Journals / Turkish Journal of Agriculture and Forestry / 2005 / Cilt: 29 - Sayı: 4

Apple Chlorotic Leaf Spot Virus (ACLSV) Status in Turkey and Sensitive Detection Using Advanced Techniques

Pages
251–257
Publication Date
2005-04-01
DOI
—
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AI Summary & Key Takeaways

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

The successful application of RT-PCR and IC-RT-PCR for the accurate and sensitive detection of ACLSV was reported in stone fruit trees in Turkey.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The prevalence of apple chlorotic leaf spot virus (ACLSV) was investigated in all the main stone fruit growing areas of Turkey except for East Anatolia.
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Key Findings & Data:Thirteen samples were detected as infected with ACLSV using ELISA while RT-PCR revealed 51 positive samples.
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Conclusion & Impact:The successful application of RT-PCR and IC-RT-PCR for the accurate and sensitive detection of ACLSV was reported in stone fruit trees in Turkey.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Apple chlorotic leaf spot virus · Reverse transcription-polymerase chain reaction · Turkey

Abstract

The prevalence of apple chlorotic leaf spot virus (ACLSV) was investigated in all the main stone fruit growing areas of Turkey except for East Anatolia. Three hundred and sixty-nine plant samples showing virus related symptoms were collected from sweet and sour cherry, peach, nectarine, apricot and plum trees. All samples were tested using DAS-ELISA and reverse transcription-polymerase chain reaction (RT-PCR). Thirteen samples were detected as infected with ACLSV using ELISA while RT-PCR revealed 51 positive samples. The highest ACLSV incidence was in Bursa (64%), followed by Yalova (20.51%), Burdur (18.18%), Amasya (13.43%), Afyon (12.07%), Isparta (6.25%), Çanakkale (4.76%) and İzmir (2.72%). Among the collected stone fruit species, nectarine was the most infected species, followed by apricot, peach, sour cherry, plum and sweet cherry. Some ACLSV isolates were used for the adoption of an immuno capture (IC) RT-PCR system. ACLSV infected plant sap diluted up to 1:10 was detected by IC-RT-PCR. The successful application of RT-PCR and IC-RT-PCR for the accurate and sensitive detection of ACLSV was reported in stone fruit trees in Turkey.

Özet

The prevalence of apple chlorotic leaf spot virus (ACLSV) was investigated in all the main stone fruit growing areas of Turkey except for East Anatolia. Three hundred and sixty-nine plant samples showing virus related symptoms were collected from sweet and sour cherry, peach, nectarine, apricot and plum trees. All samples were tested using DAS-ELISA and reverse transcription-polymerase chain reaction (RT-PCR). Thirteen samples were detected as infected with ACLSV using ELISA while RT-PCR revealed 51 positive samples. The highest ACLSV incidence was in Bursa (64%), followed by Yalova (20.51%), Burdur (18.18%), Amasya (13.43%), Afyon (12.07%), Isparta (6.25%), Çanakkale (4.76%) and İzmir (2.72%). Among the collected stone fruit species, nectarine was the most infected species, followed by apricot, peach, sour cherry, plum and sweet cherry. Some ACLSV isolates were used for the adoption of an immuno capture (IC) RT-PCR system. ACLSV infected plant sap diluted up to 1:10 was detected by IC-RT-PCR. The successful application of RT-PCR and IC-RT-PCR for the accurate and sensitive detection of ACLSV was reported in stone fruit trees in Turkey.

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Cite This Article

ULUBAŞ, Ç., ERTUNÇ, F. (2005). Apple Chlorotic Leaf Spot Virus (ACLSV) Status in Turkey and Sensitive Detection Using Advanced Techniques. Turkish Journal of Agriculture and Forestry, Cilt: 29 - Sayı: 4, 251–257. https://ajindex.com/articles/179779

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References (10)

  1. Brunt, H.A., K. Crabtree, M.J. Dallawitz, A.J. Gibbs and L. Watson. 1996.
  2. Viruses of plants. CAB International, Cambridge, UK. Ça¤layan Yildizgördü, K. and S. Çal›. 1994. Occurrence and detection of virus and virus like diseases of plum and apricot trees in the East Mediterranean. In: Proc. of 9th Cong. of the Mediter. Phytopath. Union. Sept. 18-24, Kufladas›-Ayd›n Türkiye. 551-553. Ça¤layan, K., and M.H. Gazel. 1998. Virus and virus-like diseases of stone fruits in the Eastern Mediterranean area of Turkey (Eds: A. Hadidi). Proc. 17th Int. Symp. on Fruit Tree Virus Diseases, Acta Hort. 472: 527-529.
  3. Candresse, T., M. Lanneau, F. Revers, N. Grasseau, G. Macquaire, S. German, T. Malinowski and J. Dunez. 1995. An immuno-capture PCR assay adapted to the detection and the analysis of the molecular variability of the apple chlorotic leaf spot virus. Acta Hort. 386: 136-147.
  4. Cieslinska, M., T. Malinowski and B.J. Zawadzka. 1995. Studies on several strains of apple chlorotic leaf spot virus (ACLSV) isolated from different fruit tree species. Acta Hort. 386: 63-71.
  5. Desvignes, J.C. and R. Boye. 1989. Different diseases caused by chlorotic leaf spot virus on the fruit trees. Acta Hort. 235: 31-38.
  6. Dunez, J. 1986. Preliminary observations on virus and virus like diseases of stone fruit trees in Mediterranean and Near East countries. FAO Plant Protection Bulletin, 34: 43-48. Elibüyük, ‹.Ö. 1998. Malatya ilinde yetifltirilen sert çekirdekli meyve a¤açlar›ndaki virusler›n tan›lanmas› üzerinde araflt›rmalar. Doktora tezi, Ankara Üniversitesi, Fen Bilimleri Enstitüsü, pp 120, Ankara.
  7. Fidan, Ü. and S. Özdemir. 1998. Kiraz a¤açlar›nda görülen virüslerin DAS-ELISA ile belirlenmesi. Zirai Mücadele Araflt›rma Enstitüsü, Bornova/‹zmir. German S., T. Candresse, M. Lanneau and J. Dunez. 1992. Genomic organisation of apple chlorotic leaf spot closterovirus (ACLSV). Acta Hort. 309: 31-8.
  8. German, S., T. Candresse, M. Lanneau, J.C. Huet, J.C. Pernollet and J. Dunez. 1990. Nucleotide sequence and genomic organisation of apple chlorotic leaf spot virus. Virology 179: 104-112.
  9. Helguera, P.R., D.M. Docampo, F. Nome and D.A. Ducasse. 2002. Enhanced detection of Prune dwarf virus in peach leaves by immunocapture-reverse transcription-polymerase chain reaction with nested polymerase chain reaction (IC-RT-PCR nested PCR). J. Phytopathology 150: 94-96.
  10. Helguera, P.R., T. Taborda, D.M. Docampo and D.A. Ducasse. 2001. Immuno capture reverse transcription-polymerase chain reaction combined with