By Elaine I. Tuomanen (auth.), Timo K. Korhonen, Tapani Hovi, P. Helena Mäkelä (eds.)

ISBN-10: 146136325X

ISBN-13: 9781461363255

ISBN-10: 1461530385

ISBN-13: 9781461530381

A very early step in microbial colonization and pathogenesis is that related to recog­ nition of the host by means of the microbe. within the bottom line such popularity is because of interplay among particular molecules at the aspects, with out which host and microbe might forget about one another. it's accordingly intriguing to benefit the foundations that govern host-microbe interplay at to a wide quantity determines even if we're contaminated via the molecular point, which influenza virus, leishmanias, staphylococci and different pathogens. This publication is a compendium of the addresses added at a symposium on molecular interplay at Porvoo, Finland in August 1991. figuring out that there are not any a priori range­ ences in receptor attractiveness in viruses, eukaryotic parasites and micro organism, we freely inter­ mingled those microbes on the symposium, and during this ebook. We came across the interdisciplinary discussions and comparisons either educative and stimulating. therefore the booklet is split into elements that concentrate on host phone receptors, on microbial popularity molecules and molecules that mediate microbial interplay with a number telephone receptor and, in short, at the molecular occasions that stick to. even though many microbes and lots of mobile receptors are lacking from the e-book -owing to the restricted length and measurement of the symposium -the articles awarded right here represent a magnificent physique of examples of the way preliminary host-microbe interplay can happen. We think that as such the booklet is an invaluable and engaging evaluate of the mechanisms and ideas all in favour of those interactions.

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Chagasi promastigotes, hybridized with the sequence for gp63. 7 kb gp63 RNA is detected in lane b. The lanes were washed and reprobed with the sequence for T. brucei rhodesiense a and ~ tubulin (lanes c and d), demonstrating similar amounts of the one a and three ~ tubulin RNAs. [From reference 61. 1- 1- L oligo: S L S B4 Figure 6. Cleavage of the 3' un translated region from gp63 RNAs localizes the 300 bp difference between the two sizes of gp63 RNAs. Total RNA from L. d. chagasi promastigotes in log (L) or early stationary (S) phase of growth was hybridized with either no oligonucleotide (-), or an oligonucleotide complementary to the sequence immediately downstream of the gp63 stop codon (B4).

L69:5633 (1987). 5. AE. R. Johnson, EL. W. Wannamaker, Factors influencing antibody responses to streptococcal M proteins in humans, J. Inject. Dis. 147:1 (1983). 6. EJ. P. Cleary, Identification of a divergent M protein gene and an M protein related gene family in serotype 49 Streptococcus pyogenes, J. Bacteriol. 171:6397 (1989). 7. E. Frithz, L-O. Heden, and G. Lindahl, Extensive sequence homology between IgA receptor and M protein in Streptococcus pyogenes, Molec. Microbiol. 3:1111 (1989). 8.

Erickson, C3bi receptor (complement receptor type 3) recognizes a region of complement protein C3 containing the sequence Arg-Gly-Asp, Proc. Natl. Acad. Sci. USA 84:1965 (1987). 54. LL. R. McMaster, Molecular cloning of the major surface antigen of Leishmania, J. Exp. Med. 167:724 (1988). 55. A. G. Reed, and M. Parsons, Leishmania gp63 molecule implicated in cellular adhesion lacks an Arg-G1y-Asp sequence, Mol. Biochem. Parasitol. 39:267 (1990). 56. G. Russell, P. Talamas-Rohana, and J. Zelechowski, Antibodies raised agaist synthetic peptides from the Arg-Gly-Asp-containing region of Leishmania surface protein gp63 cross-react with human C3 and interfere with gp63-mediated binding to macrophages, Infect.

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Molecular Recognition in Host-Parasite Interactions by Elaine I. Tuomanen (auth.), Timo K. Korhonen, Tapani Hovi, P. Helena Mäkelä (eds.)


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