Evidence map›Paper›PMID 38698140›Full record

ArticleArchives of microbiology2024

Molecular phylogeny and secondary structure analysis of hop stunt viroid (HSVd) associated with Mulberry (Morus alba) in India.

Shilpa N, Teruo Sano, Takashi Naoi, Janardhana G R

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Article in Archives of microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Shilpa NMolecular Phytodiagnostic Laboratory, Department of Studies in Botany, University of Mysore, Manasagangotri, Mysuru, Karnataka, 570 006, India.
Teruo SanoFaculty of Agriculture and Life Science, Hirosaki University, Bunkyo-cho, 3, Hirosaki, 036-8561, Japan.
Takashi NaoiFaculty of Agriculture and Life Science, Hirosaki University, Bunkyo-cho, 3, Hirosaki, 036-8561, Japan.
Janardhana G RMolecular Phytodiagnostic Laboratory, Department of Studies in Botany, University of Mysore, Manasagangotri, Mysuru, Karnataka, 570 006, India. grjbelur@gmail.com.

Funding

University of Mysore ViGha 03/06/2017-18 Dated 3rd October 2017
6 · The paper itself

Abstract

Hop stunt viroid (HSVd), a small, single stranded, circular, non-coding infectious RNA known to cause infection in various economically important crop plants. In the present investigation, a study was conducted in the southern part of Karnataka districts of India to detect the possible association of HSVd infection in mulberry plants. A total of 41 mulberry plants showing typical viroid-like symptoms along with asymptomatic samples were collected and screened using conventional Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) using a specific set of HSVd-Fw/ HSVd-Re primers. Out of 41 samples, the study confirmed the presence of HSVd in six samples of mulberry collected from Ramanagara (1 sample), Chikkaballapur (3 samples) and Doddaballapura (2 samples) regions with an expected HSVd amplicon size of ∼ 290-300 nucleotides. The mechanical transmission of HSVd was also confirmed on cucumber (cv. Suyo) seedlings through bioassay, which was reconfirmed by RT-PCR. The amplicons were cloned, sequenced, and the representative nucleotide sequences were deposited in the NCBI GenBank. Subsequently, molecular phylogenetic analysis showed that HSVd mulberry isolates from this study were most closely related to grapevine isolates, indicating a common origin. On the other hand, it was shown to belong to a different group from mulberry isolates so far reported from Iran, Italy, Lebanon, and China. The secondary structure analysis of HSVd mulberry Indian isolates exhibited substitutions in the terminal left, pathogenicity, and variable regions compared to those of the Indian grapevine isolates. As far as this study is concerned, HSVd was detected exclusively in some mulberry plants with viral-like symptoms, but the pathogenesis and symptom expression needs to be further investigated to establish the relationship between HSVd and the disease symptoms in the mulberry plants.

Indexed as

MorusPhylogenyPlant DiseasesPlant VirusesViroidsIndiaNucleic Acid ConformationRNA, ViralRNA, ViralBioassayHop stunt viroidMulberryReverse transcription PCRSecondary structure analysis

Identifiers

PMID38698140

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