Cytokine profiles of HeLa and human diploid cells induced by different fractions of Vibrio parahaemolyticus cultures exposed to stress conditions (original) (raw)
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The role of proteins expressed under the stress condition in virulence of some Vibrio strains
Roumanian Archives of Microbiology and Immunology, 2008
ROMANIAN ARCHIVES OF MICROBIOLOGY AND IMMUNOLOGY Aims and Scope Romanian Archives of Microbiology and Immunoloy, an international journal dedicated to original research work, publishes papers focusing on various aspects of microbiology and immunology. Romanian Archives of Microbiology and Immunology is indexed in MEDLINE. The frequency of the Journal is currently four issues per year. Categories of manuscripts Full-length articles are full-length descriptions of original research (up to 10 printed pages) Reviews are comprehensive appraisals of research in a field of current interest. All reviews are subject to the normal review process (up to 15 printed pages) Rapid Communications are brief, definitive reports of highly significant and timely findings in the field (up to 5 printed pages)
African Journal of …, 2011
Vibrio parahaemolyticus is an estuarine bacterium widely distributed in natural aquatic environments and also a well-known food-borne pathogen, and like other enteropathogenic bacteria, it survives both in its natural environment and in its host. The transition from one state to another requires a high capacity to adapt to different physico-chemical parameters, process which increases the synthesis of specific proteins, including heat-shock proteins (HSPs). In order to investigate the immunogenicity of heat shock proteins from different cellular fractions of V. parahaemolyticus grown under sub-lethal heat and osmotic shock, we analyzed the response of holoxenic mice to V. parahaemolyticus cellular fractions injected intraperitoneally by examining the anti-HSP antibodies response to stressful conditions and the immune protection installed after several immunizations. The supernatant and total cellular extract of heat or simultaneously heat and osmotically-stressed bacterial cultures induced the early occurrence of anti-HSP antibodies (after 4 immunizations), while after 8 immunizations, the anti-HSP antibodies were present in the majority of the tested batches, the most immunogenic fraction proving to be the heat-stressed culture supernatants.
Journal of Infectious Diseases, 2003
In patients with diarrhea caused by Vibrio parahaemolyticus, antibody-secreting cell responses to thermostable direct hemolysin (TDH), lipopolysaccharide (LPS), and whole-cell bacteria were seen. TDH-and LPS-specific responses were seen in serum samples, and immunoglobulin A antibody responses were observed in stool. Levels of C-reactive protein and nitric oxide metabolites increased in the systemic circulation at the onset of illness. Tumor necrosis factor-a and lactoferrin levels were high during the acute stage in mucosal secretions and in plasma, whereas interleukin-1b levels were high only in mucosal secretions. Duodenal and rectal biopsy specimens obtained at the onset of illness showed an acute inflammatory response. The lamina propria showed edema, congestion of blood vessels, and hemorrhage, with an increase in levels of polymorphonuclear neutrophils and macrophages. Strains belonging to different serotypes exhibited varying resistance to killing by serum; the O8:K21 strain was most sensitive. Infection with V. parahaemolyticus results in B cell responses and an acute inflammatory response that is self-limiting.
Infection and Immunity, 2010
Vibrio parahaemolyticus is an inhabitant of estuarine and marine environments that causes seafood-borne gastroenteritis worldwide. Recently, a type 3 secretion system (T3SS2) able to secrete and translocate virulence factors into the eukaryotic cell has been identified in a pathogenicity island (VP-PAI) located on the smaller chromosome. These virulence-related genes have previously been detected only in clinical strains. Classical virulence genes for this species (tdh, trh) are rarely detected in environmental strains, which are usually considered to lack virulence potential. However, during screening of a collection of environmental V. parahaemolyticus isolates obtained in the North Adriatic Sea in Italy, a number of marine strains carrying virulencerelated genes, including genes involved in the T3SS2, were detected. In this study, we investigated the pathogenic potential of these marine V. parahaemolyticus strains by studying their adherence ability, their cytotoxicity, their effect on zonula occludin protein 1 (ZO-1) of the tight junctions, and their effect on transepithelial resistance (TER) in infected Caco-2 cells. By performing a reverse transcription-PCR, we also tested the expression of the T3SS2 genes vopT and vopB2, encoding an effector and a translocon protein, respectively. Our results indicate that, similarly to clinical strains, marine V. parahaemolyticus strains carrying vopT and vopB2 and that other genes included in the VP-PAI are capable of adhering to human cells and of causing cytoskeletal disruption and loss of membrane integrity in infected cells. On the basis of data presented here, environmental V. parahaemolyticus strains should be included in coastal water surveillance plans, as they may represent a risk for human health.
Fish & Shellfish Immunology, 2017
Marine bivalves are exposed to different types of bacteria in the surrounding waters, in particular of the Vibrio genus. In the hemocytes of the mussel Mytilus spp. immune responses to different vibrios have been largely characterized. However, little information is available on the hemocyte responses to human pathogenic vibrios commonly detected in coastal waters and bivalve tissues that are involved in seafoodborne diseases. In this work, functional parameters of the hemocytes from the Mediterranean mussel M. galloprovincialis were evaluated in response to in vitro challenge with different vibrios isolated from environmental samples of the Adriatic sea (Italy): V. parahaemolyticus Conero, V. alginolyticus 1513 and V. vulnificus 509. V. parahaemolyticus ATCC 43996 was used for comparison. At the 50:1 bacteria hemocyte ratio, only V. parahaemolyticus strains induced significant lysosomal membrane destabilisation. Stimulation of extracellular lysozyme release, total ROS, O 2 À and NO production were observed, although to different extents and with distinct time courses for different vibrios, V. vulnificus 509 in particular. Further comparisons between V. parahaemolyticus Conero and V. vulnificus 509 showed that only the latter induced dysregulation of the phosphorylation state of p38 MAP Kinase and apoptotic processes. The results indicate that mussel hemocytes can mount an efficient immune response towards V. parahaemolyticus and V. alginolyticus strains, whereas V. vulnificus 509 may affect the hemocyte function. This is the first report on immune responses of mussels to local environmental isolates of human pathogenic vibrios. These data reinforce the hypothesis that Mytilus hemocytes show specific responses to different vibrio species and strains.
2002
In patients with diarrhea caused by Vibrio parahaemolyticus, antibody-secreting cell responses to thermostable direct hemolysin (TDH), lipopolysaccharide (LPS), and whole-cell bacteria were seen. TDH-and LPS-specific responses were seen in serum samples, and immunoglobulin A antibody responses were observed in stool. Levels of C-reactive protein and nitric oxide metabolites increased in the systemic circulation at the onset of illness. Tumor necrosis factor-a and lactoferrin levels were high during the acute stage in mucosal secretions and in plasma, whereas interleukin-1b levels were high only in mucosal secretions. Duodenal and rectal biopsy specimens obtained at the onset of illness showed an acute inflammatory response. The lamina propria showed edema, congestion of blood vessels, and hemorrhage, with an increase in levels of polymorphonuclear neutrophils and macrophages. Strains belonging to different serotypes exhibited varying resistance to killing by serum; the O8:K21 strain was most sensitive. Infection with V. parahaemolyticus results in B cell responses and an acute inflammatory response that is self-limiting. Vibrio parahaemolyticus strains are becoming an increasing cause of concern as causative agents of acute gastroenteritis in a number of locations, including India [1], Bangladesh [2, 3], Japan [4], Taiwan [5], and the United States [6]. The serogroups O3:K6, O4:K68, and O1:KUT are believed to have acquired pandemic potential [2, 7, 8]. V. parahaemolyticus is responsible mainly for gastro
The pathogenesis, detection, and prevention of Vibrio parahaemolyticus
Vibrio parahaemolyticus, a Gram-negative motile bacterium that inhabits marine and estuarine environments throughout the world, is a major food-borne pathogen that causes life-threatening diseases in humans after the consumption of raw or undercooked seafood. The global occurrence of V. parahaemolyticus accentuates the importance of investigating its virulence factors and their effects on the human host.This review describes the virulence factors of V. parahaemolyticus reported to date, including hemolysin, urease, two type III secretion systems and two type VI secretion systems, which both cause both cytotoxicity in cultured cells and enterotoxicity in animal models. We describe various types of detection methods, based on virulence factors, that are used for quantitative detection of V. parahaemolyticus in seafood. We also discuss some useful preventive measures and therapeutic strategies for the diseases mediated by V. parahaemolyticus, which can reduce, to some extent, the damage to humans and aquatic animals attributable to V. parahaemolyticus. This review extends our understanding of the pathogenic mechanisms of V. parahaemolyticus mediated by virulence factors and the diseases it causes in its human host. It should provide new insights for the diagnosis, treatment, and prevention of V. parahaemolyticus infection.
Journal of Physics: Conference Series, 2019
Polyclonal antibodies are antibody proteins formed from interaction between antigens that enter a body. It results in immunogenicity. The process of generating polyclonal antibodies begins with purifying a membrane protein. A membrane protein that is potential to make an antibody is the outer membrane protein (OMP) of bacterium V. parahaemolyticus. These proteins are injects into an animal's body as the target antigen so that an antibody can be produced. The antibody was obtained by taking the animal's blood sample. It is then isolated in a serum until it generates a polyclonal antibody. ELISA (Enzyme-Linked Immunosorbent Assay) is a technique normally used to measure the concentration of an antibody or an antigen in blood or to detect their existence in a sample. The aim of this research was to analyse the immunogenicity of polyclonal antibodies produced from Vibrio Parahaemolyticus membranes that was induce using ELISA method. Research findings indicate that the highest OD value of ELISA (0, 404) was obtained on the third week of 1/100 dilution. The highest value of antigens and antibodies interaction was found on 1/100 dilution. Immunization before booster generated relatively small antibody titres because the rat's body was not ready to provide an immune response.
Journal of food protection, 2007
The ability of only a subset of Vibrio parahaemolyticus strains to cause human infection underscores the need for an analytical method that can effectively differentiate between pathogenic strains and those that do not cause disease. We tested the feasibility of a tissue culture-based assay to determine whether clinical isolates could be differentiated from nonclinical isolates based on relative isolate cytopathogenicity. To screen for cytotoxic capability, we measured relative extracellular lactate dehydrogenase as an indicator of host cell damage in five different mammalian cell lines in the presence of V. parahaemolyticus. Isolates originating from clinical sources exhibited 15.5 to 59.3% relative cytotoxicity, whereas those originating from food sources exhibited 4.4 to 54.9% relative cytotoxicity. In the presence of -1.2 x 10(6) cells, cytotoxicity was 1.6- to 3.5-fold higher (P < 0.05) for clinical isolates than for nonclinical isolates in L2, Henle 407, and Caco-2 cell lin...
Virulence of the human pathogen, V. vulnificus, is associated with encapsulation, serum complement resistance, and genotype. The C-genotype of this bacterium is correlated (>90%) with virulence and with isolation source (clinical settings). E-genotype strains are highly correlated with environmental isolation (93%) but appear less virulent. In this study, we characterized the importance of genotype, encapsulation, serum complement, and in situ exposure to estuarine water on the survival of the two genotypes in human serum. Results confirmed the superior ability of C-genotype strains to survive exposure to human serum, as well as the significance of complement, and revealed that lack of capsule allowed serum killing of both C- and E-genotypes. Cells incubated in situ responded similarly to cells incubated in vitro with the exception of E-environmental strains. Interestingly, our studies found that those cells of the E-genotype, typically considered non-pathogenic, which were isolated from wound infections demonstrated serum survival similar to that of virulent, C-genotype, strains.