Abstract

Simple SummaryStaphylococci are the most prevalent bacteria isolated from bovine mammary secretions. They not only originate from cases of intramammary infections, but also from teat canal, skin and other environmental sources. They are usually divided into coagulase-negative staphylococci (CNS) and Staphylococcus (S.) aureus. In contrast to the contagious nature of most S. aureus infections, the epidemiology of CNS is less clear. Results of our observational study suggest that both, CNS and S. aureus, can be associated with clinical and subclinical mastitis but may also appear as colonizers and remain undetected in cows without inflammatory signs. As a result, the consequences differ, especially with the increased emphasis on reducing antibiotic use as a means of limiting antimicrobial resistance (AMR). A positive S. aureus test result requires antibiotic treatment of infected cows after evaluation of the probability of bacteriological cure, and, where necessary, implementation of management strategies to limit new infections. In contrast, treatment of CNS in cows without increase in somatic cell count should be avoided. Thus, these findings emphasize the value of regular bacteriological examination of clinical and subclinical cases and a thorough evaluation of any staphylococcal presentation before treatment.Staphylococcus (S.) aureus is considered as a major mastitis pathogen, with considerable epidemiological information on such infections while the epidemiology of coagulase-negative staphylococci (CNS) is more controversial. The aim of this study was to use matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) technology for identification of staphylococci isolated from bovine milk at species level and to characterize them in reference to presentation, somatic cell count (SCC), bacterial shedding (cfu) and antimicrobial resistance patterns. A total of 200 staphylococcal isolates (S. aureus n = 100; CNS n = 100) originating from aseptically collected quarter milk samples from different quarters of dairy cows were included in the study. They originated from cases of clinical (CM) and subclinical mastitis (SCM) or were isolated from milk with SCC ≤ 100,000 cells/mL in pure culture. We found staphylococci predominantly in cases of SCM (n = 120). In low-SCC cows, 12 S. aureus and 32 CNS isolates were detected. Eighteen percent of each were associated with CM. Eleven CNS species were identified, S. chromogenes (n = 26) and S. xylosus (n = 40) predominated. CNS, particularly those in low-SCC cows, showed higher MIC90 (minimal inhibitory concentration) values for penicillin, ampicillin, cefoperazone, pirlimycin and marbofloxacin. Based on the present results, a careful interpretation of laboratory results is recommended to avoid antimicrobial therapy of staphylococci without clinical relevance and to ensure prudent use of antimicrobials.

Highlights

  • Mastitis is the main reason for antimicrobial treatment in dairy cattle

  • We found 32 coagulase-negative staphylococci (CNS) and 12 S. aureus isolates to act as colonizers (Table 1)

  • We wanted to determine the species differences between the various staphylococci isolated from quarter milk samples with regard to their presentation and antibiotic resistance profile and to assess the therapy concepts of veterinarians regarding Staphylococcus spp. positive culture results

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Summary

Introduction

Mastitis is the main reason for antimicrobial treatment in dairy cattle. Pathogen specific treatments of mastitis have been shown to decrease antimicrobial use without affecting clinical and bacteriological cure outcomes [1,2]. A major factor in obtaining a bacteriological cure of intramammary infections (IMI). IMI are detected frequently through milk culturing. Regular monitoring of mastitis pathogens within a herd facilitates treatment decisions in case of clinical mastitis [5,6]. Due to the time delay between sampling and culture results, treatment of mastitis is usually based on bacteriological examination of a single sample. Factors involved in diagnosing an IMI are the number of colonies, isolation in pure or mixed culture, and inflammatory signs [4,6]

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