Mastitis pathogens in Bavaria, Southern Germany: apparent prevalence and herd-level risk factors

Authors

  • Lucie Groh Tiergesundheitsdienst Bayern e.V. https://orcid.org/0000-0001-8588-755X
  • Rolf Mansfeld Klinik für Wiederkäuer mit Ambulanz und Bestandsbetreuung, Tierärztliche Fakultät der Ludwig-Maximilians-Universität München, 85764 Oberschleißheim, Germany https://orcid.org/0000-0002-7448-9246
  • Christian Baumgartner Milchprüfring Bayern e.V., 85283 Wolnzach, Germany https://orcid.org/0000-0002-3725-8414
  • Ulrike S. Sorge Tiergesundheitsdienst Bayern e.V., 85586 Poing, Germany

Keywords:

mastitis pathogens, prevalence, cross-sectional study, management practices

Abstract

The aim of this cross-sectional study was to determine the prevalence of mastitis pathogens in Bavaria and to identify management practices as possible risk factors for the presence and within-herd prevalence of the four most common pathogens .

For this purpose, aseptic quarter milk samples of 6,188 dairy cows on 152 Bavarian dairy farms were collected and a California mastitis test was performed. Udder and leg hygiene scores as well as teat end condition scores were recorded at cow-level. Teat end hygiene score after udder preparation was evaluated for about ten cows per herd. Herd information and information on management practices were obtained using a standardized checklist. To determine herd-level risk factors, Fisher’s exact test for categorical, and Student’s t-test or Mann-Whitney-U test for continuous data were performed.

The most frequently detected pathogens at quarter-level were coagulase-negative staphylococci (4.4%), Staphylococcus aureus (2.9%), Streptococcus dysgalactiae (0.9%), and Streptococcus uberis (0.9%).  Each of these four pathogens was detected in more than half of the herds (90%, 70%, 61%, and 54%, respectively). Free stall housing and larger herds were associated with detection of coagulase-negative staphylococci and Streptococcus uberis. The usage of post-milking teat disinfection was associated with a lower within-herd prevalence of Staphylococcus aureus. The use of internal teat sealants and blanket dry cow therapy reduced the odds for detection of Streptococcus dysgalactiae at the herd-level. However, the latter practices were implemented by only a minority of herds. The study shows for the first time the apparent prevalence of mastitis pathogens in Bavaria using an unbiased sample. Coagulase-negative staphylococci were found to be the most frequently isolated pathogens, further studies on the etiology and reduction of these pathogens should be considered.

Author Biography

Lucie Groh, Tiergesundheitsdienst Bayern e.V.

Second affiliation:

Klinik für Wiederkäuer mit Ambulanz und Bestandsbetreuung, Tierärztliche Fakultät der Ludwig-Maximilians-Universität München,
85764 Oberschleißheim, Germany

References

Artursson K, Schelin J, Thisted Lambertz S, Hansson I, Olsson Engvall E. Foodborne pathogens in unpasteurized milk in Sweden. Int. J. Food Microbiol. 2018;284:120–7. doi:10.1016/j.ijfoodmicro.2018.05.015.

Jamali H, Paydar M, Radmehr B, Ismail S, Dadrasnia A. Prevalence and antimicrobial resistance of Staphylococcus aureus isolated from raw milk and dairy products. Food Control. 2015;54:383–8. doi:10.1016/j.foodcont.2015.02.013.

Siivonen J, Taponen S, Hovinen M, Pastell M, Lensink BJ, Pyörälä S, Hänninen L. Impact of acute clinical mastitis on cow behaviour. Appl. Anim. Behav. Sci. 2011;132:101–6. doi:10.1016/j.applanim.2011.04.005.

Medrano-Galarza C, Gibbons J, Wagner S, Passillé AM de, Rushen J. Behavioral changes in dairy cows with mastitis. J Dairy Sci. 2012;95:6994–7002. doi:10.3168/jds.2011-5247.

Bramley AJ, Dodd FH. Reviews of the progress of Dairy Science: Mastitis control – progress and prospects. J. Dairy Res. 1984;51:481–512. doi:10.1017/s0022029900023797.

Hillerton JE, Booth JM. The Five-Point Mastitis Control Plan - a revisory tutorial [Conference Paper] Conference: 57th Annual Meeting of the National Mastitis Council. 2018. Available from: https://www.ruminantia.it/wp-content/uploads/2018/03/NATIONAL-MASTITIS-COUNCIL-2018.pdf (cited 2022 Nov 01).

Krishnamoorthy P, Goudar AL, Suresh KP, Roy P. Global and countrywide prevalence of subclinical and clinical mastitis in dairy cattle and buffaloes by systematic review and meta-analysis. Res Vet Sci. 2021;136:561–86. doi:10.1016/j.rvsc.2021.04.021.

Sorge US. Verteilung von Mastitiserregern bei klinischen Mastitiden (2015-2020) [Conference Paper]. DVG Vet-Congress; Buiatrik-Tagung, Berlin, Germany. 2021.

Huber-Schlenstedt R, Schierling K, Gey A, Sorge US. Mastitis? TGD checkt die Erreger. MiPu. 2017:18–24.

Schreiner DA, Ruegg PL. Relationship Between Udder and Leg Hygiene Scores and Subclinical Mastitis. J. Dairy Sci. 2003;86:3460–5. doi:10.3168/jds.S0022-0302(03)73950-2.

National Milk Producers Federation (NMPF). Animal Care Reference Manual. 2013 Available from: https://www.nmpf.org/wp-content/uploads/2015/08/FARM_manual_2013_WEB.pdf (cited 2022 Nov 01).

National Mastitis Council (NMC). Guidelines for Evaluating Teat Skin Condition. [Internet]. 2007. Available from: http://www.nmconline.org/wp-content/uploads/2016/09/Guidelines-for-Evaluating.pdf (cited 2022 Nov 01).

Cook N, Reinemann D. A Tool Box for Assessing Cow, Udder and Teat Hygiene. In annual meeting of the NMC 2007 Jan 21.

Barnum D.A., Newbould FHS. The use of the California Mastitis Test for the detection of bovine mastitis. Can. vet. J. 1961;2:83–90.

German Veterinarian Association. Leitlinien zur Entnahme von Milchproben unter antiseptischen Bedingungen und Leitlinien zur Isolierung und Identifizierung von Mastitiserregern, 2., überarb. Aufl. Gießen: Verlag der Deutschen Veterinärmedizinischen Gesellschaft e.V.; 2009.

Statistisches Bundesamt (Destatis). Viehbestand - Fachserie 3 Reihe 4.1. 2020 Available from: https://www.destatis.de/DE/Themen/BranchenUnternehmen/Landwirtschaft-Forstwirtschaft-Fischerei/Tiere-TierischeErzeugung/Publikationen/Downloads-Tiere-und-tierische-Erzeugung/viehbestand2030410205314.pdf;=publicationFile (cited 2022 Nov 01).

Tenhagen B-A, Köster G, Wallmann J, Heuwieser W. Prevalence of Mastitis Pathogens and Their Resistance Against Antimicrobial Agents in Dairy Cows in Brandenburg, Germany. J. Dairy Sci. 2006;89:2542–51. doi:10.3168/jds.S0022-0302(06)72330-X.

Schwarz D, Diesterbeck US, Failing K, König S, Brügemann K, Zschöck M, et al. Somatic cell counts and bacteriological status in quarter foremilk samples of cows in Hesse, Germany - a longitudinal study. J. Dairy Sci. 2010;93:5716–28. doi:10.3168/jds.2010-3223.

Ericsson Unnerstad H, Lindberg A, Persson Waller K, Ekman T, Artursson K, Nilsson-Ost M, Bengtsson B. Microbial aetiology of acute clinical mastitis and agent-specific risk factors. Vet Microbiol. 2009;137:90–7. doi:10.1016/j.vetmic.2008.12.005.

Hill AW, Shears AL, Hibbitt KG. The elimination of serum-resistant Escherichia coli from experimentally infected single mammary glands of healthy cows. Res. Vet. Sci. 1978;25:89–93. doi:10.1016/S0034-5288(18)33015-7.

Menzies FD, McBride SH, McDowell SWJ, McCoy MA, McConnell W, Bell C. Clinical and laboratoy findings in cases of toxic mastitis in Northern Ireland. Vet Rec. 2000;147:123–8. doi:10.1136/vr.147.5.123.

Tikofsky LL, Zadoks RN. Cross-Infection Between Cats and Cows: Origin and Control of Streptococcus canis Mastitis in a Dairy Herd. J. Dairy Sci. 2005;88:2707–13. doi:10.3168/JDS.S0022-0302(05)72949-0.

Pitkäla A, Haveri M, Pyörälä S, Myllys V, Honkanen-Buzalski T. Bovine Mastitis in Finland 2001-Prevalence, Distribution of Bacteria, and Antimicrobial Resistance. J. Dairy Sci. 2004;87:2433–41. doi:10.3168/jds.S0022-0302(04)73366-4.

Persson Waller K, Bengtsson B, Lindberg A, Nyman A, Ericsson Unnerstad H. Incidence of mastitis and bacterial findings at clinical mastitis in Swedish primiparous cows- influence of breed and stage of lactation. Vet Microbiol. 2009;134:89–94. doi:10.1016/j.vetmic.2008.09.004.

Curone G, Filipe J, Cremonesi P, Trevisi E, Amadori M, Pollera C, et al. What we have lost: Mastitis resistance in Holstein Friesians and in a local cattle breed. Res. Vet. Sci. 2018;116:88–98. doi:10.1016/j.rvsc.2017.11.020.

Lakew M, Tolosa T, Tigre W. Prevalence and major bacterial causes of bovine mastitis in Asella, South Eastern Ethiopia. Trop. Anim. Health Prod. 2009;41:1525–30. doi:10.1007/s11250-009-9343-6.

Devriese LA, Keyser H de. Prevalence of different species of coagulase-negative staphylococci on teats and in milk samples from dairy cows. J. Dairy Res. 1980;47:155–8. doi:10.1017/s0022029900020999.

Pyörälä S, Taponen S. Coagulase-negative staphylococci-emerging mastitis pathogens. Vet Microbiol. 2009;134:3–8. doi:10.1016/j.vetmic.2008.09.015.

Barkema HW, Green MJ, Bradley AJ, Zadoks RN. Invited review: The role of contagious disease in udder health. J Dairy Sci. 2009;92:4717–29. doi:10.3168/jds.2009-2347.

Capurro A, Aspán A, Ericsson Unnerstad H, Persson Waller K, Artursson K. Identification of potential sources of Staphylococcus aureus in herds with mastitis problems. J. Dairy Sci. 2010;93:180–91. doi:10.3168/jds.2009-2471.

Petersson-Wolfe CS, Mullarky IK, Jones GM. Staphylococcus aureus Mastitis: Cause, Detection, and Control. VA Coop. Ext. 2010:1–7.

National Mastitis Council (NMC). Post-milking teat disinfection fact sheet. 2020 Available from: https://www.nmconline.org/wpcontent/uploads/2020/09/formatted-Postmilking-Teat-Disinfection_Final- _072920.pdf (cited 2022 Nov 01).

Contreras LL, Ryan CM, Overton TR. Effects of Dry Cow Grouping Strategy and Prepartum Body Condition Score on Performance and Health of Transition Dairy Cows. J. Dairy Sci. 2004;87:517–23. doi:10.3168/jds.S0022-0302(04)73191-4.

Suriyasathaporn W, Heuer C, Noordhuizen-Stassen EN, Schukken YH. Hyperketonemia and the impairment of udder defense: a review. Vet Res. 2000;31:397–412. doi:10.1051/vetres:2000128.

Godden S, Rapnicki P, Stewart S, Fetrow J, Johnson A, Bey R, Farnsworth R. Effectiveness of an Internal Teat Seal in the Prevention of New Intramammary Infections During the Dry and Early-Lactation Periods in Dairy Cows when used with a Dry Cow Intramammary Antibiotic. J. Dairy Sci. 2003;86:3899–911. doi:10.3168/jds.S0022-0302(03)73998-8.

Parker KI, Compton KI, Anniss FM, Weir A, Heuer C, McDougall S. Subclinical and Clinical Mastitis in Heifers Following the Use of a Teat Sealant Precalving. J. Dairy Sci. 2007;90:207–18. doi:10.3168/jds.S0022-0302(07)72622-X.

Rabiee AR, Lean IJ. The effect of internal teat sealant products (Teatseal and Orbeseal) on intramammary infection, clinical mastitis, and somatic cell counts in lactating dairy cows: a meta-analysis. J Dairy Sci. 2013;96:6915–31. doi:10.3168/jds.2013-6544.

Barkema HW, Schukken YH, Lam TJGM, Beiboer ML, Benedictus G, Brand A. Management Practices Associated with the Incidence Rate of Clinical Mastitis. J Dairy Sci. 1999;82:1643–54. doi:10.3168/jds.S0022-0302(99)75393-2.

Wente N, Krömker V. Streptococcus dysgalactiae-Contagious or Environmental? Animals. 2020;10:2185. doi:10.3390/ani10112185.

Smith KL, Hogan JS. Environmental Mastitis. Vet Clin North Am Food Anim Pract. 1993;9:489–98. doi:10.1016/S0749-0720(15)30616-2.

Hogan JS, Smith, K.L. Bacteria Counts in Sawdust Bedding. J Dairy Sci. 1997;80:1600–5. doi:10.3168/jds.S0022-0302(97)76090-9.

Wente N, Klocke D, Paduch J-H, Zhang Y, Seeth MT, Zoche-Golob V, et al. Associations between Streptococcus uberis strains from the animal environment and clinical bovine mastitis cases. J. Dairy Sci. 2019;102:9360–9. doi:10.3168/jds.2019-16669.

Bramley AJ. Sources of Streptococcus uberis in the dairy herd: I. Isolation from bovine faces and from straw bedding of cattle. J. Dairy Res. 1982;49:369–73. doi:10.1017/S0022029900022500.

Zadoks RN, Allore HG, Barkema HW, Sampimon OC, Gröhn YT, Schukken YH. Analysis of an Outbreak of Streptococcus uberis Mastitis. J. Dairy Sci. 2001;84:590–9. doi:10.3168/jds.S0022-0302(01)74512-2.

Phuektes P, Mansell PD, Dyson RS, Hooper ND, Dick JS, Browning GF. Molecular epidemiology of Streptococcus uberis isolates from dairy cows with mastitis. J Clin Microbiol. 2001;39:1460–6. doi:10.1128/JCM.39.4.1460-1466.2001.

Godinho KS, Bramley AJ. The efficacy of teat dips of differing persistence on teat skin in preventing intramammary infection by Streptococcus uberis and Escherichia coli in dry cows. Br Vet J. 1980;136:574–9. doi:10.1016/s0007-1935(17)32137-1.

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Published

2023-04-28 — Updated on 2023-06-12

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