mechanisms for eliminating pathogens and tolerating commensal microorganisms. Toll-like receptors mediate recognition of microbial patterns to eliminate pathogens. In contrast, commensal bacteria exploit the TLR pathway to actively suppress immunity in order to establish host-microbial symbiosis. Activating anti-inflammatory response in the host via pattern recognition receptor signaling maintains homeostasis. Moreover, it has been shown that the intestinal microbiota composition exerts an effect on the development of immune response to certain vaccine antigens. Thus microbiota along with host human cells form a complex ecosystem which, as a whole interactively performs various biological processes. Their genomes are tightly linked forming an integral part of common metagenome.

1. Introduction. 2. Techniques for the study of human microbiome. 3. The NIH human microbiome project. 4. Additional advantages of launching the human microbiome Project. 5. Human intestinal microbiota. 6. Quality and function of microbiota based on metagenomics sequence data. 7. Microbiota and maintenance of homeostasis. 8. Does the microbiome affect the efficacy of vaccines? 9. Conclusions

CHOROBY SERCA JAKO PÓŹNE POWIKŁANIA ZAKAŻEŃ ODZWIERZĘCYCH PRZENOSZONYCH PRZEZ KLESZCZE

Heart disease as a late complications of zoonosis transmitted by a ticks
I. Mączka, S. Tylewska -Wierzbanowska
1. Wstęp. 2. Bartoneloza. 3. Borelioza z Lyme. 4. Gorączka Q. 5. Riketsjoza. 6. Diagnostyka. 7. Leczenie. 8. Podsumowanie
Abstract: Many bacterial species can be a cause of various heart diseases. The pathogens that trigger these disorders are very often fastidious, uncultured bacteria, such as: Borrelia burgdorferi sensu lato, Coxiella burnetii, Bartonella spp. and Rickettsia spp. The following symptoms: myocarditis, endocarditis, pancarditis, perimyocarditis, dilated cardiomyopathy (DCM), conduction and rhythm disturbances and atherosclerotic, cardiovascular and valvular disease may indicate a bacterial etiology of the disease. Detection of significant titers of specific antibodies allows to identify the origin of the disease. A research performed recently has shown the presence of Bartonella spp., B. afzeli and C. burnetii bacteria in malfunctioning human hearts. It indicates that these pathogens, occur ring in the natural environment in ticks and other wild animals, play a significant role in constation of cardiovascular diseases.
1. Introduction. 2. Bartonellosis. 3. Lyme borreliosis. 4. Q fever. 5. Rickettsial disease. 6. Diagnostics. 7. Treatment. 8. Summary

ZAKAŻENIA BARTONELLA SPP. ZE SZCZEGÓLNYM UWZGLĘDNIENIEM CHORÓB OCZU

Bartonella spp. infections with particular emphasis on eye diseases
B. Fiecek, T. Chmielewski, S. Tylewska - Wierzbanowska
1. Wstęp. 2. Bartonella sp. – wewnątrzkomórkowy patogen. 3. Chorobotwórczość bakterii Bartonella sp. dla zwierząt. 4. Chorobotwórczość Bartonella sp. dla ludzi. 4.1. Bartonella henselae – patogen wywołujący choroby oczu. 5. Podsumowanie
Abstract: Bartonellosis is a zoonosis caused by bacteria of the genus Bartonella which are transmitted by vectors such as feas, lice and ticks. It causes mainly cat scratch disease (CSD), but also endocarditis, meningitis, peliosis hepatitis, bacillary angiomatosis and pneumonia. It has been established that about 5–25% of infections caused by Bartonella spp. may have a form of infammatory process within the eyeball. Tese diseases include optic neuritis, anterior uveitis, focal retinal vasculitis or focal choroiditis, lesions in the optic disc region, infammation of the vitreous and the branch retinal arteriolar or venular occlusions. Ophthalmic bartonellosis should be particularly suspected in patients who have contact with a cat and develop a sudden fever with loss of vision.
1. Introduction. 2. Bartonella sp. intracellular pathogen. 3. Pathogenicity of Bartonella sp. in animals. 4. Pathogenicity Bartonella sp. in people. 4.1. Bartonella henselae a pathogen causing eye diseases. 5. Summary