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1.
Microorganisms ; 11(1)2023 Jan 09.
Article in English | MEDLINE | ID: mdl-36677460

ABSTRACT

We have previously reported the draft genome sequences of 59 endospore-forming Gram-positive bacterial strains isolated from Vietnamese crop plants due to their ability to suppress plant pathogens. Based on their draft genome sequence, eleven of them were assigned to the Brevibacillus and one to the Lysinibacillus genus. Further analysis including full genome sequencing revealed that several of these strains represent novel genomospecies. In vitro and in vivo assays demonstrated their ability to promote plant growth, as well as the strong biocontrol potential of Brevibacilli directed against phytopathogenic bacteria, fungi, and nematodes. Genome mining identified 157 natural product biosynthesis gene clusters (BGCs), including 36 novel BGCs not present in the MIBiG data bank. Our findings indicate that plant-associated Brevibacilli are a rich source of putative antimicrobial compounds and might serve as a valuable starting point for the development of novel biocontrol agents.

2.
J Gen Virol ; 93(Pt 1): 106-112, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21940410

ABSTRACT

Lactate dehydrogenase-elevating virus (LDV) exacerbates mouse susceptibility to endotoxin shock through enhanced tumour necrosis factor (TNF) production by macrophages exposed to lipopolysaccharide (LPS). However, the in vivo enhancement of TNF production in response to LPS induced by the virus largely exceeds that found in vitro with cells derived from infected animals. Infection was followed by a moderate increase of Toll-like receptor (TLR)-4/MD2, but not of membrane CD14 expression on peritoneal macrophages. Peritoneal macrophages from LDV-infected mice unresponsive to type I interferons (IFNs) did not show enhanced expression of TLR-4/MD2 nor of CD14, and did not produce more TNF in response to LPS than cells from infected normal counterparts, although the in vivo response of these animals to LPS was strongly enhanced. In contrast, the virus triggered a sharp increase of soluble CD14 and of LPS-binding protein serum levels in normal mice. However, production of these LPS soluble receptors was similar in LDV-infected type I IFN-receptor deficient mice and in their normal counterparts. Moreover, serum of LDV-infected mice that contained these soluble receptors had little effect if any on cell response to LPS. These results suggest that enhanced response of LDV-infected mice to LPS results mostly from mechanisms independent of LPS receptor expression.


Subject(s)
Arterivirus Infections/veterinary , Lactate dehydrogenase-elevating virus/physiology , Lipopolysaccharide Receptors/genetics , Rodent Diseases/genetics , Rodent Diseases/virology , Acute-Phase Proteins/genetics , Acute-Phase Proteins/immunology , Animals , Arterivirus Infections/genetics , Arterivirus Infections/immunology , Arterivirus Infections/virology , Carrier Proteins/genetics , Carrier Proteins/immunology , Cells, Cultured , Down-Regulation , Female , Lactate dehydrogenase-elevating virus/immunology , Lipopolysaccharide Receptors/metabolism , Lipopolysaccharides/immunology , Lymphocyte Antigen 96/genetics , Lymphocyte Antigen 96/immunology , Macrophages, Peritoneal/immunology , Macrophages, Peritoneal/virology , Male , Membrane Glycoproteins/genetics , Membrane Glycoproteins/immunology , Mice , Mice, Inbred BALB C , Rodent Diseases/immunology , Toll-Like Receptor 4/genetics , Toll-Like Receptor 4/immunology , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/immunology
3.
PLoS One ; 6(3): e17604, 2011 Mar 08.
Article in English | MEDLINE | ID: mdl-21408132

ABSTRACT

BACKGROUND: Streptococcus suis infection, an emerging zoonosis, is an increasing public health problem across South East Asia and the most common cause of acute bacterial meningitis in adults in Vietnam. Little is known of the risk factors underlying the disease. METHODS AND FINDINGS: A case-control study with appropriate hospital and matched community controls for each patient was conducted between May 2006 and June 2009. Potential risk factors were assessed using a standardized questionnaire and investigation of throat and rectal S. suis carriage in cases, controls and their pigs, using real-time PCR and culture of swab samples. We recruited 101 cases of S. suis meningitis, 303 hospital controls and 300 community controls. By multivariate analysis, risk factors identified for S. suis infection as compared to either control group included eating "high risk" dishes, including such dishes as undercooked pig blood and pig intestine (OR(1) = 2.22; 95%CI = [1.15-4.28] and OR(2) = 4.44; 95%CI = [2.15-9.15]), occupations related to pigs (OR(1) = 3.84; 95%CI = [1.32-11.11] and OR(2) = 5.52; 95%CI = [1.49-20.39]), and exposures to pigs or pork in the presence of skin injuries (OR(1) = 7.48; 95%CI = [1.97-28.44] and OR(2) = 15.96; 95%CI = [2.97-85.72]). S. suis specific DNA was detected in rectal and throat swabs of 6 patients and was cultured from 2 rectal samples, but was not detected in such samples of 1522 healthy individuals or patients without S. suis infection. CONCLUSIONS: This case control study, the largest prospective epidemiological assessment of this disease, has identified the most important risk factors associated with S. suis bacterial meningitis to be eating 'high risk' dishes popular in parts of Asia, occupational exposure to pigs and pig products, and preparation of pork in the presence of skin lesions. These risk factors can be addressed in public health campaigns aimed at preventing S. suis infection.


Subject(s)
Streptococcal Infections/epidemiology , Streptococcus suis/physiology , Adult , Age Distribution , Animals , Carrier State/microbiology , Case-Control Studies , Female , Hospitals , Humans , Male , Middle Aged , Multivariate Analysis , Polymerase Chain Reaction , Risk Factors , Streptococcal Infections/microbiology , Streptococcus suis/genetics , Sus scrofa/microbiology , Vietnam/epidemiology
4.
J Gen Virol ; 88(Pt 11): 3063-3066, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17947531

ABSTRACT

Two distinct pathways of gamma interferon (IFN-gamma) production have been found in mice infected with lactate dehydrogenase-elevating virus. Both pathways involve natural killer cells. The first is mostly interleukin-12-independent and is not controlled by type I interferons. The second, which is suppressed by type I interferons, leads to increased levels of IFN-gamma production and requires the secretion of interleukin-12. This regulation of IFN-gamma production by type I interferons may help to control indirect pathogenesis induced by this cytokine.


Subject(s)
Interferon-gamma/biosynthesis , Killer Cells, Natural/immunology , Lactate dehydrogenase-elevating virus/immunology , Metabolic Networks and Pathways , Animals , Gene Expression Regulation , Interferon Type I/immunology , Interleukin-12/immunology , Mice
5.
Int Immunol ; 19(11): 1303-11, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17914119

ABSTRACT

The effect of mouse infection with lactate dehydrogenase-elevating virus (LDV), a usually non-pathogenic virus, on concomitant bacterial endotoxin shock was analyzed, in terms of lethality and cytokine production. A strong enhancement of susceptibility to the shock was observed in mice acutely infected with this virus. It correlated with a sharp increase of tumor necrosis factor and leukemia inhibitory factor production and was controlled by the mouse genetic background. The viral infection led to an imbalance in the cytokine response to LPS, with an enhancement of pro-inflammatory cytokines, including IL-18 and IFN-gamma and a delayed secretion of anti-inflammatory IL-10 that could result in exacerbated macrophage activation. Enhanced IFN-gamma production was involved in the virus-induced susceptibility to shock. In sharp contrast with other viral infections, IFN-alpha/beta diminished IFN-gamma production and the resulting increased response to LPS in LDV-infected animals.


Subject(s)
Arterivirus Infections/immunology , Endotoxins/toxicity , Interferons/immunology , Lactate dehydrogenase-elevating virus/immunology , Shock, Septic/immunology , Animals , Arterivirus Infections/virology , Cytokines/immunology , Female , Lactate dehydrogenase-elevating virus/pathogenicity , Mice , Mice, Inbred BALB C , Mice, Inbred DBA
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