Authors:
K. Gopal A. N. G. R. Agricultural University All India Coordinated Research Project on Tropical Fruits (Citrus) Tirupati 517 502 Andhra Pradesh India

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E. Pradeepthi A. N. G. R. Agricultural University All India Coordinated Research Project on Tropical Fruits (Citrus) Tirupati 517 502 Andhra Pradesh India

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V. Gopi A. N. G. R. Agricultural University All India Coordinated Research Project on Tropical Fruits (Citrus) Tirupati 517 502 Andhra Pradesh India

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S. Khayum Ahammed A. N. G. R. Agricultural University All India Coordinated Research Project on Tropical Fruits (Citrus) Tirupati 517 502 Andhra Pradesh India

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Y. Sreenivasulu A. N. G. R. Agricultural University All India Coordinated Research Project on Tropical Fruits (Citrus) Tirupati 517 502 Andhra Pradesh India

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M. Reddy Indian Institute of Horticultural Research Hessaragatta lake post Bangalore 560 089 India

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V. Baranwal India Agricultural Research Institute Advanced Centre for Plant Virology Pusa, New Delhi 110 012 India

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K. Purushotham A. N. G. R. Agricultural University All India Coordinated Research Project on Tropical Fruits (Citrus) Tirupati 517 502 Andhra Pradesh India

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Huanglongbing (HLB), previously known as citrus greening disease (CGD) is one of the most destructive disease of citrus and responsible for decline of citrus orchards in Andhra Pradesh (A. P) and other citrus growing areas in the country. A preliminary survey on prevalence of HLB associated with citrus was carried out in three major sweet orange growing districts of A. P and the results revealed that a high incidence of 14.5% was recorded in Prakasam district followed by Kadapa (13.18%) and Nellore (12.59%). The DNA extracted from different plant parts of acidlime, i.e. bark, midrib, vein and lamina by CTAB and SS Tris-EDTA methods were subjected to PCR amplification. An amplification product of 1150 bp was observed in bark, midrib and vein. However, no amplification was observed in leaf lamina. Between CTAB and SS Tris-EDTA method, DNA from SS Tris-EDTA method yielded bright band compared to CTAB method. Detection of HLB in sweet orange was done from December 2004 to April 2005 at fortnight interval. It was observed that an excellent amplification product of 1150 bp was observed from December 2004 to February 2005. From March onwards a mild amplification of 1150 bp was observed in both the methods. So it can be concluded that winter season will be the suitable period for detection of the pathogen. Between these two methods of DNA extraction CTAB method was useful for detection of HLB in midrib and veins while SS Tris-EDTA method was useful for detection in bark of sweet orange.

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Editor-in-Chief

Jenő KONTSCHÁN Centre for Agricultural Research, Hungary

Technical Editor

Ágnes TURÓCI Centre for Agricultural Research, Hungary

Section Editor

K SALÁNKI Centre for Agricultural Research, Hungary
 

Editorial Board

Z BOZSÓ Centre for Agricultural Research, Hungary
PE CHETVERIKOV Saint-Petersburg State University, Russia
JX CUI Henan Institute of Science and Technology, China
J FODOR Centre for Agricultural Research, Hungary
Z IMREI Centre for Agricultural Research, Hungary
BM KAYDAN Çukurova University, Turkey
L KISS University of Southern Queensland, Australia
V MARKÓ Hungarian University of Agriculture and Life Sciences, Hungary
MW NEGM Ibaraki University, Japan
L PALKOVICS Széchenyi István University, Hungary
M POGÁNY Centre for Agricultural Research, Hungary
D RÉDEI National Chung Hsing University, Taiwan
A TOLSTIKOV University of Tyumen, Russia
J VUTS Rothamsted Research, UK
GQ WANG Guangxi University, China

Acta Phytopathologica et Entomologica Hungarica
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2024  
Scopus  
CiteScore  
CiteScore rank  
SNIP  
Scimago  
SJR index 0.188
SJR Q rank Q4

2023  
Scopus  
CiteScore 1.1
CiteScore rank Q4 (Insect Science)
SNIP 0.279
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SJR index 0.22
SJR Q rank Q4

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Acta Phytopathologica et Entomologica Hungarica
Language English
Size B5
Year of
Foundation
1966
Volumes
per Year
1
Issues
per Year
2
Founder Magyar Tudományos Akadémia  
Founder's
Address
H-1051 Budapest, Hungary, Széchenyi István tér 9.
Publisher Akadémiai Kiadó
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 0238-1249 (Print)
ISSN 1588-2691 (Online)

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