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Sự lưu hành vi khuẩn Clostridium perfringens và Clostridium difficile mang gen sinh độc tố cpa, tcdA trong thịt và rau ăn lá

Tạ Thị Yến Ninh Thị Hạnh Vũ Thị Hải Hà Phạm Văn Quân Nguyễn Thành Trung
Ngày phát hành 31/03/2023

Chi tiết

Cách trích dẫn
Tạ Thị Yến, Ninh Thị Hạnh, Vũ Thị Hải Hà, Phạm Văn Quân, Nguyễn Thành Trung. "Sự lưu hành vi khuẩn Clostridium perfringens và Clostridium difficile mang gen sinh độc tố cpa, tcdA trong thịt và rau ăn lá". Tạp chí Kiểm nghiệm và An toàn thực phẩm. tập 6 - số 1, pp. 83-99, 2023
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83-99
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341

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Tóm tắt

Chi Clostridium là các trực khuẩn Gram dương, sinh bào tử. Hầu hết các loài vi khuẩn Clostridia spp. thường xuất hiện trong đất, nước, xác thực vật, xác động vật, và đóng một phần quan trọng trong các quá trình phân huỷ các chất trong tự nhiên. Thực phẩm tươi có nguồn gốc động vật và thực vật có nhiều khả năng bị nhiễm bào tử hoặc tế bào sinh dưỡng thuộc chi Clostridium. Kết quả nghiên cứu ghi nhận tỉ lệ mẫu nhiễm thịt tươi và rau ăn lá thu thập tại các chợ thuộc Quận Đống Đa, Hà Đông, Hoàng Mai nhiễm Clostridium perfringens (C. perfringens) là 26,67% (n = 150) và 26,82% (n = 220). Tỉ lệ mẫu thịt và rau nhiễm Clostridium difficile (C. Difficile) là rất thấp với 6,0% (n = 150) và 0,9% (n = 220) mẫu thịt tươi và mẫu rau ăn lá tương ứng. Các phản ứng khuếch đại gen cho thấy sự hiện diện của gen cpa trong tất cả các chủng C. perfringens và phát hiện 2 chủng C. difficile mang gen tcdA.

Từ khóa:

Clostridium perfringens và Clostridium difficile, gen cpa, gen tcdA.

Trích dẫn

[1]. World Bank, “Vietnam food safety risks management : challenges and opportunities,” Washington, D.C. : World Bank Group, 2017.
[2]. General Statistics Office, “Statistical Yearbook,” 2019 (in Vietnamese). Address: https://www.gso.gov.vn/wp-content/uploads/2020/09/Nien-giam-thong-keday-du-2019.pdf.
[3]. Directorate for Standards, Metrology and Quality, “Vietnamese Standard TCVN 4991:2005 (ISO 7937:2004) on Microorganisms in food and animal feed - Quantitative method of Clostridium perfringens on agar plate - Counting technique colonies,” 2005 (in Vietnamese).
[4]. Directorate for Standards, Metrology and Quality, “Vietnam Standard TCVN 6404:2016 (ISO 7218: 2013) Microbiology of Food and Feed - General Requirements and Guidelines for Microbiological Testing,” 2016 (in Vietnamese).
[5]. E. Catherine, B. Burghoffer and F. Barbut, “Contamination of ready-to-eat raw vegetables with Clostridium difficile in France,” Journal of Medical Microbiology, vol. 62, pp. 1435-1438, 2013.
[6]. E. Catherine, B. Burghoffer, and F. Barbut, “Evaluation of the Chromogenic Agar chromID C. difficile,” Journal of Clinical Microbiology, vol. 51, no. 3, pp. 1002-1004, 2013.
[7]. Perry J. D., “A decade of development of chromogenic culture media for clinical microbiology in an era of molecular diagnostics,” Clinical Microbiology Review, 30, pp.449-479, 2017.
[8]. Vitek MS, “Manual Instruction,” 2017.
[9]. M. Mudassar, Z. Iqbal, A. Siddique, S. Liao, M. K. Farooq Salamat, N. Qi, A. M. Din, and M. Sun, “Prevalence, Genotypic and Phenotypic Characterization and Antibiotic Resistance Profile of Clostridium perfringens Type A and D Isolated from Feces of Sheep (Ovis aries) and Goats (Capra hircus) in Punjab, Pakistan,” Toxins, vol. 12, no. 657, 2020.
[10]. L. Lemee, A. Dhalluin, S. Testelin, M-A. Mattrat, K. Maillard, J-F. Lemeland, and J-L. Pons, “Multiplex PCR targeting tpi (triose phosphate isomerase), tcdA (Toxin A), and tcdB (Toxin B) genes for toxigenic culture of Clostridium difficile,” Journal of Clinical Microbiololgy, vol. 42, no. 12, pp. 5710-5714, 2004.
[11]. L. M. Wijnands, A. van der Mey - Florijn, E. D. - van Asch, “Clostridium perfringens associated food borne disease: Final report,” National Institute for Public Health and the Environment, Ministry of Health, Welfare and Sport, the Netherland, 2011.
[12]. H. Wen-Si, H. Kim, and O. K. Koo, “Molecular genotyping, biofilm formation and antibiotic resistance of enterotoxigenic Clostridium perfringens isolated from meat supplied to school cafeterias in South Korea,” Anaerobe, 2018.
[13]. M. Bendary Mahmoud, M. I. Abd El-Hamid, R. M. El-Tarabili, A. A. Hefny, R. M. Algendy, N. A. Elzohairy, M. M. Ghoneim, M. M. Al-Sanea, M. H. Nahari, and W. H. Moustafa, “Clostridium perfringens Associated with Foodborne Infections of Animal Origins: Insights into Prevalence, Antimicrobial Resistance, Toxin Genes Profiles, and Toxinotypes,” Biology, vol. 11, no. 551, 2022.
[14]. M. Yasuhiro, K. Miyamoto, I. Kaneko-Hirano, K. Fujiuchi, and S. Akimoto, “Prevalence and Characterization of Enterotoxin Gene-Carrying Clostridium perfringens Isolates from Retail Meat Products in Japan,” Applied and Environmental Microbiology, vol/. 74, no. 17, pp. 5366-5372, 2008.
[15]. H. S. Guran and G. Oksuztepe, “Detection and typing of Clostridium perfringens from retailchicken meat parts,” Letters in Applied Microbiology, vol. 57, pp. 77-82, 2013.
[16]. E. C. Emelda, F. O. Nwaokorie, A. O. Coker, M. J. Avila-Campos, R. L. Solis, L. A. Llanco, and F. T. Ogunsola, “Detection of toxigenic Clostridium perfringens and Clostridium botulinum from food sold in Lagos, Nigeria,” Anaerobe, vol. 42, pp. 176-181, 2016.
[17]. J. Yanfen, Y. Ma, Q. Liu, T. Li, Y. Li, K. Guo, and Y. Zhang, “Tracing Clostridium perfringens strains from beef processing of slaughter house by pulsed-field gel electrophoresis, and the distribution and toxinotype of isolates in Shaanxi province, China,” Food Microbiology, vol. 101, pp. 1-10, 2022.
[18]. A. Issimov, T. Baibatyrov, A. Tayeva, S. Kenenbay, S. Abzhanova, G. Shambulova, G. Kuzembayeva, M. Kozhakhiyeva, I. Brel-Kisseleva, O. Safronova, B. Lyailya, Y. Gulzhan, B. Kainar, K. Alma, and F. A. Uzal, “Prevalence of Clostridium perfringens and Detection of its Toxins in Meat Products in Selected Areas of West Kazakhstan,” Agriculture, vol. 12, no. 1357, pp. 1-6, 2022.
[19]. A. Masoumeh, B. Nadalian, H. Alavifard, S. N. Panirani, S. M. Vand Bonab, F. Azimirad, F. Gholami, P. Jabbari, A. Yadegar, L. Busani, H. A. Aghdaei, M. R. Zali, “Microbiological survey and occurrence of bacterial foodborne pathogens in raw and ready-to-eat green leafy vegetables marketed in Tehran, Iran,” International Journal of Hygiene and Environmental Health, vol. 237, no. 113824, pp. 1-9, 2021.
[20]. S. Ghorchian, M. Douraghi, A. Rahimiforoushani, M. M. Soltan Dallal, “Isolation and identification of cpe-positive Clostridium perfringens in bulk and packed dehydrated vegetables,” Razi Journal of Medical Science, vol. 26, no. 8, pp. 23-30, 2021.
[21]. H. Atsushi, H. Suzuki, and K. Oonaka, “Prevalence of cpe-positive Clostridium perfringens in surface-attached soil of commercially available potatoes and its significance as a potential source of food poisoning,” Anaerobe, vol. 79, no. 102687, 2023.
[22]. A. A. Mahamat, “Characterization of Clostridium perfringens strains for the investigation of food poisoning outbreaks in France,” Foodborn Pathogens and Whole Genome Sequencing Joint Conference, 26-28 March, 2019.
[23]. L. Tingting, H. Bian, Z. Sun, X. Wang, F. Liu, and D. Wang, "Inactivation of clostridium perfringens C1 spores by the combination of mild heat and lactic acid," Foods, vol. 11, no. 23, 2022.
[24]. K. T. Onur, T. Uyanik, S. Kanat, Ö. Çadirci, and A. Gücükoğlu, “Detection of Clostridium perfringens and determination of enterotoxin genes (cpa and cpe) in traditional turkish chicken doner kebab,” Ankara Univ Vet Fak Derg, no. 69, pp. 117-122, 2020.
[25]. L. Yuan-Tong and R. Labbe, “Enterotoxigenicity and Genetic Relatedness of Clostridium perfringens Isolates from Retail Foods in the United States,” Applied And Environmental Microbiology, vol. 69, no. 3, pp. 1642-1646, 2003.
[26]. Tham Thi Nguyen, Hung Vu-Khac and Tan Duc Nguyen, “Isolation and characterization of Clostridium perfringens strains isolated from ostriches (Struthio camelus) in Vietnam,” Veterinary World, vol. 13, no. 8, pp. 1679-1684, 2020.
[27]. C. Rodriguez, B. Taminiau, J. Van Broeck, M. Delme´e, and G. Daube, “Clostridium difficile in Food and Animals: A Comprehensive Review,” Advances in Experimental Medicine and Biology, 2016.
[28]. A. Rodriguez-Palacios, C. Pickworth, S. Loerch, and JT. LeJeune, “Transient fecal shedding and limited animal-to-animal transmission of Clostridium difficile by naturally infected finishing feedlot cattle,” Applied and Environmental Microbiology, vol. 77, pp. 3391-3397, 2011.
[29]. P. Hawken, J. S. Weese, R. Friendship, and K. Warriner, “Carriage and dissemination of Clostridium difficile and methicillin resistant Staphylococcus aureus in pork processing,” Food Control, no. 31, pp. 433-437, 2013.
[30]. S. Bouttier, M-C. Barc, B. Felix, S.Lambert, A. Collignon, and F. Barbut, “Clostridium difficile in Ground Meat, France,” Emerging Infectious Diseases, vol. 16, no. 4, 2010.
[31]. A. Rodriguez-Palacios, S. Borgmann, T. R. Kline, “Clostridium difficile in foods and animals: history and measures to reduce exposure,” Animal Health Research Reviews, vol. 14, pp. 11-29, 2013.
[32]. R. Ebrahim, M. Jalali, and J. S.Weese, “Prevalence of Clostridium difficile in raw beef, cow, sheep, goat, camel and buffalo meat in Iran,” BMC Public Health 14, 2014.
[33]. K. Muratoglu, E. Akkaya1, H. Hampikyan, E. Baris Bingol, O. Cetin, and H. Colak, “Detection, Characterization and Antibiotic Susceptibility of Clostridioides (Clostridium) difficile in Meat Products,” Food Science and Animal. Resources, vol. 40, no. 4, pp.578-587, 2020.
[34]. K. Malihe, S. Jalilian, A. Alvandi, and R.Abiri, “Prevalence of Clostridium difficile and its toxigenic genotype in beef samples in west of Iran,” IJM Iranian Journal of Microbiology, vol. 9, no. 3, pp. 169-173, 2017.
[35]. S. Di Bella, P. Ascenzi, S. Siarakas, N. Petrosillo, and A. di Masi, “Clostridium difficile Toxins A and B: Insights into Pathogenic Properties and Extraintestinal Effects,” Toxins, vol. 8, no. 134, 2016.

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