Araştırma Makalesi
BibTex RIS Kaynak Göster

Köpek Deri Enfeksiyonlarında Staphylococcus pseudintermedius Sıklığı ve Elde Edilen İzolatların Antibiyotik Direnç Profilleri

Yıl 2020, Cilt: 31 Sayı: 2, 127 - 132, 31.12.2020
https://doi.org/10.35864/evmd.793494

Öz

Bu çalışmada, deri enfeksiyonu olan 77 köpekten 61 Staphylococcus pseudintermedius suşu izole edilmiştir. Yaygın olarak kullanılan antibiyotiklere karşı antimikrobiyal direnç, disk difüzyon yöntemi ile değerlendirildi. Penisilin ve metisilin direncinden sorumlu sırasıyla blaZ ve mecA genlerinin varlığı PCR ile araştırıldı. S. pseudintermedius izolatları tetrasiklin (% 47.5) ve penisiline (% 40.9) yüksek direnç gösterirken, tüm izolatlar amikasine (% 100) duyarlıydı. 18 metisiline dirençli S. pseudintermedius (MRSP) suşunun tümü mecA geni için pozitif iken blaZ genine sahip 25 S. pseudintermedius suşu izolatı da fenotipik olarak penisiline dirençliydi. 18 MRSP izolatından 14 S. pseudintermedius suşu, üç veya daha fazla antibiyotiğe dirençliydi, bu da bu suşların çoklu ilaç direnci (MDR) gösterdiğini ortaya koydu. Bu rapor, S. pseudintermedius'un köpek deri enfeksiyonlarından en sık izole edilen bakteri olduğuna dair önceki bulguları doğrulamaktadır. Bu çalışmada test edilen tüm S. pseudintermedius suşları amikasine duyarlı olduğundan, amikasinin S. pseudintermedius enfeksiyonlarının tedavisinde yararlı bir ajan olduğu sonucuna varılabilir.

Kaynakça

  • Ball KR, Rubin JE, Chirino-Trejo M, Dowling PM. (2008) Antimicrobial resistance and prevalence of canine uropathogens at the Western College of Veterinary Medicine Veterinary Teaching Hospital, 2002-2007. Can Vet J. 49(10), 985-990.
  • Bannoehr J, Franco A, Iurescia M, Battisti A, Fitzgerald JR. (2009) Molecular diagnostic identification of Staphylococcus pseudintermedius. J Clin Microbiol. 47(2), 469-471.
  • Bannoehr J, Guardabassi L. (2012) Staphylococcus pseudintermedius in the dog: taxonomy, diagnostics, ecology, epidemiology and pathogenicity. Vet Dermatol. 23(4), 253-E252.
  • Bardiau M, Yamazaki K, Ote I, Misawa N, Mainil JG. (2013) Characterization of methicillin-resistant Staphylococcus pseudintermedius isolated from dogs and cats. Microbiol Immunol. 57(7), 496-501.
  • Bemis DA, Jones RD, Hiatt LE, Ofori ED, Rohrbach BW, Frank LA, Kania SA. (2006) Comparison of tests to detect oxacillin resistance in Staphylococcus intermedius, Staphylococcus schleiferi, and Staphylococcus aureus isolates from canine hosts. J Clin Microbiol. 44(9), 3374-3376.
  • Bond R, Loeffler A. (2012) What's happened to Staphylococcus intermedius? Taxonomic revision and emergence of multi-drug resistance. J Small Anim Pract. 53(3), 147-154.
  • Bosgelmez-Tinaz G, Ulusoy S, Aridogan B, Coskun-Ari F. (2006) Evaluation of different methods to detect oxacillin resistance in Staphylococcus aureus and their clinical laboratory utility. Eur J Clin Microbiol Infect Dis. 25(6), 410-412.
  • Chambers HF. (1997) Methicillin resistance in staphylococci: molecular and biochemical basis and clinical implications. Clin Microbiol Rev. 10(4), 781-791.
  • Chuang CY, Yang YL, Hsueh PR, Lee PI. (2010) Catheter-Related Bacteremia Caused by Staphylococcus pseudintermedius Refractory to Antibiotic-Lock Therapy in a Hemophilic Child with Dog Exposure. J Clin Microbiol. 48(4), 1497-1498.
  • CLSI. (2018) Interpretive Criteria for Identification of Bacteria and Fungi by DNA Target Sequencing; Approved Guideline. In: Institute CaLS, ed. CLSI document MM18-A. Wayne, PA ABD.
  • CLSI. (2019) Performance Standards for Antimicrobial Susceptibility Testing. 29th ed. CLSI supplement M100. Wayne, PA ABD.
  • De Lucia M, Moodley A, Latronico F, Giordano A, Caldin M, Fondati A, Guardabassi L. (2011) Prevalence of canine methicillin resistant Staphylococcus pseudintermedius in a veterinary diagnostic laboratory in Italy. Res Vet Sci. 91(3), 346-348.
  • Devriese LA, Vancanneyt M, Baele M, Vaneechoutte M, De Graef E, Snauwaert C, Cleenwerck I, Dawyndt P, Swings J, Decostere A, Haesebrouck F. (2005) Staphylococcus pseudintermedius sp. nov., a coagulase-positive species from animals. Int J Syst Evol Microbiol. 55(4), 1569-1573.
  • Drancourt M, Roux V, Fournier PE, Raoult D. (2004) rpoB gene sequence-based identification of aerobic Gram-positive cocci of the genera Streptococcus, Enterococcus, Gemella, Abiotrophia, and Granulicatella. J Clin Microbiol. 42(2), 497-504.
  • El Zubeir IEM, Kanbar T, Alber J, Lammler C, Akineden O, Weiss R, Zschock M. (2007) Phenotypic and genotypic characteristics of methicillin/oxacillin-resistant Staphylococcus intermedius isolated from clinical specimens during routine veterinary microbiological examinations. Vet Microbiol. 121(1-2), 170-176.
  • Felten A, Grandry B, Lagrange PH, Casin I. (2002) Evaluation of three techniques for detection of low-level methicillin-resistant Staphylococcus aureus (MRSA): a disk diffusion method with cefoxitin and moxalactam, the Vitek 2 system, and the MRSA-screen latex agglutination test. J Clin Microbiol. 40(8), 2766-2771.
  • Feng YY, Tian W, Lin DC, Luo QY, Zhou YZ, Yang T, Deng YT, Liu YH, Liu JH. (2012) Prevalence and characterization of methicillin-resistant Staphylococcus pseudintermedius in pets from South China. Vet Microbiol. 160(3-4), 517-524.
  • Findik A, Ciftci A, Onyay T, Sezener MG, Kocak Y, Gulhan T. (2018) Determination of methicillin resistance and some genotypic characteristics of staphylococci isolated from dogs and their owners. Turk J Vet Anim Sci. 42(6), 549-555.
  • Fuda CC, Fisher JF, Mobashery S. (2005) Beta-lactam resistance in Staphylococcus aureus: the adaptive resistance of a plastic genome. Cell Mol Life Sci. 62(22), 2617-2633.
  • Geha DJ, Uhl JR, Gustaferro CA, Persing DH. (1994) Multiplex PCR for identification of methicillin-resistant staphylococci in the clinical laboratory. J Clin Microbiol. 32(7), 1768-1772.
  • Gomez-Sanz E, Torres C, Lozano C, Saenz Y, Zarazaga M. (2011) Detection and characterization of methicillin-resistant Staphylococcus pseudintermedius in healthy dogs in La Rioja, Spain. Comp Immunol Microbiol Infect Dis. 34(5), 447-453.
  • Kawakami T, Shibata S, Murayama N, Nagata M, Nishifuji K, Iwasaki T, Fukata T. (2010) Antimicrobial Susceptibility and Methicillin Resistance in Staphylococcus pseudintermedius and Staphylococcus schleiferi subsp coagulans Isolated from Dogs with Pyoderma in Japan. J Vet Med Sci. 72(12), 1615-1619.
  • Krapf M, Muller E, Reissig A, Slickers P, Braun SD, Muller E, Ehricht R, Monecke S. (2019) Molecular characterisation of methicillin-resistant Staphylococcus pseudintermedius from dogs and the description of their SCCmec elements. Vet Microbiol. 233, 196-203.
  • Malik S, Christensen H, Peng H, Barton MD. (2007) Presence and diversity of the beta-lactamase gene in cat and dog staphylococci. Vet Microbiol. 123(1-3), 162-168.
  • Martineau F, Picard FJ, Grenier L, Roy PH, Ouellette M, Bergeron MG. (2000) Multiplex PCR assays for the detection of clinically relevant antibiotic resistance genes in staphylococci isolated from patients infected after cardiac surgery. The ESPRIT Trial. J Antimicrob Chemother. 46(4), 527-534.
  • Mellmann A, Becker K, Von Eiff C, Keckevoet U, Schumann P, Harmsen D. (2006) Sequencing and staphylococci identification. Emerg Infect Dis. 12(2), 333-336.
  • Moodley A, Damborg P, Nielsen SS. (2014) Antimicrobial resistance in methicillin susceptible and methicillin resistant Staphylococcus pseudintermedius of canine origin: Literature review from 1980 to 2013. Vet Microbiol. 171(3-4), 337-341.
  • Murugaiyan J, Wlther B, Stamm I, Abou-Elnaga Y, Brueggemann-Schwarze S, Vincze S, Wieler LH, . Lübke-Becker A, Semmler T, Roesler U. (2014) Species differentiation within the Staphylococcus intermedius group using a refined MALDI-TOF MS database. Clin Microbiol Infect. 20, 1007–1015.
  • Nienhoff U, Kadlec K, Chaberny IF, Verspohl J, Gerlach GF, Kreienbrock L, Schwarz S, Simon D, Nolte I. (2011) Methicillin-resistant Staphylococcus pseudintermedius among dogs admitted to a small animal hospital. Vet Microbiol. 150(1-2), 191-197.
  • Ozturk D, Avki S, Turutoglu H, Yigitarslan K, Sagnak S. (2010) Methicillin Resistance Among Coagulase-positive Staphylococci Isolated from Dogs with Otitis Externa, Skin Wounds and Pyoderma. Kafkas Uni Vet Fak Derg. 16(4), 651-656.
  • Onuma K, Tanabe T, Sato H. (2012) Antimicrobial resistance of Staphylococcus pseudintermedius isolates from healthy dogs and dogs affected with pyoderma in Japan. Vet Dermatol. 23, 17-22, e15.
  • Perez LR, Antunes AL, Barth AL, D'azevedo PA. (2007) Variations of agar screen tests for detection of methicillin resistance in staphylococci: focus on cefoxitin. Eur J Clin Microbiol Infect Dis. 26(4), 267-270.
  • Petti CA, Clinical and Laboratory Standards Institute. (2008) Interpretive criteria for identification of bacteria and fungi by DNA target sequencing : approved guideline, Wayne, PA: Clinical and Laboratory Standards Institute.
  • Rosato AE, Kreiswirth BN, Craig WA, Eisner W, Climo MW, Archer GL. (2003) mecA-blaZ corepressors in clinical Staphylococcus aureus isolates. Antimicrob Agents and Chemother. 47(4), 1460-1463.
  • Rubin JE, Chirino-Trejo M. (2011) Prevalence, sites of colonization, and antimicrobial resistance among Staphylococcus pseudintermedius isolated from healthy dogs in Saskatoon, Canada. J Vet Diagn Invest. 23(2), 351-354.
  • Ruscher C, Lubke-Becker A, Semmler T, Wleklinski CG, Paasch A, Soba A, Stamm I, Kopp P, Wieler LH, Walther B. (2010) Widespread rapid emergence of a distinct methicillin- and multidrug-resistant Staphylococcus pseudintermedius (MRSP) genetic lineage in Europe. Vet Microbiol. 144(3-4), 340-346.
  • Saputra S, Jordan D, Worthing KA, Norris JM, Wong HS, Abraham R, Trott DJ, Abraham S. (2017) Antimicrobial resistance in coagulase-positive staphylococci isolated from companion animals in Australia: A one year study. Plos One. 12(4), e0176379.
  • Sareyyupoglu B, Mustak HK, Cantekin Z, Diker KS. (2014) Methicillin Resistance in Staphylococcus pseudintermedius Isolated from Shelter Dogs in Turkey. Kafkas Univ Vet Fak Derg. 20(3), 435-438.
  • Sasaki T, Kikuchi K, Tanaka Y, Takahashi N, Kamata S, Hiramatsu K. (2007a) Methicillin-resistant Staphylococcus pseudintermedius in a veterinary teaching hospital. J Clin Microbiol. 45(4), 1118-1125.
  • Sasaki T, Kikuchi K, Tanaka Y, Takahashi N, Kamata S, Hiramatsu K. (2007b) Reclassification of phenotypically identified Staphylococcus intermedius strains. J Clin Microbiol. 45(9), 2770-2778.
  • Savini V, Barbarini D, Polakowska K, Gherardi G, Bialecka A, Kasprowicz A, Polilli E, Marrollo R, Di Bonaventura G, Fazii P, D'antonio D, Miedzobrodzki J, Carretto E. (2013) Methicillin-Resistant Staphylococcus pseudintermedius Infection in a Bone Marrow Transplant Recipient. J Clin Microbiol. 51(5), 1636-1638.
  • Somayaji R, Priyantha MAR, Rubin JE, Church D. (2016) Human infections due to Staphylococcus pseudintermedius, an emerging zoonosis of canine origin: report of 24 cases. Diagn Micr and Infec Dis. 85(4), 471-476.
  • Stegmann R, Burnens A, Maranta CA, Perreten V. (2010) Human infection associated with methicillin-resistant Staphylococcus pseudintermedius ST71. J Antimicrob Chemot. 65(9), 2047-2048.
  • Strommenger B, Kettlitz C, Werner G, Witte W. (2003) Multiplex PCR assay for simultaneous detection of nine clinically relevant antibiotic resistance genes in Staphylococcus aureus. J Clin Microbiol. 41(9), 4089-4094.
  • Van Duijkeren E, Catry B, Greko C, Moreno MA, Pomba MC, Pyorala S, Ruzauskas M, Sanders P, Threlfall EJ, Torren-Edo J, Torneke K, Antimicrobials SAG. (2011) Review on methicillin-resistant Staphylococcus pseudintermedius. J Antimicrob Chemot. 66(12), 2705-2714.
  • Van Hoovels L, Vankeerberghen A, Boel A, Van Vaerenbergh K, De Beenhouwer H. (2006) First case of Staphylococcus pseudintermedius infection in a human. J Clin Microbiol. 44(12), 4609-4612.
  • Velasco D, Del Mar Tomas M, Cartelle M, Beceiro A, Perez A, Molina F, Moure R, Villanueva R, Bou G. (2005) Evaluation of different methods for detecting methicillin (oxacillin) resistance in Staphylococcus aureus. J Antimicrob Chemot. 55(3), 379-382.
  • Weese JS, Van Duijkeren E. (2010) Methicillin-resistant Staphylococcus aureus and Staphylococcus pseudintermedius in veterinary medicine. Vet Microbiol. 140(3-4), 418-429.
  • Yoon JW, Lee KJ, Lee SY, Chae MJ, Park JK, Yoo JH, Park HM. (2010) Antibiotic resistance profiles of Staphylococcus pseudintermedius isolates from canine patients in Korea. J Microbiol Biotechnol. 20(12), 1764-1768.
  • Zhu LX, Zhang ZW, Wang C, Yang HW, Zhang Q, Cheng J. (2006) Evaluation of the CLSI cefoxitin 30-microg disk-diffusion method for detecting methicillin resistance in staphylococci. Clin Microbiol Infect. 12(10), 1039-1042.
  • Zscheck KK, Murray BE. (1993) Genes Involved in the Regulation of Beta-Lactamase Production in Enterococci and Staphylococci. Antimicrob Agents Chemother. 37(9), 1966-1970.

Frequency of Staphylococcus pseudintermedius in Canine Skin Infections and Antibiotic Resistance Profiles of the Recovered Isolates

Yıl 2020, Cilt: 31 Sayı: 2, 127 - 132, 31.12.2020
https://doi.org/10.35864/evmd.793494

Öz

In this study, 61 Staphylococcus pseudintermedius strains were isolated from 77 dogs with skin infections. Antimicrobial resistance to commonly used antibiotics was evaluated by disc diffusion method. The presence of the blaZ and mecA genes responsible respectively for penicillin and methicillin resistance were investigated by PCR. The S. pseudintermedius isolates were highly resistant to tetracycline (47.5%) and penicillin (40.9%) while all isolates were susceptible to amikacin (100%). All 18 methicillin-resistant S. pseudintermedius (MRSP) strains were positive for the mecA gene while the 25 S. pseudintermedius strain isolates with the blaZ gene were also resistant to penicillin phenotypically. Of the 18 MRSP isolates, 14 S. pseudintermedius strains were resistant to three or more antibiotics, indicating that these strains showed multiple drug resistance (MDR). This report confirms previous findings that S. pseudintermedius is the most frequently isolated bacteria from dog skin infections. It can also be concluded that amikacin is a useful agent for treating S. pseudintermedius infections since all the S. pseudintermedius strains tested in this study were susceptible to amikacin.

Kaynakça

  • Ball KR, Rubin JE, Chirino-Trejo M, Dowling PM. (2008) Antimicrobial resistance and prevalence of canine uropathogens at the Western College of Veterinary Medicine Veterinary Teaching Hospital, 2002-2007. Can Vet J. 49(10), 985-990.
  • Bannoehr J, Franco A, Iurescia M, Battisti A, Fitzgerald JR. (2009) Molecular diagnostic identification of Staphylococcus pseudintermedius. J Clin Microbiol. 47(2), 469-471.
  • Bannoehr J, Guardabassi L. (2012) Staphylococcus pseudintermedius in the dog: taxonomy, diagnostics, ecology, epidemiology and pathogenicity. Vet Dermatol. 23(4), 253-E252.
  • Bardiau M, Yamazaki K, Ote I, Misawa N, Mainil JG. (2013) Characterization of methicillin-resistant Staphylococcus pseudintermedius isolated from dogs and cats. Microbiol Immunol. 57(7), 496-501.
  • Bemis DA, Jones RD, Hiatt LE, Ofori ED, Rohrbach BW, Frank LA, Kania SA. (2006) Comparison of tests to detect oxacillin resistance in Staphylococcus intermedius, Staphylococcus schleiferi, and Staphylococcus aureus isolates from canine hosts. J Clin Microbiol. 44(9), 3374-3376.
  • Bond R, Loeffler A. (2012) What's happened to Staphylococcus intermedius? Taxonomic revision and emergence of multi-drug resistance. J Small Anim Pract. 53(3), 147-154.
  • Bosgelmez-Tinaz G, Ulusoy S, Aridogan B, Coskun-Ari F. (2006) Evaluation of different methods to detect oxacillin resistance in Staphylococcus aureus and their clinical laboratory utility. Eur J Clin Microbiol Infect Dis. 25(6), 410-412.
  • Chambers HF. (1997) Methicillin resistance in staphylococci: molecular and biochemical basis and clinical implications. Clin Microbiol Rev. 10(4), 781-791.
  • Chuang CY, Yang YL, Hsueh PR, Lee PI. (2010) Catheter-Related Bacteremia Caused by Staphylococcus pseudintermedius Refractory to Antibiotic-Lock Therapy in a Hemophilic Child with Dog Exposure. J Clin Microbiol. 48(4), 1497-1498.
  • CLSI. (2018) Interpretive Criteria for Identification of Bacteria and Fungi by DNA Target Sequencing; Approved Guideline. In: Institute CaLS, ed. CLSI document MM18-A. Wayne, PA ABD.
  • CLSI. (2019) Performance Standards for Antimicrobial Susceptibility Testing. 29th ed. CLSI supplement M100. Wayne, PA ABD.
  • De Lucia M, Moodley A, Latronico F, Giordano A, Caldin M, Fondati A, Guardabassi L. (2011) Prevalence of canine methicillin resistant Staphylococcus pseudintermedius in a veterinary diagnostic laboratory in Italy. Res Vet Sci. 91(3), 346-348.
  • Devriese LA, Vancanneyt M, Baele M, Vaneechoutte M, De Graef E, Snauwaert C, Cleenwerck I, Dawyndt P, Swings J, Decostere A, Haesebrouck F. (2005) Staphylococcus pseudintermedius sp. nov., a coagulase-positive species from animals. Int J Syst Evol Microbiol. 55(4), 1569-1573.
  • Drancourt M, Roux V, Fournier PE, Raoult D. (2004) rpoB gene sequence-based identification of aerobic Gram-positive cocci of the genera Streptococcus, Enterococcus, Gemella, Abiotrophia, and Granulicatella. J Clin Microbiol. 42(2), 497-504.
  • El Zubeir IEM, Kanbar T, Alber J, Lammler C, Akineden O, Weiss R, Zschock M. (2007) Phenotypic and genotypic characteristics of methicillin/oxacillin-resistant Staphylococcus intermedius isolated from clinical specimens during routine veterinary microbiological examinations. Vet Microbiol. 121(1-2), 170-176.
  • Felten A, Grandry B, Lagrange PH, Casin I. (2002) Evaluation of three techniques for detection of low-level methicillin-resistant Staphylococcus aureus (MRSA): a disk diffusion method with cefoxitin and moxalactam, the Vitek 2 system, and the MRSA-screen latex agglutination test. J Clin Microbiol. 40(8), 2766-2771.
  • Feng YY, Tian W, Lin DC, Luo QY, Zhou YZ, Yang T, Deng YT, Liu YH, Liu JH. (2012) Prevalence and characterization of methicillin-resistant Staphylococcus pseudintermedius in pets from South China. Vet Microbiol. 160(3-4), 517-524.
  • Findik A, Ciftci A, Onyay T, Sezener MG, Kocak Y, Gulhan T. (2018) Determination of methicillin resistance and some genotypic characteristics of staphylococci isolated from dogs and their owners. Turk J Vet Anim Sci. 42(6), 549-555.
  • Fuda CC, Fisher JF, Mobashery S. (2005) Beta-lactam resistance in Staphylococcus aureus: the adaptive resistance of a plastic genome. Cell Mol Life Sci. 62(22), 2617-2633.
  • Geha DJ, Uhl JR, Gustaferro CA, Persing DH. (1994) Multiplex PCR for identification of methicillin-resistant staphylococci in the clinical laboratory. J Clin Microbiol. 32(7), 1768-1772.
  • Gomez-Sanz E, Torres C, Lozano C, Saenz Y, Zarazaga M. (2011) Detection and characterization of methicillin-resistant Staphylococcus pseudintermedius in healthy dogs in La Rioja, Spain. Comp Immunol Microbiol Infect Dis. 34(5), 447-453.
  • Kawakami T, Shibata S, Murayama N, Nagata M, Nishifuji K, Iwasaki T, Fukata T. (2010) Antimicrobial Susceptibility and Methicillin Resistance in Staphylococcus pseudintermedius and Staphylococcus schleiferi subsp coagulans Isolated from Dogs with Pyoderma in Japan. J Vet Med Sci. 72(12), 1615-1619.
  • Krapf M, Muller E, Reissig A, Slickers P, Braun SD, Muller E, Ehricht R, Monecke S. (2019) Molecular characterisation of methicillin-resistant Staphylococcus pseudintermedius from dogs and the description of their SCCmec elements. Vet Microbiol. 233, 196-203.
  • Malik S, Christensen H, Peng H, Barton MD. (2007) Presence and diversity of the beta-lactamase gene in cat and dog staphylococci. Vet Microbiol. 123(1-3), 162-168.
  • Martineau F, Picard FJ, Grenier L, Roy PH, Ouellette M, Bergeron MG. (2000) Multiplex PCR assays for the detection of clinically relevant antibiotic resistance genes in staphylococci isolated from patients infected after cardiac surgery. The ESPRIT Trial. J Antimicrob Chemother. 46(4), 527-534.
  • Mellmann A, Becker K, Von Eiff C, Keckevoet U, Schumann P, Harmsen D. (2006) Sequencing and staphylococci identification. Emerg Infect Dis. 12(2), 333-336.
  • Moodley A, Damborg P, Nielsen SS. (2014) Antimicrobial resistance in methicillin susceptible and methicillin resistant Staphylococcus pseudintermedius of canine origin: Literature review from 1980 to 2013. Vet Microbiol. 171(3-4), 337-341.
  • Murugaiyan J, Wlther B, Stamm I, Abou-Elnaga Y, Brueggemann-Schwarze S, Vincze S, Wieler LH, . Lübke-Becker A, Semmler T, Roesler U. (2014) Species differentiation within the Staphylococcus intermedius group using a refined MALDI-TOF MS database. Clin Microbiol Infect. 20, 1007–1015.
  • Nienhoff U, Kadlec K, Chaberny IF, Verspohl J, Gerlach GF, Kreienbrock L, Schwarz S, Simon D, Nolte I. (2011) Methicillin-resistant Staphylococcus pseudintermedius among dogs admitted to a small animal hospital. Vet Microbiol. 150(1-2), 191-197.
  • Ozturk D, Avki S, Turutoglu H, Yigitarslan K, Sagnak S. (2010) Methicillin Resistance Among Coagulase-positive Staphylococci Isolated from Dogs with Otitis Externa, Skin Wounds and Pyoderma. Kafkas Uni Vet Fak Derg. 16(4), 651-656.
  • Onuma K, Tanabe T, Sato H. (2012) Antimicrobial resistance of Staphylococcus pseudintermedius isolates from healthy dogs and dogs affected with pyoderma in Japan. Vet Dermatol. 23, 17-22, e15.
  • Perez LR, Antunes AL, Barth AL, D'azevedo PA. (2007) Variations of agar screen tests for detection of methicillin resistance in staphylococci: focus on cefoxitin. Eur J Clin Microbiol Infect Dis. 26(4), 267-270.
  • Petti CA, Clinical and Laboratory Standards Institute. (2008) Interpretive criteria for identification of bacteria and fungi by DNA target sequencing : approved guideline, Wayne, PA: Clinical and Laboratory Standards Institute.
  • Rosato AE, Kreiswirth BN, Craig WA, Eisner W, Climo MW, Archer GL. (2003) mecA-blaZ corepressors in clinical Staphylococcus aureus isolates. Antimicrob Agents and Chemother. 47(4), 1460-1463.
  • Rubin JE, Chirino-Trejo M. (2011) Prevalence, sites of colonization, and antimicrobial resistance among Staphylococcus pseudintermedius isolated from healthy dogs in Saskatoon, Canada. J Vet Diagn Invest. 23(2), 351-354.
  • Ruscher C, Lubke-Becker A, Semmler T, Wleklinski CG, Paasch A, Soba A, Stamm I, Kopp P, Wieler LH, Walther B. (2010) Widespread rapid emergence of a distinct methicillin- and multidrug-resistant Staphylococcus pseudintermedius (MRSP) genetic lineage in Europe. Vet Microbiol. 144(3-4), 340-346.
  • Saputra S, Jordan D, Worthing KA, Norris JM, Wong HS, Abraham R, Trott DJ, Abraham S. (2017) Antimicrobial resistance in coagulase-positive staphylococci isolated from companion animals in Australia: A one year study. Plos One. 12(4), e0176379.
  • Sareyyupoglu B, Mustak HK, Cantekin Z, Diker KS. (2014) Methicillin Resistance in Staphylococcus pseudintermedius Isolated from Shelter Dogs in Turkey. Kafkas Univ Vet Fak Derg. 20(3), 435-438.
  • Sasaki T, Kikuchi K, Tanaka Y, Takahashi N, Kamata S, Hiramatsu K. (2007a) Methicillin-resistant Staphylococcus pseudintermedius in a veterinary teaching hospital. J Clin Microbiol. 45(4), 1118-1125.
  • Sasaki T, Kikuchi K, Tanaka Y, Takahashi N, Kamata S, Hiramatsu K. (2007b) Reclassification of phenotypically identified Staphylococcus intermedius strains. J Clin Microbiol. 45(9), 2770-2778.
  • Savini V, Barbarini D, Polakowska K, Gherardi G, Bialecka A, Kasprowicz A, Polilli E, Marrollo R, Di Bonaventura G, Fazii P, D'antonio D, Miedzobrodzki J, Carretto E. (2013) Methicillin-Resistant Staphylococcus pseudintermedius Infection in a Bone Marrow Transplant Recipient. J Clin Microbiol. 51(5), 1636-1638.
  • Somayaji R, Priyantha MAR, Rubin JE, Church D. (2016) Human infections due to Staphylococcus pseudintermedius, an emerging zoonosis of canine origin: report of 24 cases. Diagn Micr and Infec Dis. 85(4), 471-476.
  • Stegmann R, Burnens A, Maranta CA, Perreten V. (2010) Human infection associated with methicillin-resistant Staphylococcus pseudintermedius ST71. J Antimicrob Chemot. 65(9), 2047-2048.
  • Strommenger B, Kettlitz C, Werner G, Witte W. (2003) Multiplex PCR assay for simultaneous detection of nine clinically relevant antibiotic resistance genes in Staphylococcus aureus. J Clin Microbiol. 41(9), 4089-4094.
  • Van Duijkeren E, Catry B, Greko C, Moreno MA, Pomba MC, Pyorala S, Ruzauskas M, Sanders P, Threlfall EJ, Torren-Edo J, Torneke K, Antimicrobials SAG. (2011) Review on methicillin-resistant Staphylococcus pseudintermedius. J Antimicrob Chemot. 66(12), 2705-2714.
  • Van Hoovels L, Vankeerberghen A, Boel A, Van Vaerenbergh K, De Beenhouwer H. (2006) First case of Staphylococcus pseudintermedius infection in a human. J Clin Microbiol. 44(12), 4609-4612.
  • Velasco D, Del Mar Tomas M, Cartelle M, Beceiro A, Perez A, Molina F, Moure R, Villanueva R, Bou G. (2005) Evaluation of different methods for detecting methicillin (oxacillin) resistance in Staphylococcus aureus. J Antimicrob Chemot. 55(3), 379-382.
  • Weese JS, Van Duijkeren E. (2010) Methicillin-resistant Staphylococcus aureus and Staphylococcus pseudintermedius in veterinary medicine. Vet Microbiol. 140(3-4), 418-429.
  • Yoon JW, Lee KJ, Lee SY, Chae MJ, Park JK, Yoo JH, Park HM. (2010) Antibiotic resistance profiles of Staphylococcus pseudintermedius isolates from canine patients in Korea. J Microbiol Biotechnol. 20(12), 1764-1768.
  • Zhu LX, Zhang ZW, Wang C, Yang HW, Zhang Q, Cheng J. (2006) Evaluation of the CLSI cefoxitin 30-microg disk-diffusion method for detecting methicillin resistance in staphylococci. Clin Microbiol Infect. 12(10), 1039-1042.
  • Zscheck KK, Murray BE. (1993) Genes Involved in the Regulation of Beta-Lactamase Production in Enterococci and Staphylococci. Antimicrob Agents Chemother. 37(9), 1966-1970.
Toplam 51 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Veteriner Bilimleri
Bölüm Araştırma Makaleleri
Yazarlar

İnci Başak Müştak 0000-0001-9180-5768

Hamit Kaan Müştak 0000-0002-3694-1959

Seyyide Sarıçam 0000-0002-2386-6857

Tuğçe Üstün 0000-0002-1711-5520

Asena Esra Erdem 0000-0001-7650-7762

Yayımlanma Tarihi 31 Aralık 2020
Gönderilme Tarihi 13 Eylül 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 31 Sayı: 2

Kaynak Göster

APA Müştak, İ. B., Müştak, H. K., Sarıçam, S., Üstün, T., vd. (2020). Frequency of Staphylococcus pseudintermedius in Canine Skin Infections and Antibiotic Resistance Profiles of the Recovered Isolates. Etlik Veteriner Mikrobiyoloji Dergisi, 31(2), 127-132. https://doi.org/10.35864/evmd.793494


15430