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Occurrence and distribution of citrus leprosis virus (CiLV-C) in Honduras, Central America
First report of alstroemeria wilt caused by Fusarium
oxysporum in India
V.
Shanmugam*, S. Kumar, M.K. Singh, R. Verma, V. Sharma
and N.S. Ajit
Floriculture Division, Institute of Himalayan Bioresource Technology,
Palampur-176061, Himachal Pradesh, India
*shanpatho@yahoo.com
Accepted for publication
25/10/06
Hybrids of
Alstroemeria (Alstroemeriaceae), commonly called Peruvian Lily, are an
exotic, rhizomatous and perennial cut flower crop widely cultivated under
protection in India. Nine
hybrids (cvs. Alladin, Amor, Capri, Cinderella, Pluto, Rosita, Serena, Tiara
and No. 14) were procured from three locations in India by the Institute of
Himalayan Bioresource Technology (IHBT) in 2000-2001. During cultivation,
plants of all cultivars exhibited leaf chlorosis and slight vein clearing on
outer leaflets, followed by leaf yellowing and abscission, discolouration of
stem vascular tissue and death.

Figure 1:
Symptoms of alstroemeria
wilt following artificial inoculation with Fusarium oxysporum
Fusarium oxysporum
was consistently isolated when sections of discoloured stem vascular tissue were
surface sterilised (2% sodium hypochlorite) and plated on potato dextrose agar
(PDA) or carnation leaf agar. Single-spore isolates were identified based on
morphological characters (Nelson et al., 1983). Conidiophores were
unbranched or branched short monophialides. Microconidia were abundant,
generally single celled, oval to kidney shaped and produced only in false heads
5-12 x 3-3.5 µm. Macroconidia were abundant, slightly sickle-shaped and
thin-walled, with an attenuated apical cell and a foot-shaped basal cell
35.0-60.0 x 3.0-5.0 µm. Chlamydospores were single or in pairs and profusely
distributed. The presence of chlamydospores and microconidia borne in false
heads on short monophialides distinguished the fungus from closely related
Fusarium species. The culture has been deposited in the Microbial Type
Culture Collection (MTCC 7677) of the Institute of Microbial Technology,
Chandigarh, India. The
identity of the culture was also established by
PCR amplification and sequencing of the internal transcript spacer (ITS) region
(White et al., 1990) (Acc. No.
AM 261761).
Pathogenicity tests
were done twice in a screen house on 8-week-old plants of cv. No. 14. Wounded
roots were submerged for 10 min in a conidial suspension (1 x 106
conidia per mL in sterile tap water), while control plants were dipped in
sterile tap water. Seedlings were transplanted into pots and maintained in a
polytunnel. Symptoms observed on inoculated plants were similar to those in
commercial glasshouses, including leaf wilt (3 weeks after inoculation) (Fig.
1), chlorosis, necrosis and plant death. The pathogen was re-isolated from the
stems of affected inoculated plants to confirm Koch’s postulates. The control
plants did not exhibit symptoms.
Root rot complex of alstroemeria caused by F. oxysporum in association
with Pythium irregulare and Rhizoctonia solani was earlier
reported in Canada (Chang & Mirza, 1993) and Germany (Chang et al.,
1994). This is the first report of Fusarium oxysporum causing
alstroemeria wilt in India.
Acknowledgement
We thank the Director, IHBT (CSIR), Palampur for support and encouragement
during the course of this investigation. IHBT Publication Number: 0641.
References
Chang KF, Barr DJS, Hwang SF, Mirza M, 1994. Effect of interactions between
Fusarium, Rhizoctonia and Pythium on root and rhizome rot of Alstroemeria.
Zeitschrift-fur-Pflanzenkrankheiten-und-Pflanzenschutz 101, 46-466.
Chang KF, Mirza A,
1993. The occurrence of root rot disease complex of Alstroemeria in Alberta.
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Nelson PE, Toussoun
TA, Marasas WFO, 1983. Fusarium Species: An illustrated Manual for
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White TJ, Bruns TD, Lee S, Taylor J, 1990. Analysis of phylogenetic
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