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Abstract

Chlorocresol nanoemulsion disinfectant (CND) is an environmental disinfectant prepared with nanoemulsion as its drug carrier. This study aimed to investigate the bactericidal effect of CND on Staphylococcus aureus ( S. aureus) and its effect on bacterial ultrastructure. The neutralizing effect of CND against S. aureus was first screened by suspension quantitative evaluation experiment procedure of neutralizer. Disinfection performance was evaluated by the determination of Minimal Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC), quantitative bactericidal experiment, and comparative experiment of disinfection performance between 0.1% CND and 0.1% chlorocresol aqueous solution. Meanwhile, the effect of CND on the ultrastructure of S. aureus was investigated with scanning electron microscope (SEM) and transmission electron microscope (TEM) to preliminarily explore the bactericidal mechanism. The results showed that 3% Tween-80 in PBS could be screened as the neutralizer of CND against S. aureus. MIC and MBC were 100 μg/mL and 200 μg/mL, respectively. The bactericidal rates were all 100% when 0.06% and 0.08% disinfectant acted for 15 and 5 min, respectively. Furthermore, compared with 0.1% chlorocresol aqueous solution, the bactericidal effect of 0.1% CND was significantly enhanced (p<0.01). After treatment with CND for 10 min, SEM observation showed that the morphology of S. aureus cells were changed and the integrity destroyed. TEM observation showed that the cell shape changed, and the structures of the cell wall, cell membrane and cytoplasm were damaged in varying degrees. CND showed the strong bactericidal effect on S. aureus and could cause ultrastructure alterations of S. aureus.
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Bibliography

References:

Abdelmonem R, Younis MK, Hassan DH, El-Sayed Ahmed M, Hassanein E, El-Batouty K, Elfaham A (2019) Formulation and characterization of chlorhexidine HCl nano-emulsion as a promising antibacterial root canal irrigant: in-vitro and ex-vivo studies. Int J Nanomedicine 14: 4697-4708.
Badruddoza AZ, Gupta A, Myerson AS, Trout BL, Doyle PS (2018) Low energy nanoemulsions as templates for the formulation of hydrophobic drugs. Adv Ther 1: 1700020.
Boyce JM (2016) Modern technologies for improving cleaning and disinfection of environmental surfaces in hospitals. Antimicrob Resist Infect Control 5: 10.
Chen LH, Cheng LC, Doyle PS (2020) Nanoemulsion-loaded capsules for controlled delivery of lipophilic active ingredients. Adv Sci 7: 2001677.
Chepurnov AA, Bakulina LF, Dadaeva AA, Ustinova EN, Chepurnova TS, Baker JR Jr (2003) Inactivation of Ebola virus with a surfactant nanoemulsion. Acta Trop 87: 315-320.
Dancer SJ (2014) Controlling hospital-acquired infection: focus on the role of the environment and new technologies for decontamination. Clin Microbiol Rev 27: 665-690.
Eissa M, Ashour ED, Mansy MS (2012) Neutralizer evaluation study of some microbial isolates against two strong disinfectants with and without the presence of synthetic detergent. World Appl Sci J 20: 823-831.
Hamouda T, Hayes MM, Cao Z, Tonda R., Johnson K, Wright DC, Brisker J, Baker JR Jr (1999) A novel surfactant nanoemulsion with broad-spectrum spori-cidal activity against Bacillus species. J Infect Dis 180: 1939-1949.
Hamouda T, Myc A, Donovan B, Shih AY, Reuter JD, Baker JR Jr (2001) A novel surfactant nanoemulsion with a unique non-irritant topical antimicrobial activity against bacteria, enveloped viruses and fungi. Microbiol Res 156: 1-7.
Han JH, Sullivan N, Leas BF, Pegues DA, Kaczmarek JL, Umscheid CA (2015) Cleaning hospital room surfaces to prevent health care-associated infections: a technical brief. Ann Intern Med 163: 598-607.
Hashemnejad SM, Badruddoza AZ, Zarket B, Ricardo Castaneda C, Doyle PS (2019) Thermoresponsive nanoemulsion-based gel synthesized through a low-energy process. Nat Commun 10: 2749.
Hidber T, Pauli U, Steiner A, Kuhnert P (2020) In vitro and ex vivo testing of alternative disinfectants to currently used more harmful substances in footbaths against Dichelobacter nodosus. PLoS One 15: e0229066.
Horstmann Risso N, Ottonelli Stopiglia CD, Oliveira MT, Haas SE, Ramos Maciel T, Reginatto Lazzari N, Kelmer EL, Pinto Vilela JA, Beckmann DV (2020) Chlorhexidine nanoemulsion: a new antiseptic formulation. Int J Nanomedicine 15: 6935-6944.
Hu GZ, Qiu YS (2010) Medicines commonly used in poultry and their rational use. Henan Science and Technology Press, Zhengzhou, p 27.
Matsubara T, Maki S, Toshimori Y (2021) The effectiveness of a nonalcoholic disinfectant containing metal ions, with broad antimicrobial activity. Sci Rep 11: 1072.
Ministry of Health of the People’s Republic of China (2008) Technical standard for disinfection. Ministry of Health of the People’s Republic of China, Beijing, pp 21-52.
Mu SY, Liu DY, Bai YZ, Yang WY, Shi YL, Li S, Ning MX, Yang XF (2016) Disinfection efficacy of chlorocresol nanoemulsion disin-fectant. Chin J Vet Med 52: 35-37.
Ramalingam K, Frohlich NC, Lee VA (2013) Effect of nanoemulsion on dental unit waterline biofilm. J Dent Sci 8: 333-336.
Roedel A, Vincze S, Projahn M, Roesler U, Robé C, Hammerl JA, Noll M, Al Dahouk S, Dieckmann R (2021) Genetic but no phenotypic associations between biocide tolerance and antibiotic resistance in Escherichia coli from german broiler fattening farms. Microorganisms 9: 651.
Wei QH, Zhang WF, Wang CD, Lu Y, Wang JY, Zhang M (2004) Experimental observation on properties of a compound germicidal nanoemulsion. Chin J Dis 21: 1-4.
Yang XF, Qi YH, Ning HM, Wang QH (2012) Preparation and quality evaluation of enrofloxacin nanoemulsion. J Zhejiang Univ (Agric & Life Sci) 38: 693-699.
Yang XF, Sun YW, Mu SY, Liu DY, Hu JH, Xu YZ, Bai YZ, Shi YL (2016) Evaluation of characterization and disinfection efficacy of chlorocresol nanoemulsion disinfectant. RSC Adv 6: 12730-12736.
Yin M, Zhang DL, Sun YJ, Li XH, Li YY, Xu P, Xue MQ, Jin MY, Yang XF (2020) Fungicidal effect of chlorcresol nanoemulsion disinfectant. J Northwest A&F Univ (Nat Sci Ed) 48: 18-23.
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Authors and Affiliations

Y.F. Zhang
1
Y.W. Sun
1
X.H. Liu
1
Z.X. An
1
X.F. Yang
1

  1. College of Animal Science and Veterinary Medicine, Henan Institute of Science and Technology, Hualan Road No. 90, Xinxiang City, Henan Province, 453003, China
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Abstract

The study was carried out in Polish goat population to estimate the prevalence of the nasal cavity infection with various staphylococcal species including methicillin-resistant Staphylococcus aureus (MRSA), investigate the potential permissive role of small ruminant lentivirus (SRLV) infection and determine the level of clonality of S. aureus nasal isolates. Nasal swabs and blood samples were collected from 1300 clinically healthy adult goats from 21 Polish goat herds. Blood samples were serologically screened for SRLV. Staphylococci were isolated from nasal swabs and identified using classical microbiological methods, MALDI-TOF, multiplex-PCR, and their clonality was assessed using PFGE. Antimicrobial resistance was determined on the basis of minimum inhibitory concentration and by demonstration of the presence of the mecA gene encoding the multiplex-PCR PBP2a protein and of the five main types of staphylococcal cassette chromosome mec. The apparent prevalence of staphylococcal and S. aureus infection of the nasal cavity was 29.1% (CI 95%: 26.9%, 31.5%) and 7.3% (CI 95%: 6.1%, 8.8%), respectively. No relationship was found between the SRLV-infection and the presence of any staphylococcal species including S. aureus (p=0.143). Only 9.8% of S. aureus isolates were resistant to amoxicillin/clavulanic acid and 5.9% to chloramphenicol and ciprofloxacin. All tested isolates proved to be phenotypically and genotypically sensitive to methicillin, which yielded the apparent prevalence of MRSA of 0% (CI 95%: 0%, 7.0%). S. aureus isolates show high genetic similarity within goat herds, however vary considerably between herds. Goats do not appear to be an important source of S. aureus for humans in Poland.

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Authors and Affiliations

A. Moroz
O. Szaluś-Jordanow
M. Czopowicz
K. Brodzik
V. Petroniec
E. Augustynowicz-Kopeć
A. Lutyńska
M. Roszczynko
A. Gołoś-Wójcicka
A. Korzeniowska-Kowal
A. Gamian
M. Mickiewicz
T. Frymus
H. Petelicka
J. Kaba
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Abstract

In Northern Cyprus, around 51% of halloumi cheese is produced from sheep milk, and there­fore the livelihood of the farmers mostly depends on the sheep milk production. However masti­tis, an inflammation of the udder, significantly affects this production. Due to a lack of sufficient data concerning the prevalence, etiology, and antimicrobial resistance of sheep mastitis, there remains no effective method to control the disease. This study aims to estimate the prevalence of subclinical mastitis (SCM) and identify bacterial etiological agents and the antimicrobial sus­ceptibility profiles of bacterial isolates in sheep in Northern Cyprus. A total of 227 milk samples taken from sheep were analysed using somatic cell count (SCC), bacteriological isolation-identi­fication, and antimicrobial susceptibility procedures. Pathogens were isolated in 62 (27.3%) sheep milk samples. Somatic cell counts of more than 500000 cells/ml were found in 56 (24.6%). S. aureus (12.8%) was the most common isolate from the milk samples, followed by NAS (non-Aureus staphylococci) species (11.9%), Escherichia coli (0.9%), Streptococci (0.4%), Bacillus spp. (0.9%) and Staph spp. (0.4%). While a high resistance to sulphamethaxazole/trime­toprim (81.5%) was found, no resistance to gentamicin (10.6%) was found. The study findings indicate that subclinical mastitis is a serious problem in Cyprus. Therefore, continuous observa­tion of subclinical mastitis and application of antibiogram tests to combat mastitis and antibiotic resistance and reduce economic losses are needed.

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Bibliography

Abdalhamed AM, Zeedan GSG, Zeina HAAA (2018) Isolation and identification of bacteria causing mastitis in small ruminants and their susceptibility to antibiotics, honey, essential oils, and plant extracts. Vet World 11: 355-362.

Ahmed G, Timms LL, Morrical DG, Brackelsberg PO (1992) Dynamics and significance of ovine subclinical intramammary infections and their effects on lamb performance. Sheep Res J 8: 25-29.

Alba DF, da Rosa G, Hanauer D, Saldanha TF, Souza CF, Baldissera MD, Da Silva dos Santos D, Piovezan AP, Girardini LK, Da Silva AS (2019) Subclinical mastitis in Lacaune Sheep: causative agents, impacts on milk production, milk quality, oxidative profiles and treatment efficacy of Ceftiofur. Microb Pathog 137: 103732.

Alekish MO, Alshehabat MA, Abutarbush SM (2014) The prevalence and etiology of subclinical mastitis in Awassi sheep; emphasis on the relationship between the ısolated organisms and the somatic cell count. EJVM 8: 1-13.

Al-Majali AM, Jawabieh S (2003) Period prevalence and etiology of subclinical mastitis in Awassi sheep in Southern Jordan. Small Rumin Res 47: 243-248.

Attili AR, Preziuso S, Ngwa VN, Cantalamessa A, Moriconi M, Cuteri V (2016) Clinical evaluation of the use of Enrofloxacin against staphylococcus aureus clinical mastitis in sheep. Small Rumin Res 136: 72-77.

Bauer AW, Kirby WM, Sherris JC, Turck M (1996) Antibiotic susceptibility testing by standardised single disk method. Am J Clin Pathol 45: 493–6.

Bergonier D, Berthelot X (2003) New advances in epizootiology and control of ewe mastitis. Livest Prod Sci 79: 1-16.

Berthelot X, Lagriffoul G, Concordet D, Barillet F, Bergonier D (2006) Physiological and pathological thresholds of somatic cell counts in ewe milk. Small Rumin Res 62: 27-31.

Bradley AJ (2002) Bovine mastitis: an evolving disease. Vet J 164: 116-128.

Caboni P, Manis C, Ibba I, Contu M, Coroneo V, Scano P (2017) Compositional profile of ovine milk with a high somatic cell count: a metabolomics approach. Int Dairy J 69: 33-39.

Contreras GA, Rodríguez JM (2011) Mastitis: comparative etiology and epidemiology. J Mammary Gland Biol Neoplasia 16: 339-356.

da Silva ER, Siqueira AP, Martins JC, Ferreira WP, da Silva N (2004) Identification and in vitro antimicrobial susceptibility of Staphylococcus species isolated from goat mastitis in the Northeast of Brazil. Small Rumin Res 55: 45-49.

Daniel WW (1999) Biostatistics: a foundation for analysis in the health sciences. 7th ed., John Wiley & Sons, New York.

Dore S, Liciardi M, Amatiste S, Bergagnacy S, Bolzoni G, Caligiuri V, Cerrone A, Farina G, Montagna CO, Saletti MA, Scatassa ML, Sotgiu G, Cannas EA (2016) Survey on small ruminant bacterial mastitis in Italy, 2003-2014. Small Rum Res 141: 91-93.

El-Jakee J, Hableel HS, Kandil M, Hassan OF, Khairy EA, Marouf SA (2013) Antibiotic resistance patterns of Streptococcus agalactiae isolated from mastitic cows and ewes in Egypt. Glob Vet 10: 264-270.

Ergun Y, Aslantas O, Dogruer G, Kirecci E, Sarıbay MK, Ates CT, Ulku A, Demir C (2009) Prevalence and etiology of subclinical mastitis in Awassi dairy ewes in Southern Turkey. Turk J Vet Anim Sci 33: 5.

Fragkou IA, Boscos CM, Fthenakis GC (2014) Diagnosis of clinical or subclinical mastitis in ewes. Small Rumin Res 118: 86-92.

Gebrewahid TT, Abera BH, Menghistu HT (2012) Prevalence and etiology of subclinical mastitis in small ruminants of Tigray Regional State, North Ethiopia. Vet World 5: 103-109.

Gelasakis AI, Mavrogianni VS, Petridis IG, Vasileiou NG, Fthenakis GC (2015) Mastitis in sheep–the last 10 years and the future of research. Vet Microbiol 181: 136-146.

Gokhan M, Gulaydin O (2020) Prevalance and antimicrobial susceptibility of bacterial species isolated from ovine clinical mastitis cases in Van province. Etlik Vet Mikrobiyol Derg 31: 39-46.

Guler L, Ok U, Gunduz K, Gulcu Y, Hadimli HH (2005) Antimicrobial susceptibility and coagulase gene typing of Staphylococcus aureus ısolated from bovine clinical mastitis cases in Turkey. J Dairy Sci 88: 3149-3154.

Hariharan H, Donachie W, Macaldowie C, Keefe G (2004) Bacteriology and somatic cell counts in milk samples from ewes on a Scottish farm. Can J Vet Res 68: 188-192.

Harmon RJ (2001) Somatic cell count: A primer. In: Annual Meeting National Mastitis Council Reno, Proceedings. Madison: National Mastitis Council 40: 3-9.

Hawari AD, Obeidat M, Awaisheh SS, Al-Daghistani HI, Al-Abbadi AA, Omar SS, Qrunfleh IM, Al-Dmoor HM, El-Qudah J (2014) Prevalence of mastitis pathogens and their resistance against antimicrobial agents in Awassi sheep in Al-Balqa Province of Jordan. Am J Anim Vet Sci 9: 116-121.

Holko I, Tančin V, Tvarožková K, Supuka P, Supuková A, Mačuhová L (2019) Occurrence and antimicrobial resistance of common udder pathogens ısolated from sheep milk in Slovakia. Potr Slov J F and Sci 13: 258-261.

Jones JE (1984) An Investigation of Mastitis in Sheep in Cyprus. Report to the Veterinary Department, Ministry of Agriculture, Nicosia, p 47.

Kaskous S, Farschtschi S, Pfaffl MW (2022) Physiological aspects of milk somatic cell count in small ruminants – A Review. Dairy 4: 26-42.

Kern G, Traulsen I, Kemper N, Krieter J (2013) Analysis of somatic cell counts and risk factors associated with occurrence of bacteria in ewes of different primary purposes. Livest Sci 157: 597-604.

Kiossis E, Brozos CN, Petridou E, Boscos C (2007) Program for the control of subclinical mastitis in dairy Chios breed ewes during lactation. Small Rumin Res 73: 194-199.

Kunz F, Corti S, Giezendanner N, Stephan R, Wittenbrink MM, Zweifel C (2011) Antimicrobial resistance of Staphylococcus aureus and coagulase negative Staphylococci isolated from mastitis milk samples from sheep and goats. Schweiz Arch Tierheilkd 153: 63-69.

Leitner G, Silanikove N, Merin U (2008) Estimate of milk and curd yield loss of sheep and goat with intrammamary infection and its relation to somatic cell count. Small Rumin Res 74: 221-225.

Lollai SA, Ziccheddu M, Di Mauro C, Manunta D, Nudda A, Leori G (2008) Profile and evolution of antimicrobial resistance of ovine mastitis pathogens (1995-2004). Small Rumin Res 74: 249–254.

Martins HB, Selis ND, Nascimento FS, de Carvalho SP, Gusmão LD, Nascimento JD, Brito AK, de Souza SI, de Oliveira MV, Timenetsky J, Yatsuda R, Uetanabaro AP, Marques LM (2017) Anti-inflammatory activity of the essential oil citral in experimental infection with Staphylococcus aureus in a model air pouch. Evid Based Complement Alternat Med 2017: 2505610.

Maurer J, Schaeren W (2007) Udder health and somatic cell count in ewes. Agrarforschung 14: 162-167.

Mavrogenis AP, Koumas A, Kakoyiannis CK, Taliotis CH (1995) Use of somatic cell counts for the detection of subclinical mastitis in sheep. Small Rumin Res 17: 79-84.

McDougall S, Pankey W, Delaney C, Barlow J, Murdough PA, Scruton D (2002) Prevalence and incidence of subclinical mastitis in goats and dairy ewes in Vermont, USA. Small Rumin Res 46: 115-121.

Moawad AA, Osman SA (2005) Prevalence and etiology of subclinical mastitis in dairy ewes at Fayoum Governorate, Egypt. Assiut Vet Med J 51: 1-15.

Moroni P, Pisoni G, Varisco G, Boettcher P (2007) Effect of intramammary infection in Bergamasca meat sheep on milk parameters and lamb growth. J Dairy Res 74: 340-344.

Naccari F, Martino D, Giofrè F, Passantino A, De Montis P (2003) Therapeutic efficacy of Tilmicosin in ovine mammary infections. Small Rumin Res 47: 1-9.

Novick JR, William J (1989). Development of in vitro susceptibility testing criteria and quality control parameters. Clin. Microbiol. Newsl 11: 60-62.

Nunes GR, Blagitz MG, Freitas CB, Souza FN, Ricciardi M, Stricagnolo CR, Sanches BG, Azedo MR, Sucupira MC, Della Libera AM (2008) Evaluation of the indicators of inflammation in the diagnosis of ovine mastitis. Arq Inst Biol 75: 271-281.

Olivares-Pérez J, Kholif AE, Rojas-Hernández S, Elghandour MM, Salem AZM, Bastida AZ, Velázquez-Reynoso D, Cipriano-Salazar M, Camacho-Díaz LM, María Uxúa Alonso-Fresán MU, DiLorenzo N (2015) Prevalence of bovine subclinical mastitis, its etiology and diagnosis of antibiotic resistance of dairy farms in four municipalities of a tropical region of Mexico. Trop Anim Health Prod 47: 1497-1504.

Oliver SP, Murinda SE (2012) Antimicrobial resistance of mastitis pathogens. Vet Clin North Am Food Anim Prat 28: 165-185.

Ozenc E, Seker E, Baki Acar D, Birdane MK, Darbaz I, Dogan N (2011) The importance of Staphylococci and threshold value of somatic cell count for diagnosis of sub-clinical mastitis in Pirlak sheep at mid-lactation. Reprod Domest Anim 46: 970-974.

Paterna A, Contreras A, Gómez-Martín A, Amores J, Tatay-Dualde J, Prats-van der Ham M, Corrales JC, Sanchez A, De la Fe C (2014) The Diagnosis of mastitis and contagious agalactia in dairy goats. Small Rumin Res 121: 36-41.

Petersson-Wolfe CS, Mullarky IK, Jones GM (2010) Staphylococcus Aureus Mastitis: Cause, Detection, and Control; VirginiaTech: Blacksburg, VA, USA, 2010.

Podhorecka K, Borkova M, Sulc M, Seydlova R, Dragounova H, Svejcarova M, Peroutkova J, Elich O (2021) Somatic cell count in goat milk: an indirect quality indicator. FoodS 10: 1046.

Queiroga MC (2017) Prevalence and aetiology of sheep mastitis in Alentejo regions of Portugal. Small Rumin Res 153: 123-130.

Quinn PJ, Markey BK, Leonard FC, Fitzpatrick ES, Fanning S, Hartigan PJ (2011) Veterinary Microbiology and Microbial Disease, 2nd ed. West Sussex: Wiley-Blackwell, 837-850.

Quinn PJ, Markey BK, Carter ME, Donelly WJ, Leonard FC (2002) Veterinary Microbiology and Microbial Disease, Blackwell Science Ltd, a Blackwell Publishing Company, 465 475.

Rall VL, Miranda ES, Castilho IG, Camargo CH, Langoni H, Guimarães FF, Araújo Júnior JP, Fernandes Júnior A (2014) Diversity of Staphylococcus species and prevalence of enterotoxin genes isolated from milk of healthy cows and cows with subclinical mastitis. J Dairy Sci 97: 829-837.

Raynal-Ljutovac K, Pirisi A, De Crémoux R, Gonzalo C (2007) Somatic cells of goat and sheep milk: analytical sanitary, productive and technological aspects. Small Rumin Res 68: 126-144.

Riggio V, Pesce LL, Morreale S, Portolano B (2013) Receiveroperating characteristic curves for somatic cell scores and california mastitis test in Valle del Belice dairy sheep. Vet J 196: 528-532.

Sevi A, Albenzio M, Taibi L, Dantone D, Massa S, Annicchiarico G (1999) Changes of somatic cell count through lactation and their effects on nutritional, renneting and bacteriological characteristics of ewe’s milk. Adv Food Sci 21: 122-127.

Stocco G, Summer A, Cipolat-Gotet C, Zanini L, Vairani D, Dadousis C, Zecconi A (2020) Differential somatic cell count as a novel indicator of milk quality in dairy cows. Animals (Basel) 10: 753.

Świderek WP, Charon KM, Winnicka A, Gruszczyńska J, Pierzchała M (2016) Physiological threshold of somatic cell count in milk of polish heath sheep and polish lowland sheep. Ann Anim Sci 16: 155-170.

Tvarožková K, Tančin V, Holko I, Uhrinčať M, Mačuhová L (2019) Mastitis in ewes: somatic cell counts, pathogens and antibiotic resistance. J Microbiol Biotech Food Sci 9: 661-670.

Tvarožková K, Tančin V, Uhrincat M, Hleba L, Mačuhová L (2020) Mastitis pathogens and somatic cell count in ewes milk. Potravinarstvo Slovak J Food Sci 14: 164-169.

Tvarozkova K, Vasicek J, Uhrinca M, Macuhova L, Hleba L, Tancin V (2021) The presence of pathogens in milk of ewes in relation to the somatic cell count and subpopulations of leukocytes. Czech J Anim Sci 66: 315-322.

Vasıľ M, Elečko J, Farkašová Z, Zigo F (2018) Development of resistance to antibiotics in bacteria Staphylococcus sp. isolated from milk samples in the sheep breedings on East of Slovakia. Potravinarstvo Slovak J Food Sci 12: 273-278.

Vasileiou NG, Cripps PJ, Ioannidi KS, Chatzopoulos DC, Gougoulis DA, Sarrou S, Orfanou DC, Politis AP, Gonzalez-Valerio TC, Argyros S, Mavrogianni VS, Petinaki E, Fthenakis GC (2018) Extensive countrywide field investigation of subclinical mastitis in sheep in Greece. J Dairy Sci 101: 7297-7310.

Wald R, Hess C, Urbantke V, Wittek T, Baumgartner M (2019) Characterization of Staphylococcus species isolated from bovine quarter milk samples. Animals (Basel) 9: 200.

Zafalon LF, Santana RC, Pilon LE, Fim Júnior GA (2016) Diagnosis of subclinical mastitis in Santa Ines and Morada Nova sheep in Southeastern Brazil. Trop Anim Health Prod 48: 967-72.

Zdragas A, Tsakos P, Kotzamanidis C, Anatoliotis K, Tsaknakis I (2005) Outbreak of mastitis in ewes caused by Streptococcus Agalactiae. J Hellenic Vet Med Society 6: 114-121.

Zigo F, Vasiľ M, Kadáši M, Elečko J, Farkašová Z (2011) Bacteria Staphylococcus spp. izolated from mastitis of sheep and their enterotoxigenic properties. Potravinarstvo 5: 70-72.

 

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Authors and Affiliations

O. Ergene
1
H. Baloglu
2
V. Haciogullari
2
H.E. Çolakoğlu
3

  1. Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Near East University, 99158Nicosia, North Cyprus, Mersin-10, Turkey
  2. Directorate of Veterinary Department, Nicosia, Cyprus
  3. Ankara University, Faculty of Veterinary Medicine, Department of Obstetrics and Gynecology, 06110,Ankara, Turkey
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Abstract

Taraxacum Officinale, commonly called dandelion, is herbaceous perennial belonging to the family of Asteraceae, having good antibacterial effects which are related to its phenolic substances. In this study, the effect of phenolic contents as well as the antibiofilm activity against Staphylococcus aureus of phenolic extract from T. Officinale were evaluated in vitro. With 70% metha- nol-water (v/v) as a solvent, the dandelion was extracted by ultrasonic assisted extraction method. Subsequent identification and quantification of phenol in extract was carried out using High Performance Liquid Chromatography (HPLC). The minimum inhibitory concentration and anti- bacterial kinetic curve of dandelion phenolic extract were analyzed by spectrophotometry. Changes in extracellular alkaline phosphatase (AKP) contents, electrical conductivity, intracellular protein contents, and DNA of S. aureus after the action of dandelion phenolic extract were determined to study its effect on the permeability of S. aureus cell wall and cell membrane. The results showed that chlorogenic acid (1.34 mg/g) was present in higher concentration, followed by luteolin (1.08 mg/g), ferulic acid (0.22 mg/g), caffeic acid (0.21 mg/g), and rutin (0.19 mg/g) in the dandelion phenolic extract. The minimum inhibitory concentration (MIC) of dandelion phenolic extract against S. aureus was 12.5 mg/mL. The antibacterial kinetic curve analysis showed that the inhibitory effect of dandelion phenolic extract on S. aureus was mainly in the exponential growth phase. After applying the dandelion phenolic extract, the growth of S. aureus was signifi- cantly inhibited entering into the decay phase early. Furthermore, after the action of dandelion, the extracellular AKP contents of S. aureus, the electrical conductivity and the extracellular protein contents were all increased. The phenolic extract also affected the normal reproduction of S. aureus. These results suggest that dandelion has an inhibitory effect on S. aureus, and the mechanism of its action was to destroy the integrity of the cell walls and cell membranes.
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Authors and Affiliations

P. Xu
1 2 3
X.B. Xu
1
A. Khan
4
T. Fotina
3
S.H. Wang
2

  1. School of Life Science and Basic Medicine, Xinxiang University, Jinsui St. 191, 453003 Xinxiang, China
  2. College of Animal Science and Veterinary Medicine, Henan Institute of Science and Technology, Eastern Hua Lan Street, 453003 Xinxiang, China
  3. Department of Veterinary Medicine, Sumy National Agrarian University, Herasima Kondratieva St. 160, 40021 Sumy, Ukraine
  4. College of Animal Science and Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi 030801, P.R. China
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Abstract

Currently, we are facing the ever-increasing phenomenon of bacteria being resistant to antibiotics. It is the consequence of excessive and incorrect use of drugs. The phenomenon is a global problem affecting bacteria both in their hospital population and in the natural environment. Municipal waste is an environment conducive to the development of microorganisms, therefore it contains various groups of bacteria, including drug-resistant staphylococci. The aim of the study was to identify species of bacteria, determine their antibiotic resistance, and assess the occurrence of genes responsible for methicillin resistance in Staphylococcus aureus isolated from mixed municipal waste. Strains were isolated by Koch’s serial dilution method with the use of microbiological media. Species were identified using the MALDI TOF-MS technique, whereas the drug resistance profile was determined by disk diffusion and molecular PCR methods. 250 isolates of S. aureus were collected. The highest resistance found was to cefoxitin, erythromycin and tetracycline. Among the bacteria collected, resistance to 1, 2, 3 or 4 antibiotics at the same time was the most common, with a maximum of 10. Additionally, 45 (18%) MDR (multidrug-resistant) isolates were detected. Methicillin resistance was found by the disk diffusion test in 60 (24%) strains, while the mecA gene was detected in as many as 180 (72%) isolates.
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Authors and Affiliations

Katarzyna Wolny-Koładka
1
ORCID: ORCID

  1. University of Agriculture in Krakow, Department of Microbiology and Biomonitoring, al. Mickiewicza 24/28, 30-059 Kraków, Poland
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Abstract

Studies were carried out in the summer seasons of l 995-1999 (from June to September) on the quantitative and qualitative composition of Enterobacteriaceae bacteria (including Escherichia coli and Salmonella sp.), and potentially pathogenic bacteria Aeromonas hydrophila, Pseudomonas aeruginosa and Staphylococcus sp. in the water of 8 bathing sites of the Lake Wigry. Aeromonas hydrophila occurred in the all samples of studied water and was the most numerous in water sampled from sites of increased trophic levels. Irrespective of the site and time of sampling Pseudomonas aeruginosa was rarely isolated. In the total of 160 samples of water analysed Salmonella sp.. Escherichia coli and Staphyloccocus aureus were determined in 32 (22.6%), 68 (42.4%) and 90 (55%) samples, respectively. Pathogenic bacteria of the genus Salmonella sp. and potentially pathogenic Staphylococcus aureus and Aeromonas hydrophila identified in the analysed offshore waters (also when Escherichia coli were absent) suggest that the use of the Lake Wigry waters for swimming, falling into account faecal bacterial counts, may not be sufficient to fully reflect safety conditions for bathers. The results of the research suggest that the evaluation of the Lake Wigry surface waters for recreational use should include the frequency of the occurrence of Salmonella sp., Staphylococcus aureus, Aeromonas hydrophila and Pseudomonas aeruginosa. These three species, which arc not directly linked to faecal contamination, can cause various diseases of the skin, nasal and oral cavities, eyes, internal car and other problems in people swimming in contaminated water.
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Authors and Affiliations

Ewa Korzeniewska
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Abstract

The free-living Acanthamoeba sp. causes various diseases. Treatment of them is very difficult and not always effective because of encystation, making it highly resistant to antiamoebic drugs. Gram-positive bacteria Staphylococcus aureus, Gram-negative bacteria Escherichia coli, and an yeast Candida albicans also exhibit outstanding resistance to antimicrobial substances. The search for new natural amoebicidal and antimicrobial agents of plant origin is still of current interest. The aim of the study was to investigate the amoebicidal activity of the extracts obtained from tissue culture and a field-grown plant of Chaenomeles japonica against pathogenic trophozoites of Acanthamoeba spp. and antimicrobial effect against S. aureus, E. coli, and C. albicans. The extracts of C. japonica had an inhibitory effect on the proliferation of Acanthamoeba trophozoites as compared to the non-treated control. Among the crude extracts tested, the extract of leaves, from both shoot culture and the field-grown plant had remarkable amoebicidal action against the trophozoites but also antibacterial activity against Gram-positive bacteria Staphylococcus aureus. The extract from leaves from shoot culture, already on the second and third days of treatment, showed an antiamoebicidal effect at a concentration of 1 mg mL-1 (inhibition of trophozoites 87.5% and 91.8%, respectively). In addition to leaves from shoot culture (a conc. 5 mg mL-1, 2nd day inhibition of trophozoites 85.7% and 3rd day 97.2%), leaves from a field-grown plant (a conc. 5 mg mL-1, 2nd day 91.0% and 3rd day 94.4%) and callus (a conc. 5 mg mL-1, 2nd day 90.0% and 3rd day – 95.4%) also exhibited a good antiamoebicidal activity. Out of the four extracts, the extracts from leaves from both shoot culture and a field-grown plant were reported to be the most active against Gram-positive S. aureus, which was determined by the values of MIC = 5.0 mg mL-1 and MIC = 2.5 mg mL-1, respectively. The inhibitory potential depends on the yield and composition of mainly bioactive compounds: pentacyclic terpenoids (mainly betulinic, ursolic, and oleanolic acids) and polyphenols (mainly chlorogenic acid and its isomers, epicatechin, dimeric, and trimeric proanthocyanidins, quercetin and kaempferol derivatives).

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Authors and Affiliations

Małgorzata Kikowska
Monika Derda
Barbara Thiem
Agata Włodarczyk
Jolanta Długaszewska
Anna Stochmal
Jerzy Żuchowski
Edward Hadaś

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