scholarly journals Use of Green Fluorescent Protein-Transgenic Strains to Study Pathogenic and Nonpathogenic Lifestyles in Colletotrichum acutatum

2002 ◽  
Vol 92 (7) ◽  
pp. 743-749 ◽  
Author(s):  
Sigal Horowitz ◽  
Stanley Freeman ◽  
Amir Sharon

Colletotrichum acutatum, which causes anthracnose disease on strawberry, can also persist on several other plant species without causing disease symptoms. The genetic and molecular bases that determine pathogenic and nonpathogenic lifestyles in C. acutatum are unclear. We developed a transformation system for C. acutatum by electroporation of germinating conidia, and transgenic isolates that express the green fluorescent protein (GFP) were produced. Details of the pathogenic and nonpathogenic lifestyles of C. acutatum were determined by using GFP-transgenic isolates. Major differences between colonization-mediating processes of strawberry and of other plants were observed. On the main host, strawberry, the germinating conidia formed branched, thick hyphae, and large numbers of appressoria were produced that were essential for plant penetration. In strawberry, the fungus developed rapidly, filling the mesophyll with dense mycelium that invaded the cells and caused necrosis of the tissue. In nonpathogenic interactions on pepper, eggplant, and tomato, the conidia germinated, producing thin, straight germ tubes. Appressoria were produced but failed to germinate and penetrate leaf tissue, resulting in epiphytic growth without invasion of the plant. Penetration of the plant occurred only several days after inoculation and was restricted to the intercellular spaces of the first cell layers of infected tissue without causing any visible damage. Much of the new fungal biomass continued to develop on the surface of inoculated organs in the nonpathogenic interaction. The differences in fungal development on strawberry compared with the other plant species suggest that signal molecules, which may be present only in strawberry, trigger appressorial germination and penetration of the primary host.

2007 ◽  
Vol 51 (1) ◽  
pp. 49-55 ◽  
Author(s):  
G. P. Sansebastiano ◽  
L. Renna ◽  
M. Gigante ◽  
M. Caroli ◽  
G. Piro ◽  
...  

2010 ◽  
Vol 76 (18) ◽  
pp. 6119-6127 ◽  
Author(s):  
Putthapoom Lumjiaktase ◽  
Claudio Aguilar ◽  
Tom Battin ◽  
Kathrin Riedel ◽  
Leo Eberl

ABSTRACT Many bacteria utilize quorum sensing (QS) systems to communicate with each other by means of the production, release, and response to signal molecules. N-Acyl homoserine lactone (AHL)-based QS systems are particularly widespread among the Proteobacteria, in which they regulate various functions. It has become evident that AHLs can also serve as signals for interspecies communication. However, knowledge on the impact of AHLs for the ecology of bacteria in their natural habitat is scarce, due mainly to the lack of tools that allow the study of QS in bacterial communities in situ. Here, we describe the construction of self-mobilizable green fluorescent protein (GFP)-based AHL sensors that utilize the conjugation and replication properties of the broad-host-range plasmid RP4. We show that these novel AHL sensor plasmids can be easily transferred to different bacterial species by biparental mating and that they give rise to green fluorescent cells in case the recipient is an AHL producer. We also demonstrate that these sensor plasmids are capable of self-spreading within mixed biofilms and are a suitable tool for the identification of AHL-producing bacteria in lake sediment.


2019 ◽  
Vol 20 (22) ◽  
pp. 5637 ◽  
Author(s):  
Lifang Zou ◽  
Bingwei Yu ◽  
Xing-Liang Ma ◽  
Bihao Cao ◽  
Guoju Chen ◽  
...  

Chinese kale (Brassica oleracea var. chinensis Lei) is an important vegetable crop in South China, valued for its nutritional content and taste. Nonetheless, the thermal tolerance of Chinese kale still needs improvement. Molecular characterization of Chinese kale’s heat stress response could provide a timely solution for developing a thermally tolerant Chinese kale variety. Here, we report the cloning of multi-protein bridging factor (MBF) 1c from Chinese kale (BocMBF1c), an ortholog to the key heat stress responsive gene MBF1c. Phylogenetic analysis showed that BocMBF1c is highly similar to the stress-response transcriptional coactivator MBF1c from Arabidopsis thaliana (AtMBF1c), and the BocMBF1c coding region conserves MBF1 and helix-turn-helix (HTH) domains. Moreover, the promoter region of BocMBF1c contains three heat shock elements (HSEs) and, thus, is highly responsive to heat treatment. This was verified in Nicotiana benthamiana leaf tissue using a green fluorescent protein (GFP) reporter. In addition, the expression of BocMBF1c can be induced by various abiotic stresses in Chinese kale which indicates the involvement of stress responses. The BocMBF1c-eGFP (enhanced green fluorescent protein) chimeric protein quickly translocated into the nucleus under high temperature treatment in Nicotiana benthamiana leaf tissue. Overexpression of BocMBF1c in Arabidopsis thaliana results in a larger size and enhanced thermal tolerance compared with the wild type. Our results provide valuable insight for the role of BocMBF1c during heat stress in Chinese kale.


2006 ◽  
Vol 84 (2) ◽  
pp. 179-188 ◽  
Author(s):  
Stephen J. Dinka ◽  
Manish N. Raizada

Vast numbers of crop, fungal, and animal accessions as well as insect vectors and evolving eukaryotic pathogens await molecular analysis. Inexpensive methods are required to make map-based gene isolation accessible to more of the world’s researchers. Today, positional cloning relies on genotyping and phenotyping large numbers of progeny to detect chromosome recombination events that break linkage between the trait of interest and flanking molecular markers following meiosis. In the postgenome era, positional cloning will no longer be limited by the availability of high-density molecular markers but rather by the skilled labour and the expense of genotyping and phenotyping 103−104 progeny to detect rare recombination events in a narrow chromosome block flanking the target gene of interest. Here, we review how linked, mapped transgenes that encode dominant, visible traits such as green fluorescent protein can be used to preselect meiotic recombinants inexpensively, thus reducing progeny genotyping and phenotyping requirements by >95% during positional cloning. Because transgene markers such as green fluorescent protein are genotype independent, transgenes created in one inbred line may be used to fine-map genetic variation in large numbers of genotypes.


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