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Fiziksel ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri

Yıl 2018, , 149 - 153, 27.12.2018
https://doi.org/10.31196/huvfd.508964

Öz

DNA virusları tamir mekanizmaları ve RNA viruslarına
göre daha stabil olmaları sayesinde çevre şartlarına dirençli bir yapı
gösterirler. Sahip oldukları bu direnç mutasyonel değişiklikleri elimine
ederek, virusun korunmuş bölgelerinin kolaylıkla amplifikasyonu sağlamasına
rağmen, uygun olmayan laboratuvar koşulları ve inhibe edici ajanlar, viral DNA
tespitine engel olabilmektedir. Viral DNA eldesinde çeşitli yöntemlerin
karşılaştırılmasının yapıldığı bu çalışmada aynı zamanda farklı fiziksel ve
kimyasal koşulların viral nükleik asite olan etkileri de sorgulandı. Bu amaçla
biri konvansiyonel metot olmak üzere toplam dört farklı ekstraksiyon yöntemi
bir parapoxvirus olan ecythma contagiosumun DNA’sını tespit amacıyla kullanıldı.
Elde edilen DNA’lar verimlilikleri yönünden kıyaslandıktan sonra çeşitli
fiziksel (basınç, UV) ve kimyasal (deterjan) koşullara maruz bırakıldı. Basınçlı
buhar otoklavına maruziyetten sonra viral DNA amplifikasyonu gerçekleşirken;
tween 20 ve uv radyasyon viral DNA amplifikasyonu inhibe ettiler. Ticari kitlerin
çoğu DNA ekstraksiyonunun süresini kısaltmaya yardımcı olurken konvansiyonel
yöntem viral DNA tespiti açısından en yüksek verimliliği sağladı.

Kaynakça

  • Akkutay-Yoldar Z, Oguzoglu TC, Akça Y, 2016: Diagnosis and phylogenetic analysis of orf virus in Aleppo and Saanen goats from an outbreak in Turkey. Virol Sin, 31(3), 270-273.
  • Arnal C, Ferre-Aubineau V, Besse B, Mignotte B, Schwartzbrod L, Billaudel S, 1999: Comparison of seven RNA extraction methods on stool and shellfish samples prior to hepatitis A virus amplification. J Virol Methods, 77(1), 17-26.
  • Besaratinia A, Pfeifer GP, 2012: Measuring the formation and repair of UV damage at the DNA sequence level by ligation-mediated PCR. In “DNA Repair Protocols”, Ed; Bjergbaek, L, Humana Press, Totowa, NJ, pp. 189-202.
  • Bickley JA, Hopkins DA, 1999: Inhibitors and enhancers of PCR. In “Analytical Molecular Biology: quality and validation”, Ed; Saunders GC and Parkers HC., pp.81-102.
  • Chacon-Cortes D, Griffiths LR, 2014: Methods for extracting genomic DNA from whole blood samples: current perspectives. J Biorep Sci App Med, 2, 1-9.
  • Choi WS, Rodríguez RA, Sobsey MD, 2014: Persistence of viral genomes after autoclaving. J Virol Methods, 198, 37-40.
  • Deng MY, Wang H, Ward GB, Beckham TR, McKenna TS, 2005: Comparison of six RNA extraction methods for the detection of classical swine fever virus by real-time and conventional reverse transcription–PCR. J Vet Diagn Invest, 17(6), 574-578.
  • Eischeid AC, Meyer JN, Linden KG, 2009: UV disinfection of adenoviruses: molecular indications of DNA damage efficiency. Appl Environ Microbiol, 75(1), 23-28.
  • Eskandani M, Hamishehkar H, Ezzati Nazhad Dolatabadi J, 2013: Cyto/Genotoxicity study of polyoxyethylene (20) sorbitan monolaurate (tween 20). DNA Cell Biol, 32(9), 498-503.
  • Inoshima Y, Morooka A, Sentsui H, 2000: Detection and diagnosis of parapoxvirus by the polymerase chain reaction. J Virol Methods, 84, 201–208.
  • Knowles DP, 2011: Poxviridae. In “Fenner's Veterinary Virology”, 4th Eds., Academic Press, Elsevier, Ed; N. Maclachlan N, Dubovi EJ, pp. 151-65.
  • Murphy FA, Gibbs EPJ, Horzinek MC, Studdert MJ, 1999: Veterinary Virology. Third ed. San Diego: Academic Press, pp. 335-342.
  • Reha-Krantz LJ, 2010: DNA polymerase proofreading: Multiple roles maintain genome stability. Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics, 1804(5), 1049-1063.
  • Sambrook J, Russell DW, 2001: Molecular cloning: a laboratory manual. Cold Spring Harbor: Cold Spring Harbor Laboratory Press.
  • Scherer K, Johne R, Schrader C, Ellerbroek L, Schulenburg J, Klein G, 2010: Comparison of two extraction methods for viruses in food and application in a norovirus gastroenteritis outbreak. J Virol Methods, 169(1), 22-27.
  • Skinner MA, Buller RM, Damon IK, Lefkowitz EJ, McFadden G, Mc Innes CJ, Mercer AA, Moyer RW, Upton C, 2012: Poxviridae. In: Virus taxonomy: classification and nomenclature of viruses: Ninth Report of the International Committee on Taxonomy of Viruses. King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ (Eds.), Elsevier Academic Press, San Diego, pp. 291-309.
  • Wilson IG, 1997: Inhibition and facilitation of nucleic acid amplification. Appl Environ Microbiol, 63(10), 3741.
  • Xin Z, Velten JP, Oliver MJ, Burke JJ, 2003: High-throughput DNA extraction method suitable for PCR. Biotechniques, 34(4), 820-827.
  • Zimmer C, 2015: A planet of viruses. University of Chicago Press, pp. 1-30.

The Effects of Physical and Chemical Conditions on Viral DNA Obtained by Various Methods

Yıl 2018, , 149 - 153, 27.12.2018
https://doi.org/10.31196/huvfd.508964

Öz

DNA viruses are more resistant to environmental
conditions than RNA viruses due to their repair mechanisms and stablity of
their genetic material. Despite these advantages, inadequate laboratory
conditions and inhibitory agents can interfere with viral DNA detection. In
this study, which compares various methods of viral DNA obtainment, the effects
of different physical and chemical conditions on viral nucleic acid were also
questioned. For this purpose, a total of four different extraction methods, one
of which was the conventional method, have been used to detect the DNA of the
parapox virus causing ecythma contagiosum. The isolated DNAs were exposed to
various physical (pressure, uv) and chemical treatment (detergent) conditions before
PCR amplification. While viral DNA amplification occured after exposure to autoclave
pressure steam sterilizer; Tween 20 and UV radiation inhibited viral DNA amplification.
While most commercial kits helped to shorten the duration of DNA extraction,
the conventional method provided the highest efficiency for viral DNA
detection.

Kaynakça

  • Akkutay-Yoldar Z, Oguzoglu TC, Akça Y, 2016: Diagnosis and phylogenetic analysis of orf virus in Aleppo and Saanen goats from an outbreak in Turkey. Virol Sin, 31(3), 270-273.
  • Arnal C, Ferre-Aubineau V, Besse B, Mignotte B, Schwartzbrod L, Billaudel S, 1999: Comparison of seven RNA extraction methods on stool and shellfish samples prior to hepatitis A virus amplification. J Virol Methods, 77(1), 17-26.
  • Besaratinia A, Pfeifer GP, 2012: Measuring the formation and repair of UV damage at the DNA sequence level by ligation-mediated PCR. In “DNA Repair Protocols”, Ed; Bjergbaek, L, Humana Press, Totowa, NJ, pp. 189-202.
  • Bickley JA, Hopkins DA, 1999: Inhibitors and enhancers of PCR. In “Analytical Molecular Biology: quality and validation”, Ed; Saunders GC and Parkers HC., pp.81-102.
  • Chacon-Cortes D, Griffiths LR, 2014: Methods for extracting genomic DNA from whole blood samples: current perspectives. J Biorep Sci App Med, 2, 1-9.
  • Choi WS, Rodríguez RA, Sobsey MD, 2014: Persistence of viral genomes after autoclaving. J Virol Methods, 198, 37-40.
  • Deng MY, Wang H, Ward GB, Beckham TR, McKenna TS, 2005: Comparison of six RNA extraction methods for the detection of classical swine fever virus by real-time and conventional reverse transcription–PCR. J Vet Diagn Invest, 17(6), 574-578.
  • Eischeid AC, Meyer JN, Linden KG, 2009: UV disinfection of adenoviruses: molecular indications of DNA damage efficiency. Appl Environ Microbiol, 75(1), 23-28.
  • Eskandani M, Hamishehkar H, Ezzati Nazhad Dolatabadi J, 2013: Cyto/Genotoxicity study of polyoxyethylene (20) sorbitan monolaurate (tween 20). DNA Cell Biol, 32(9), 498-503.
  • Inoshima Y, Morooka A, Sentsui H, 2000: Detection and diagnosis of parapoxvirus by the polymerase chain reaction. J Virol Methods, 84, 201–208.
  • Knowles DP, 2011: Poxviridae. In “Fenner's Veterinary Virology”, 4th Eds., Academic Press, Elsevier, Ed; N. Maclachlan N, Dubovi EJ, pp. 151-65.
  • Murphy FA, Gibbs EPJ, Horzinek MC, Studdert MJ, 1999: Veterinary Virology. Third ed. San Diego: Academic Press, pp. 335-342.
  • Reha-Krantz LJ, 2010: DNA polymerase proofreading: Multiple roles maintain genome stability. Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics, 1804(5), 1049-1063.
  • Sambrook J, Russell DW, 2001: Molecular cloning: a laboratory manual. Cold Spring Harbor: Cold Spring Harbor Laboratory Press.
  • Scherer K, Johne R, Schrader C, Ellerbroek L, Schulenburg J, Klein G, 2010: Comparison of two extraction methods for viruses in food and application in a norovirus gastroenteritis outbreak. J Virol Methods, 169(1), 22-27.
  • Skinner MA, Buller RM, Damon IK, Lefkowitz EJ, McFadden G, Mc Innes CJ, Mercer AA, Moyer RW, Upton C, 2012: Poxviridae. In: Virus taxonomy: classification and nomenclature of viruses: Ninth Report of the International Committee on Taxonomy of Viruses. King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ (Eds.), Elsevier Academic Press, San Diego, pp. 291-309.
  • Wilson IG, 1997: Inhibition and facilitation of nucleic acid amplification. Appl Environ Microbiol, 63(10), 3741.
  • Xin Z, Velten JP, Oliver MJ, Burke JJ, 2003: High-throughput DNA extraction method suitable for PCR. Biotechniques, 34(4), 820-827.
  • Zimmer C, 2015: A planet of viruses. University of Chicago Press, pp. 1-30.
Toplam 19 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Araştıma
Yazarlar

Zeynep Akkutay Yoldar Bu kişi benim

Yayımlanma Tarihi 27 Aralık 2018
Gönderilme Tarihi 30 Nisan 2018
Kabul Tarihi 19 Kasım 2018
Yayımlandığı Sayı Yıl 2018

Kaynak Göster

APA Akkutay Yoldar, Z. (2018). Fiziksel ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri. Harran Üniversitesi Veteriner Fakültesi Dergisi, 7(2), 149-153. https://doi.org/10.31196/huvfd.508964
AMA Akkutay Yoldar Z. Fiziksel ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri. Harran Univ Vet Fak Derg. Aralık 2018;7(2):149-153. doi:10.31196/huvfd.508964
Chicago Akkutay Yoldar, Zeynep. “Fiziksel Ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri”. Harran Üniversitesi Veteriner Fakültesi Dergisi 7, sy. 2 (Aralık 2018): 149-53. https://doi.org/10.31196/huvfd.508964.
EndNote Akkutay Yoldar Z (01 Aralık 2018) Fiziksel ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri. Harran Üniversitesi Veteriner Fakültesi Dergisi 7 2 149–153.
IEEE Z. Akkutay Yoldar, “Fiziksel ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri”, Harran Univ Vet Fak Derg, c. 7, sy. 2, ss. 149–153, 2018, doi: 10.31196/huvfd.508964.
ISNAD Akkutay Yoldar, Zeynep. “Fiziksel Ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri”. Harran Üniversitesi Veteriner Fakültesi Dergisi 7/2 (Aralık 2018), 149-153. https://doi.org/10.31196/huvfd.508964.
JAMA Akkutay Yoldar Z. Fiziksel ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri. Harran Univ Vet Fak Derg. 2018;7:149–153.
MLA Akkutay Yoldar, Zeynep. “Fiziksel Ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri”. Harran Üniversitesi Veteriner Fakültesi Dergisi, c. 7, sy. 2, 2018, ss. 149-53, doi:10.31196/huvfd.508964.
Vancouver Akkutay Yoldar Z. Fiziksel ve Kimyasal Koşulların Çeşitli Yöntemlerle Elde Edilmiş Viral DNA’ya Etkileri. Harran Univ Vet Fak Derg. 2018;7(2):149-53.