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Plant Disease Journal - 98(8):1161 - Abstract
apsjournals.apsnet.org /doi/abs/10.1094/PDIS-01-14-0002-PDN
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August 2014, Volume 98, Number 8
Page 1161
http://dx.doi.org/10.1094/PDIS-01-14-0002-PDN
Disease Notes
First Report of Iris yellow spot virus Infecting Allium
tuberosum in India
S. J. Gawande, V. S. Gurav, A. A. Ingle, and J. Gopal, Directorate of Onion and Garlic
Research, Rajgurunagar, Pune, India
Allium tuberosum L., commonly known as garlic chives, is an important spice in
northeastern India as well as in many other parts of the world. Iris yellow spot virus
(IYSV; genus Tospovirus, family Bunyaviridae) is an important pathogen of onion (4)
and other related Alliums such as garlic (3) and leek (2). During April 2013, symptoms
potentially induced by IYSV such as chlorotic and straw-colored spindle-like lesions
were observed on leaves of A. tuberosum accession Hanzong Winter (CGN 20779)
plants in the wild species garden at the Directorate of Onion and Garlic Research
(DOGR), Rajgurunagar, Pune, Maharashtra, India. Ten plant samples of A. tuberosum
were randomly collected from the wild species garden and the upper, middle, and
lower portions of the leaves were pooled and tested by double-antibody sandwich
(DAS)-ELISA using a commercially available kit (Agdia Inc., Elkhart, IN) for IYSV. All of
them showed positive results for IYSV incidence. Total RNA from the ELISA positive
leaf samples of A. tuberosum was extracted using the RNeasy Plant Mini kit (Qiagen
GmbH, Hilden, Germany). The primer pair IYSV-F (5′-TCAGAAATCGAGAAACTT-3′)
and IYSV-R (5′-TAATTATATCTATCTTTCTTGG-3′) (1) was used for RT-PCR. The
primer pair was specific to amplify 797 bp of the nucleocapsid (N) gene of IYSV. The
amplified product derived from A. tuberosum isolate was purified by QIAquick PCR
Purification Kit (Qiagen) and cloned using the vector pDrive (Qiagen). The
recombinant clone was sequenced (Accession No. KF624624). Sequence analysis
performed on CLC Main Workbench Version 6.8.4 confirmed that the fragment was of
IYSV. Nucleotide sequence comparison of our virus with other IYSV isolates revealed
that the highest nucleotide identity (99%) was with the IYSV garlic isolate
(HM173691) from India. Further, maximum 96% protein identity was with IYSV onion
isolate (ACA09432) and garlic isolate (ADK56108) from India. To our knowledge, this
is the first report of IYSV naturally occurring on A. tuberosum in India. It is evident
from previous studies that IYSV causes significant losses in onions (1) and from this
study, that its symptoms have direct impact on quality of garlic chives. Further detailed
studies are required to assess the magnitude of the impact of IYSV infection on yield
and quality of A. tuberosum.
References: (1) A. Bulajic et al. Plant Dis. 93:976, 2009. (2) M. C. Córdoba-Sellés et
al. Plant Dis. 91:1365, 2007. (3) S. J. Gawande et al. Plant Dis. 94:1066, 2010. (4) B.
Mandal et al. Plant Dis. 96:468, 2012.

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apsjournals.apsnet.org-Plant_Disease_Journal__9881161__Abstract

  • 1. Plant Disease Journal - 98(8):1161 - Abstract apsjournals.apsnet.org /doi/abs/10.1094/PDIS-01-14-0002-PDN Welcome Sign in | Register | Mobile
  • 2. Previous Article | Next Article August 2014, Volume 98, Number 8 Page 1161 http://dx.doi.org/10.1094/PDIS-01-14-0002-PDN Disease Notes First Report of Iris yellow spot virus Infecting Allium tuberosum in India S. J. Gawande, V. S. Gurav, A. A. Ingle, and J. Gopal, Directorate of Onion and Garlic Research, Rajgurunagar, Pune, India Allium tuberosum L., commonly known as garlic chives, is an important spice in northeastern India as well as in many other parts of the world. Iris yellow spot virus (IYSV; genus Tospovirus, family Bunyaviridae) is an important pathogen of onion (4) and other related Alliums such as garlic (3) and leek (2). During April 2013, symptoms potentially induced by IYSV such as chlorotic and straw-colored spindle-like lesions were observed on leaves of A. tuberosum accession Hanzong Winter (CGN 20779) plants in the wild species garden at the Directorate of Onion and Garlic Research (DOGR), Rajgurunagar, Pune, Maharashtra, India. Ten plant samples of A. tuberosum were randomly collected from the wild species garden and the upper, middle, and lower portions of the leaves were pooled and tested by double-antibody sandwich (DAS)-ELISA using a commercially available kit (Agdia Inc., Elkhart, IN) for IYSV. All of them showed positive results for IYSV incidence. Total RNA from the ELISA positive leaf samples of A. tuberosum was extracted using the RNeasy Plant Mini kit (Qiagen GmbH, Hilden, Germany). The primer pair IYSV-F (5′-TCAGAAATCGAGAAACTT-3′) and IYSV-R (5′-TAATTATATCTATCTTTCTTGG-3′) (1) was used for RT-PCR. The primer pair was specific to amplify 797 bp of the nucleocapsid (N) gene of IYSV. The amplified product derived from A. tuberosum isolate was purified by QIAquick PCR Purification Kit (Qiagen) and cloned using the vector pDrive (Qiagen). The recombinant clone was sequenced (Accession No. KF624624). Sequence analysis performed on CLC Main Workbench Version 6.8.4 confirmed that the fragment was of IYSV. Nucleotide sequence comparison of our virus with other IYSV isolates revealed that the highest nucleotide identity (99%) was with the IYSV garlic isolate (HM173691) from India. Further, maximum 96% protein identity was with IYSV onion isolate (ACA09432) and garlic isolate (ADK56108) from India. To our knowledge, this is the first report of IYSV naturally occurring on A. tuberosum in India. It is evident from previous studies that IYSV causes significant losses in onions (1) and from this study, that its symptoms have direct impact on quality of garlic chives. Further detailed studies are required to assess the magnitude of the impact of IYSV infection on yield and quality of A. tuberosum. References: (1) A. Bulajic et al. Plant Dis. 93:976, 2009. (2) M. C. Córdoba-Sellés et al. Plant Dis. 91:1365, 2007. (3) S. J. Gawande et al. Plant Dis. 94:1066, 2010. (4) B. Mandal et al. Plant Dis. 96:468, 2012.