期刊论文详细信息
BMC Veterinary Research
Isolation of coagulase-positive staphylococci from bitches’ colostrum and milk and genetic typing of methicillin-resistant Staphylococcus pseudintermedius strains
Stefan Börjesson3  Alessio Bortolami1  Ilenia Drigo1  Michela Corrò1  Ada Rota2 
[1] Istituto Zooprofilattico Sperimentale delle Venezie, viale dell’Università 10, Legnaro, 35020, PD, Italy;Department of Veterinary Science, University of Turin, Largo Paolo Braccini 2, Grugliasco, 10090, TO, Italy;Department of Animal Health and Antimicrobial Strategies, National Veterinary Institute (SVA), Uppsala, SE-751 89, Sweden
关键词: Milk;    Colostrum;    Dog;    MRSP;    Coagulase-positive staphylococci;   
Others  :  1224424
DOI  :  10.1186/s12917-015-0490-x
 received in 2015-03-16, accepted in 2015-07-16,  发布年份 2015
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【 摘 要 】

Background

Among the coagulase-positive, potentially pathogenic staphylococci, Staphylococcus pseudintermedius has been frequently isolated from bitches’ milk. This organism colonizes the mammary gland or causes infection, while S. aureus has been only occasionally reported. The objective of this study was to investigate the occurrence and persistence of coagulase-positive staphylococci in the colostrum and milk of postpartum bitches, either treated or untreated with antimicrobials, and to assess the incidence, antibiotic resistance profile and genetic type of the methicillin-resistant strains.

On postpartum D1, D7 and D15, drops of secretion were collected from the mammary glands of 27 postpartum bitches, nine of which were treated with antimicrobials. Coagulase-positive staphylococci were identified, antimicrobial susceptibility and the presence of mecA were tested and the genetic profile of methicillin-resistant strains was assessed.

Results

Staphylococcus pseudintermedius was the only coagulase-positive staphylococcus isolated, and its presence was detected in 21 out of 27 bitches and in 66 out of 145 swabs. In a single bitch, it caused puerperal mastitis. In untreated bitches, the frequency of isolation was lower in colostrum than in milk. All of the isolates except one were resistant to at least three antimicrobial classes, while 14 out of 66 S. pseudintermedius strains were methicillin-resistant mecA positive (MRSP) and were isolated from eight bitches housed in the same breeding kennel. A significant association was found between antimicrobial treatment and the presence of MRSP. Six of the 12 typed isolates belonged to spa-type t02 carrying SCCmec II/III, and another six were non-typeable with spa carrying SCCmec IV. The t02-SCCmec II/III isolates were sequence type (ST) 71; four NT-SCCmec IV isolates were ST258 and two were ST369. PFGE showed that isolates from the same dog had identical band patterns, while isolates from different dogs had unique band patterns. MRSP strains showed multidrug resistance profiles.

Conclusions

Our results confirm that S. pseudintermedius is the most frequently isolated coagulase-positive staphylococcus from bitches’ milk. The isolation of several different strains of MRSP with different genetic characteristics in the same kennel and the fact that two of the strains belonged to a sequence type (ST) described for the first time are noteworthy findings.

【 授权许可】

   
2015 Rota et al.

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【 参考文献 】
  • [1]Kuhn G, Pohl S, Hingst V. Investigations on bacteria in the milk of healthy lactiferous bitches. Berl Munch Tierarztl Wochenschr. 1991; 104:130-3.
  • [2]Walser K, Henschelchen O. Contribution to the etiology of acute mastitis in the bitch. Berl Munch Tierarztl Wochenschr. 1983; 96:195-7.
  • [3]Sager M, Remmers C. Some aspects of perinatal mortality in the dog. A clinical, bacteriological and pathological study. Tierarztl Prax. 1990; 18:415-9.
  • [4]Schäfer-Somi S, Spergser J, Breitenfellner J, Aurich JE. Bacteriological status of canine milk and septicaemia in neonatal puppies—a retrospective study. J Vet Med B Infect Dis Vet Public Health. 2003; 50:343-6.
  • [5]Fitzgerald JR. The Staphylococcus intermedius group of bacterial pathogens: species reclassification, pathogenesis and the emergence of meticillin resistance. Vet Dermatol. 2009; 20:490-5.
  • [6]Bannoehr J, Guardabassi L. Staphylococcus pseudintermedius in the dog: taxonomy, diagnostics, ecology, epidemiology and pathogenicity. Vet Dermatol. 2012; 23:253-66.
  • [7]Loeffler A, Linek M, Moodley A, Guardabassi L, Sung JML, Winkler M et al.. First report of multiresistant, mecA-positive Staphylococcus intermedius in Europe: 12 cases from a veterinary dermatology referral clinic in Germany. Vet Dermatol. 2007; 18:412-21.
  • [8]Ruscher C, Lübke-Becker A, Wleklinski CG, Soba A, Wieler LH, Walther B. Prevalence of methicillin-resistant Staphylococcus pseudintermedius isolated from clinical samples of companion animals and equidaes. Vet Microbiol. 2009; 136:197-201.
  • [9]Rota A, Milani C, Drigo I, Drigo M, Corrò M. Isolation of methicillin-resistant Staphylococcus pseudintermedius from breeding dogs. Theriogenology. 2011; 75:115-21.
  • [10]van Duijkeren E, Kamphuis M, van der Mije IC, Laarhoven LM, Duim B, Wagenaar JA et al.. Transmission of methicillin-resistant Staphylococcus pseudintermedius between infected dogs and cats and contact pets, humans and the environment in households and veterinary clinics. Vet Microbiol. 2011; 150:338-43.
  • [11]Bergström A, Gustafsson C, Leander M, Fredriksson M, Grönlund U, Trowald-Wigh G. Occurrence of methicillin-resistant Staphylococci in surgically treated dogs and the environment in a Swedish animal hospital. J Small Anim Pract. 2012; 53:404-10.
  • [12]Nienhoff U, Kadlec K, Chaberny IF, Verspohl J, Gerlachm GF, Kreienbrock L et al.. Methicillin-resistant Staphylococcus pseudintermedius among dogs admitted to a small animal hospital. Vet Microbiol. 2011; 150:191-7.
  • [13]Weese JS, Faires MC, Frank LA, Reynolds LM, Battisti A. Factors associated with methicillin-resistant versus methicillin-susceptible Staphylococcus pseudintermedius infection in dogs. J Am Vet Med Assoc. 2012; 240:1450-5.
  • [14]Rota A, Milani C, Corrò M, Drigo I, Börjesson S. Misuse of antimicrobials and selection of methicillin-resistant Staphylococcus pseudintermedius strains in breeding kennels: genetic characterization of bacteria after a two-year interval. Reprod Dom Anim. 2013; 48:1-6.
  • [15]Lehner G, Linek M, Bond R, Lloyd DH, Prenger-Berninghoff E, Thom N et al.. Case-control risk factor study of methicillin-resistant Staphylococcus pseudintermedius (MRSP) infection in dogs and cats in Germany. Vet Microbiol. 2014; 168:154-60.
  • [16]Perreten V, Kadlec K, Schwarz S, Gronlund Andersson U, Finn M, Greko C et al.. Clonal spread of methicillin-resistant Staphylococcus pseudintermedius in Europe and North America: an international multicentre study. J Antimicrob Chemother. 2010; 65:1145-54.
  • [17]CLSI. Performance Standard for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated from Animals; Approved Standard-Forth Edition. Vol 33 n.7 Vet 01-A4, Wayne, PA; 2013a.
  • [18]CLSI. Performance Standard for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated from Animals; Second Informational Supplement. Vol 33 n.8 Vet 01-S2, Wayne, PA; 2013b.
  • [19]Louie L, Goodfellow J, Mathieu P, Glatt A, Louie M, Simor AE. Rapid detection of methicillin-reistant staphylococci from blood culture bottles by using a multiplex PCR assay. J Clin Microbiol. 2002; 40:2786-90.
  • [20]Holm BR, Petersson U, Mörner A, Bergström K, Franklin A, Greko C. Antimicrobial resistance in staphylococci from canine pyoderma: a prospective study of first-time and recurrent cases in Sweden. Vet Rec. 2002; 151:600-5.
  • [21]Moodley A, Stegger M, Ben Zakour NL, Fitzgerald JR, Guardabassi L. Tandem repeat sequence analysis of staphylococcal protein A (spa) gene in methicillin-resistant Staphylococcus pseudintermedius. Vet Microbiol. 2009; 135:320-6.
  • [22]Solyman SM, Black CC, Duim B, Perreten V, van Duijkeren E, Wagenaar JA et al.. Multilocus sequence typing for characterization of Staphylococcus pseudintermedius. J Clin Microbiol. 2013; 51:306-10.
  • [23]Börjesson S, Bergström M, Landén A, Grönlund-Andersson U. Methicillin-resistant Staphylococcus pseudintermedius (MRSP) in Sweden. Microb Drug Resist. 2012; 18:597-603.
  • [24]Murchan S, Kaufmann ME, Deplano A, de Ryck R, Struelens M, Zinn CE et al.. Harmonization of pulsed-field gel electrophoresis protocols for epidemiological typing of strains of methicillin-resistant Staphylococcus aureus: a single approach developed by consensus in 10 European laboratories and its application for tracing the spread of related strains. J Clin Microbiol. 2003; 41:1574-85.
  • [25]Ververidis HN, Mavrogianni VS, Fragkou IA, Orfanou DC, Gougoulis DA, Tzivara A, Gouletsou PG, Athanasiou L, Boscos CM, Fthenakis GC. Experimental staphylococcal mastitis in bitches: clinical, bacteriological, cytological, haematological and pathological features. Vet Microbiol. 2007; 124:95-106.
  • [26]Osland AM, Vestby LK, Fanuelsen H, Slettemeås JS, Sunde M. Clonal diversity and biofilm-forming ability of methicillin-resistant Staphylococcus pseudintermedius. J Antimicrob Chemother. 2012; 67:841-8.
  • [27]Damborg P, Moodley A, Guardabassi L. High genetic diversity among methicillin-resitant Staphylococcus pseudintermedius isolated from canine infection in Denmark. In: Proceeding of the 3rd ASM-ESCMID Conference in Methicillin-resistant Staphylococci in Animals: 4-7 November 2013, Copenhagen, Denmark. Edited by American Society for Microbiology, 80.
  • [28]Haennia M, de Moraesa NA, Alves N, Châtrea P, Médailleb C, Moodleyc A et al.. Characterisation of clinical canine meticillin-resistant and meticillin-susceptible Staphylococcus pseudintermedius in France. J Glob Antimicrob Resist. 2014; 2:119-23.
  • [29]Windahl U, Reimegård E, Holst BS, Egenvall A, Fernström L, Fredriksson M et al.. Carriage of methicillin-resistant Staphylococcus pseudintermedius in dogs-a longitudinal study. BMC Vet Res. 2012; 8:34. BioMed Central Full Text
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