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Institution

University of Costa Rica

EducationSan José, Costa Rica
About: University of Costa Rica is a education organization based out in San José, Costa Rica. It is known for research contribution in the topics: Population & Venom. The organization has 9817 authors who have published 16781 publications receiving 238208 citations. The organization is also known as: UCR & Universidad de Costa Rica.


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Journal ArticleDOI
01 May 2007-Blood
TL;DR: It is suggested that 92714C>G, a nonsynonymous SNP encoding the B-domain substitution D1241E, was significantly associated with FVIII:C level, which is a highly heritable quantitative trait that is strongly correlated with thrombosis risk.

93 citations

Journal ArticleDOI
TL;DR: The results showed that LPS is the main cause of B. abortus' resistance to bactericidal cationic peptides, the OM-disturbing action of divalentcationic chelants, and OM permeability to hydrophobic substances, and it is proposed that these three features are related to the ability of Brucella bacteria to multiply within phagocytes.
Abstract: A rough (R) Brucella abortus 45/20 mutant was more sensitive to the bactericidal activity of polymyxin B and lactoferricin B than was its smooth (S) counterpart but considerably more resistant than Salmonella montevideo. The outer membrane (OM) and isolated lipopolysaccharide (LPS) of S. montevideo showed a higher affinity for these cationic peptides than did the corresponding B. abortus OM and LPS. We took advantage of the moderate sensitivity of R B. abortus to cationic peptides to construct live R B. abortus-S-LPS chimeras to test the activities of polymyxin B, lactoferricin B, and EDTA. Homogeneous and abundant peripheral distribution of the heterologous S-LPS was observed on the surface of the chimeras, and this coating had no effect on the viability or morphology of the cells. When the heterologous LPS corresponded to the less sensitive bacterium S B. abortus S19, the chimeras were more resistant to cationic peptides; in contrast, when the S-LPS was from the more sensitive bacterium S. montevideo, the chimeras were more susceptible to the action of peptides and EDTA. A direct correlation between the amount of heterologous S-LPS on the surface of chimeric Brucella cells and peptide sensitivity was observed. Whereas the damage produced by polymyxin B in S. montevideo and B. abortus-S. montevideo S-LPS chimeras was manifested mainly as OM blebbing and inner membrane rolling, lactoferricin B caused inner membrane detachment, vacuolization, and the formation of internal electron-dense granules in these cells. Native S and R B. abortus strains were permeable to the hydrophobic probe N-phenyl-1-naphthylamine (NPN). In contrast, only reduced amounts of NPN partitioned into the OMs of the S. montevideo and B. abortus-S. montevideo S-LPS chimeras. Following peptide exposure, accelerated NPN uptake similar to that observed for S. montevideo was detected for the B. abortus-S. montevideo LPS chimeras. The partition of NPN into native or EDTA-, polymyxin B-, or lactoferricin B-treated LPS micelles of S. montevideo or B. abortus mimicked the effects observed with intact cells, and this was confirmed by using micelle hybrids of B. abortus and S. montevideo LPSs. The results showed that LPS is the main cause of B. abortus' resistance to bactericidal cationic peptides, the OM-disturbing action of divalent cationic chelants, and OM permeability to hydrophobic substances. It is proposed that these three features are related to the ability of Brucella bacteria to multiply within phagocytes.

92 citations

Journal ArticleDOI
TL;DR: The establishment of venom proteomic profiles offers a fundamental platform to assess the detailed immunorecognition of individual venom components by therapeutic or experimental antivenoms, an evolving methodology for which the term 'antivenomics' was coined.

92 citations

Journal ArticleDOI
TL;DR: A brief and updated overview of these toxic PLA(2) homologues is presented, emphasizing their various biological activities, both in vivo and in vitro and the relevance of these bioactivities in relation to their possible adaptive roles for the snakes is discussed.
Abstract: A particular subgroup of toxins with phospholipase A(2) (PLA(2)) structure, but devoid of this enzymatic activity, is commonly found in the venoms of snakes of the family Viperidae, and known as the PLA(2) homologues. Among these, the most frequent type presents a lysine residue at position 49 (Lys49), in substitution of the otherwise conserved aspartate (Asp49) of catalytically-active PLA(2)s. A brief and updated overview of these toxic PLA(2) homologues is presented, emphasizing their various biological activities, both in vivo and in vitro. The relevance of these bioactivities in relation to their possible adaptive roles for the snakes is discussed. Finally, experiments designed to assess the validity of such hypothetical roles are suggested, to stimulate future studies in this field.

92 citations

Journal ArticleDOI
16 Nov 2010-PLOS ONE
TL;DR: Genomic techniques are employed to demonstrate that the bacterial pathogen causing Pierce's disease of grapevine is not native to the US as previously assumed, but descended from a single genotype introduced from Central America.
Abstract: Invasive diseases present an increasing problem worldwide; however, genomic techniques are now available to investigate the timing and geographical origin of such introductions. We employed genomic techniques to demonstrate that the bacterial pathogen causing Pierce's disease of grapevine (PD) is not native to the US as previously assumed, but descended from a single genotype introduced from Central America. PD has posed a serious threat to the US wine industry ever since its first outbreak in Anaheim, California in the 1880s and continues to inhibit grape cultivation in a large area of the country. It is caused by infection of xylem vessels by the bacterium Xylella fastidiosa subsp. fastidiosa, a genetically distinct subspecies at least 15,000 years old. We present five independent kinds of evidence that strongly support our invasion hypothesis: 1) a genome-wide lack of genetic variability in X. fastidiosa subsp. fastidiosa found in the US, consistent with a recent common ancestor; 2) evidence for historical allopatry of the North American subspecies X. fastidiosa subsp. multiplex and X. fastidiosa subsp. fastidiosa; 3) evidence that X. fastidiosa subsp. fastidiosa evolved in a more tropical climate than X. fastidiosa subsp. multiplex; 4) much greater genetic variability in the proposed source population in Central America, variation within which the US genotypes are phylogenetically nested; and 5) the circumstantial evidence of importation of known hosts (coffee plants) from Central America directly into southern California just prior to the first known outbreak of the disease. The lack of genetic variation in X. fastidiosa subsp. fastidiosa in the US suggests that preventing additional introductions is important since new genetic variation may undermine PD control measures, or may lead to infection of other crop plants through the creation of novel genotypes via inter-subspecific recombination. In general, geographically mixing of previously isolated subspecies should be avoided.

92 citations


Authors

Showing all 9922 results

NameH-indexPapersCitations
Alberto Ascherio13646269578
Gervasio Gomez133184499695
Myron M. Levine12378960865
Hong-Cai Zhou11448966320
Edward O. Wilson10140689994
Mary Claire King10033647454
Olga Martín-Belloso8638423428
José María Gutiérrez8460726779
Cesare Montecucco8438227738
Rodolphe Clérac7850622604
Kim R. Dunbar7447020262
Paul J. Hanson7025119504
Hannia Campos6921015164
Jean-Pierre Gorvel6723115005
F. Albert Cotton66102327647
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202325
2022155
2021865
20201,009
2019894
2018834