Biological properties of staphylococci derived from cats and dogs

Authors

  • Y. Vishovan National University of Life and Environmental Sciences of Ukraine image/svg+xml
  • V. Ushkalov National University of Life and Environmental Sciences of Ukraine image/svg+xml
  • L. Vygovska National University of Life and Environmental Sciences of Ukraine image/svg+xml
  • O. Machuskyy National University of Life and Environmental Sciences of Ukraine image/svg+xml
  • A. Hranat National University of Life and Environmental Sciences of Ukraine image/svg+xml
  • A. Shaiko National University of Life and Environmental Sciences of Ukraine image/svg+xml
  • S. Boianovskiy National University of Life and Environmental Sciences of Ukraine image/svg+xml

DOI:

https://doi.org/10.31548/ujvs2020.03.006

Abstract

 

Dogs and cats play an important role in human life, and they are often a source of zoonotic agents. The purpose of the study was to investigate domestic dogs and cats for staphylococcus carriers and to study their biological properties, biofilm ability, and antibiotic resistance in isolated cultures. Staphylococci were detected in 54% of all samples selected 25 cultures of Staphylococcus spp. Plasma coagulation reaction was negative in 100% of strains isolated from cats, and positive in 2 strains isolated from dogs (18%). Lecithinase activity was shown by 85.8% of strains isolated from cats and 72.8% from dogs. 71.5% of the strains isolated from cats and 63.7% from dogs had the ability to hemolysis. Mannitol was fermented in 50.0% of strains isolated from cats and 54.6% from dogs. 78.6% of strains isolated from cats and 91.0% isolated from dogs grew on crystal violet lactose agar in the form of blue colonies. Simultaneously showed lecithinase activity, hemolysis, fermented mannitol and grew on crystal violet lactose agar 28.5% isolated from cats and 27.2% isolated from dogs strains. The derived strains from cats and dogs had multiple resistance to Oxacillin, two or more groups of antibiotics.  All 100% of the isolated isolates from dogs had a high (OD> 1.0) ability to form a biofilm. Only 21.4% of strains isolated from cats had a medium (OD> 0.5 <1.0), and the remaining 78.5 high (OD> 1.0) ability to form a biofilm.

Keywords: Staphylococcus spp., coagulase-positive coagulase-negative, biofilms, antibiotic resistance.

References

Ahmadrajabi, R., Layegh-Khavidaki, S., Kalantar-Neyestanaki, D., & Fasihi, Y. (2017). Molecular analysis of immune evasion cluster (IEC) genes and intercellular adhesion gene cluster (ICA) among methicillin-resistant and methicillin-sensitive isolates of Staphylococcus aureus. Journal of preventive medicine and hygiene, 58(4), E308-E314. https://doi.org/10.15167/2421-4248/jpmh2017.58.4.711

EFSA and ECDC (European Food Safety Authority and European Centre for Disease Prevention and Control), (2019). The European Union One Health 2018 Zoonoses Report. EFSAJournal 2019;17(12):5926, 276 pp.

https://doi.org/10.2903/j.efsa.2019.5926

Eucast. The european committee on antimicrobial susceptibility testing (2020). Available from: http://www.eucast.org/ [Accessed 10th February 2020].

Gómez-Sanz E, Ceballos S,Ruiz-Ripa L, Zarazaga M and Torres C (2019) Clonally Diverse Methicillin and Multidrug Resistant Coagulase Negative Staphylococci Are Ubiquitous and Pose Transfer Ability Between Pets and Their Owners. Front. Microbiol. 10:485.

https://doi.org/10.3389/fmicb.2019.00485

Hatch, S., Sree, A., Tirrell, S., Torres, B., & Rothman, A. L. (2012). Metastatic complications from Staphylococcus intermedius, a zoonotic pathogen. Journal of clinical microbiology, 50(3), 1099-1101.

https://doi.org/10.1128/JCM.05170-11

Kizerwetter-Świda, M., Chrobak-Chmiel, D. & Rzewuska, M. (2019) High-level mupirocin resistance in methicillin-resistant staphylococci isolated from dogs and cats. BMC Vet Res 15, 238 https://doi.org/10.1186/s12917-019-1973-y

Kozytska T., Garkavenko T. (2019) Circulation of Methicillin-resistant Staphylococcus (MRS) in Livestock and Domestic Animals. Proceedings of the BTRP Ukraine Regional One Health Research Symposium. https://labukraineblog.files.wordpress.com/2019/05/2019-swmp-symposium-program-final-lowres.pdf

Kukhtyn, M., , Krushelnytska, N.(2014) Forming of biofilms of microorganisms obtained from milking equipment. The Animal Biology, 16, (1),

Lee, G. Y., Lee, H. H., Hwang, S. Y., Hong, J., Lyoo, K. S., & Yang, S. J. (2019). Carriage of Staphylococcus schleiferi from canine otitis externa: antimicrobial resistance profiles and virulence factors associated with skin infection. Journal of veterinary science, 20(2), e6. https://doi.org/10.4142/jvs.2019.20.e6

Loncaric, I., Tichy, A., Handler, S., Szostak, M. P., Tickert, M., Diab-Elschahawi, M., Spergser, J., & Künzel, F. (2019). Prevalence of Methicillin-Resistant Staphylococcus sp. (MRS) in Different Companion Animals and Determination of Risk Factors for Colonization with MRS. Antibiotics (Basel, Switzerland), 8(2), 36. https://doi.org/10.3390/antibiotics8020036

Ministry of health of Ukraine. Determination of susceptibility of microorganisms to antibacterial drugs (2009). Available from: https://zakon.rada.gov.ua/rada/show/v0167282-07 [Accessed 10th February 2020].

Otto M. (2018). Staphylococcal Biofilms. Microbiology spectrum, 6(4), 10.1128 /microbialspec. GPP3-0023-2018. https://doi.org/10.1128/microbiolspec.GPP3-0023-2018

Paharik, A. E., & Horswill, A. R. (2016). The Staphylococcal Biofilm: Adhesins, Regulation, and Host Response. Microbiology spectrum, 4(2), 10.1128/microbiolspec.VMBF-0022-2015. https://doi.org/10.1128/microbiolspec.VMBF-0022-2015

Quitoco, I. M., Ramundo, M. S., Silva-Carvalho, M. C., Souza, R. R., Beltrame, C. O., de Oliveira, T. F., Araújo, R., Del Peloso, P. F., Coelho, L. R., & Figueiredo, A. M. (2013). First report in South America of companion animal colonization by the USA1100 clone of community-acquired meticillin-resistant Staphylococcus aureus (ST30) and by the European clone of methicillin-resistant Staphylococcus pseudintermedius (ST71). BMC research notes, 6, 336.

https://doi.org/10.1186/1756-0500-6-336

Rahman et al. (2018) Investigation of methicillin-resistant Staphylococcus aureus among clinical isolates from humans and animals by culture methods and multiplex PCR BMC Veterinary Research 14:300 https://doi.org/10.1186/s12917-018-1611-0

Savini, V., Barbarini, D., Polakowska, K., Gherardi, G., Białecka, 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. Journal of clinical microbiology, 51(5), 1636-1638. https://doi.org/10.1128/JCM.03310-12

Stewart, E. J., Payne, D. E., Ma, T. M., Van Epps, J. S., Boles, B. R., Younger, J. G., & Solomon, M. J. (2017). Effect of Antimicrobial and Physical Treatments on Growth of Multispecies Staphylococcal Biofilms. Applied and environmental microbiology, 83(12), e03483-16. https://doi.org/10.1128/AEM.03483-16

Turko, I., & Ushkalov, V. (2018). Biofilm-forming ability of coccus forms of the caecal microflora of laying hens when using the probiotic and nanonutrition cobalt. Scientific Messenger of LNU of Veterinary Medicine and Biotechnologies. Series: Veterinary Sciences, 20(87), 60-64. https://doi.org/10.15421/nvlvet8712

Vitale, M., Galluzzo, P., Buffa, P. G., Carlino, E., Spezia, O., & Alduina, R. (2019). Comparison of Antibiotic Resistance Profile and Biofilm Production of Staphylococcus aureus Isolates Derived from Human Specimens and Animal-Derived Samples. Antibiotics (Basel, Switzerland), 8(3), 97. https://doi.org/10.3390/antibiotics8030097

Weese, J. S., & van Duijkeren, E. (2010). Methicillin-resistant Staphylococcus aureus and Staphylococcus pseudintermedius in veterinary medicine. Veterinary Microbiology, 140(3-4), 418-429. https://doi.org/10.1016/j.vetmic.2009.01.039

Worthing, K. A., Brown, J., Gerber, L., Trott, D. J., Abraham, S., & Norris, J. M. (2018). Methicillin-resistant staphylococci amongst veterinary personnel, personnel-owned pets, patients and the hospital environment of two small animal veterinary hospitals. Veterinary microbiology, 223, 79-85. https://doi.org/10.1016/j.vetmic.2018.07.021

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2020-09-09

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