Journals / Turkish Journal of Veterinary and Animal Sciences / 2005 / Cilt: 29 - Sayı: 5

İlk izolasyon aşamasında escherichia coli 0157' nin şüpheli identifikasyonu amacıyla salisin-Ramnoz-Sellobiyoz-4-Metilumbelliferil-Beta-D Glukuronit-sorbitol MacConkey (SRC-MUG-SMAC) ayırıcı katı besiyerinin kullanılması

Use of salicin-rhamnose-cellobiose-4-methylumbelliferyl-Beta-D Glucuronide-sorbitol MacConkey (SRC-MUG-SMAC) differential agar for the presumptive identification of Escherichia coli 0157 from the primary isolation step

Pages
1137–1141
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

As a result, the testing of presumptive E. coli O157 colonies using a differential agar plate including MUG and 3 (or more) sugars that are not fermented by this organism is a rapid, easy, precise and relatively inexpensive isolation procedure, and it is particularly ideal for use in routine screening laboratories.

📌 3 Key Takeaways

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Objective & Hypothesis:A differential agar for the further detection of presumptive Escherichia coli O157 strains among typical sorbitol negative and cefixime-tellurite resistant strains was investigated.
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Key Findings & Data:For this purpose, in parallel to colonies of 8 reference strains, 1130 suspect colonies picked from the surface of cefixime-tellurite (CT)-sorbitol MacConkey (SMAC) (CT-SMAC) agar plates of food samples (white cheese, raw milk and ground beef) were transferred to differential agar plates.
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Conclusion & Impact:As a result, the testing of presumptive E. coli O157 colonies using a differential agar plate including MUG and 3 (or more) sugars that are not fermented by this organism is a rapid, easy, precise and relatively inexpensive isolation procedure, and it is particularly ideal for use in routine screening laboratories.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

A differential agar for the further detection of presumptive Escherichia coli O157 strains among typical sorbitol negative and cefixime-tellurite resistant strains was investigated. For this purpose, in parallel to colonies of 8 reference strains, 1130 suspect colonies picked from the surface of cefixime-tellurite (CT)-sorbitol MacConkey (SMAC) (CT-SMAC) agar plates of food samples (white cheese, raw milk and ground beef) were transferred to differential agar plates. After a 6-h incubation period at 42 ºC, only 47 (4.15%) of the 1130 colonies appeared as typical E. coli O157 on the differential agar plates (100 x 15 mm) gridded into 25 numbered sections. Salicin (S), rhamnose (R) and cellobiose (C) were tested separately and together in combination with MUG. The best results were obtained from the combined use of the 3 in SMAC medium (SRC-MUG-SMAC). When violet red bile lactose agar (VL) was used in the same manner as SRC-MUG-SMAC, only 16 (1.41%) of the 1130 colonies remained typical. In this procedure, no biochemical test was required for further identification. The use of an SRC-MUG-SMAC plate immediately after the colony selection step appeared to be more discriminative than the addition of these sugars and MUG to the primary isolation media. As a result, the testing of presumptive E. coli O157 colonies using a differential agar plate including MUG and 3 (or more) sugars that are not fermented by this organism is a rapid, easy, precise and relatively inexpensive isolation procedure, and it is particularly ideal for use in routine screening laboratories.

Özet

Bu çalışmada, sorbitoi negatif ve sefiksim-tellurite dirençli tipik suşlar arasından şüpheli Escherichia coli 0157 suşlarının izolasyonu için bir ayırıcı katı besiyeri araştırıldı. Bu amaç için, 8 referans suş kolonisine paralel olarak gıda örneklerine (beyaz peynir, çiğ süt ve kıyma) ait sefiksim-tellurit (CT) içeren sorbitoi MacConkey (CT-SMAC) besiyeri yüzeyinden seçilen 1130 şüpheli koloni ayırıcı katı besiyerine transfer edildi. Şalisin (S), ramnoz (R), sellobiyoz (C) hem ayrı ayrı, hem de üçü birlikte MUG ile kombine edilerek test edildi. SRC ve MUG içeren ve dıştan çizimle 25 numaralı bölmeye ayrılan ayırıcı katı besiyeri (SRC-MUG-SMAC) plaklarının (100 x 15 mm) 42 °C'de 6 saat inkübasyonundan sonra, 1130 susun sadece 47 (% 4,15)'sinin tipik E. Coli O157 özelliği gösterdiği gözlendi. Violet red bile lactose agar (VL) aynı tarzda kullanıldığında ise 1130 susun sadece 16 (% 1,41)'sı tipik özellik gösterdi. Bu prosedürde ileri identifikasyon için başka bir biyokimyasal teste ihtiyaç duyulmadı. Koloni seçim aşamasında SRC-MUG-SMAC katı besiyerinin kullanılmasının ilk izolasyon katı besiyerlerine bu şekerlerin ve MUG'un katılmasına kıyasla daha ayırıcı olduğu görüldü. Sonuç olarak, şüpheli E. coli 0157 identiftkasyonunda MUG ile birlikte susun fermente edemediği 3 veya daha fazla şeker içeren bir ayırıcı agar plağı kullanmanın hızlı, kolay, kesin ve göreceli olarak ucuz olması nedeniyle özellikle rutin tarama laboratuarları için ideal olduğu görüldü.

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Cite This Article

VATANSEVER, L., GÜLMEZ, M., SEZER, Ç., GÜVEN, A., DUMAN, B. (2022). İlk izolasyon aşamasında escherichia coli 0157' nin şüpheli identifikasyonu amacıyla salisin-Ramnoz-Sellobiyoz-4-Metilumbelliferil-Beta-D Glukuronit-sorbitol MacConkey (SRC-MUG-SMAC) ayırıcı katı besiyerinin kullanılması. Turkish Journal of Veterinary and Animal Sciences, Cilt: 29 - Sayı: 5, 1137–1141. https://ajindex.com/articles/615495

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References (12)

  1. MacRae, M., Rebate, T., Johnston, M., Ogden, I.D.: The sensitivity of Escherichia coli 0157 to some antimicrobials by conventional and conductance assays. Lett. Appl. Microbiol., 1997; 25: 135-137
  2. Blais, B.W., Booth, R.A., Phillippe, L.M., Yamazaki, H.: Effect of temperature and agitation on enrichment of Escherichia coli 0157:H7 in ground beef using modified EC broth with novobiocin. Int. J. Food Microbiol., 1997; 36: 221-225
  3. Chapman, P.A.: Methods available for the detection of Escherichia coli 0157 in clinical, food and environmental samples. World J. Microbiol. Biotechnol., 2000; 16: 733-740
  4. Johnson, J.L., Brooke, C.L., Fristchel, S.J.: Comparison of the BAX for screening/E. coli 0157:H7 method with conventional methods for detection of extremely low levels of Escherichia coli 0157:H7 in ground beef. Appl. Environ. Microbiol., 1998; 64: 4390-4395
  5. Fujisawa, T., Sata, S., Aikawa, K., Takahashi, T., Yamai, S., Shimada, T: Evaluation of sorbitol-salicin MacConkey medium containing cefixime and tellurite (CT-SSMAC medium) for isolation of Escherichia coli 0157:H7 from raw vegetables. Int. J. Food Microbiol., 2002; 74: 161-163
  6. Ratnam, S., March, S.B., Ahmed, R., Bezanson, G.S., Kasatiya, S.: Characterization of Escherichia coli serotype 0157:H7. J. Clin. Microbiol., 1988: 26: 2006-2012
  7. Chapman, P.A., Siddons, C.A., Zadik, P.M., Jewes, L.: An improved selective medium for the isolation of Escherichia coli 0157. J. Med. Microbiol., 1991; 35: 107-110
  8. Hitchins, A.D., Feng, P., Watkins, W.D., Rippey, S.R. Chandler, L.A.: Bacteriological Analytical Manual, Edition 8, Revision A, Chapter 4. U.S. Food & Drug Administration Center for Food Safety & Applied Nutrition. 1998
  9. Leclercq, A., Lambert, B., Pierard, D., Mahillon, J.: Particular biochemical profiles for enterohemorrhagic Escherichia coli 0157:H7 isolates on the ID 32E system. J. Clin. Microbiol., 2001; 39: 1161-1164
  10. Thompson, J.S., Hodge, D.S., Smith, D.E., Yong, Y.A.: Use of tri- gas incubator for routine culture of Campylobacter species from fecal specimens. J. Clin. Microbiol., 1990; 28: 2802-2803
  11. Fujisawa, T., Sata, S., Aikawa, K., Takahashi, T., Yamai, S., Shimada, T.: Modification of sorbitol MacConkey medium containing cefixime and tellurite for isolation of Escherichia coli 0157:H7 from radish sprouts. Appl. Environ. Microbiol., 2000; 66:3117-3118
  12. Okrend. A.J.G., Rose, B.E., Lattuada, C.P.: Use of 5-bromo-4- chloro-3-indoxyl-b-D- glucuronide in MacCon