Cíntia Renata Costa Rocha
Federal University of Pernambuco
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Publication
Featured researches published by Cíntia Renata Costa Rocha.
Human Immunology | 2008
Vilma Guimaraes; Rafael Lima Guimarães; Lucas André Cavalcanti Brandão; Maria Fernanda Piffer Tomasi Baldez da Silva; Michele Milanese; Ludovica Segat; Henrique Castelletti; Danielly Bruneska; José Luiz de Lima Filho; Antonio Carlos de Freitas; Luiz Claudio Arraes; Cíntia Renata Costa Rocha; Sergio Crovella
We studied the association between high-risk human papillomavirus (HPV) infection and MBL2 functional polymorphisms in a group of 180 high-risk HPV-infected women and 180 healthy control subjects. The most frequent high-risk HPV genotypes were 16 (47.2%), 31 (11.7%), 33 (5%), and 18 (2.2%), respectively. Of the 180 HPV-infected women, 99 presented with uterine cervical cancer and 81 did not. No differences in MBL2 genotype or in allelic or haplotype frequencies were found between HPV patients who developed cervical uterine cancer and those who did not. When considering combined genotypes grouped according to MBL production (designated as high, low, and deficient producers), we detected a significant difference between healthy controls and high-risk HPV-positive patients, the latter group showing increased frequencies of deficient-producer genotypes (14.4% vs 9.4% in the healthy control group, corrected p = 0.04). In conclusion, a correlation between MBL2 polymorphisms and high-risk HPV infection was found in this study.
Current Microbiology | 2011
Dyana Leal Veras; Luiz Carlos Alves; Fábio André Brayner; Duschinka Ribeiro Duarte Guedes; Maria Amélia Vieira Maciel; Cíntia Renata Costa Rocha; Ana Catarina de Souza Lopes
The aim of this study was to determine the prevalence of the blaSHV gene in Klebsiella pneumoniae isolates from hospital and community infections and from the normal microbiota of healthy individuals in Recife, PE, Brazil. Fifty-two K. pneumoniae isolates were analyzed regarding the presence of the blaSHV gene, using PCR, and eight isolates were analyzed by DNA sequencing. This gene was detected in 16 isolates from hospital infections, four from community infections, and nine from the normal microbiota. This was the first study to find the blaSHV gene in K. pneumoniae isolates from the normal microbiota. Through DNA sequencing of eight K. pneumoniae isolates from hospital and community infections, with a resistance phenotype indicative of extended-spectrum β-lactamase production, a new SHV variant named SHV-122 was found. We also detected the presence of blaSHV-1, blaSHV-11, blaSHV-28, and blaSHV-108. The results show that in Recife, Brazil, K. pneumoniae isolates that presented resistance to oxyimino-β-lactams had high prevalence and diversity of the blaSHV gene. We also conclude that there was a high presence of the blaSHV gene among isolates from the normal microbiota of healthy individuals.
Brazilian Journal of Microbiology | 2015
Karina Maria Olbrich dos Santos; A. D. S. Vieira; Hévila Oliveira Salles; Jacqueline da Silva Oliveira; Cíntia Renata Costa Rocha; Maria de Fátima Borges; Laura Maria Bruno; Bernadette Dora Gombossy de Melo Franco; Svetoslav Dimitrov Todorov
This study aimed to characterize the safety and technological properties of Enterococcus faecium strains isolated from Brazilian Coalho cheeses. High levels of co-aggregation were observed between Enterococcus faecium strains EM485 and EM925 and both Escherichia coli and Clostridium perfringens . Both strains presented low levels of hydrophobicity. E. faecium EM485 and EM925 were both able to grow in the presence of 0.5% of the sodium salts of taurocholic acid (TC), taurodeoxycholic acid (TDC), glycocholic acid (GC), and glycodeoxycholic acid (GDC), although they showed the ability to deconjugate only GDC and TDC. Both strains showed good survival when exposed to conditions simulating the gastro intestinal tract (GIT). When tested for the presence of virulence genes, only tyrosine decarboxylase and vancomycin B generated positive PCR results.
International Journal of Dermatology | 2010
Ludovica Segat; Rafael Lima Guimarães; Lucas André Cavalcanti Brandão; Cíntia Renata Costa Rocha; Valentina Zanin; Chiara Trevisiol; José Luiz de Lima Filho; Sergio Crovella
Background Atopic dermatitis (AD) is a common inflammatory skin disease resulting from the interplay between environmental, immunological and genetic factors. In our study, we investigated the role of three single nucleotide polymorphisms (SNPs) at 5′‐UTR of DEFB1 gene, encoding for the human beta defensin‐1, on the susceptibility to develop AD in a group of Brazilian children and adolescents.
International Journal of Biological Macromolecules | 2017
Vanir Reis Pinto-Junior; Vinicius Jose Silva Osterne; Mayara Queiroz Santiago; Jorge Luis Almeida Correia; Francisco Nascimento Pereira-Junior; Rodrigo Bainy Leal; Maria Gonçalves Pereira; Larissa da Silva Chicas; Celso Shiniti Nagano; Bruno Anderson Matias Rocha; José Caetano Silva-Filho; Wandemberg Paiva Ferreira; Cíntia Renata Costa Rocha; Kyria S. Nascimento; Ana Maria Sampaio Assreuy; Benildo Sousa Cavada
The three-dimensional structure of Dioclea reflexa seed lectin (DrfL) was studied in detail by a combination of X-ray crystallography, molecular docking and molecular dynamics. DrfL was purified by affinity chromatography using Sephadex G-50 matrix. Its primary structure was obtained by mass spectrometry, and crystals belonging to orthorhombic space group P212121 were grown by the vapor diffusion method at 293K. The crystal structure was solved at 1.765Å and was very similar to that of other lectins from the same subtribe. The structure presented Rfactor and Rfree of 21.69% and 24.89%, respectively, with no residues in nonallowed regions of Ramachandran plot. Similar to other Diocleinae lectins, DrfL was capable of relaxing aortic rings via NO induction, with CRD participation, albeit with low intensity (32%). In silico analysis results demonstrated that DrfL could strongly interact with complex N-glycans, components of blood vessel glycoconjugates. Despite the high similarity among Diocleinae lectins, it was also reported that each lectin has unique CRD properties that influence carbohydrate binding, resulting in different biological effects presented by these molecules.
Autoimmunity | 2009
Rafael Lima Guimarães; Ludovica Segat; Cíntia Renata Costa Rocha; Lucas André Cavalcanti Brandão; Valentina Zanin; J. Araujo; M. S. Naslavsky; J.L. de Lima Filho; Sergio Crovella
We analyzed three functional 5′ un-translated region β-defensin 1 (DEFB1) single nucleotide polymorphism (SNPs) in a group of 170 type 1 diabetes (T1D) patients. In order to evaluate the SNPs influence on the disease onset and the development of other autoimmune disorder, such as celiac disease (CD) and autoimmune thyroid disease (AITD), patients were stratified according to the presence of AITD, CD, and both AITD and CD. As control group, we studied 191 healthy children and adolescent not presenting a familiar historic of T1D, CD or AITD. DEFB1 SNPs were in Hardy–Weinberg equilibrium both in healthy controls and T1D patients, as well in the T1D patients stratified according to the presence of other autoimmune disorder(s). Allele, genotype, and haplotype frequencies of T1D patients globally considered were comparable to healthy controls ones. No evidence of any association of DEFB1 SNPs with the onset of AIDT, CD, and both AITD and CD on T1D patients was evidenced. Only a minor trend was found for an increased frequency of the − 20 G allele in T1D patients only presenting AITD vs. T1D patients not presenting AITD or CD, as well as an increase of those haplotypes comprising the − 20 G allele when compared with the GCA haplotype. We also evaluated the influence of functional DEFB1 SNPs on the age of T1D onset: no significant statistical conclusion was achieved. Further studies are envisaged, in order to elucidate the possible role of functional DEFB1 polymorphisms in the onset of TD1 and other autoimmune-related disorders.
Biochimie | 2017
Vanir Reis Pinto-Junior; Vinicius Jose Silva Osterne; Mayara Queiroz Santiago; Claudia Figueiredo Lossio; Celso Shiniti Nagano; Cíntia Renata Costa Rocha; Jessica Catarine Frutuoso do Nascimento; Francisco Lucas Faustino Nascimento; Ivanice Bezerra da Silva; Antônia Simoni de Oliveira; Jorge Luis Almeida Correia; Rodrigo Bainy Leal; Ana Maria Sampaio Assreuy; Benildo Sousa Cavada; Kyria S. Nascimento
Lectins are proteins, or glycoproteins, capable of reversibly binding to specific mono- or oligosaccharides via a noncatalytic domain. The Diocleinae subtribe presents lectins with high structural similarity, but different effects based on biological activity assays. This variability results from small structural differences. Therefore, in this context, the present study aimed to perform a structural analysis of the lectin from Dioclea lasiophylla Mart. ex Benth seeds (DlyL) and evaluate its inflammatory effect. To accomplish this, DlyL was purified in a single step by affinity chromatography on Sephadex® G-50 matrix. DlyL primary structure was determined through a combination of tandem mass spectrometry and DNA sequencing. DlyL showed high similarity with other species from the same genus. Its theoretical three-dimensional structure was predicted by homology modelling, and the protein was subjected to ligand screening with monosaccharides, oligosaccharides and complex N-glycans by molecular docking. Stability and binding of the lectin with α-methyl-d-mannoside were assessed by molecular dynamics. DlyL showed acute inflammatory response with hypernociceptive effect in the paw edema model, possibly by interaction with glycans present at the cell surface.
International Journal of Biological Macromolecules | 2018
Benildo Sousa Cavada; Mayara Torquato Lima Silva; Vinicius Jose Silva Osterne; Vanir Reis Pinto-Junior; Ana Paula Machado Nascimento; Ingrid Alessandra Victoria Wolin; Isabella A. Heinrich; Clareane Avelino Simplicio Nobre; Cleane Gomes Moreira; Claudia Figueiredo Lossio; Cíntia Renata Costa Rocha; Jorge Luiz Martins; Kyria S. Nascimento; Rodrigo Bainy Leal
CaBo is a mannose/glucose-specific lectin purified from seeds of Canavalia bonariensis. In the present work, we report the CaBo crystal structure determined to atomic resolution in the presence of X-man, a specific ligand. Similar to the structural characteristics of other legume lectins, CaBo presented the jellyroll motif, a metal binding site occupied by calcium and manganese ions close to the carbohydrate-recognition domain (CRD). In vitro test of CaBo cytotoxicity against glioma cells demonstrated its ability to decrease the cellular viability and migration by induction of autophagy and cell death. Molecular docking simulations corroborate previous data indicating that the lectins biological activities occur mostly through interactions with glycoproteins since the lectin interacted favorably with several N-glycans, especially those of the high-mannose type. Together, these results suggest that CaBo interacts with glycosylated cell targets and elicits a remarkable antiglioma activity.
The International Journal of Biochemistry & Cell Biology | 2017
Kyria S. Nascimento; Mayara Queiroz Santiago; Vanir Reis Pinto-Junior; Vinicius Jose Silva Osterne; Francisco William Viana Martins; Ana Paula Machado Nascimento; Ingrid Alessandra Victoria Wolin; Isabella A. Heinrich; Maria Gleiciane Queiroz Martins; Mayara Torquato Lima Silva; Claudia Figueiredo Lossio; Cíntia Renata Costa Rocha; Rodrigo Bainy Leal; Benildo Sousa Cavada
Lectins are multidomain proteins that specifically recognize various carbohydrates. The structural characterization of these molecules is crucial in understanding their function and activity in systems and organisms. Most cancer cells exhibit changes in glycosylation patterns, and lectins may be able to recognize these changes. In this work, Dioclea lasiocarpa seed lectin (DLL) was structurally characterized. The lectin presented a high degree of similarity with other lectins isolated from legumes, presenting a jelly roll motif and a metal-binding site stabilizing the carbohydrate-recognition domain. DLL demonstrated differential interactions with carbohydrates, depending on type of glycosidic linkage present in ligands. As observed by the reduction of cell viability in C6 cells, DLL showed strong antiglioma activity by mechanisms involving activation of caspase 3.
International Journal of Biological Macromolecules | 2018
Rodrigo Bainy Leal; Vanir Reis Pinto-Junior; Vinicius Jose Silva Osterne; Ingrid Alessandra Victoria Wolin; Ana Paula Machado Nascimento; Antonio Hadson Bastos Neco; David Alencar Araripe; Priscilla Gomes Welter; Corneville Correia Neto; Jorge Luis Almeida Correia; Cíntia Renata Costa Rocha; Kyria S. Nascimento; Benildo Sousa Cavada
Abstract Lectins are a class of carbohydrate-binding proteins or glycoproteins with diverse specificities and functions. The determination and characterization of the three-dimensional structures of these proteins are keys to understanding their biological effects. Recent studies have explored the anticancer potential of Diocleinae lectins (from Leguminoseae family), evaluating their antiproliferative effect and their ability to induce glioma cell death via apoptosis and autophagy. In this work, the three-dimensional structure of Dioclea lasiophylla seed lectin (DlyL) complexed with Xman (5-bromo-6-chloro-3-indolyl-α- d -mannopyranoside) was determined by X-ray crystallography. Moreover, interactions with relevant N-glycans were evaluated by molecular docking. DlyL presented the jellyroll motif, and both metal binding site (MBS) and carbohydrate-recognition domain (CRD) were determined and characterized. Molecular docking simulations indicated that DlyL interacts favorably with N-glycans, especially those of the complex and hybrid types, unlike previously studied Diocleinae lectins. DlyL also showed antitumor potential against rat C6 glioma cells impairing cell migration, inducing autophagy and cell death via activation of caspase 3. These results indicate that small structural differences among Diocleinae lectins can, in turn, result in differential modulation of autophagy and cell apoptosis processes.
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Jessica Catarine Frutuoso do Nascimento
Federal University of Pernambuco
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