نتایج جستجو برای: mycobacteria

تعداد نتایج: 8178  

2003
CHARLES C. SHEPARD

The cytoplasm of HeLa cells provides a favorable site for the rapid multiplication of tubercle bacilli and several other species of mycobacteria pathogenic for humans (1). The purpose of the present study was to learn the comparative suitability for the growth of mycobacteria of some other human and simian cells growing in tissue culture of the monolayer type. Human amnlon and monkey kidney cel...

Journal: :Infection and immunity 2002
Shannon K Roach Jeffrey S Schorey

Mycobacteria are the etiologic agents of numerous diseases which account for significant morbidity and mortality in humans and other animal species. Many mycobacteria are intramacrophage pathogens and therefore the macrophage response to infection, which includes synthesis of cytokines such as tumor necrosis factor alpha (TNF-alpha) and production of nitric oxide, has important consequences for...

2015
Brilliant B. Luthuli Georgiana E. Purdy Frederick K. Balagaddé Jérôme Nigou

Tuberculosis (TB) is the world's deadliest curable disease, responsible for an estimated 1.5 million deaths annually. A considerable challenge in controlling this disease is the prolonged multidrug chemotherapy (6 to 9 months) required to overcome drug-tolerant mycobacteria that persist in human tissues, although the same drugs can sterilize genetically identical mycobacteria growing in axenic ...

Journal: :Journal of immunology 2015
Chien-Hsiung Yu Massimo Micaroni Andreas Puyskens Thomas E Schultz Jeremy Changyu Yeo Amanda C Stanley Megan Lucas Jade Kurihara Karen M Dobos Jennifer L Stow Antje Blumenthal

Cytokines are key regulators of adequate immune responses to infection with Mycobacterium tuberculosis. We demonstrate that the p110δ catalytic subunit of PI3K acts as a downstream effector of the TLR family member RP105 (CD180) in promoting mycobacteria-induced cytokine production by macrophages. Our data show that the significantly reduced release of TNF and IL-6 by RP105(-/-) macrophages dur...

Journal: :Journal of clinical microbiology 1997
L F Kox H M Jansen S Kuijper A H Kolk

Rapid identification of infecting mycobacterial species enables appropriate medical care decisions to be made. Our aim was to demonstrate the clinical usefulness of the multiplex PCR assay, a test based on PCR, which permits direct identification of 12 mycobacterial species in clinical specimens. A total of 259 specimens from 177 patients who had clinical symptoms of mycobacterial disease but f...

2011
Susanne Herbst Ulrich E. Schaible Bianca E. Schneider

Mycobacterium tuberculosis is an intracellular pathogen of macrophages and escapes the macrophages' bactericidal effectors by interfering with phagosome-lysosome fusion. IFN-γ activation renders the macrophages capable of killing intracellular mycobacteria by overcoming the phagosome maturation block, nutrient deprivation and exposure to microbicidal effectors including nitric oxide (NO). While...

2012
Hasan Shojaei Hashemi Abodolrazagh Parvin Heidarieh Fazel Pourahmad Daei Naser Daei Naser

OBJECTIVES In addition to several molecular methods and in particular 16S rDNA analysis, the application of a more discriminatory genetic marker, i.e., 16S-23S internal transcribed spacer gene sequence has had a great impact on identification and classification of mycobacteria. In the current study we aimed to apply this sequencing power to conclusive identification of some Iranian clinical str...

Journal: :The Journal of Experimental Medicine 1990
D Kabelitz A Bender S Schondelmaier B Schoel S H Kaufmann

We report that M. tuberculosis organisms, but neither PHA nor allogeneic stimulator cells, preferentially activate gamma/delta+ cells within E rosette-purified peripheral blood T cells. gamma/delta+ T cells from purified protein derivative (PPD)-nonimmune healthy donors were enriched by depletion of CD4+ and CD8+ cells; double-negative (DN) cells contained 65-92% gamma/delta+ T cells. Limiting ...

Journal: :Emerging Infectious Diseases 2009

Journal: :Microbiology Australia 2004

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