Listeria monocytogenes in mussels (Mytilus galloprovincialis) harvested from North Aegean coastal area

One hundred and two samples of mussels (Mytilus galloprovincialis), harvested from approved shellfish coastal water in northern Greece, were screened for the presence and antimicrobial resistance of Listeria monocytogenes. Listeria spp. were isolated according to International Organization for Standardization method 11290-1: 1996/FDAM 1: 2004(E) and identified using a multiplex polymerase chain reaction (PCR) system. The serovar identity of L. monocytogenes isolates was also determined with a multiplex PCR assay. The antimicrobial profile of the isolates was determined by the disk diffusion method. Listeria spp. were present in 8 of 102 samples tested (8%) and only 1 (1%) yielded L. monocytogenes. The isolate identified as L. monocytogenes was defined as serogroup I and found to be resistant to nalidixic acid and streptomycin. In conclusion, this study demonstrated that L. monocytogenes is not commonly found in mussels harvested in the North Aegean Sea, whereas there is a higher possibility of mussels’ contamination with other Listeria species.

Listeria monocytogenes in mussels (Mytilus galloprovincialis) harvested from North Aegean coastal area

One hundred and two samples of mussels (Mytilus galloprovincialis), harvested from approved shellfish coastal water in northern Greece, were screened for the presence and antimicrobial resistance of Listeria monocytogenes. Listeria spp. were isolated according to International Organization for Standardization method 11290-1: 1996/FDAM 1: 2004(E) and identified using a multiplex polymerase chain reaction (PCR) system. The serovar identity of L. monocytogenes isolates was also determined with a multiplex PCR assay. The antimicrobial profile of the isolates was determined by the disk diffusion method. Listeria spp. were present in 8 of 102 samples tested (8%) and only 1 (1%) yielded L. monocytogenes. The isolate identified as L. monocytogenes was defined as serogroup I and found to be resistant to nalidixic acid and streptomycin. In conclusion, this study demonstrated that L. monocytogenes is not commonly found in mussels harvested in the North Aegean Sea, whereas there is a higher possibility of mussels’ contamination with other Listeria species.

___

  • General Secretariat of National Statistical Service of Greece. Quantity of Seafoods. Table B4. Athens, Greece: General Secretariat of National Statistical Service of Greece; 2009.
  • Swaminathan B, Cabanes D, Zhang W, Cossart P. L. monocytogenes. In: Doyle MP, Beuchat LR, editors. Food Microbiology: Fundamentals and Frontiers. Washington, DC, USA: ASM Press; 2007. pp. 457–491.
  • Jay JM, Loessner MJ, Golden DA. Modern Food Microbiology. 7th ed. New York, NY, USA: Springer Science and Business Media; 2005.
  • Croonenbergs RE. Contamination of shellfish-growing waters. In: Martin RE, Carter EP, Flick GJ Jr, Davis LM, editors. Marine and Freshwater Products Handbook. Lancaster, PA, USA: Technomic Publishing Company Inc.; 2000. pp. 665–693.
  • Rodas-Suárez OR, Flores-Pedroche JF, Betacourt-Rule JM, Quinõnes-Ramírez EI, Vazquez-Salinas C. Occurrence and antibiotic sensitivity of L. monocytogenes strains isolated from oysters, fish, and estuarine water. Appl Environ Microb 2006; 72: 7410–7412. de Simon M, Terrago C, Ferrer MD. Incidence of L. monocytogenes in fresh foods in Barcelona (Spain). Int J Food Microbiol 1992; 16: 153–156.
  • Monfort P, Minet J, Rocourt J, Piclet G, Cormier M. Incidence of Listeria spp. in Breton live shellfish. Lett Appl Microbiol 1998; 26: 205–208.
  • Jacquet C, Gouin E, Jeannel D, Cossart P, Rocourt J. Expression of ActA, Ami, InlB, and listeriolysin O in L. monocytogenes of human and food origin. Appl Environ Microb 2002; 68: 616– 6
  • Kathariou S. L. monocytogenes virulence and pathogenicity, a food safety perspective. J Food Prot 2002; 65: 1811–1829.
  • Doumith M, Buchrieser C, Glaser P, Jacquet C, Martin P. Differentiation of the major L. monocytogenes serovars by multiplex PCR. J Clin Microbiol 2004; 42: 3819–3822.
  • Chen Y, Knabel SJ. Multiplex PCR for simultaneous detection of the genus Listeria, Listeria minocytogenes, and major serotypes and epidemic clones of L. monocytogenes. Appl Environ Microb 2007; 73: 6299–6304.
  • Aureli P, Ferrini AM, Mannoni V, Hodzic S, Wedell-Weergaard C, Oliva B. Susceptibility of L. monocytogenes isolated from food in Italy to antibiotics. Int J Food Microbiol 2003; 83: 325–330.
  • European Food Safety Authority (EFSA). The European Union summary report on trends and sources of zoonoses, zoonotic agents, antimicrobial resistance and foodborne outbreaks in 20 EFSA J 2012; 10: 2597. de Cesare A, Manfreda G, Macri M, Cantoni C. Application of automated ribotyping to support the evaluation of the L. monocytogenes source in a Taleggio producing plant and to predict the risk human health linked to the accidental sale of contaminated cheese. Arch Vet Ital 2006; 57: 231–240 .
  • Antunes P, Reu C, Sousa JC, Pestana N, Peixe L. Incidence and susceptibility to antimicrobials agents of Listeria spp. and L. monocytogenes isolated from poultry carcasses in Porto, Portugal. J Food Prot 2002; 65: 1888–1893.
  • Yusel N, Citak S, Onder M. Prevalence and antibiotic resistance of Listeria species in meat products in Ankara, Turkey. Food Microbiol 2005; 22: 241–245.
  • Arslan S, Özdemir F. Prevalence and antimicrobial resistance of Listeria spp. in homemade white cheese. Food Control 2008; 19: 360–363.
  • International Organization for Standardization. Microbiology of food and animal feeding. Horizontal method for the detection and enumeration of L. monocytogenes. ISO 11290-1: 1996/
  • FDAM 1: 2004 (E). Geneva, Switzerland: ISO; 2004.
  • Lawrence LM, Gilmour A. Incidence of Listeria spp. and L. monocytogenes in a poultry processing environment and in poultry products and their rapid confirmation by multiplex PCR. Appl Environ Microb 1994; 60: 4600–4604.
  • Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing; 14th Informational Supplement M100–S14. Vol. 24, No 1. Wayne, PA, USA: CLSI; 2004.
  • El Marrakchi A, Boumhandi R, Hamama A. Performance of a new chromogenic plating medium for the isolation of L. monocytogenes from marine environments. Lett Appl Microbiol 2005; 40: 87–91.
  • Ferrer MD, de Simon M. Isolation of Salmonella spp., V. parahemolyticus, Y. enterocolytica and L. monocytogenes in bivalve mollusks. Alimentaria 1993; 30: 33–35.
  • Vernocchi P, Maffei M, Lanciotti R, Suzzi G, Gardini F. Characterization of Mediterranean mussels (Mytilus galloprovincialis) harvested in Adriatic Sea (Italy). Food Control 2007; 18: 1575–1583.
  • Bremer PJ, Fletcher GC, Osborne C. L. monocytogenes in seafood. Auckland, New Zealand: New Zealand Institute for Crop & Food Research Limited; 2003.
  • Brett MSY, Short P, McLauchlin J. A small outbreak of listeriosis associated with smoked mussels. Int J Food Microbiol 1998; 43: 223–229.
  • Inoue S, Nakama A, Arai Y, Kokubo Y, Maruyama T, Salto A, Yoshida T, Terao M, Yamamoto S, Kumagai S. Prevalence and contamination levels of L. monocytogenes in retail food in Japan. Int J Food Microbiol 2000; 59: 73–77.
  • Pinto AL, Teixeira P, Castilho F, Felicio MT, Pombal F, Eibbs PA. Prevalence and serotyping of L. monocytogenes in Portuguese live bivalve molluscs sampled in various steps along the sanitary control process. Aquac Res 2006; 37: 1112–1116.
  • Kueh CSW, Chan K. Bacteria in bivalve shellfish with special reference to the oyster. J Appl Bacteriol 1985; 59: 41–47.
  • International Commission on Microbiological Specifications for Foods. Microorganisms in Foods 6. Microbial Ecology of Food Commodities. 2nd ed. New York, NY, USA: Kluwer Academic; 200 Aarestrup FM. Other pathogens. In: Aarestrup FM, editor. Antimicrobial Resistance in Bacteria of Animal Origin. Washington, DC, USA: ASM Press; 2006. pp. 249–267.
Turkish Journal of Veterinary and Animal Sciences-Cover
  • ISSN: 1300-0128
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Ractopamine efect on lipid metabolism and GLUT4 amount of fnishing pigs

Laura Cristina PORTO JARDIM, Erica MARIO GUILHEN, Luciano Jose PEREIRA, Matheus Soares FERREIRA DA SILVA, Marcelo Henrique NAPIMOGA, Leida Maria BOTION, Raimundo Vicente DE SOUSA, Tiago Santos ARAUJO, Marcio Gilberto ZANGERONIMO

Oral and dental disorders in pet hedgehogs

Tzvetan CHAPRAZOV, Rosen DIMITROV, Kamelia Stamatova YOVCHEVA, Krasimira UZUNOVA

Antioxidant effect of rosehip seed powder in raw and cooked meatballs during refrigerated storage

Huri İLYASOĞLU

Evaluating the effects of chitosan, plant oils, and different diets on rumen metabolism and protozoan population in sheep

Monika WENCELOVA, Zora VÁRADYOVA, Katarína MIHALIKOVA

The lumbar dorsal rami of the wild pig: the intermediate branch

İbrahim KÜRTÜL, Sevinç ATEŞ, Erdal ÖZMEN, Lutfi TAKCI, Hanno STEINKE

Comparison of manual measurements and computer-assisted image analysis in fish morphometry

Miloslav PETRTYL, Lukas KALOUS, Devrim MEMİŞ

Isolation and molecular identifcation of Avibacterium paragallinarum in suspected cases of infectious coryza

Nader AZAD, Omid MADADGAR, Mahdi BADOUEI ASKARI, Avesta SADRZADEH, Patrick BLACKALL, Saeid CHARKHKAR

Genetic characterization of paramphistomes of bufalo by HAT-RAPD analysis

Giregowdanahalli PUTTALAKSHMAMMA, Umed RAMANI, Krishna SINGH, Amrutlal PATEL, Abdul PATEL, Chaitanya JOSHI

The effect of oviductal cells on in vitro maturation of canine oocytes in diferent culture media

Asiye İzem SANDAL, Mehmet Can GÜNDÜZ, Sinem Özlem ENGİNLER, Alper BARAN, Çağatay TEK, Ramazan ARICI, Israa Faris MOHAMMED, Elif Merve ÇINAR, Özen Banu ÖZDAŞ, Ezgi ERTÜRK

Insertion/deletion polymorphism of the sterol regulatory element-binding protein 1 gene in different cattle breeds

Witold Stanislaw PROSKURA