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Crop Research

Pathogenicity and molecular characterization of Candidatus Liberibacter asiaticus (CLas) of acid lime crop 


DOI: 10.31830/2454-1761.2026.CR-1145    | Article Id: CR-1145
SANDHIYA R, REECHA J AND SUJHEE P sandhiyapat17@gmail.com
Address : School of Agriculture, Bharath Institute of Higher Education and Research, Chennai - 600 073, Tamil Nadu, India
Submitted Date : 6-09-2026
Accepted Date : 21-10-2026
Online Published:

Abstract

The pathogen Candidatus Liberibacter asiaticus (CLas) is the cause of Huanglongbing (HLB) or citrus greening (CG) disease, which is one of the devastating diseases causing a significant crop reduction in citrus crops (Family: Rutaceae). It is a systemic pathogen which lives in citrus crop phloem tissues. Detection of Ca. L. asiaticus (CLas) casuing citrus Huanglongbing (HLB) disease was facilitated by taking samples from three different citrus orchards located in Tirupattur, Dharmapuri, Krishnagiri district. Midrib injection method by using syringe needle or microneedles used has early transmission of Ca. L. asiaticus (CLas) in phloem tissue of acid lime leaves. Total genomic DNA is extracted from inoculation of citrus leaves using a modified CTAB method to identify DNA from both healthy and infected samples. A 100 mg leaf midrib sample was crushed in liquid nitrogen, homogenized in 500 µl CTAB, incubated for 45 minutes at 60°C in a water bath, centrifuged for 5 minutes at 12000 rpm, and the supernatant was then transferred to a fresh tube, to which 5 µl of RNase-A was added, and incubated for 20 minutes at 37°C. For phase separation, an equal volume of chloroform/isoamyl alcohol (24:1) was added, vortexed for five minutes, and centrifuged for two minutes at 12000 rpm. The upper phase was then transferred to a new tube, in which 500µl of chilling isopropanol was added, kept at -20°C for 15 minutes, centrifuged at 12000 rpm, and the pallet was cleaned twice with 70% ethanol. The specific primers OI1/OI2c and A2/J5 had been used in a polymerase chain reaction (PCR) for detection, and they showed a specific band of 1160 bp and 703 bp, respectively. These were amplified from diseased leaves whereas no product from healthy citrus plant.

Keywords

Acid lime citrus greening disease midrib injection method modified CTAB method PCR 

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