Agroclimatic zone-wise prevalence of biofilm forming methicillin resistant staphylococcus aureus in West Bengal


351 / 319 / 95

Authors

  • RAJARSHI BARDHAN West Bengal University of Animal and Fishery Sciences, Belgachia, Kolkata, West Bengal 700 037 India image/svg+xml
  • ADITYA PAUL West Bengal University of Animal and Fishery Sciences, Belgachia, Kolkata, West Bengal 700 037 India image/svg+xml
  • INDRANIL SAMANTA West Bengal University of Animal and Fishery Sciences, Belgachia, Kolkata, West Bengal 700 037 India image/svg+xml
  • KUNAL BATABYAL West Bengal University of Animal and Fishery Sciences, Belgachia, Kolkata, West Bengal 700 037 India image/svg+xml
  • SAMIR DEY West Bengal University of Animal and Fishery Sciences, Belgachia, Kolkata, West Bengal 700 037 India image/svg+xml
  • UTTAM SARKAR West Bengal University of Animal and Fishery Sciences, Belgachia, Kolkata, West Bengal 700 037 India image/svg+xml
  • SIDDHARTHA NARAYAN JOARDAR West Bengal University of Animal and Fishery Sciences, Belgachia, Kolkata, West Bengal 700 037 India image/svg+xml

https://doi.org/10.56093/ijans.v94i8.147438

Keywords:

Agro-climatic zones, Biofilm, Cattle, Milk, Methicillin resistance

Abstract

The present study envisages the prevalence of biofilm producing, methicillin resistant Staphylococcus aureus, isolated from cattle milk of different agro-climatic zones of an eastern state of India, West Bengal. The milk samples (n=168) were collected from three predominant agro- climatic zones of South Bengal, viz. new alluvial, coastal saline and red laterite. A total of 146 Staphylococcus aureus isolates were recovered, confirmed by biochemical tests and polymerase chain reaction (PCR). Through PCR of mecA gene, it was found that 45 strains were methicillin resistant, encompassing 28.57% new alluvial zone, 30.19% red laterite region and 29.16% coastal saline region. Determination of biofilm formation was done, both phenotypically by microtiter plate method and genotypically by PCR of icaA and icaD genes, specific for biofilm formation in Staphylococcus aureus. Phenotypic study revealed that 14 isolates were strong biofilm producers, 79 were moderate and the 47 were weak biofilm producers. PCR studies also showed that a total of 30 isolates were icaA positive and 25 isolates were icaD positive. Although no significant difference was found in the occurrence of icaA positive isolates, the possession of icaD by the Staphylococcus aureus isolates varied significantly according to different agro-climatic zones.

Downloads

Download data is not yet available.

References

Abebe R, Hatiya H, Abera M, Megersa B and Asmare K. 2016. Bovine mastitis: Prevalence, risk factors and isolation of Staphylococcus aureus in dairy herds at Hawassa milk shed, South Ethiopia. BMC Veterinary Research 12: 270.

Ali R, Al-Achkar K, Al-Mariri A and Safi M. 2014. Role of polymerase chain reaction (PCR) in the detection of antibiotic- resistant Staphylococcus aureus. Egyptian Journal of Medical Human Genetics 15(3): 293–98.

Bandyopadhyay S, Samanta I, Bhattacharyya D, Nanda P K, Kar J, Chowdhury J, Dandapat P, Das A K, Natul N, Mondal B, Dutta T K, Das G, Das B C, Naskar U, Bandyopadhyay U K, Das S C and Bandyopadhyay S. 2015. Co-infection of methicillin-resistant Staphylococcus epidermidis, methicillin-resistant Staphylococcus aureus and extended spectrum β-lactamase producing Escherichia coli in bovine mastitis–three cases reported from India. Veterinary Quarterly 35: 56–61.

Bardhan R, Samanta I, Batabyal K, Dey S and Joardar S N. 2023. Occurrence of nuc gene in Staphylococcus aureus from milk samples of different regions of West Bengal. Indian Journal of Animal Health.

Basanisi M G, La Bella G, Nobili G, Franconieri I and La Salandra G. 2017. Genotyping of methicillin-resistant Staphylococcus aureus (MRSA) isolated from milk and dairy products in South Italy. Food Microbiology 62: 141–46.

Basanisi M G, Nobili G, La Bella G, Russo R, Spano G, Normanno G and La Salandra G. 2016. Molecular characterization of Staphylococcus aureus isolated from sheep and goat cheeses in southern Italy. Small Ruminant Research 135: 17–19.

DAHD (2019). Available at: https://dahd.nic.in/sites/default/ filess/District-wise%20cattle%20population%202019_1.pdf; accessed on 05/06/24.

Donlan R M 2002. Biofilms: Microbial life on surfaces. Emerging Infectious Diseases 8(9): 881–90.

Joshi S and Gokhale S. 2006. Status of mastitis as an emerging disease in improved and periurban dairy farms in India. Annals of the New York Academy of Sciences 1081(2006): 74–83.

Khan M Z. and Khan A. 2006. Basic facts of mastitis in dairy animals: A review. Pakistan Veterinary Journal 26(4): 204–8.

Kumar R, Yadav B R and Singh R S. 2010. Genetic determinants of antibiotic resistance in Staphylococcus aureus isolates from milk of mastitic crossbred cattle. Current Microbiology 60: 379–86.

Lowy F D. 1998. Staphylococcus aureus infections. New England Journal of Medicine 339: 520–32.

Mahanti A, Joardar S N, Bandyopadhyay S, Banerjee J, Ghosh J, Batabyal K, Sar T K, Dutta T K, and Samanta I. 2020. Characterization of methicillin-resistant and enterotoxins producing Staphylococcus aureus in bovine milk in India. Journal of Agriculture and Food Research 2:100017.

Mistry H, Sharma P, Mahato S, Saravanan R, Ananad Kumar P and Vadari P. 2016. Prevalence and characterization of oxacillin susceptible mecA-positive clinical isolates of Staphylococcus aureus causing bovine mastitis in India. PLoS One 11(9): e0162256.

Notcovich S, DeNicolo G, Flint S H, Williamson N B, Gedye K, Grinberg A and Lopez- Villalobos N. 2018. Biofilm-forming potential of Staphylococcus aureus isolated from bovine mastitis in New Zealand. Veterinary Sciences 5(1): 8.

Otter J A and French G L. 2011. Community associated methicillin- resistant Staphyllococcus aureus strains as a cause of healthcare-associated infection. Journal of Hospital infection 79 (3):189–93.

Pérez-Conesa D, Cao J, Chen L, McLandsborough L and Weiss J. 2011. Inactivation of Listeria monocytogenes and Escherichia coli O157: H7 biofilms by micelle-encapsulated eugenol and carvacrol. Journal of Food Protection 74(1): 55–62.

Prashanth K, Rao K R, Reddy P V, Saranathan R and Makki AR. 2011. Genotypic characterization of Staphylococcus aureus obtained from humans and bovine mastitis samples in India. Journal of Global Infectious Diseases 3(2): 115–22.

Quinn P J. 1994. Clinical Veterinary Microbiology. Wolfe Publications, London, UK.

Rosenberg M and Kjelleberg S. 1986. Hydrophobic interactions in bacterial adhesion. Advances in Microbial Ecology 9: 353–93.

Salina A, Guimarães F F, Pereira, V B, Menozzi B D and Rall V L M and Langoni H. 2020. Detection of icaA, icaD, and bap genes and biofilm production in Staphylococcus aureus and non-aureus staphylococci isolated from subclinical and clinical bovine mastitis. Arquivo Brasileiro de Medicina Veterinária e Zootecnia 72: 1034–38.

Santos F F, Mendacona L C, Reis D R L, Guimaraes, A S, Lange C, Ribeiro J B, Machado M A and Brito M A V P. 2016. Presence of mecA-positive multidrug-resistant Staphylococcus epidermidis in bovine milk samples in Brazil. Journal of Dairy Science 99(2): 1374–82.

Shah M S, Qureshi S, Kashoo Z, Farooq S, Wani SA, Hussain MI, Banday M S, Khan A A, Gull B, Habib A, Khan S M and Dar B A. 2019. Methicillin resistance genes and in vitro biofilm formation among Staphylococcus aureus isolates from bovine mastitis in India. Comparative Immunology, Microbiology and Infectious Diseases 64: 117–24.

Stefani S, Chung D R, Lindsay J A, Friedrich A W, Kearns A M, Westh H and Mackenzie F M. 2012. Meticillin-resistant Staphylococcus aureus (MRSA): Global epidemiology and harmonisation of typing methods. International Journal of Antimicrobial Agents 39(4): 273–82.

Stegger M, Andersen P S, Kearns A, Pichon B, Holmes M A, Edwards G, Laurent F, Teale C, Skov R and Larsen A R. 2012. Rapid detection, differentiation and typing of methicillin- resistant Staphylococcus aureus harbouring either mecA or the new mecA homologue mecALGA251. Clinical Microbiology and Infection 18: 395–400.

Stepanović S, Vuković D, Hola V, Bonaventura G D, Djukic S, Cirkovic I and Ruzicka F. 2007. Quantification of biofilm in microtiter plates: Overview of testing conditions and practical recommendations for assessment of biofilm production by staphylococci. Acta Pathologica, Microbiologica, et Immunologica Scandinavica 115(8): 891–99.

van Belkum A, Melles D C, Nouwen J, van Leeuwen W B, van Wamel W, Vos M C, Wertheim HFL and Verbrugh H A. 2009. Co-evolutionary aspects of human colonisation and infection by Staphylococcus aureus. Infection, Genetics and Evolution 9(1): 32–47.

Vasudevan P, Nair M K M, Annamalai T and Venkitanarayanan K S. 2003. Phenotypic and genotypic characterization of bovine mastitis isolates of Staphylococcus aureus for biofilm formation. Veterinary Microbiology 92(1-2): 179–85.

Submitted

2024-01-13

Published

2024-08-06

Issue

Section

Short-Communication

How to Cite

BARDHAN, R. ., PAUL, A. ., SAMANTA, I. ., BATABYAL, K. ., DEY, S. ., SARKAR, U. ., & JOARDAR, S. N. . (2024). Agroclimatic zone-wise prevalence of biofilm forming methicillin resistant staphylococcus aureus in West Bengal. The Indian Journal of Animal Sciences, 94(8), 681–685. https://doi.org/10.56093/ijans.v94i8.147438
Citation