scholarly journals In vitro growth and cell wall degrading enzyme production by Argentinean isolates of Macrophomina phaseolina, the causative agent of charcoal rot in corn

2016 ◽  
Vol 48 (4) ◽  
pp. 267-273 ◽  
Author(s):  
Araceli M. Ramos ◽  
Marcela Gally ◽  
Gala Szapiro ◽  
Tatiana Itzcovich ◽  
Maira Carabajal ◽  
...  
2015 ◽  
Vol 105 ◽  
pp. 97-105 ◽  
Author(s):  
Pedro Ricardo V. Hamann ◽  
Dayane L. Serpa ◽  
Amanda Souza Barreto da Cunha ◽  
Brenda R. de Camargo ◽  
Karen Ofuji Osiro ◽  
...  

2009 ◽  
Vol 191 (7) ◽  
pp. 2163-2168 ◽  
Author(s):  
Katherine E. Price ◽  
Andrew Camilli

ABSTRACT Streptococcus pneumoniae is the causative agent of multiple diseases, including otitis media, pneumonia, bacteremia, and meningitis. Pneumolysin (Ply), a member of the cholesterol-dependent cytolytic pore-forming toxins, is produced by virtually all clinical isolates of S. pneumoniae, and strains in which the Ply gene has been deleted are severely attenuated in mouse models of infection. In contrast to all other members of the cholesterol-dependent cytolysin family, Ply lacks a signal peptide for export. Instead, Ply has been hypothesized to be released upon autolysis or, alternatively, via a nonautolytic mechanism that remains ill defined. We determined by use of cell fractionation and Western blotting that, during in vitro growth, exported Ply is localized primarily to the cell wall compartment in 18 different serotypes in the absence of detectable cell lysis. Hemolytic assays revealed that this cell wall-localized Ply is active. Additionally, cell wall-localized Ply is accessible to extracellular protease and is detergent releasable.


1989 ◽  
Vol 2 (3) ◽  
pp. 270-277 ◽  
Author(s):  
P J Blackall

There are four currently recognized taxa to accommodate the avian haemophili: Haemophilus paragallinarum, Pasteurella avium, Pasteurella volantium, and Pasteurella species A (the last three being formerly united as Haemophilus avium). A range of other taxa has also been recognized, but they have been neither named nor assigned to a genus. All of these various taxa, legitimate and otherwise, have the common characteristic of requiring V factor, but not X factor, for in vitro growth. Several recent studies have established the phenotypic properties that allow the differentiation of the recognized taxa, both named and unnamed. The serological properties of H. paragallinarum, the causative agent of infectious coryza of chickens, has received considerable recent attention. In contrast, many questions on the pathogenicity and virulence mechanisms of H. paragallinarum remain unanswered. Another area requiring further work is the identification of those antigens responsible for inducing protective immunity in vaccinated or naturally infected chickens.


2013 ◽  
Vol 20 (6) ◽  
pp. 846-853 ◽  
Author(s):  
Jin-A Jeon ◽  
Seo-Jun Park ◽  
Soo-Hwan Yeo ◽  
Ji-Ho Choi ◽  
Han-Seok Choi ◽  
...  

2019 ◽  
Vol 12 (6) ◽  
pp. 1286-1292 ◽  
Author(s):  
Roxane Raulo ◽  
Egon Heuson ◽  
Ali Siah ◽  
Vincent Phalip ◽  
Renato Froidevaux

mSphere ◽  
2019 ◽  
Vol 4 (3) ◽  
Author(s):  
Haofu Hu ◽  
Rafael Rodrigues da Costa ◽  
Bo Pilgaard ◽  
Morten Schiøtt ◽  
Lene Lange ◽  
...  

ABSTRACT Termites forage on a range of substrates, and it has been suggested that diet shapes the composition and function of termite gut bacterial communities. Through comparative analyses of gut metagenomes in nine termite species with distinct diets, we characterize bacterial community compositions and use peptide-based functional annotation method to determine biomass-degrading enzymes and the bacterial taxa that encode them. We find that fungus-growing termite guts have relatively more fungal cell wall-degrading enzyme genes, while wood-feeding termite gut communities have relatively more plant cell wall-degrading enzyme genes. Interestingly, wood-feeding termite gut bacterial genes code for abundant chitinolytic enzymes, suggesting that fungal biomass within the decaying wood likely contributes to gut bacterial or termite host nutrition. Across diets, the dominant biomass-degrading enzymes are predominantly coded for by the most abundant bacterial taxa, suggesting tight links between diet and gut community composition, with the most marked difference being the communities coding for the mycolytic capacity of the fungus-growing termite gut. IMPORTANCE Understanding functional capacities of gut microbiomes is important to improve our understanding of symbiotic associations. Here, we use peptide-based functional annotation to show that the gut microbiomes of fungus-farming termites code for a wealth of enzymes that likely target the fungal diet the termites eat. Comparisons to other termites showed that fungus-growing termite guts have relatively more fungal cell wall-degrading enzyme genes, whereas wood-feeding termite gut communities have relatively more plant cell wall-degrading enzyme genes. Across termites with different diets, the dominant biomass-degrading enzymes are predominantly coded for by the most abundant bacterial taxa, suggesting tight links between diet and gut community compositions.


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