Microbiologic profile of endodontic infections from HIV− and HIV+ patients using Multiple-Displacement Amplification and Checkerboard DNA-DNA Hybridization
Oral Diseases (2012) 18, 558–567 Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV‐negative and HIV‐positive subjects. Materials and Methods: Root canal samples from necrotic pulp were collected from 40 HIV− and 20 HIV+ subjects. Pulps were amplified using mul...
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Published in | Oral diseases Vol. 18; no. 6; pp. 558 - 567 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.09.2012
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1354-523X 1601-0825 1601-0825 |
DOI | 10.1111/j.1601-0825.2012.01908.x |
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Abstract | Oral Diseases (2012) 18, 558–567
Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV‐negative and HIV‐positive subjects.
Materials and Methods: Root canal samples from necrotic pulp were collected from 40 HIV− and 20 HIV+ subjects. Pulps were amplified using multiple displacement amplification (MDA). Then, checkerboard DNA–DNA hybridization was employed to assess the levels of 107 microbial taxa. The percentage of DNA probe count and the percentage of teeth colonized by each test species were investigated. Significant differences between groups regarding proportions of taxa and prevalence of the test species were sought using the Mann–Whitney test and the Chi‐square analysis, respectively.
Results: The most prevalent taxa detected were Dialister pneumosintes, Stenotrophomonas maltophilia, Streptococcus sobrinus, Corynebacterium diphteriae, and Helicobacter pylori among HIV‐ subjects and D. pneumosintes, Prevotella tannerae, Porphyromonas gingivalis, Parvimonas micra, Prevotella nigrescens, and Corynebacterium diphtheriae among HIV+ individuals. D. pneumosintes, C. diphtheria, and C. albicans were the most abundant species in the HIV‐ group, whereas the predominant taxa in HIV+ samples were P. tannerae, D. pneumosintes and Olsenella uli. P. tannerae, O. uli, Veilonella dispar, Bacteroides fragilis, and Actinomyces meyeri were significantly more abundant in HIV+ samples.
Conclusions: There were significant differences in the prevalence and proportions of specific microbial taxa between HIV− and HIV+ individuals. The root canal microbiota may represent a reservoir of important oral and medical pathogens, mainly in HIV+ individuals. |
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AbstractList | Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects. Materials and Methods: Root canal samples from necrotic pulp were collected from 40 HIV- and 20 HIV+ subjects. Pulps were amplified using multiple displacement amplification (MDA). Then, checkerboard DNA-DNA hybridization was employed to assess the levels of 107 microbial taxa. The percentage of DNA probe count and the percentage of teeth colonized by each test species were investigated. Significant differences between groups regarding proportions of taxa and prevalence of the test species were sought using the Mann-Whitney test and the Chi-square analysis, respectively. Results: The most prevalent taxa detected were Dialister pneumosintes, Stenotrophomonas maltophilia, Streptococcus sobrinus, Corynebacterium diphteriae, and Helicobacter pylori among HIV- subjects and D. pneumosintes, Prevotella tannerae, Porphyromonas gingivalis, Parvimonas micra, Prevotella nigrescens, and Corynebacterium diphtheriae among HIV+ individuals. D. pneumosintes, C. diphtheria, and C. albicans were the most abundant species in the HIV- group, whereas the predominant taxa in HIV+ samples were P. tannerae, D. pneumosintes and Olsenella uli. P. tannerae, O. uli, Veilonella dispar, Bacteroides fragilis, and Actinomyces meyeri were significantly more abundant in HIV+ samples. Conclusions: There were significant differences in the prevalence and proportions of specific microbial taxa between HIV- and HIV+ individuals. The root canal microbiota may represent a reservoir of important oral and medical pathogens, mainly in HIV+ individuals.Original Abstract: Oral Diseases (2012) 18, 558-567 Oral Diseases (2012) 18, 558-567 Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects. Materials and Methods: Root canal samples from necrotic pulp were collected from 40 HIV- and 20 HIV+ subjects. Pulps were amplified using multiple displacement amplification (MDA). Then, checkerboard DNA-DNA hybridization was employed to assess the levels of 107 microbial taxa. The percentage of DNA probe count and the percentage of teeth colonized by each test species were investigated. Significant differences between groups regarding proportions of taxa and prevalence of the test species were sought using the Mann-Whitney test and the Chi-square analysis, respectively. Results: The most prevalent taxa detected were Dialister pneumosintes, Stenotrophomonas maltophilia, Streptococcus sobrinus, Corynebacterium diphteriae, and Helicobacter pylori among HIV- subjects and D. pneumosintes, Prevotella tannerae, Porphyromonas gingivalis, Parvimonas micra, Prevotella nigrescens, and Corynebacterium diphtheriae among HIV+ individuals. D. pneumosintes, C. diphtheria, and C. albicans were the most abundant species in the HIV- group, whereas the predominant taxa in HIV+ samples were P. tannerae, D. pneumosintes and Olsenella uli. P. tannerae, O. uli, Veilonella dispar, Bacteroides fragilis, and Actinomyces meyeri were significantly more abundant in HIV+ samples. Conclusions: There were significant differences in the prevalence and proportions of specific microbial taxa between HIV- and HIV+ individuals. The root canal microbiota may represent a reservoir of important oral and medical pathogens, mainly in HIV+ individuals. [PUBLICATION ABSTRACT] To compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects.OBJECTIVETo compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects.Root canal samples from necrotic pulp were collected from 40 HIV- and 20 HIV+ subjects. Pulps were amplified using multiple displacement amplification (MDA). Then, checkerboard DNA-DNA hybridization was employed to assess the levels of 107 microbial taxa. The percentage of DNA probe count and the percentage of teeth colonized by each test species were investigated. Significant differences between groups regarding proportions of taxa and prevalence of the test species were sought using the Mann-Whitney test and the Chi-square analysis, respectively.MATERIALS AND METHODSRoot canal samples from necrotic pulp were collected from 40 HIV- and 20 HIV+ subjects. Pulps were amplified using multiple displacement amplification (MDA). Then, checkerboard DNA-DNA hybridization was employed to assess the levels of 107 microbial taxa. The percentage of DNA probe count and the percentage of teeth colonized by each test species were investigated. Significant differences between groups regarding proportions of taxa and prevalence of the test species were sought using the Mann-Whitney test and the Chi-square analysis, respectively.The most prevalent taxa detected were Dialister pneumosintes, Stenotrophomonas maltophilia, Streptococcus sobrinus, Corynebacterium diphteriae, and Helicobacter pylori among HIV- subjects and D. pneumosintes, Prevotella tannerae, Porphyromonas gingivalis, Parvimonas micra, Prevotella nigrescens, and Corynebacterium diphtheriae among HIV+ individuals. D. pneumosintes, C. diphtheria, and C. albicans were the most abundant species in the HIV- group, whereas the predominant taxa in HIV+ samples were P. tannerae, D. pneumosintes and Olsenella uli. P. tannerae, O. uli, Veilonella dispar, Bacteroides fragilis, and Actinomyces meyeri were significantly more abundant in HIV+ samples.RESULTSThe most prevalent taxa detected were Dialister pneumosintes, Stenotrophomonas maltophilia, Streptococcus sobrinus, Corynebacterium diphteriae, and Helicobacter pylori among HIV- subjects and D. pneumosintes, Prevotella tannerae, Porphyromonas gingivalis, Parvimonas micra, Prevotella nigrescens, and Corynebacterium diphtheriae among HIV+ individuals. D. pneumosintes, C. diphtheria, and C. albicans were the most abundant species in the HIV- group, whereas the predominant taxa in HIV+ samples were P. tannerae, D. pneumosintes and Olsenella uli. P. tannerae, O. uli, Veilonella dispar, Bacteroides fragilis, and Actinomyces meyeri were significantly more abundant in HIV+ samples.There were significant differences in the prevalence and proportions of specific microbial taxa between HIV- and HIV+ individuals. The root canal microbiota may represent a reservoir of important oral and medical pathogens, mainly in HIV+ individuals.CONCLUSIONSThere were significant differences in the prevalence and proportions of specific microbial taxa between HIV- and HIV+ individuals. The root canal microbiota may represent a reservoir of important oral and medical pathogens, mainly in HIV+ individuals. Oral Diseases (2012) 18, 558–567 Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV‐negative and HIV‐positive subjects. Materials and Methods: Root canal samples from necrotic pulp were collected from 40 HIV− and 20 HIV+ subjects. Pulps were amplified using multiple displacement amplification (MDA). Then, checkerboard DNA–DNA hybridization was employed to assess the levels of 107 microbial taxa. The percentage of DNA probe count and the percentage of teeth colonized by each test species were investigated. Significant differences between groups regarding proportions of taxa and prevalence of the test species were sought using the Mann–Whitney test and the Chi‐square analysis, respectively. Results: The most prevalent taxa detected were Dialister pneumosintes, Stenotrophomonas maltophilia, Streptococcus sobrinus, Corynebacterium diphteriae, and Helicobacter pylori among HIV‐ subjects and D. pneumosintes, Prevotella tannerae, Porphyromonas gingivalis, Parvimonas micra, Prevotella nigrescens, and Corynebacterium diphtheriae among HIV+ individuals. D. pneumosintes, C. diphtheria, and C. albicans were the most abundant species in the HIV‐ group, whereas the predominant taxa in HIV+ samples were P. tannerae, D. pneumosintes and Olsenella uli. P. tannerae, O. uli, Veilonella dispar, Bacteroides fragilis, and Actinomyces meyeri were significantly more abundant in HIV+ samples. Conclusions: There were significant differences in the prevalence and proportions of specific microbial taxa between HIV− and HIV+ individuals. The root canal microbiota may represent a reservoir of important oral and medical pathogens, mainly in HIV+ individuals. Oral Diseases (2012) 18, 558–567 Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV‐negative and HIV‐positive subjects. Materials and Methods: Root canal samples from necrotic pulp were collected from 40 HIV− and 20 HIV+ subjects. Pulps were amplified using multiple displacement amplification (MDA). Then, checkerboard DNA–DNA hybridization was employed to assess the levels of 107 microbial taxa. The percentage of DNA probe count and the percentage of teeth colonized by each test species were investigated. Significant differences between groups regarding proportions of taxa and prevalence of the test species were sought using the Mann–Whitney test and the Chi‐square analysis, respectively. Results: The most prevalent taxa detected were Dialister pneumosintes , Stenotrophomonas maltophilia , Streptococcus sobrinus , Corynebacterium diphteriae , and Helicobacter pylori among HIV‐ subjects and D. pneumosintes , Prevotella tannerae , Porphyromonas gingivalis , Parvimonas micra , Prevotella nigrescens , and Corynebacterium diphtheriae among HIV+ individuals. D. pneumosintes , C. diphtheria , and C. albicans were the most abundant species in the HIV‐ group, whereas the predominant taxa in HIV+ samples were P. tannerae , D. pneumosintes and Olsenella uli . P. tannerae , O. uli , Veilonella dispar , Bacteroides fragilis , and Actinomyces meyeri were significantly more abundant in HIV+ samples. Conclusions: There were significant differences in the prevalence and proportions of specific microbial taxa between HIV− and HIV+ individuals. The root canal microbiota may represent a reservoir of important oral and medical pathogens, mainly in HIV+ individuals. To compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects. Root canal samples from necrotic pulp were collected from 40 HIV- and 20 HIV+ subjects. Pulps were amplified using multiple displacement amplification (MDA). Then, checkerboard DNA-DNA hybridization was employed to assess the levels of 107 microbial taxa. The percentage of DNA probe count and the percentage of teeth colonized by each test species were investigated. Significant differences between groups regarding proportions of taxa and prevalence of the test species were sought using the Mann-Whitney test and the Chi-square analysis, respectively. The most prevalent taxa detected were Dialister pneumosintes, Stenotrophomonas maltophilia, Streptococcus sobrinus, Corynebacterium diphteriae, and Helicobacter pylori among HIV- subjects and D. pneumosintes, Prevotella tannerae, Porphyromonas gingivalis, Parvimonas micra, Prevotella nigrescens, and Corynebacterium diphtheriae among HIV+ individuals. D. pneumosintes, C. diphtheria, and C. albicans were the most abundant species in the HIV- group, whereas the predominant taxa in HIV+ samples were P. tannerae, D. pneumosintes and Olsenella uli. P. tannerae, O. uli, Veilonella dispar, Bacteroides fragilis, and Actinomyces meyeri were significantly more abundant in HIV+ samples. There were significant differences in the prevalence and proportions of specific microbial taxa between HIV- and HIV+ individuals. The root canal microbiota may represent a reservoir of important oral and medical pathogens, mainly in HIV+ individuals. |
Author | Haffajee, AD Brito, LCN Teles, RP Vieira, LQ Socransky, SS Teles, FRF Sobrinho, AP Ribeiro |
Author_xml | – sequence: 1 givenname: LCN surname: Brito fullname: Brito, LCN organization: Department of Operative Dentistry, School of Dentistry, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil – sequence: 2 givenname: AP Ribeiro surname: Sobrinho fullname: Sobrinho, AP Ribeiro organization: Department of Operative Dentistry, School of Dentistry, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil – sequence: 3 givenname: RP surname: Teles fullname: Teles, RP organization: Department of Periodontology, The Forsyth Institute, Cambridge, MA, USA – sequence: 4 givenname: SS surname: Socransky fullname: Socransky, SS organization: Department of Periodontology, The Forsyth Institute, Cambridge, MA, USA – sequence: 5 givenname: AD surname: Haffajee fullname: Haffajee, AD organization: Department of Periodontology, The Forsyth Institute, Cambridge, MA, USA – sequence: 6 givenname: LQ surname: Vieira fullname: Vieira, LQ organization: Department of Biochemistry and Immunology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil – sequence: 7 givenname: FRF surname: Teles fullname: Teles, FRF organization: Department of Periodontology, The Forsyth Institute, Cambridge, MA, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22335194$$D View this record in MEDLINE/PubMed |
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Nandakumar R, Whiting J, Fouad AF (2008). Identification of selected respiratory pathogens in endodontic infections. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 106: 145-151. Miranda TT, Vianna CR, Rodrigues L, Monteiro AS, Rosa CA, Correa A Jr (2009). Diversity and frequency of yeasts from the dorsum of the tongue and necrotic root canals associated with primary apical periodontitis. Int Endod J 42: 839-844. Aas JA, Barbuto SM, Alpagot T, Olsen I, Dewhirst FE, Paster BJ (2007). Subgingival plaque microbiota in HIV positive patients. J Clin Periodontol 34: 189-195. de Brito LC, da Rosa MA, Lopes VS, e Ferreira EF, Vieira LQ, Sobrinho AP (2009). Brazilian HIV-infected population: assessment of the needs of endodontic treatment in the post-highly active antiretroviral therapy era. J Endod 35: 1178-1181. Teles FR, Teles RP, Uzel NG et al (2011). Early microbial succession in redeveloping dental biofilms in periodontal health and disease. J Periodontal Res 47(1): 95-104. Navazesh M, Mulligan R, Pogoda J et al (2005). The effect of HAART on salivary microbiota in the Women's Interagency HIV Study (WIHS). Oral Surg Oral Med Oral Pathol Oral Radiol Endod 100: 701-708. Roças IN, Siqueira JF Jr (2005). Species-directed 16S rRNA gene nested PCR detection of Olsenella species in association with endodontic diseases. Lett Appl Microbiol 41: 12-16. Dean FB, Hosono S, Fang L et al (2002). Comprehensive human genome amplification using multiple displacement amplification. Proc Natl Acad Sci U S A 99: 5261-5266. Teles F, Haffajee AD, Socransky SS (2007). Multiple displacement amplification as an aid in checkerboard DNA-DNA hybridization. Oral Microbiol Immunol 22: 118-125. Rams TE, Andriolo M Jr, Feik D, Abel SN, McGivern TM, Slots J (1991). Microbiological study of HIV-related periodontitis. J Periodontol 62: 74-81. Scannapieco FA, Rethman MP (2003). The relationship between periodontal diseases and respiratory diseases. Dent Today 22: 79-83. Socransky SS, Haffajee AD, Smith C et al (2004). Use of checkerboard DNA-DNA hybridization to study complex microbial ecosystems. Oral Microbiol Immunol 19: 352-362. Contreras A, Doan N, Chen C, Rusitanonta T, Flynn MJ, Slots J (2000). Importance of Dialister pneumosintes in human periodontitis. Oral Microbiol Immunol 15: 269-272. Xia T, Baumgartner JC, David LL (2000). Isolation and identification of Prevotella tannerae from endodontic infections. Oral Microbiol Immunol 15: 273-275. Mager DL, Ximenez-Fyvie LA, Haffajee AD, Socransky SS (2003). Distribution of selected bacterial species on intraoral surfaces. J Clin Periodontol 30: 644-654. Panos GZ, Xirouchakis E, Tzias V et al (2007). Helicobacter pylori infection in symptomatic HIV-seropositive and -seronegative patients: a case-control study. AIDS Res Hum Retroviruses 23: 709-712. Colombo AP, Boches SK, Cotton SL et al (2009). Comparisons of subgingival microbial profiles of refractory periodontitis, severe periodontitis, and periodontal health using the human oral microbe identification microarray. J Periodontol 80: 1421-1432. Gonçalves LS, Soares Ferreira SM, Souza CO, Souto R, Colombo AP (2007). Clinical and microbiological profiles of human immunodeficiency virus (HIV)-seropositive Brazilians undergoing highly active antiretroviral therapy and HIV-seronegative Brazilians with chronic periodontitis. J Periodontol 78: 87-96. Zou QH, Li RQ (2011). Helicobacter pylori in the oral cavity and gastric mucosa: a meta-analysis. J Oral Pathol Med 40: 317-324. Smith GL, Socransky SS, Smith CM (1989). Rapid method for the purification of DNA from subgingival microorganisms. Oral Microbiol Immunol 4: 47-51. Siqueira JF Jr, Roças IN (2002). Dialister pneumosintes can be a suspected endodontic pathogen. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 94: 494-498. Socransky SS, Haffajee AD (2005). Periodontal microbial ecology. Periodontol 2000 38: 135-187. Tavares WL, Neves de Brito LC, Teles RP et al (2011). Microbiota of deciduous endodontic infections analysed by MDA and Checkerboard DNA-DNA hybridization. Int Endod J 44: 225-235. Back-Brito GN, Mota AJ, Vasconcellos TC et al (2009). Frequency of Candida spp. in the oral cavity of Brazilian HIV-positive patients and correlation with CD4 cell counts and viral load. Mycopathologia 167: 81-87. Möller AJ (1966). Microbiological examination of root canals and periapical tissues of human teeth. Methodological studies. Odontol Tidskr 74(Suppl. 1): 1-380. Rasmussen BA, Bush K, Tally FP (1997). Antimicrobial resistance in anaerobes. Clin Infect Dis 24(Suppl 1): S110-S120. Shchipkova AY, Nagaraja HN, Kumar PS (2010). Subgingival microbial profiles of smokers with periodontitis. J Dent Res 89: 1247-1253. Didilescu AC, Skaug N, Marica C, Didilescu C (2005). Respiratory pathogens in dental plaque of hospitalized patients with chronic lung diseases. Clin Oral Investig 9: 141-147. Teles RP, Patel M, Socransky SS, Haffajee AD (2008). Disease progression in periodontally healthy and maintenance subjects. J Periodontol 79: 784-794. Shetty K, Garcia J, Leigh J (2006). Success of root canal therapy in HIV-positive patients. Gen Dent 54: 397-402. Siqueira JF Jr, Roças IN, Cunha CD, Rosado AS (2005). Novel bacterial phylotypes in endodontic infections. J Dent Res 84: 565-569. Coogan MM, Greenspan J, Challacombe SJ (2005). Oral lesions in infection with human immunodeficiency virus. Bull World Health Organ 83: 700-706. Cannon RD, Chaffin WL (1999). Oral colonization by Candida albicans. Crit Rev Oral Biol Med 10: 359-383. Scully C, Porter SR, Mutlu S, Epstein JB, Glover S, Kumar N (1999). Periodontopathic bacteria in English HIV-seropositive persons. AIDS Patient Care STDS 13: 369-374. Domaneschi C, Massarente DB, de Freitas RS et al (2011). Oral colonization by Candida species in AIDS pediatric patients. Oral Dis 17: 393-398. Romanelli F, Smith KM, Murphy BS (2007). Does HIV infection alter the incidence or pathology of Helicobacter pylori infection? AIDS Patient Care STDS 21: 908-919. Mai M, Hoyer JD, McClure RF (2004). Use of multiple displacement amplification to amplify genomic DNA before sequencing of the alpha and beta haemoglobin genes. J Clin Pathol 57: 637-640. Siqueira JF Jr, Roças IN (2009). Diversity of endodontic microbiota revisited. J Dent Res 88: 969-981. Socransky SS, Haffajee AD, Cugini MA, Smith C, Kent RL Jr (1998). Microbial complexes in subgingival plaque. J Clin Periodontol 25: 134-144. Scannapieco FA, Bush RB, Paju S (2003). Associations between periodontal disease and risk for nosocomial bacterial pneumonia and chronic obstructive pulmonary disease. A systematic review. Ann Periodontol 8: 54-69. UNAIDS (2011). Report on the global AIDS epidemic. WHO: Geneva, Switzerland. Quesnell BT, Alves M, Hawkinson RW Jr, Johnson BR, Wenckus CS, BeGole EA (2005). The effect of human immunodeficiency virus on endodontic treatment outcome. J Endod 31: 633-636. Haffajee AD, Socransky SS, Patel MR, Song X (2008). Microbial complexes in supragingival plaque. Oral Microbiol Immunol 23: 196-205. Tsang CS, Samaranayake LP (2001). Predominant cultivable subgingival microbiota of healthy and HIV-infected ethnic Chinese. APMIS 109: 117-126. Alley BS, Buchanan TH, Eleazer PD (2008). Comparison of the success of root canal therapy in HIV/AIDS patients and non-infected controls. Gen Dent 56: 155-157. Uzel NG, Teles FR, Teles RP et al (2011). Microbial shifts during dental biofilm re-development in the absence of oral hygiene in periodontal health and disease. J Clin Periodontol 38: 612-620. de Souza Gonçalves L, Souto R, Colombo AP (2009). Detection of Helicobacter pylori, Enterococcus faecalis, and Pseudomonas aeruginosa in the subgingival biofilm of HIV-infected subjects undergoing HAART with chronic periodontitis. Eur J Clin Microbiol Infect Dis 28: 1335-1342. Gao J, Li Y, Wang Q, Qi C, Zhu S (2011). Correlation between distribution of Helicobacter pylori in oral cavity and chronic stomach conditions. J Huazhong Univ Sci Technolog Med Sci 31: 409-412. Lizardi PM, Huang X, Zhu Z, Bray-Ward P, Thomas DC, Ward DC (1998). Mutation detection and single-molecule counting using isothermal rolling-circle amplification. Nat Genet 19: 225-232. Perello R, Miro O, Marcos MA et al (2010). Predicting bacteremic pneumonia in HIV-1-infected patients consulting the ED. Am J Emerg Med 28: 454-459. Suchina JA, Levine D, Flaitz CM, Nichols CM, Hicks MJ (2006). Retrospective clinical and radiologic evaluation of nonsurgical endodontic treatment in human immunodeficiency virus (HIV) infection. J Contemp Dent Pract 7: 1-8. Chattin BR, Ishihara K, Okuda K, Hirai Y, Ishikawa T (1999). Specific microbial colonizations in the periodontal sites of HIV-infected subjects. Microbiol Immunol 43: 847-852. Chaudhry R, Kalra N, Talwar V, Thakur R (1997). Anaerobic flora in endodontic infections. Indian J Med Res 105: 262-265. Sassone L, Fidel R, Figueiredo L, Fidel S, Faveri M, Feres M (2007). Evaluation of the microbiota of primary endodontic infections using checkerboard DNA-DNA hybridization. Oral Microbiol Immunol 22: 390-397. Baradkar VP, Kum 2009; 88 2009; 42 2009; 80 2002; 94 2002; 99 2005; 20 1999; 43 2008; 106 2008; 79 2003; 18 2011; 17 1997; 3 2007; 34 2007; 78 2001; 109 1992; 7 1997; 105 1998; 19 2009; 54 2000; 15 2005; 100 2010; 28 2004; 37 2003; 8 1999; 13 2009; 167 2008; 23 2005; 31 1999; 10 2003; 82 2007; 21 2005; 38 2007; 22 2007; 23 1989; 4 1983; 132 2011 2006; 54 2006; 17 1997; 24 2011; 40 2008; 17 2011; 31 2005; 84 2006; 7 2005; 41 2008; 56 2005; 83 2011; 38 2003; 30 2007; 13 1966; 74 1998; 25 2009; 28 2010; 89 2009; 35 2004; 19 2005; 9 2004; 57 1991; 62 2011; 44 2011; 47 2007; 45 2003; 22 e_1_2_7_5_1 e_1_2_7_9_1 e_1_2_7_7_1 e_1_2_7_19_1 e_1_2_7_60_1 e_1_2_7_17_1 e_1_2_7_62_1 e_1_2_7_15_1 e_1_2_7_41_1 e_1_2_7_64_1 Chaudhry R (e_1_2_7_10_1) 1997; 105 e_1_2_7_13_1 e_1_2_7_43_1 e_1_2_7_66_1 e_1_2_7_11_1 e_1_2_7_45_1 e_1_2_7_47_1 e_1_2_7_26_1 e_1_2_7_49_1 Coogan MM (e_1_2_7_14_1) 2005; 83 e_1_2_7_50_1 e_1_2_7_25_1 e_1_2_7_31_1 e_1_2_7_52_1 e_1_2_7_23_1 e_1_2_7_33_1 e_1_2_7_54_1 e_1_2_7_21_1 e_1_2_7_35_1 e_1_2_7_56_1 e_1_2_7_37_1 e_1_2_7_58_1 e_1_2_7_39_1 e_1_2_7_6_1 e_1_2_7_4_1 Shetty K (e_1_2_7_46_1) 2006; 54 UNAIDS (e_1_2_7_63_1) 2011 e_1_2_7_8_1 e_1_2_7_18_1 e_1_2_7_16_1 e_1_2_7_40_1 e_1_2_7_61_1 e_1_2_7_2_1 e_1_2_7_12_1 e_1_2_7_44_1 e_1_2_7_65_1 e_1_2_7_67_1 e_1_2_7_48_1 e_1_2_7_27_1 Suchina JA (e_1_2_7_55_1) 2006; 7 e_1_2_7_29_1 e_1_2_7_51_1 Alley BS (e_1_2_7_3_1) 2008; 56 Möller AJ (e_1_2_7_28_1) 1966; 74 e_1_2_7_30_1 e_1_2_7_53_1 e_1_2_7_24_1 e_1_2_7_32_1 e_1_2_7_22_1 e_1_2_7_34_1 e_1_2_7_57_1 e_1_2_7_20_1 e_1_2_7_36_1 e_1_2_7_59_1 e_1_2_7_38_1 Scannapieco FA (e_1_2_7_42_1) 2003; 22 |
References_xml | – reference: Back-Brito GN, Mota AJ, Vasconcellos TC et al (2009). Frequency of Candida spp. in the oral cavity of Brazilian HIV-positive patients and correlation with CD4 cell counts and viral load. Mycopathologia 167: 81-87. – reference: Contreras A, Doan N, Chen C, Rusitanonta T, Flynn MJ, Slots J (2000). Importance of Dialister pneumosintes in human periodontitis. Oral Microbiol Immunol 15: 269-272. – reference: Shchipkova AY, Nagaraja HN, Kumar PS (2010). Subgingival microbial profiles of smokers with periodontitis. J Dent Res 89: 1247-1253. – reference: Cannon RD, Chaffin WL (1999). Oral colonization by Candida albicans. Crit Rev Oral Biol Med 10: 359-383. – reference: Möller AJ (1966). Microbiological examination of root canals and periapical tissues of human teeth. Methodological studies. Odontol Tidskr 74(Suppl. 1): 1-380. – reference: Socransky SS, Haffajee AD (2005). Periodontal microbial ecology. Periodontol 2000 38: 135-187. – reference: Dean FB, Hosono S, Fang L et al (2002). Comprehensive human genome amplification using multiple displacement amplification. Proc Natl Acad Sci U S A 99: 5261-5266. – reference: Mager DL, Ximenez-Fyvie LA, Haffajee AD, Socransky SS (2003). Distribution of selected bacterial species on intraoral surfaces. J Clin Periodontol 30: 644-654. – reference: Shetty K, Garcia J, Leigh J (2006). Success of root canal therapy in HIV-positive patients. Gen Dent 54: 397-402. – reference: Teles FR, Teles RP, Uzel NG et al (2011). Early microbial succession in redeveloping dental biofilms in periodontal health and disease. J Periodontal Res 47(1): 95-104. – reference: Nandakumar R, Whiting J, Fouad AF (2008). Identification of selected respiratory pathogens in endodontic infections. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 106: 145-151. – reference: Colombo AP, Boches SK, Cotton SL et al (2009). 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Snippet | Oral Diseases (2012) 18, 558–567
Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV‐negative and HIV‐positive subjects.... Oral Diseases (2012) 18, 558–567 Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV‐negative and HIV‐positive subjects.... To compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects. Root canal samples from necrotic pulp were... Oral Diseases (2012) 18, 558-567 Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects.... To compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects.OBJECTIVETo compare the microbiota of... Objective: To compare the microbiota of endodontic infections in necrotic pulp from HIV-negative and HIV-positive subjects. Materials and Methods: Root canal... |
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SubjectTerms | Actinomyces - isolation & purification Actinomyces meyeri Adolescent Adult Bacteria - classification Bacteriology Bacteroides fragilis Bacteroides fragilis - isolation & purification Candida albicans - isolation & purification checkerboard Child Corynebacterium Corynebacterium diphtheriae Corynebacterium diphtheriae - isolation & purification Dental pulp Dental Pulp Cavity - microbiology Dental Pulp Necrosis - microbiology Deoxyribonucleic acid Diphtheria DNA DNA Probes endodontic infections Female Gram-Negative Anaerobic Straight, Curved, and Helical Rods - classification Helicobacter pylori HIV Seronegativity HIV Seropositivity - microbiology HIV-positive patients Human immunodeficiency virus Humans Infection Male MDA Middle Aged Nucleic Acid Amplification Techniques Nucleic Acid Hybridization - methods Pathogens Peptostreptococcus - isolation & purification Porphyromonas gingivalis Porphyromonas gingivalis - isolation & purification Prevotella Prevotella - classification Prevotella nigrescens Prevotella nigrescens - isolation & purification root canals Stenotrophomonas maltophilia Stenotrophomonas maltophilia - isolation & purification Streptococcus sobrinus Streptococcus sobrinus - isolation & purification Teeth Veillonella - isolation & purification Young Adult |
Title | Microbiologic profile of endodontic infections from HIV− and HIV+ patients using Multiple-Displacement Amplification and Checkerboard DNA-DNA Hybridization |
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