Sequence Types and Antimicrobial Resistance Profiles of Streptococcus uberis Isolated From Bovine Mastitis

Bovine mastitis is one of the most common diseases among dairy cows and causes high economic losses in dairy industries worldwide. Streptococcus uberis is one of the most frequently identified pathogens causing the disease. In this study, 153 S. uberis strains isolated from mastitis milk samples were analyzed for their genetic diversity using multi locus sequence typing (MLST). Moreover, antibiotic susceptibility testing was performed using a microdilution assay and 11 antimicrobial agents including penicillin, which is the first line agent for treatment of bovine mastitis in Switzerland. MLST was successful for 152 (99.3%) of the strains. Overall, 103 different sequence types (STs) were determined, including 91 novel STs. S. uberis belonging to clonal complex (CC) 5 represented 47 (30.7%) of the mastitis cases. Two (1.3%) of the strains belonged to CC86 and one (0.7%) to CC143. The population structure identified in this work suggests that environmental transmission is the predominant route of infection in herds in Switzerland. Antimicrobial susceptibility testing determined a resistance rate of 11.8% for pirlimycin and elevated MIC90-values for marbofloxacin as well as for erythromycin. This study highlights the importance of genetic characterization of S. uberis and the need for veterinary breakpoints for surveillance of antimicrobial resistance in S. uberis.

[1]  D. Calavas,et al.  Antimicrobial resistance in bacteria isolated from mastitis in dairy cattle in France, 2006-2016. , 2018, Journal of dairy science.

[2]  B. Luisi,et al.  RNase E and the High-Fidelity Orchestration of RNA Metabolism , 2018, Microbiology spectrum.

[3]  J. Madec,et al.  Antimicrobial Resistance in Streptococcus spp , 2018, Microbiology spectrum.

[4]  J. Małaczewska,et al.  Biofilm production and other virulence factors in Streptococcus spp. isolated from clinical cases of bovine mastitis in Poland , 2017, BMC Veterinary Research.

[5]  H. Egberink,et al.  Sensitivity and specificity of a real-time reverse transcriptase polymerase chain reaction detecting feline coronavirus mutations in effusion and serum/plasma of cats to diagnose feline infectious peritonitis , 2017, BMC Veterinary Research.

[6]  S. Taponen,et al.  Bacteriological etiology and treatment of mastitis in Finnish dairy herds , 2017, Acta Veterinaria Scandinavica.

[7]  I. Dolka,et al.  Experimental tumor growth of canine osteosarcoma cell line on chick embryo chorioallantoic membrane (in vivo studies) , 2017, Acta Veterinaria Scandinavica.

[8]  Richard D Emes,et al.  Molecular Epidemiology of Streptococcus uberis Clinical Mastitis in Dairy Herds: Strain Heterogeneity and Transmission , 2015, Journal of Clinical Microbiology.

[9]  R. Almeida,et al.  Role of Streptococcus uberis adhesion molecule in the pathogenesis of Streptococcus uberis mastitis. , 2015, Veterinary microbiology.

[10]  R. Boss,et al.  Phenotypic and genotypic identification of streptococci and related bacteria isolated from bovine intramammary infections , 2013, Acta Veterinaria Scandinavica.

[11]  G. Overesch,et al.  Antimicrobial susceptibility of gram-positive udder pathogens from bovine mastitis milk in Switzerland. , 2013, Schweizer Archiv fur Tierheilkunde.

[12]  E. Märtlbauer,et al.  Short communication: Streptococcus species isolated from mastitis milk samples in Germany and their resistance to antimicrobial agents. , 2012, Journal of dairy science.

[13]  S. Schwarz,et al.  A proposal of interpretive criteria for cefoperazone applicable to bovine mastitis pathogens. , 2012, Veterinary microbiology.

[14]  M. Bhuvana,et al.  Molecular characterization of Streptococcus agalactiae and Streptococcus uberis isolates from bovine milk , 2012, Tropical Animal Health and Production.

[15]  J. Madec,et al.  ermB-mediated erythromycin resistance in Streptococcus uberis from bovine mastitis. , 2011, Veterinary journal.

[16]  M. Lasagno,et al.  Distribution of virulence-associated genes in Streptococcus uberis isolated from bovine mastitis. , 2011, FEMS microbiology letters.

[17]  Henk Hogeveen,et al.  Economic aspects of mastitis: New developments , 2011, New Zealand veterinary journal.

[18]  E. Morignat,et al.  Distribution and antimicrobial resistance of clinical and subclinical mastitis pathogens in dairy cows in Rhône-Alpes, France. , 2010, Foodborne pathogens and disease.

[19]  Alexandre P. Francisco,et al.  Global optimal eBURST analysis of multilocus typing data using a graphic matroid approach , 2009, BMC Bioinformatics.

[20]  J. Fitzpatrick,et al.  Changing trends in mastitis , 2009, Irish veterinary journal.

[21]  R. Bexiga,et al.  Molecular epidemiology and population structure of bovine Streptococcus uberis. , 2008, Journal of dairy science.

[22]  M. Maiden,et al.  Multilocus-sequence typing analysis reveals similar populations of Streptococcus uberis are responsible for bovine intramammary infections of short and long duration. , 2007, Veterinary microbiology.

[23]  H Hogeveen,et al.  Economic effects of bovine mastitis and mastitis management: A review , 2007, The Veterinary quarterly.

[24]  Keith A. Jolley,et al.  First Insights into the Evolution of Streptococcus uberis: a Multilocus Sequence Typing Scheme That Enables Investigation of Its Population Biology , 2006, Applied and Environmental Microbiology.

[25]  A. Bradley Bovine mastitis: an evolving disease. , 2002, Veterinary journal.

[26]  J. Leigh,et al.  Streptococcus uberis: a permanent barrier to the control of bovine mastitis? , 1999, Veterinary journal.

[27]  S. Simjee,et al.  Monitoring of antimicrobial susceptibility of udder pathogens recovered from cases of clinical mastitis in dairy cows across Europe: VetPath results. , 2018, Veterinary microbiology.

[28]  E. Munch-Petersen,et al.  Further notes on a lytic phenomenon shown by group B streptococci. , 1945, The Australian journal of experimental biology and medical science.