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Staphylococcus aureus em tonsilas de pacientes com faringotonsilite aguda recorrente: prevalência, perfil de suscetibilidade e caracterização genotípica / Staphylococcus aureus in the tonsils of patients with acute recurrent pharyngotonsillitis: prevalence, susceptibility profile and genotypic characterization

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Previous issue date: 2013-10-17 / Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPq / The bacterial pharyngotonsillitis are infections of the upper airways that occurs predominantly in children and adolescents. Due to the composition of the oral microbiota is difficult to clarify the role of each organism in the etiology of the disease. The presence of bacteria that produce beta-lactamase interferes with the effectiveness of beta-lactam antibiotics, the most commonly drug used in treatment of these infections, promoting the recurrence of the disease. S. aureus is one of the most common pathogen in the etiology of tonsillitis and its relevance is due to the ability of antimicrobial resistance and persistence in the tissues of the tonsils. Tonsillectomy is indicated in cases of recurrent tonsillitis after several failures in the antibiotic terapy. The aim of this study was to determine the prevalence of S. aureus in the tonsils of patients undergoing tonsillectomy, in a teaching hospital in Goiânia, the antimicrobial susceptibility profile and the genetic characterization of isolates. Tonsils obtained from 123 patients were processed, the microorganisms identified and submitted to antibiogram by conventional techniques. The isolates that presented cefoxitin resistance were submitted to tests to determine the minimum inhibitory concentration - MIC for oxacillin and to detect the presence of the mecA gene. All isolates were subjected to PCR for detection of Panton-Valentine leukocidin gene and to PFGE to determine the genetic similarity among them. It was identified 60 S. aureus isolates from 49 patients (39.8%). There were no significant difference in prevalence by sex and, the average age of male patients was lower (8.2 years) (p<0.001) than the female patients (15.3 years). Nine out 49 patients(18.4%) presented two or more different S. aureus isolates. The isolates presented resistance of 85.0%, 10.0%, 15.0%, 3.3%, 10.0%, 3.3%, 18.3% and 8.3% to penicillin, amoxicillin + ácido clavulânico, cefoxitin, ceftriaxone, erythromycin, trimethoprim/sulfamethoxazole, ciprofloxacin and tetracycline, respectively. All isolates were sensitive to linezolid and rifampin. Six erythromycin-resistant isolates (10.0%) showed inducible resistance (MLSbi) to clindamycin and quinupristin/dalfopristin. Eight isolates (13.3%) were resistant to three or more classes of antimicrobials. Despite the resistance to cefoxitin be considered a marker of the presence of the mecA gene only in two resistant isolates it has been found,
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suggesting that the cefoxitin resistance should be mediated by other mechanisms, such as the overproduction of beta-lactamases. None of these isolates showed resistance to more than two classes of antimicrobials. Among the sixty S. aureus isolates, only carried the gene encoding the Panton-Valentine leukocidin. This isolate presented resistance to five classes of antimicrobials and phenotype D. PFGE analysis grouped 36 (60,0%) of 60 isolates in 10 clusters (>80% similarity), since no one specific clone was associated with colonization of the tonsils. It was observed different patients carrying S. aureus isolates genetically identical or with a high level of similarity (>80%), suggesting in these cases, a common origin. The high prevalence of S. aureus in tonsils suggests an ability to colonize the surface and/or the persistence in the tissues of the tonsils. The isolation of MDR bacteria can promote cross-resistance to other bacteria commonly associated with recurrent tonsillitis. The results point to change the paradigm of diagnosis and treatment of recurrent tonsillitis in order to enable the correct use of antimicrobials to reduce the recurrence which is the main cause of tonsillectomy. / As faringotonsilites bacterianas são infecções das vias aéreas superiores que ocorrem predominantemente em crianças e adolescentes. Devido à composição da microbiota oral é difícil o esclarecimento da participação de cada microrganismo na etiologia da doença. A presença de bactérias produtoras de β-lactamases interfere na eficácia de antimicrobianos β-lactâmicos, os mais utilizados no tratamento destas infecções, favorecendo a recorrência da doença. S. aureus é um dos patógenos mais frequentes na etiologia das tonsilites e sua relevância se deve à capacidade de resistência aos antimicrobianos e à persistência nos tecidos internos das tonsilas. A tonsilectomia é indicada nos casos de tonsilite recorrente após várias falhas na antibioticoterapia. O objetivo deste trabalho foi determinar a prevalência de S. aureus em tonsilas de pacientes submetidos à tonsilectomia, em um hospital escola de Goiânia; o perfil de suscetibilidade aos antimicrobianos e a caracterização genética dos isolados. Tonsilas obtidas de 123 pacientes foram processadas, os microrganismos identificados e submetidos ao antibiograma por técnicas convencionais. Nos isolados resistentes à cefoxitina, foi realizada a determinação da concentração inibitória mínima - CIM para oxacilina e a detecção da presença do gene mecA por PCR. Todos os isolados foram submetidos à PCR para detecção da leucocidina Panton-Valentine e ao PFGE para determinação da similaridade genética. Foram identificados 60 isolados de S. aureus de 49 pacientes (39,8%). Não houve diferença significativa da prevalência por sexo e a média de idade dos pacientes do sexo masculino foi menor (8,2 anos) (p<0,001) do que das pacientes (15,3 anos). Em nove (18,4%) dos 49 pacientes houve a identificação de dois ou mais isolados diferentes de S. aureus. Os isolados apresentaram resistência de 85,0%, 10,0%, 15,0%, 3,3%, 10,0%, 3,3%, 18,3% e 8,3% para penicilina, amoxacilina + ácido clavulânico, cefoxitina, ceftriaxona, eritromicina, sulfametoxazol/trimetoprim, ciprofloxacina e tetraciclina respectivamente. Todos os isolados foram sensíveis à linezolida e rifampicina. Seis isolados (10,0%) resistentes à eritromicina apresentaram fenótipo de resistência induzível (MLSbi) à clindamicina e quinupristina/dalfopristina. Oito isolados (13,3%) foram resistentes a três ou mais classes de antimicrobianos. Apesar da resistência à cefoxitina ser considerada o
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marcador da presença do gene mecA, somente em dois isolados resistentes, o mesmo foi detectado sugerindo que a resistência à cefoxitina pudesse ser mediada por outro mecanismo, como a hiperprodução de β-lactamases. Nenhum desses isolados apresentou resistência a mais de duas classes de antimicrobianos. Dos 60 S. aureus isolados, somente um apresentou o gene que codifica a leucocidina Panton-Valentine. Neste isolado ainda foi observada resistência a cinco classes de antimicrobianos e fenótipo D. A análise por PFGE agrupou 36 (60,0%) dos 60 isolados em 10 clusters (>80% similaridade), não sendo detectado um clone específico associado à colonização das tonsilas. Porém observamos pacientes diferentes portando S. aureus geneticamente idênticos ou com alto grau de similaridade (>80%), sugerindo nestes casos, uma origem comum. A alta prevalência de S. aureus nas tonsilas sugere uma capacidade de colonização da superfície e/ou persistência nos tecidos internos das tonsilas. O isolamento de bactérias MDR pode favorecer resistência cruzada de outras bactérias comumente associadas à tonsilite recorrente. Os resultados apontam para mudança no paradigma de diagnóstico e tratamento de tonsilites recorrentes com vistas a viabilizar o uso correto de antimicrobianos e diminuir a recorrência que é a principal causa de tonsilectomia

Identiferoai:union.ndltd.org:IBICT/oai:repositorio.bc.ufg.br:tede/3173
Date17 October 2013
CreatorsCavalcanti, Veraluce Paolini
ContributorsAndré, Maria Cláudia Dantas Porfirio Borges, Braga, Carla Afonso da Silva Bitencourt, André, Maria Cláudia Dantas Porfirio Borges, Cardoso, Juliana Lamaro, Cardoso, Alessandra Marques
PublisherUniversidade Federal de Goiás, Programa de Pós-graduação em Biologia das Interações PH (IPTSP), UFG, Brasil, Instituto de Patologia Tropical e Saúde Pública - IPTSP (RG)
Source SetsIBICT Brazilian ETDs
LanguagePortuguese
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis
Formatapplication/pdf
Sourcereponame:Biblioteca Digital de Teses e Dissertações da UFG, instname:Universidade Federal de Goiás, instacron:UFG
Rightshttp://creativecommons.org/licenses/by-nc-nd/4.0/, info:eu-repo/semantics/openAccess
Relation6367159433410056917, 600, 600, 600, 600, -7769011444564556288, 8648187577661350585, -2555911436985713659, Acar JF, Goldstein FW. Trends in bacterial resistance to fluoroquinolones. Clin Infect Dis 24 (Suppl 1): S67-S73, 1997. 2. Ahmad N, Ruzan IN, Ghani MKA, Hussin A, Nawi S, Aziz MN, Maning N, Eow VLK. Characteristics of community- and hospital- acquired meticillin-resistant Staphylococcus aureus strains carrying SCC mec type IV isolated in Malaysia. J Med Microbiol 58: 1213-1218, 2009. 3. Aires de Sousa M, Parente CE, Vieira-da-Motta O, Bonna IC, Silva DA, Lencastre H. Characterization of Staphylococcus aureus isolates from buffalo, bovine, ovine, and caprine milk samples collected in Rio de Janeiro State, Brazil. Appl Environ Microbiol 73: 3845-3849, 2007. 4. Alekshun MN, Levy SB. Molecular mechanisms of antibacterial multidrug resistance. Cell 128: 1037-1050, 2007. 5. Almeida LC, Pimenta-Rodrigues MV, Moris DV, Fortaleza CMCB, Cunha MLRS. Avaliação fenotípica e genotípica do perfil de resistência de amostras de Staphylococcus aureus isoladas de culturas clínicas e de vigilância de um hospital de ensino brasileiro. Colloquium Vitae 4 (2): 68-78, 2012. 6. Al-Mazrou KA, Al-Khattaf AS. Adherent biofilms in adenotonsillar disease in children. Arch Otolaryngol Head Neck Surg 134: 20-23, 2008. 7. Al-Najjar FYA, Uduman SA. Clinical utility of a new rapid test for the detection of group A Streptococcus and discriminate use of antibiotics for bacterial pharyngitis in an outpatient setting. Int J Infect Dis 12: 308-311, 2008. 8. Alós JI. Quinolonas. Enferm Infect Microbiol Clin 27 (5): 290- 297, 2009. 9. Appelbaum PC. The emergence of vancomycin-intermediate and vancomycin-resistant Staphylococcus aureus. Clin Microbiol Infect 12: 16-23, 2006. 10. Averono G, Vidali M, Olina M, Basile M, Bagnati M, Bellomo G, Aluffi P. Evaluation of amoxicillin plasma and tissue levels in pediatric patients undergoing tonsillectomy. Int J Pediatr Otorhinolaryngol 74: 995-998, 2010. 11. Avcia IY, Kilicb S, Acikelb CH, Hasdeb MUM, Eyiguna CP, Pahsaa A, Cetinerd S. Outpatient prescription of oral antibiotics in a training hospital in Turkey: Trends in the last decade. J Infect 52: 9-14, 2006. 51 12. Avilés AGP, Zaragoza COM. Streptococcus pyogenes: susceptibilidad in vitro y papel de las bacterias productoras de betalactamasa en la persistencia de la faringoamigdalitis estreptocócica. Aten Primaria 25: 542-545, 2000. 13. Balbani APS, Montovani JC, Carvalho LR. Pharyngotonsillitis in children: view from a sample of pediatricians and otorhinolaryngologists. Rev Bras Otorrinolaringol 75: 139-146, 2009. 14. Banerjee R, Gretes M, Basuino L, Strynadka N, Chambers HF. In vitro selection and characterization of ceftobiprole-resistant methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother 52 (6): 2089-2096, 2008. 15. Banerjee R, Gretes M, Harlem C, Basuino L, Chambers HF. A mecA-negative strain of methicillin-resistant Staphylococcus aureus with high-level β-Lactam resistance contains mutations in three genes. Antimicrob Agents Chemother 54 (11): 4900-4902, 2010. 16. Baranovich T, Zaraket H, Shabana II, Nevzorova V, Turcutyuicov V, Suzuki H. Molecular characterization and susceptibility of methicillin-resistant and methicillin-susceptible Staphylococcus aureus isolates from hospitals and the community in Vladivostok, Russia. Clin Microbiol Infect 16: 575-582, 2010. 17. Bartoloni A, Bartalesi F, Mantella A, Dell’Amico E, Roselli M, Strohmeyer M, Barahona HG, Barrón VP, Paradisi F, Rossolini GM. High Prevalence of Acquired Antimicrobial Resistance Unrelated to Heavy Antimicrobial Consumption. J Infect Dis 189: 1291-1294, 2004. 18. Bauer AW, Kirby WM, Sherris JC, Turck M. Antibiotic susceptibility testing by a standardized single disk method. Am J Clin Pathol 45: 493-496, 1966. 19. Berquó LS, Barros AJD, Lima RC, Bertoldi AD. Utilização de medicamentos para tratamento de infecções respiratórias na comunidade. Rev Saúde Pública 38: 358-364, 2004. 20. Bhattacharyya N, Kepnes LJ, Shapiro J. Efficacy and quality-of-life impact of adult tonsillectomy. Arch Otolaryngol Head Neck Surg 127: 1347-50, 2001. 21. Bisno AL, Gerber MA, Gwaltney Jr JM, Kaplan EL, Schwartz RH. Practice guidelines for the diagnosis and management of group A Streptococcal pharyngitis. Clin Infect Dis 35: 113–125, 2002. 52 22. Braoios A, Oliveira LR, Lima IBS, Kendrew E. Portadores Assintomáticos de Streptococcus pyogenes e Staphylococcus aureus entre crianças atendidas em uma creche. Colloquium Vitae 1: 25-29, 2009. 23. Brodsky L. Modern assesment of tonsils and adenoids. Pediatr Clin North America 36 (6): 1551-1569, 1989. 24. Brodsky L, Nagy M, Volk M, Stanievich J, Moore L. The relationship of tonsil bacterial concentration to surface and core cultures in chronic tonsillar disease in children. Int J Pediatr Otorhinolaryngol 21: 33-39, 1991. 25. Brodsky L, Koch RJ. Bacteriology and immunology of formal and diseased adenoids in children. Arch Otolaryngo head Neck Surg 119: 821-829, 1993. 26. Brook I. The role of β-lactamase producing bacteria and bacterial interference in streptococcal tonsillitis. Int J Antimicrob Agents 17: 439-442, 2001. 27. Brook I. The role of bacterial interference in otitis, sinusitis and tonsillitis. Otolaryngol - Head and Neck Surg 133: 139-146, 2005. 28. Brook I, Gober AE. Recovery of interfering and β-lactamase-producing bacteria from group A β-haemolytic streptococci carriers and non-carriers. J Med Microbiol 55: 1741–1744, 2006. 29. Brook I, Foote PA. Isolation of methicillin resistant Staphylococcus aureus from the surface and core of tonsils in children. Int J Pediatr Otorhinolaryngol 70: 2099-2102, 2006. 30. Brook I. Overcoming penicillin failures in the treatment of group A streptococcal pharyngo-tonsillitis. Int J Pediatr Otorhinolaryngol 71: 1501-1508, 2007a. 31. Brook I. Penicillin failure in the treatment of acute and relapsing tonsillopharyngitis is associated with copathogens and alteration of microbial balance: a role for cephalosporins. Clin Pediatr 46 (4S): 17S-24S, 2007b. 32. Brook I, Gober AE. Failure to eradicate streptococci and β-lactamase producing bacteria. Acta Paediatr 97: 193-195, 2008. 33. Brook I, Gober AE. Rate of eradication of group A β-hemolytic streptococci in children with pharyngo-tonsillitis by amoxicillin and cefdinir. Int J Pediatr Otorhinolaryngol 73: 757-759, 2009. 53 34. Brook I. Penicillin failure in the treatment of Streptococcal pharyngo-tonsillitis. Curr Infect Dis Rep 15: 232-235, 2013. 35. Bush K, Jacoby GA, Medeiros AA. A functional classification scheme for β-lactamases and its correlation with molecular structure. Antimicrob Agents Chemother 39: 1211-1233, 1995. 36. Bush K, Jacoby GA. Updated functional classification of β-Lactamases. Antimicrob Agents Chemother 54 (3): 969-976, 2010. 37. Carriço JA, Pinto FR, Simas C, Nunes S, Sousa NG, Frazao N, de Lencastre H, Almeida JS. Assessment of band-based similarity coefficients for automatic type and subtype classification of microbial isolates analyzed by pulsed-field gel electrophoresis. J Clin Microbiol 43: 5483-5490, 2005. 38. Cartwright EJP, Paterson GK, Raven KE, Harrison EM, Gouliouris T, Kearns A, Pichon B, Edwards G, Skov RL, Larsen AR, Holmes MA, Parkhill J, Peacock SJ, Töröka ME. Use of Vitek 2 antimicrobial susceptibility profile to identify mecC in methicillin-resistant Staphylococcus aureus. J Clin Microbiol 51 (8): 2732-2734, 2013. 39. Casey JR, Pichichero ME. The evidence base for cephalosporin superiority overpenicillin in streptococcal pharyngitis. Diagn Micr Infec Dis 57: 39S-45S, 2007. 40. Cetin ES, Gunes H, Kaya S, Aridogan BC, Demirci M. Distribution of genes encoding resistance to macrolides, lincosamides and streptogramins among clinical staphylococcal isolates in a Turkish University Hospital. J Microbiol Immunol Infect 43 (6): 524-529, 2010. 41. Chambers HF, Archer G, Matsuhashi M. Low-level methicillin resistance in strains of Staphylococcus aureus. Antimicrob Agents Chemother 33 (4): 424-428, 1989. 42. Chambers HF. Methicillin Resistance in Staphylococci: Molecular and biochemical basis and clinical implications. Clin Microbiol Rev 10 (4): 781-791, 1997. 43. Chambers HF. The Changing epidemiology of Staphylococcus aureus? Emerg Infect Dis 7 (2): 178-182, 2001. 44. Chen FJ, Hiramatsu K, Huang IW, Wanga CH, Lauderdale TLY. Panton –Valentine leukocidin (PVL)-positive methicillin-susceptible and resistant 54 Staphylococcus aureus in Taiwan: identification of oxacillin-susceptible mecA -positive methicillin-resistant S. aureus. Diagn Microbiol Infect Dis 65: 351-357, 2009. 45. Chole RA, Faddis BT. Anatomical evidence of microbial biofilms in tonsillar tissues: a possible mechanism toexplain chronicity. Arch Otolaryngol Head Neck Surg 129: 634-636, 2003. 46. Chung MLH, Matthews P, Tomasz A, Adamsson I, Aires de Sousa M, Camou T, Cocuzza C, Corso A, Couto I, Dominguez A, Gniadkowski M, Goering R, Gomes A, Kikuchi K, Marchese A, Mato R, Melter O, Oliveira D, Palacio R, Sá-Leão R, Santos Sanches I, Song JH, Tassios PT, Villari P. Multilaboratory Project Collaborators 2000. Molecular typing of methicillin-resistant Staphylococcus aureus by pulsed-field gel electrophoresis: comparison of results obtained in a multilaboratory effort using identical protocols and MRSA strains. Microb Drug Resist 6: 189-198, 2000. 47. CLSI. Clinical Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing; Twenty-third informational supplement. CLSI document M100-S23, 2013. 48. Conley J, Olson ME, Cook LS, Ceri H, Pahn V, Davies HD. Biofilm formation by group A streptococci: is there a relationship with treatment failure? J Clin Microbiol 41: 4043-4048, 2003. 49. Conlon BJ, Donnelly MJ, Mcshane DP. Improvements in health and behavior following childhood tonsillectomy: a parental perspective at 1 year. Int J Pediatr Otorhinolaringol 41: 155-161, 1997. 50. Costa FN, Santos O, Weckx LLM, Pignatari SSN. Estudo microbiológico do core e superfície das amígdalas palatinas em crianças portadoras de faringoamigdalites de repetição e hipertrofia adenoamigdaliana. Rev Bras Otorrinolaringol 69: 181-184, 2003. 51. Cuirolo A, Canigia LF, Gardella N, Fernández S, Gutkind G, Rosato A, Mollerach M. Oxacillin- and cefoxitin-susceptible meticillin-resistant Staphylococcus aureus (MRSA). Int J Antimicrob Agents 37: 174–185, 2011. 52. Cunnington A, Brick T, Cooper M, Danin J, Hunt D, Jeanes A, Kearns AM, Nolan M, Lyall H. Severe invasive Panton-Valentine leucocidin positive 55 Staphylococcus aureus infections in children in London, UK. J Infect 59 (1): 28-36, 2009. 53. Dal Rio ACC, Nicola EDN, Teixeira ARF. Halitose: proposta de um protocolo de avaliação. Rev Bras Otorrinolaringol 73: 835-842, 2007. 54. DATASUS. Ministério da Saúde [Internet]. Acesso em set. 2013. Informações de Saúde. Assistência à Saúde. Disponível em: <http://www.datasus.gov.br> 2013. 55. Dell'Aringa AR, Juares AJC, Melo C, Nardi JC, Kobari K, Filho RMP. Análise histopatológica de produtos de adenotonsilectomia de janeiro de 2001 a maio de 2003. Rev Bras Otorrinolaringol 71 (1): 18-22, 2005. 56. Dice LR. Measures of the amount of ecologic association between species. Ecology 26 (3): 297-302, 1945. 57. Discolo CM, Darrow DH, Koltai PJ. Infectious indications for tonsillectomy. Pediatr Clin of North America 50: 445-458, 2003. 58. Donnio PY, Oliveira DC, Faria NA, Wilhelm N, Le Coustumier A, Lencastre H. Partial excision of the chromosomal cassete containing the methicillin resistance determinant results in methicillin-susceptible Staphylococcus aureus. J Clin Microbiol 43: 4191-4193, 2005. 59. Dos Santos AGP, Berezin EM. Comparative analysis of clinical and laboratory methods for diagnosing streptococcal sore throat. Jornal de Pediatria 81: 23-28, 2005. 60. Drawz SM, Bonomo RA. Three decades of β-Lactamase inhibitors. Clin Microbiol Rev 23: 160-201, 2010. 61. Drinkovic D, Fuller ER, Shore KP, Holland DJ, Ellis-Pegler R. Clindamycin treatment of Staphylococcus aureus expressing inducible clindamycin resistance. J Antimicrob Chemother 48: 315-316, 2001. 62. Ebert MD, Sheth S, Fishman EK. Necrotizing pneumonia caused by community-acquired methicillin-resistant Staphylococcus aureus: an increasing cause of ‘mayhem in the lung’. Emerg Radiol 16: 159-162, 2009. 63. Edwards AM, Massey RC, Clarke SR. Molecular mechanisms of Staphylococcus aureus nasopharyngeal colonization. Mol Oral Microbiol 27: 1-10, 2012. 56 64. Ejzenberg B, Nascimento SL, Gilio AE, Lotufo JP, Okay Y. Faringoamigdalites episódicas e recorrentes. Pediatria (São Paulo) 20: 191-210, 1998. 65. Eliasson I, Holst E, Molstad S, Kamme C. Emergence and persistence of β-lactamase-producing bacteria in the upper respiratory tract in children treated with β-lactam antibiotics. American J Medicine 88 (Suppl. 5A): 51S-55S, 1990. 66. Falser N, Dalhoff A, Weuta H. Ciprofloxacin concentrations in tonsils following single or multiple administrations. Infection 16 (Suppl. 1): S14-S18, 1988. 67. Figueiredo CR, Pignatari SSN, Valera FPC, Avelino MAG. Rinossinusites e faringotonsilites em crianças. Pediatria Moderna 37: 647-659, 2001. 68. Filho OL. Anatomia cirúrgica das amígdalas palatinas. In: Temas de Otorrinolaringologia. Editora Manole Ltda. São Paulo. 1aEd., p 23-60, 1980. 69. Filizzola VCC, Dualibi APFF, Solé D, Weckx LLM. Risk factors for recurrent acute tonsillitis in children. Rev Bras Alerg Imunopatol 21 (4): 100-104, 1998. 70. Fujihara K, Goto H, Hiraoka M, Hayashi M, Hotomi M, Tamura S, Kuki K, Yamanaka N, Koltai PJ. Tonsillitis index: An objective tool for quantifying the indications for tonsillectomy for recurrent acute tonsillitis. Int J Ped Otorhinolaryngol 69: 1515-1520, 2005. 71. García-Álvarez L, Holden, MTG, Lindsay H, Webb CR, Brown DFJ, Curran MD, Walpole E, Brooks K, Pickard DJ, Teale C, Parkhill J, Bentley SD, Edwards GF, Girvan EK, Kearns AM, Pichon B, Hill RLR, Larsen AR, Skov RL, Peacock SJ, Maskell DJ, Holmes MA. Meticillin-resistant Staphylococcus aureus with a novel mecA homologue in human and bovine populations in the UK and Denmark: a descriptive study. Lancet Infect Dis 11 (8): 595-603, 2011. 72. Gasch O, Hornero A, Domínguez MA, Fernández A, Suárez C, Gómez S, Camoez M, Linares J, Ariza J, Pujol M. Methicillin-susceptible Staphylococcus aureus clone related to the early pandemic phage type 80/81 causing an outbreak among residents ofthree occupational centres in Barcelona, Spain. Clin Microbiol Infect 18: 662-667, 2012. 57 73. Gillet Y, Issartel B, Vanhems P, Fournet JC, Lina G, Bes M, Vandenesch F, Piémont Y, Brousse N, Floret D, Etienne J. Association between Staphylococcus aureus strains carrying genefor Panton-Valentine leukocidin and highly lethal necrotizing pneumonia in young immunocompetent patients. Lancet 359: 753-759, 2002. 74. Glover JA. The incidence of tonsillectomy in school children. Int J Epidemiol 37: 9-19, 2008. 75. Gowrishankar S, Thenmozhi R, Balaji K, Pandian SK. Emergence of methicillin-resistant, vancomycin-intermediate Staphylococcus aureus among patients associated with group A Streptococcal pharyngitis infection in southern India. Infect Genet Evol 14: 383-389, 2013. 76. Grossman RF. The role of fluoroquinolones in respiratory tract infections. J Antimicrob Agents Chemother 40 (Suppl. A): 59-62, 1997. 77. Guerra AFM, Gonçalves DU, Cortes MCJW, Alves CRL, Lima TMA. Otorrinolaringologia pediátrica no Sistema Público de Saúde de Belo Horizonte. Rev Saúde Públ 41: 719-725, 2007. 78. Gul M, Okur E, Ciragil P, Yildirim I, Aral M, Kilic MA. The comparison of tonsillar surface and core cultures in recurrent tonsillitis. American J Otolaryngol–Head Neck Med Surg 28: 173–176, 2007. 79. Gunnarsson RK, Holm SE, Soderstrom M. The prevalence of potencial pathogenic bacteria in nasopharyngeal samples from individuals with a respiratory tract infection and a sore throat – implications for the diagnosis of pharyngotonsillitis. Family Practice 18: 266-271, 2001. 80. Gurdal Y, Kemalettin A. Detection and prevalence of inducible clindamycin resistance in staphylococci. J Med Microbiol 56: 342-345, 2007. 81. Hackbarth CJ, Kocagoz T, Kocagoz S, Chambers HF. Point mutations in Staphylococcus aureus PBP2 gene affect penicillin-binding kinetics and are associated with resistance. Antimicrob Agents Chemother 39 (1): 103-106, 1995. 82. Harputluoglu U, Egeli E, Sahin I, Oghan F, Ozturka O. Nasopharyngeal aerobic bacterial flora and Staphylococcus aureus nasal carriage in deaf children. Int J Pediat Otorhinolaryngol 69: 69-74, 2005. 58 83. Henze UU, Berger-Bachi B. Penicillin-binding protein 4 overproduction increases β-Lactam resistance in Staphylococcus aureus. Antimicrob Agents Chemother 40 (9): 2121-2125, 1996. 84. Hirakata Y, Yanagihara K, Miyazaki Y, Tomono K, Kobayashi I, Kohno S. Antimicrobial susceptibilities of potential bacterial pathogens in adults with acute respiratory tract infections prospective epidemiological network investigating community-acquired infection surveillance in Nagasaki (Penicillin) study. Diag Microbiol Infect Dis 51: 271-280, 2005. 85. Hiramatsu K, Hanki H, Ino T, Yabuta K, Oguri T,Tenover FC. Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility. J Antimicrob Chemother 40: 135-136, 1997. 86. Hungria H. O problema das amígdalas e vegetações adenóides. In: Otorrinolaringologia. Guanabara Koogan, Rio de Janeiro, p 167-170, 2000. 87. Huang H, Flynn NM, King JH, Monchaud C, Morita M, Cohen SH. Comparisons of community-associated methicillin-resistant Staphylococcus aureus (MRSA) and hospital-associated MRSA infections in Sacramento, California. J Clin Microbiol 44 (7): 2423-2427, 2006. 88. Huang YH, Tseng SP, Hu JM, Tsai JC, Hsueh PR, Teng LJ. Clonal spread of SCCmec type IV methicillin-resistant Staphylococcus aureus between community and hospital. Clin Microbiol Infect 13: 717-724, 2007. 89. Ito T, Hiramatsu K, Tomasz A, Lencastre H, Perreten V, Holden MTG, Coleman DC, Goering R, Giffard PM, Skov RL, Zhang K, Westh H, O’Brien F, Tenover FC, Oliveira DC, Boyle-Vavra S, Laurent F, Kearns AM, Kreiswirth B, Ko KS, Grundmann H, Sollid JE, John JF, Daum R, Soderquist B, Buistx G. Guidelines for reporting novel mecA gene homologues. Antimicrob Agents Chemother October 56 (10): 4997-4999, 2012. 90. Jensen A, Fago-Olsen H, Sorensen CH, Kilian M. Molecular mapping to species level of the tonsillar crypt microbiota associated with health and recurrent tonsillitis. PLoS ONE 8 (2): 2013. 91. Júnior RGC, Brandão FH, Carvalho MRMS, Aquino JEP, Pereira SH, Eiras B. Perfil de pacientes submetidos à adenoidectomia, amigdalectomia e adenoamigdalectomia pela disciplina de otorrinolaringologia da UNISA. Arq Int Otorrinolaringol 12 (2): 189-193, 2008. 59 92. Kaiser TDL, Pacheco FC, Lima AA, Pereira EM,Santos KRN, Nunes APF. Avaliação de métodos comumente usados em laboratórios para a determinação da suscetibilidade à oxacilina entre amostras de Staphylococcus sp, isoladas de um hospital de Vitória, Estado do Espírito Santo. Rev Soc Bras Med Trop 43 (3): 298-303, 2010. 93. Khosravi AD, Hoveizavi H, Farshadzadeh Z. The prevalence of genes encoding leukocidins in Staphylococcus aureus strains resistant and sensitive to methicillin isolated from burn patients in Taleghani hospital, Ahvaz, Iran. Burns 38: 247-251, 2012. 94. Kielmovitch IH, Keleti G, Bluestone CD, Wald ER, Gonzáles C. Microbiology of obstructive tonsillar hypertrophy and recurrent tonsillitis. Arch Otolaryngol Head Neck Surg 115: 721-724, 1989. 95. Kim C, Milheiriço C, Gardete S, Holmes MA, Holden MTG, Hermínia de Lencastre H, Tomasz A. Properties of a novel PBP2A protein homolog fromStaphylococcus aureus strain LGA251 and its contribution to the β-lactam-resistant phenotype. J Biol Chem 287 (44): 36854-36863, 2012. 96. Kumar VA, Steffy K, Chatterjee M, Sugumar M, Dinesh KR, Manoharan A, Karim S, Biswas R. Detection of oxacillin-susceptible mecA-positive Staphylococcus aureus isolates by use of chromogenic medium MRSA ID. J Clin Microbiol 51 (1): 318-319, 2013. 97. Leclercq R. Mechanisms of resistance to macrolides and lincosamides: nature of the resistance elements and their clinical implications. Clin Infect Dis 34: 482-492, 2002. 98. Lewis II JS, Jorgensen JH. Inducible clindamycin resistance in Staphylococci: should clinicians and microbiologists be concerned? Clin Infect Dis 40: 280-285, 2005. 99. Lim JA, Kwon AE, Kim SK, Cong Y, Lee K, Choi EC. Prevalence of resistance to macrolide, lincosamide and streptogramin antibiotics in Gram-positive cocci isolated in Korean hospital. J Antimicrob Chemother 49: 489-495, 2002. 100. Lina G, Piémont Y, Godail-Gamot F, Bes M, Peter MO, Gauduchon V, Vandenesch F, Etienne J. Involvement of Panton-Valentine leukocidin- 60 producing Staphylococcus aureus in primary skin infections and pneumonia. Clin Infect Dis 29: 1128-1232, 1999. 101. Lowy FD. Staphylococcus aureus infections. N Engl J Med 339: 520-532, 1998. 102. Lowy FD. Antimicrobial resistance: the example of Staphylococcus aureus. J Clin Invest 111: 1265-1273, 2003. 103. Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, Harbarth S, Hindler JF, Kahlmeter G, Olsson-Liljequist B, Paterson DL, Rice LB, Stelling J, Struelens MJ, Vatopoulos A, Weber JT, Monnet DL. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect 18: 268-281, 2012. 104. Makgotlho PE, Kock MM, Hoosen A, Lekalakala R, Omar S, Dove M, Ehlers MM. Molecular identification and genotyping of MRSA isolates. FEMS Immunol Med Microbiol 57: 104-115, 2009. 105. Marchese A, Balistreri G, Tonoli E, Debbia A,Schito GC. Heterogeneous vancomycin resistance in methicillin-resistant Staphylococcus aureusstrains isolated in a large italian hospital. J Clin Microbiol 38: 866-869, 2000. 106. Maroto DP, Quezel NM, Rodríguez IL, Veja EM, Morente JCC, Rodríguez VP, Ruiz EF, Jiménez MC. Situación actual de las resistencias a antimicrobianos em infecciones amigdalares. Acta Otorrinolaringol Esp 57: 171-175, 2006. 107. Matos FS, Reale JA, Neto JS, Barata L, Pamponet LO, Brito RMPX, Costa VCNB, Viana VMS, Carvalho CMN. Antibiotics use in Streptococcal tonsillitis. Gazeta Média da Bahia 77: S23-S27, 2007. 108. Mcdougal LK, Thornsberry C. Role of β-lactamase in Staphylococcal resistance to penicillinase-resistant penicillins and cephalosporins. J Clin. Microbiol 23 (5): 832-839, 1986. 109. Mckinney TK, Sharma VK, Craig WA, Archer GL. Transcription of the gene mediating methicillin resistance in Staphylococcus aureus (mecA) is corepressed but not coinduced by cognate mecA and β-Lactamase regulators. J Bacteriol 183 (23): 6862-6868, 2001. 61 110. Medrano FL, Aguado JM. Staphylococcus aureus con sensibilidad disminuida a vancomicina. Nuevos problemas para el clínico. Med Clin (Barc) 135 (4): 160-161, 2010. 111. Mena Viveros N. Biofilms en otorrinolaringología. Acta Otorrinolaringol Esp. 2012. http://dx.doi.org/10.1016/j.otorri.2012.08.005. 112. Mertz D, Frei R, Jaussi B, Tietz A, Stebler C, Fluckiger U, Widmer AF. Throat Swabs Are Necessary to Reliably Detect Carriers of Staphylococcus aureus. Clin Infect Dis 45: 475-477, 2007. 113. Morag A, Ocra PL. Immunologic aspect of tonsils. Ann Otol Rhinol Laryngol 84 (Supp. 19): 37-43, 1975. 114. Morais S, Teles A, Ramalheira E, Roseta J. Amigdalite estreptocócica - presunção clínica versus diagnóstico. Acta Medica Portuguesa 22: 773-778, 2009. 115. Murakami K, Minamide W,Wada K, Nakamura E, Teraoka H, Watanabe S. Identification of methicillin-resistant strains of staphylococci by polymerase chain reaction. J Clin Microbiol 29: 2240-2244, 1991. 116. Murray PR, Rosenthal KS, Pfaller MA. Staphylococcus e microrganismos relacionados. In: Microbiologia Médica. Elsevier Editora Ltda, Rio de Janeiro, p 215-230, 2006. 117. Naimi TS, LeDell KH, Como-Sabetti K, Borchardt SM, Boxrud DJ, Etienne J, Johnson SK, Vandenesch F, Fridkin S, O'Boyle C, Danila RN, Lynfield R. Comparison of community- and health care-associated methicillin-resistant Staphylococcusaureusinfection. JAMA 290 (22): 2976-2984, 2003. 118. Narita S, Kaneko J, Chiba J, Piemont Y, Jarraud S, Etienne J, Kamio Y. Phage conversion of Panton-Valentine leukocidinin Staphylococcus aureus: molecular analysis of a PVL-converting phage, φSLT. Gene 268: 195-206, 2001. 119. Nascimento-Carvalho CM, Marques HHS. Recomendação do Departamento de Infectologia da Sociedade Brasileira de Pediatria para conduta de crianças e adolescentes com faringoamigdalites agudas. Jornal de Pediatria 82: 79-80, 2006. 62 120. Nilsson P, Ripa T. Staphylococcus aureus throat colonization is more frequent than colonization in the anterior nares. J Clin Microbiol 44 (9): 3334-3339, 2006. 121. Oplustil CP, Zoccoli CM, Tobouti NR, Sinto SI. Cultura de amostras do tratro respiratório superior. In: Procedimentos básicos em Microbiologia Clínica. Elsevier Editora Ltda, 3º Ed., São Paulo, p 224-230, 2010. 122. Palavecino E. Community-acquired methicillin-resistant Staphylococcus aureus infections. Clin Lab Med 24 (2): 403-418, 2004. 123. Pascuala A, Bañob JR, Arellanoa ER, Molac J, Martínez LM. Sensibilidad disminuida a vancomicina en cepas isogénicas de Staphylococcus aureus aisladas del mismo paciente. Med Clin (Barc) 117: 416-418, 2001. 124. Pereira C. Noções anatômicas. In: Otorrinolaringologia para uso do médico prático. Editora Guanabara, Koogan S.A., 3aEd., Rio de Janeiro, p 33-69, 1957. 125. Pereira LMP, Juman S, Bekele I, Seepersadsingh N, Adesiyun AA. Achado de bactérias selecionadas em crianças de Trinidad com doença amigdaliana crônica. Rev Bras Otorrinolaringol 74: 903-911, 2008. 126. Petinaki E, Kontos F, Maniatis NA. Emergence of two oxacillin-susceptible mecA-positive Staphylococcus aureus clones in a Greek hospital. J Antimicrob Chemother 50: 1090-1091, 2002. 127. Pichichero ME. Group A β-hemolytic streptococcal infections. Pediatr Rev 19 (9): 291-302, 1998. 128. Pichichero ME, Casey JR. Systematic review of factors contributing to penicillin treatment failure in Streptococcus pyogenes pharyngitis. Otolaryngol-Head and Neck Surgery 137 (6): 851-857, 2007. 129. Pitrez PMC, Pitrez JLB. Acute upper respiratory tract infections: outpatient diagnosis and treatment. J Pediatr 79: S77-S86, 2003. 130. Podbielski A, Beckertb S, Schattkec R, Leithauser F, Lestina F, Gobler B, Kreikemeyer B. Epidemiology and virulence gene expression of intracellular group A streptococci in tonsils of recurrently infected adults. Int J Med Microbiol 293: 179-190, 2003. 131. Pottumarthy S, Fritsche TR, Jones RN. Evaluation of alternative disk diffusion methods for detecting mecA-mediated oxacillin resistance in an 63 international collection of staphylococci: Validation report from the SENTRY Antimicrobial Surveillance Program. Diagn Microbiol Infect Dis 51: 57-62, 2005. 132. Raju G, Selvam EM. Evaluation of microbial flora in chronictonsillitis and the role of tonsillectomy. Bangladesh J Otorhinolaryngol 18 (2): 109-113, 2012. 133. Ripoll MA, Orero A, González J. Prescripción de antimicrobianos en atención primaria en España. Motivos y características. Med Gen 48: 785-790, 2002. 134. Rodríguez-Noriega E, Seas C. The changing pattern of methicillin-resistant Staphylococcus aureus clones in Latin America: implications for clinical practice in the region. Braz J Infect Dis 14 (Suppl. 2): S87-S96, 2010. 135. Ross MH, Reith EJ, Romrell LJ. Sistema Linfático (Órgãos Linfáticos ou Sistema Imunológico). In: Histologia texto e atlas. Editora Médica Panamericana.São Paulo. 2aEd., p 307-328, 1993. 136. Rossney AS, Shore AC, Morgan PM, Fitzgibbon MM, O’Connell B, Coleman DC. The emergence and importation of diverse genotypes of methicillin-resistant Staphylococcus aureus (MRSA) harboring the Panton-Valentine leukocidin gene (pvl) reveal that pvl is a poor marker for community-acquired MRSA strains in Ireland. J Clin Microbiol 45 (8): 2554-2563, 2007. 137. Rozenbaum R, Sampaio MG, Batista GS, Garibaldi AM, Terra GMF, Souza MJ, Vieira EN, Silva-Carvalho MC, Teixeira LA, Figueiredo AMS. The first report in Brazil of severe infection caused by community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA). Braz J Med Biolog Res 42: 756-760, 2009. 138. Santos AL, Santos DO, Freitas CC, Ferreira BLA, Afonso IF, Rodrigues CR, Castro HC. Staphylococcus aureus: visitando uma cepa de importância hospitalar. J Bras Patol Med Lab 43 (6): 413-423, 2007. 139. Scalabrin R, Buss GD, Iamaguchi KCS, Cardoso CL, Garcia LB. Isolation of Streptococcus pyogenes in individuals with pharyngotonsillitis and antimicrobial susceptibility testing. Rev Bras Otorrinolaringol 69: 814-818, 2003. 140. Schaechter M, Engleberg NC, Eisenstein BI, Medoff G. Flora microbiana normal. In: Microbiologia- mecanismos das doenças infecciosas. Editora Guanabara Koogan, 3aEd, Rio de janeiro, p 10-15, 2002. 64 141. Schmitz FJ, Verhoef J, Fluit AC. Prevalence of resistance to MLS antibiotics in 20 European university hospitals participating in the European Sentry surveillance programme. J Antimicrob Chemother 43 (6): 783-792, 1999. 142. Schwartz B. Tonsilite viral ou bacteriana? In: Sih T. Infectologia pediátrica. Rio de Janeiro: Revinter, p.47-51, 2001. 143. Seppala H, Klaukka T, Vuopio-Varkila J. The effect of changes in the consumption of macrolide antibiotics on erythromycin resistance in group A streptococci in Finland. Finnish Study Group for Anti-microbial Resistance. N Engl J Med 337 (7): 441-446, 1997. 144. Shallcross LJ, Fragaszy E, Johnson AM, Hayward AC. The role of the Panton-Valentine leucocidin toxin in staphylococcal disease: a systematic review and meta-analysis. Lancet Infect Dis 13: 43-54, 2013. 145. Sih TM, Bricks LF. Optimizing the management of the main acute infections in pediatric ORL: tonsillitis, sinusitis, otitis media. Rev Bras Otorrinolaringol 74: 755-762, 2008. 146. Smith RD, Coast J. Antimicrobial resitance: a global response. Bull World Health Organization 80: 126-133, 2002. 147. Sneath PH, Sokal RR. Numerical taxonomy: The principles and practice of numerical classification. San Francisco: W.H. Freeman, 573p, 1973. 148. Sollid JUE, Furberg AS, Hanssen AM, Johannessen M. Staphylococcus aureus: Determinants of human carriage. Infect Genet Evol 2013. http://dx.doi.org/10.1016/j.meegid.2013.03.020. 149. Stegger M, Andersen PS, Kearns A, Pichon B, Holmes MA, Edwards G, Laurent F, Teale C, Skov R, Larsen AR. Rapid detection, differentiation and typing of methicillin-resistant Staphylococcus aureus harbouring either mecA or the new mecA homologue mecA LGA25. Clin Microbiol Infect 18: 395-400, 2012. 150. Stuck BA, Windfuhr JP, Genzwurker H, Schroten H, Tenenbaum T, Gotte K. Tonsillectomy in Children. Rev Deutsches Ärzteblatt International 105: 852-861, 2008. 151. Swenson JM, Skov R, Patel JB. The Cefoxitin Disk Test - What a Clinical Microbiologist Needs To Know. Clin Microbiol Newsletter 29 (5): 33-40, 2007. 65 152. Swidsinski A, Goktas O, Bessler C, Loening-Baucke V, Hale LP, Andree H, Weizenegger M, Holzl M, Scherer H, Lochs H. Spatial organization of microbiota in quiescent adenoiditis and tonsillitis. J Clin Pathol 60: 253-260, 2007. 153. Tavares W. Resistência bacteriana. In: Manual de antimicrobianos e quimioterápicos antiinfecciosos, Atheneu, 3ª Ed., São Paulo, p. 79, 2001. 154. Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, Swaminathan B. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 33: 2233-2239, 1995. 155. Timon CI, Mcallister VA, Walsh M, Cafferkey MT. Changes in t

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