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[PMID]: 27613234 [Au] Autor: Shkoporov AN; Efimov BA; Kondova I; Ouwerling B; Chaplin AV; Shcherbakova VA; Langermans JA [Ad] Endereço: 1​Department of Microbiology and Virology, Pirogov Russian National Research Medical University, Moscow 117997, Russia. [Ti] Título: Peptococcus simiae sp. nov., isolated from rhesus macaque faeces and emended description of the genus Peptococcus. [So] Source: Int J Syst Evol Microbiol;66(12):5187-5191, 2016 Dec. [Is] ISSN: 1466-5034 [Cp] País de publicação: England [La] Idioma: eng [Ab] Resumo: A study of the faecal microbiome in three healthy female rhesus macaques revealed the presence of a novel obligately anaerobic, chemoorganoheterotrophic, non-sporing, coccoid, non-motile, Gram-stain-positive bacterial species. Three strains of this species, designated as M108T, M916-1/1, and M919-2/1, were non-haemolytic, H2S-positive, catalase-positive, bile- and NaCl-sensitive and required peptone for growth. Strains also were asaccharolytic, able to utilize sulfite, thiosulfate and elemental sulfur as electron acceptors, and produced acetic and butyric acids as metabolic end-products. Strain M108T is characterized by the prevalence of C14 : 0, C16 : 0 and C18 : 1ω9cis dimethyl acetal among the cellular fatty acids, and the presence of MK-10 menaquinone. The DNA G+C content was found to be 51 mol%. Phylogenetic analysis of partial 16S rRNA gene sequences of strains M108T, M916-1/1 and M919-2/1 placed these strains into the genus Peptococcus (family Peptococcaceae). On the basis of phenotypic and genotypic properties we conclude that these strains represent a novel bacterial species for which the name Peptococcus simiae sp. nov. is proposed. The type strain is M108T (=DSM 100347T=VKM B-2932T). [Mh] Termos MeSH primário: Macaca mulatta/microbiologia Peptococcus/classificação Filogenia [Mh] Termos MeSH secundário: Animais Técnicas de Tipagem Bacteriana Composição de Bases DNA Bacteriano/genética Ácidos Graxos/química Fezes/microbiologia Feminino Peptococcus/genética Peptococcus/isolamento & purificação RNA Ribossômico 16S/genética Análise de Sequência de DNA Ubiquinona/análogos & derivados Ubiquinona/química [Pt] Tipo de publicação: JOURNAL ARTICLE [Nm] Nome de substância: 0 (DNA, Bacterial); 0 (Fatty Acids); 0 (RNA, Ribosomal, 16S); 1339-63-5 (Ubiquinone); EJ27X76M46 (coenzyme Q10) [Em] Mês de entrada: 1707 [Cu] Atualização por classe: 170817 [Lr] Data última revisão: 170817 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 160911 [St] Status: MEDLINE [do] DOI: 10.1099/ijsem.0.001494

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[PMID]: 26091682 [Au] Autor: Kanengoni AT; Chimonyo M; Tasara T; Cormican P; Chapwanya A; Ndimba BK; Dzama K [Ad] Endereço: Agricultural Research Council-Animal Production Institute, Private Bag X2, Irene, 0062, South Africa Department of Animal Sciences, Stellenbosch University, Private Bag X1, Matieland, 7602, South Africa Arnoldk@arc.agric.za. [Ti] Título: A comparison of faecal microbial populations of South African Windsnyer-type indigenous pigs (SAWIPs) and Large White × Landrace (LW × LR) crosses fed diets containing ensiled maize cobs. [So] Source: FEMS Microbiol Lett;362(13):fnv100, 2015 Jul. [Is] ISSN: 1574-6968 [Cp] País de publicação: England [La] Idioma: eng [Ab] Resumo: Faecal microbial communities in South African Windsnyer-type indigenous pigs (SAWIPs) and Large White × Landrace (LW × LR) crosses were investigated using high-throughput sequencing of the 16S rDNA genes. The faecal microbial communities in LW × LR crosses and SAWIPs fed control (CON) and high maize cob (HMC) diets were evaluated through parallel sequencing of 16S rDNA genes. Butrivibrio, Faecalibacterium and Desulfovibrio, although present in LW × LR pigs, were absent from the SAWIP microbial community. Bacteroides, Succiniclasticum, Peptococcus and Akkermansia were found in SAWIPs but not in LW × LR crosses. The ratios of Bacteroidia to Clostridia on the CON and HMC diets were similar (0.37 versus 0.39) in SAWIPs but different (0.24 versus 0.1) in LW × LR crosses. The faecal microbial profiles determined were different between the LW × LR and SAWIP breeds but not between pigs fed the CON and HMC diets. The composition of faecal bacterial communities in SAWIPs was determined for the first time. The differences in microbial communities detected may explain the enhanced ability of SAWIPs to digest fibrous diets compared with the LW × LR crosses. [Mh] Termos MeSH primário: Ração Animal Fezes/microbiologia Intestinos/microbiologia Consórcios Microbianos Sus scrofa/classificação Sus scrofa/microbiologia Zea mays [Mh] Termos MeSH secundário: Animais Bacteroides/genética Bacteroides/isolamento & purificação Clostridium/genética Clostridium/isolamento & purificação Desulfovibrio/genética Desulfovibrio/isolamento & purificação Dieta/normas Dieta/veterinária Fibras na Dieta/metabolismo Fermentação Sequenciamento de Nucleotídeos em Larga Escala Metagenômica Peptococcus/genética Peptococcus/isolamento & purificação África do Sul Sus scrofa/fisiologia Suínos [Pt] Tipo de publicação: COMPARATIVE STUDY; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T [Em] Mês de entrada: 1603 [Cu] Atualização por classe: 171116 [Lr] Data última revisão: 171116 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 150621 [St] Status: MEDLINE

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[PMID]: 25797348 [Au] Autor: Patel R; Neill A; Liu H; Andrien B [Ad] Endereço: Product Characterization, Alexion Pharmaceuticals, Inc, USA. Electronic address: patelr@alxn.com. [Ti] Título: IgG subclass specificity to C1q determined by surface plasmon resonance using Protein L capture technique. [So] Source: Anal Biochem;479:15-7, 2015 Jun 15. [Is] ISSN: 1096-0309 [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: Recombinant monoclonal antibodies (mAbs) have become an important category of biological therapeutics. mAbs share the same structures and biological functions as endogenous IgG molecules. One function is complement-dependent cytotoxicity (CDC) initiation by binding of C1q. Traditionally, ELISA methods have been utilized to measure C1q binding. A new robust capture method was established in this study to measure the binding affinity of C1q to antibodies by surface plasmon resonance (SPR). The utility of this method was demonstrated by determination of the difference in IgG subclass specificity of C1q binding. [Mh] Termos MeSH primário: Complemento C1q/imunologia Imunoglobulina G/imunologia Ressonância de Plasmônio de Superfície/métodos [Mh] Termos MeSH secundário: Animais Anticorpos Monoclonais/análise Anticorpos Monoclonais/imunologia Proteínas de Bactérias/química Células CHO Cricetulus Seres Humanos Proteínas Imobilizadas/química Imunoglobulina G/análise Peptococcus/química Proteínas Recombinantes/análise Proteínas Recombinantes/imunologia [Pt] Tipo de publicação: JOURNAL ARTICLE [Nm] Nome de substância: 0 (Antibodies, Monoclonal); 0 (Bacterial Proteins); 0 (Ig L-binding protein, Peptostreptococcus); 0 (Immobilized Proteins); 0 (Immunoglobulin G); 0 (Recombinant Proteins); 80295-33-6 (Complement C1q) [Em] Mês de entrada: 1601 [Cu] Atualização por classe: 150511 [Lr] Data última revisão: 150511 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 150324 [St] Status: MEDLINE

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[PMID]: 24508414 [Au] Autor: Garrett A; Carnish E; Das N; Slome M; Measley R [Ad] Endereço: Department of Medicine, Thomas Jefferson University Hospital, Philadelphia. Electronic address: andrew.garrett@jeffersonhospital.org. [Ti] Título: Once universally fatal: pylephlebitis. [So] Source: Am J Med;127(7):595-7, 2014 Jul. [Is] ISSN: 1555-7162 [Cp] País de publicação: United States [La] Idioma: eng [Mh] Termos MeSH primário: Infecções por Bacteroides Infecções por Bactérias Gram-Positivas Peptococcus Flebite/microbiologia Veia Porta [Mh] Termos MeSH secundário: Seres Humanos Masculino Meia-Idade Flebite/diagnóstico Supuração [Pt] Tipo de publicação: CASE REPORTS; JOURNAL ARTICLE [Em] Mês de entrada: 1408 [Cu] Atualização por classe: 140627 [Lr] Data última revisão: 140627 [Sb] Subgrupo de revista: AIM; IM [Da] Data de entrada para processamento: 140211 [St] Status: MEDLINE

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[PMID]: 24144750 [Au] Autor: Zhang T; Chen Y; Wang Z; Zhou Y; Zhang S; Wang P; Xie S; Jiang B [Ad] Endereço: Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangdong Provincial Key Laboratory of Gastroenterology, Guangzhou 510515, China. E-mail: zhangtingyikeda@126.com. [Ti] Título: [Changes of fecal flora and its correlation with inflammatory indicators in patients with inflammatory bowel disease]. [So] Source: Nan Fang Yi Ke Da Xue Xue Bao;33(10):1474-7, 2013 Oct. [Is] ISSN: 1673-4254 [Cp] País de publicação: China [La] Idioma: chi [Ab] Resumo: OBJECTIVE: To investigate the changes in fecal flora and its correlation with the occurrence and progression of inflammatory bowel disease (IBD). METHODS: We collected fresh fecal specimens from 167 IBD patients (including 113 with ulcerative colitis and 54 with Crohn's disease) and 54 healthy volunteers. The fecal flora was analyzed by gradient dilution method and the data of inflammatory markers including WBC, PLT, CRP and ESR were collected to assess the association between the fecal flora and the inflammatory markers. RESULTS: The species Enterrococcus (6.60∓0.23, P<0.01), Saccharomyces (2.22∓0.27, P<0.05), Bacteriodes (5.57∓0.28, P<0.001), Bifidobacterium (5.08∓0.30, P<0.01), Peptococcus (6.22∓0.25, P<0.001), Lactobacillus (6.00∓0.26, P<0.001), and Clostridium (3.57∓0.30, P<0.05) all increased significantly, while Eubacterium (1.56∓0.24, P<0.01) reduced markedly in patients with ulcerative colitis compared with those in the control subjects. Enterrococcus (6.93∓0.28, P<0.01), Saccharomyces (2.73∓0.37, P<0.01), Bacteriodes (4.32∓0.52, P<0.05), Bifidobacterium (4.88∓0.42, P<0.05), Peptococcus (6.19∓0.32, P<0.01) and Lactobacillus (4.73∓0.47, P<0.001) all increased significantly and Eubacterium (1.01∓0.29, P<0.01) and Clostridium (0.87∓0.31, P<0.01) decreased in patients with Crohn's disease. The positivity rates of bacterial culture were consistent with the results of quantitative analysis of the fecal flora. The changes in fecal flora did not show a significant correlation with these inflammatory markers. CONCLUSION: IBD patients have fecal flora imbalance compared with the healthy controls, and this imbalance may contribute to the occurrence and progression of IBD. The decline of Eubacterium contributes to the occurrence and development of IBD. [Mh] Termos MeSH primário: Bactérias/isolamento & purificação Eubacterium/isolamento & purificação Fezes/microbiologia Doenças Inflamatórias Intestinais/microbiologia [Mh] Termos MeSH secundário: Adulto Bacteroides/isolamento & purificação Bifidobacterium/isolamento & purificação Biomarcadores/análise Clostridium/isolamento & purificação Colite Ulcerativa/microbiologia Doença de Crohn/microbiologia Enterococcus/isolamento & purificação Feminino Seres Humanos Doenças Inflamatórias Intestinais/etiologia Lactobacillus/isolamento & purificação Masculino Peptococcus/isolamento & purificação Saccharomyces/isolamento & purificação [Pt] Tipo de publicação: ENGLISH ABSTRACT; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T [Nm] Nome de substância: 0 (Biomarkers) [Em] Mês de entrada: 1405 [Cu] Atualização por classe: 151119 [Lr] Data última revisão: 151119 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 131023 [St] Status: MEDLINE

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[PMID]: 23489056 [Au] Autor: Bizzarro S; Loos BG; Laine ML; Crielaard W; Zaura E [Ad] Endereço: Department of Periodontology, Academic Centre for Dentistry Amsterdam, University of Amsterdam and VU University Amsterdam, Amsterdam, The Netherlands. s.bizzarro@acta.nl [Ti] Título: Subgingival microbiome in smokers and non-smokers in periodontitis: an exploratory study using traditional targeted techniques and a next-generation sequencing. [So] Source: J Clin Periodontol;40(5):483-92, 2013 May. [Is] ISSN: 1600-051X [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: AIM: To compare the results of two targeted techniques to an open-ended technique in periodontitis patients, differentiated on the basis of smoking habit. MATERIALS & METHODS: Thirty periodontitis patients (15 smokers and 15 non-smokers) provided subgingival plaque samples for 16S rRNA gene amplicon sequencing, culturing and quantitative polymerase chain reaction (qPCR). RESULTS: No differences were found in the composition of the subgingival microbiome between smokers and non-smokers with culture and qPCR. With pyrosequencing, operational taxonomic units (OTUs) classified to genera Fusobacterium, Prevotella and Selenomonas were more abundant in smokers, while OTUs belonging to the genera Peptococcus and Capnocytophaga were more abundant in non-smokers. Principal coordinate analysis identified two clusters; one was composed mainly of smokers (80%) and revealed significantly lower taxonomic diversity, higher attachment loss and higher proportion of the genera Fusobacterium, Paludibacter and Desulfobubus. CONCLUSION: In periodontitis, there is a difference in the composition of the subgingival microbiome between smokers and non-smokers, as revealed by pyrosequencing. This difference was not identified by the targeted techniques. Low taxonomic diversity was associated with higher disease severity, especially in smokers. This supports the hypothesis of the ecological microbial-host interaction in the severity of periodontal disease. [Mh] Termos MeSH primário: Placa Dentária/microbiologia Metagenoma Periodontite/microbiologia Fumar [Mh] Termos MeSH secundário: Técnicas Bacteriológicas Capnocytophaga/classificação Feminino Fusobacterium/classificação Marcação de Genes Gengiva/microbiologia Bactérias Anaeróbias Gram-Negativas/classificação Interações Hospedeiro-Patógeno Seres Humanos Masculino Meia-Idade Peptococcus/classificação Perda da Inserção Periodontal/microbiologia Índice Periodontal Bolsa Periodontal/microbiologia Reação em Cadeia da Polimerase Prevotella/classificação RNA Bacteriano/análise RNA Ribossômico 16S/análise Selenomonas/classificação Análise de Sequência de RNA Treponema/classificação [Pt] Tipo de publicação: COMPARATIVE STUDY; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T [Nm] Nome de substância: 0 (RNA, Bacterial); 0 (RNA, Ribosomal, 16S) [Em] Mês de entrada: 1309 [Cu] Atualização por classe: 130405 [Lr] Data última revisão: 130405 [Sb] Subgrupo de revista: D; IM [Da] Data de entrada para processamento: 130316 [St] Status: MEDLINE [do] DOI: 10.1111/jcpe.12087

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[PMID]: 23057830 [Au] Autor: Xia Z; Das P; Shakhnovich EI; Zhou R [Ad] Endereço: Computational Biology Center, IBM Thomas J. Watson Research Center, Yorktown Heights, New York 10598, USA. [Ti] Título: Collapse of unfolded proteins in a mixture of denaturants. [So] Source: J Am Chem Soc;134(44):18266-74, 2012 Nov 07. [Is] ISSN: 1520-5126 [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: Both urea and guanidinium chloride (GdmCl) are frequently used as protein denaturants. Given that proteins generally adopt extended or unfolded conformations in either aqueous urea or GdmCl, one might expect that the unfolded protein chains will remain or become further extended due to the addition of another denaturant. However, a collapse of denatured proteins is revealed using atomistic molecular dynamics simulations when a mixture of denaturants is used. Both hen egg-white lysozyme and protein L are found to undergo collapse in the denaturant mixture. The collapse of the protein conformational ensembles is accompanied by a decreased solubility and increased non-native self-interactions of hydrophobic residues in the urea/GdmCl mixture. The increase of non-native interactions rather than the native contacts indicates that the proteins experience a simple collapse transition from the fully denatured states. During the protein collapse, the relatively stronger denaturant GdmCl displays a higher tendency to be absorbed onto the protein surface due to their stronger electrostatic interactions with proteins. At the same time, urea molecules also accumulate near the protein surface, resulting in an enhanced "local crowding" for the protein near its first solvation shell. This rearrangement of denaturants near the protein surface and crowded local environment induce the protein collapse, mainly by burying their hydrophobic residues. These findings from molecular simulations are then further explained by a simple analytical model based on statistical mechanics. [Mh] Termos MeSH primário: Proteínas de Bactérias/química Proteínas de Ligação a DNA/química Guanidina/química Muramidase/química Peptococcus/química Desdobramento de Proteína Ureia/química [Mh] Termos MeSH secundário: Animais Galinhas Modelos Moleculares Conformação Proteica [Pt] Tipo de publicação: JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T [Nm] Nome de substância: 0 (Bacterial Proteins); 0 (DNA-Binding Proteins); 0 (L-protein, Peptococcus magnus); 8W8T17847W (Urea); EC 3.2.1.- (hen egg lysozyme); EC 3.2.1.17 (Muramidase); JU58VJ6Y3B (Guanidine) [Em] Mês de entrada: 1304 [Cu] Atualização por classe: 131121 [Lr] Data última revisão: 131121 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 121013 [St] Status: MEDLINE [do] DOI: 10.1021/ja3031505

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[PMID]: 22876624 [Au] Autor: Kogan MI; Pasechnik DG; Naboka IuL; Ibishev KhS; Gazaev ZI; Gudima IA [Ti] Título: [Non-clostridial anaerobic bacteria can cause acute pyelonephritis (an experimental trial)]. [So] Source: Urologiia;(2):8-13, 2012 Mar-Apr. [Is] ISSN: 1728-2985 [Cp] País de publicação: Russia (Federation) [La] Idioma: rus [Ab] Resumo: Acute obstructive pyelonephritis (PN) caused by Peptococcus niger (Pn), E. coli and mixed infection (Pn + E. coli) was modeled in rabbits. Morphologic examination showed that in animals with peptococcal infection renal lesions were identical to those in escherichial PN. Hemorrhagic infarctions and vasculitis develop in animals with mixed infection. These morphological findings were confirmed bacteriologically. The experimental trial confirms the role of Pn in development of acute obstructive PN in animals. [Mh] Termos MeSH primário: Infecções por Bactérias Gram-Positivas/microbiologia Infecções por Bactérias Gram-Positivas/patologia Peptococcus Pielonefrite/microbiologia Pielonefrite/patologia [Mh] Termos MeSH secundário: Doença Aguda Animais Modelos Animais de Doenças Masculino Coelhos [Pt] Tipo de publicação: ENGLISH ABSTRACT; JOURNAL ARTICLE [Em] Mês de entrada: 1209 [Cu] Atualização por classe: 120810 [Lr] Data última revisão: 120810 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 120811 [St] Status: MEDLINE

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[PMID]: 22432920 [Au] Autor: Wales DJ; Head-Gordon T [Ad] Endereço: University Chemical Laboratories, Lensfield Road, Cambridge CB2 1EW, UK. dw34@cam.ac.uk [Ti] Título: Evolution of the potential energy landscape with static pulling force for two model proteins. [So] Source: J Phys Chem B;116(29):8394-411, 2012 Jul 26. [Is] ISSN: 1520-5207 [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: The energy landscape is analyzed for off-lattice bead models of protein L and protein G as a function of a static pulling force. Two different pairs of attachment points (pulling directions) are compared in each case, namely, residues 1/56 and 10/32. For the terminal residue pulling direction 1/56, the distinct global minimum structures are all extended, aside from the compact geometry that correlates with zero force. The helical turns finally disappear at the highest pulling forces considered. For the 10/32 pulling direction, the changes are more complicated, with a variety of competing arrangements for beads outside the region where the force is directly applied. These alternatives produce frustrated energy landscapes, with low-lying minima separated by high barriers. The calculated folding pathways in the absence of force are in good agreement with previous work. The N-terminal hairpin folds first for protein L and the C-terminal hairpin for protein G, which exhibits an intermediate. However, for a relatively low static force, where the global minimum retains its structure, the folding mechanisms change, sometimes dramatically, depending on the protein and the attachment points. The scaling relations predicted by catastrophe theory are found to hold in the limit of short path lengths. [Mh] Termos MeSH primário: Proteínas de Bactérias/química Proteínas de Ligação a DNA/química Peptococcus/química Dobramento de Proteína Streptococcus/química [Mh] Termos MeSH secundário: Simulação por Computador Modelos Moleculares Conformação Proteica Estrutura Secundária de Proteína Termodinâmica [Pt] Tipo de publicação: JOURNAL ARTICLE [Nm] Nome de substância: 0 (Bacterial Proteins); 0 (DNA-Binding Proteins); 0 (IgG Fc-binding protein, Streptococcus); 0 (L-protein, Peptococcus magnus) [Em] Mês de entrada: 1211 [Cu] Atualização por classe: 120726 [Lr] Data última revisão: 120726 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 120322 [St] Status: MEDLINE [do] DOI: 10.1021/jp211806z

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[PMID]: 22417294 [Au] Autor: Kumar PS; Mason MR; Brooker MR; O'Brien K [Ad] Endereço: Division of Periodontology, College of Dentistry, The Ohio State University, Columbus, OH, USA. [Ti] Título: Pyrosequencing reveals unique microbial signatures associated with healthy and failing dental implants. [So] Source: J Clin Periodontol;39(5):425-33, 2012 May. [Is] ISSN: 1600-051X [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: AIM: Although it is established that peri-implantitis is a bacterially induced disease, little is known about the bacterial profile of peri-implant communities in health and disease. The purpose of the present investigation was to examine the microbial signatures of the peri-implant microbiome in health and disease. MATERIALS AND METHODS: Subgingival and submucosal plaque samples were collected from forty subjects with periodontitis, peri-implantitis, periodontal and peri-implant health and analysed using 16S pyrosequencing. RESULTS: Peri-implant biofilms demonstrated significantly lower diversity than subgingival biofilms in both health and disease, however, several species, including previously unsuspected and unknown organisms, were unique to this niche. The predominant species in peri-implant communities belonged to the genera Butyrivibrio, Campylobacter, Eubacterium, Prevotella, Selenomonas, Streptococcus, Actinomyces, Leptotrichia, Propionibacterium, Peptococcus, Lactococcus and Treponema. Peri-implant disease was associated with lower levels of Prevotella and Leptotrichia and higher levels of Actinomyces, Peptococcus, Campylobacter, non-mutans Streptococcus, Butyrivibrio and Streptococcus mutans than healthy implants. These communities also demonstrated lower levels of Prevotella, non-mutans Streptococcus, Lactobacillus, Selenomonas, Leptotrichia, Actinomyces and higher levels of Peptococcus, Mycoplasma, Eubacterium, Campylobacter, Butyrivibrio, S. mutans and Treponema when compared to periodontitis-associated biofilms. CONCLUSION: The peri-implant microbiome differs significantly from the periodontal community in both health and disease. Peri-implantitis is a microbially heterogeneous infection with predominantly gram-negative species, and is less complex than periodontitis. [Mh] Termos MeSH primário: Biofilmes/classificação Implantes Dentários/microbiologia Peri-Implantite/microbiologia [Mh] Termos MeSH secundário: Actinomyces/classificação Adulto Carga Bacteriana Butyrivibrio/classificação Campylobacter/classificação DNA Bacteriano/genética Placa Dentária/microbiologia Falha de Restauração Dentária Eubacterium/classificação Feminino Seres Humanos Lactobacillus/classificação Lactococcus/classificação Leptotrichia/classificação Masculino Metagenoma/genética Mycoplasma/classificação Peptococcus/classificação Periodontite/microbiologia Prevotella/classificação Propionibacterium/classificação RNA Ribossômico 16S/genética Selenomonas/classificação Análise de Sequência de DNA Streptococcus/classificação Treponema/classificação [Pt] Tipo de publicação: JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, NON-U.S. GOV'T [Nm] Nome de substância: 0 (DNA, Bacterial); 0 (Dental Implants); 0 (RNA, Ribosomal, 16S) [Em] Mês de entrada: 1209 [Cu] Atualização por classe: 161019 [Lr] Data última revisão: 161019 [Sb] Subgrupo de revista: D; IM [Da] Data de entrada para processamento: 120316 [St] Status: MEDLINE [do] DOI: 10.1111/j.1600-051X.2012.01856.x

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