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  • 1
    Publication Date: 2009-02-03
    Description: Microbial symbioses are essential for the normal development and growth of animals. Often, symbionts must be acquired from the environment during each generation, and identification of the relevant symbiotic partner against a myriad of unwanted relationships is a formidable task. Although examples of this specificity are well-documented, the genetic mechanisms governing it are poorly characterized. Here we show that the two-component sensor kinase RscS is necessary and sufficient for conferring efficient colonization of Euprymna scolopes squid by bioluminescent Vibrio fischeri from the North Pacific Ocean. In the squid symbiont V. fischeri ES114, RscS controls light-organ colonization by inducing the Syp exopolysaccharide, a mediator of biofilm formation during initial infection. A genome-level comparison revealed that rscS, although present in squid symbionts, is absent from the fish symbiont V. fischeri MJ11. We found that heterologous expression of RscS in strain MJ11 conferred the ability to colonize E. scolopes in a manner comparable to that of natural squid isolates. Furthermore, phylogenetic analyses support an important role for rscS in the evolution of the squid symbiosis. Our results demonstrate that a regulatory gene can alter the host range of animal-associated bacteria. We show that, by encoding a regulator and not an effector that interacts directly with the host, a single gene can contribute to the evolution of host specificity by switching 'on' pre-existing capabilities for interaction with animal tissue.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713604/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713604/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mandel, Mark J -- Wollenberg, Michael S -- Stabb, Eric V -- Visick, Karen L -- Ruby, Edward G -- F32 GM078760/GM/NIGMS NIH HHS/ -- F32 GM078760-03/GM/NIGMS NIH HHS/ -- R01 GM059690/GM/NIGMS NIH HHS/ -- R01 GM059690-07/GM/NIGMS NIH HHS/ -- R01 GM059690-08/GM/NIGMS NIH HHS/ -- R01 RR012294/RR/NCRR NIH HHS/ -- R01 RR012294-13/RR/NCRR NIH HHS/ -- T32 GM007215/GM/NIGMS NIH HHS/ -- T32 GM007215-33/GM/NIGMS NIH HHS/ -- England -- Nature. 2009 Mar 12;458(7235):215-8. doi: 10.1038/nature07660. Epub 2009 Feb 1.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medical Microbiology and Immunology, University of Wisconsin School of Medicine and Public Health, 1550 Linden Drive, Madison, Wisconsin 53706, USA. mmandel@wisc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19182778" target="_blank"〉PubMed〈/a〉
    Keywords: Aliivibrio fischeri/*genetics/*growth & development ; Animal Structures/microbiology ; Animals ; Biofilms/growth & development ; Decapodiformes/*microbiology ; Molecular Sequence Data ; Pacific Ocean ; Phylogeny ; Polysaccharides, Bacterial/genetics/metabolism ; Protein Kinases/genetics/metabolism ; Symbiosis/genetics/*physiology
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2004-11-13
    Description: Tracheal cytotoxin (TCT), a fragment of the bacterial surface molecule peptidoglycan (PGN), is the factor responsible for the extensive tissue damage characteristic of whooping cough and gonorrhea infections. Here, we report that Vibrio fischeri also releases TCT, which acts in synergy with lipopolysaccharide (LPS) to trigger tissue development in its mutualistic symbiosis with the squid Euprymna scolopes. As components of PGN and LPS have commonly been linked with pathogenesis in animals, these findings demonstrate that host interpretation of these bacterial signal molecules is context dependent. Therefore, such differences in interpretation can lead to either inflammation and disease or to the establishment of a mutually beneficial animal-microbe association.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koropatnick, Tanya A -- Engle, Jacquelyn T -- Apicella, Michael A -- Stabb, Eric V -- Goldman, William E -- McFall-Ngai, Margaret J -- NCRR12294/RR/NCRR NIH HHS/ -- R01-AI50661/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Nov 12;306(5699):1186-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Pacific Biomedical Research Center, Kewalo Marine Laboratory, University of Hawaii, 41 Ahui Street, Honolulu, HI 96813, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15539604" target="_blank"〉PubMed〈/a〉
    Keywords: Aliivibrio fischeri/growth & development/metabolism/*physiology ; Animals ; Apoptosis ; Bacterial Toxins/metabolism/pharmacology ; Chromatography, High Pressure Liquid ; Cytotoxins/*metabolism/pharmacology ; Decapodiformes/cytology/*growth & development/*microbiology ; Epithelial Cells/cytology/physiology ; Epithelium/microbiology/physiology ; Hemocytes/physiology ; Lipopolysaccharides/*metabolism ; Morphogenesis ; Peptidoglycan/chemistry/*metabolism ; *Symbiosis
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2000-08-29
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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