Pathological and molecular characterisation of lettuce big- vein virus and associated virus from Egypt

Other Title(s)

التوصيف المرضي الجزيئي لفيروس العرق الكبير في الخس و الفيرويات المرتبطة في مصر

Joint Authors

Atiyyah, Shayma Ahmad Mahmud
Wajih, al-Sayyid al-Sayyid
Fath Allah, Mirfat Mustafa

Source

Alexandria Journal of Agricultural Sciences

Issue

Vol. 64, Issue 3 (30 Jun. 2019), pp.193-202, 10 p.

Publisher

Alexandria University Faculty of Agriculture

Publication Date

2019-06-30

Country of Publication

Egypt

No. of Pages

10

Main Subjects

Agriculture

Topics

Abstract EN

Lettuce (Lactuca sativa) is known to be attacked by many viruses causing disease epidemics among which Lettuce
big-vein virus (s) is (are) shown here to cause considerable quality and yield losses.

In winter 2014, samples suspected of
being infected with lettuce big-vein disease viruses (Mirafiori lettuce big-vein virus, MLBVV and Lettuce big-vein
associated virus, LBVaV) were collected from naturally infected plants grown at different locations, from two
governorates in Egypt (El-Qalyubia and El-Fayoum).

The characteristic symptom of the disease was seen as the
development of a clear region along the major veins of leaf due to the disappearance of chlorophyll making the veins
appear as if they were bigger than normal.

Along with this symptom, leaves were crinkled and head size was reduced and
assumed elongated shape.

Three isolates (two of MLBVV, 1 and 2 and one of LBVaV) were detected in lettuce specimens
giving negative reaction to cucumber mosaic virus (CMV) and lettuce mosaic virus(LMV)to specific polyclonal antisera
using DAS-ELISA.

Detection was based on the RT-PCR technique with a pair of specific primers for coat protein gene of
both MLBVV and LBVaV as it resulted in the generation of a unique PCR amplification product of approximately 233 bp
for MLBVV and approximately 360bp for LBVaV.

It was also proven that MLBVV and LBVaV isolated here are
transmissible by the fungal vector Olpidium virulentus.

The fungus was isolated from plant roots and seeds andits identity
was confirmed using the PCR technique.

The length of the product amplified was approximately 632 bp using a specific
pair of primers for the fungal ITS region.

Purification of MLBVV and LBVaV was achieved and the two viruses were
detectable and distinguishable by polymerase chain reaction (PCR) and electron microscopy.

Samples with symptoms that
were positive by RT-PCR to MLBVV and LBVaV were gel-purified and sequenced using specific forward and reverse
primers.

Sequences related to the three virus isolates (MLBVV1, MLBVV2 and LBVaV1) were submitted to Genbank
database under the accession numbers, LT721898, LT721899 and LT721900.

The highest similarity percentage was
observed between MLBVV1 and MLBVV2 and a Spain isolate was 70.3% and 69.7% , respectively.

While, the highest
similarity percentage between LBVaV1 and Brazil isolate was 100% .

To the best of our knowledge this is the first report
of lettuce big-vein disease in Egypt.

American Psychological Association (APA)

Atiyyah, Shayma Ahmad Mahmud& Wajih, al-Sayyid al-Sayyid& Fath Allah, Mirfat Mustafa. 2019. Pathological and molecular characterisation of lettuce big- vein virus and associated virus from Egypt. Alexandria Journal of Agricultural Sciences،Vol. 64, no. 3, pp.193-202.
https://search.emarefa.net/detail/BIM-1072800

Modern Language Association (MLA)

Atiyyah, Shayma Ahmad Mahmud…[et al.]. Pathological and molecular characterisation of lettuce big- vein virus and associated virus from Egypt. Alexandria Journal of Agricultural Sciences Vol. 64, no. 3 (2019), pp.193-202.
https://search.emarefa.net/detail/BIM-1072800

American Medical Association (AMA)

Atiyyah, Shayma Ahmad Mahmud& Wajih, al-Sayyid al-Sayyid& Fath Allah, Mirfat Mustafa. Pathological and molecular characterisation of lettuce big- vein virus and associated virus from Egypt. Alexandria Journal of Agricultural Sciences. 2019. Vol. 64, no. 3, pp.193-202.
https://search.emarefa.net/detail/BIM-1072800

Data Type

Journal Articles

Language

English

Notes

-

Record ID

BIM-1072800