New Disease Reports (2015) 31, 4. [http://dx.doi.org/10.5197/j.2044-0588.2015.031.004]
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First report of the rust Puccinia porri on cultivated Allium vineale 'Hair'

C. Sansford 1*, E.J. Beal 2, G. Denton 2 and J.O. Denton 2

*claire.sansford@btinternet.com

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Received: 16 Dec 2014; Published: 01 Feb 2015

Keywords: Puccinia allii, crow garlic, wild garlic, fungal plant disease

Allium vineale is native in the UK and temperate Europe and naturalised elsewhere. In North America, amongst other places, it is considered to be an exotic invasive weed. A. vineale is also cultivated as an ornamental plant, including the variety A. vineale 'Hair'. In June 2014, all stems of this variety (ca. 50 plants), established from commercial bulbs in a private garden in York in 2004, exhibited multiple eye-shaped lesions for the first time, with dark edges and golden-yellow centres, ca. 10mm long x 5mm wide (Fig. 1). Infected plant material was deposited in the Kew fungarium under accession number K(M)193813. The causal agent was suspected to be Puccinia porri (synonym Puccinia allii).

In August, stem samples (Fig. 2) were confirmed as being infected by P. porri based on morphological characteristics and molecular diagnostics. Teliospores measured 34-50 µm (mean 43 µm) x 18.75-28 µm (mean 21 µm) (Fig. 3); matching conventional descriptions (e.g. McNabb, 1966). As only resting spores (teliospores) were present on the sample at this stage, it was not possible to perform Koch’s postulates. Molecular diagnosis used primers ITS1F and RUST1 for analysis of the ITS region, as described by Anikster et al. (2004). Sequences isolated from infected A. vineale ‘Hair’ samples (GenBank Accession Nos. KP205384 and KP205385) were 99% identical to P. allii isolates from cultivated chives (Allium schoenoprasum; AF511087) and garlic (Allium sativum; AF511075). In addition, the large ribosomal subunit (LSU) was amplified and sequenced using primers NL1 and NL4 (Maier et al., 2003). Although the isolated LSU sequences (KP205382 and KP205383) matched P. allii sequences in GenBank (AF511087 and AF511075; 98% and 99% respectively), they additionally closely matched LSU sequences of P. hordei (AF511086; 98%) and Uromyces scillarum (AF511085; 99%). However, morphological characteristics of our isolates do not match these two species.

Phylogenetic analysis of the ITS region was undertaken using KP205384, KP205385 and the top 18 matching sequences retrieved through NCBI megablast (see Fig. 4). The rust on A. vineale ‘Hair’ falls within P. porri (as the synonym P. allii). Anikster et al. (2004) observed a geographical split, supported by morphological and molecular data, but stated more work was needed before splitting P. porri. This finding indicates a potential new group within P. porri sensu lato. If research separates P. porri into two species, the rust on A. vineale ‘Hair’ may also represent a new species.

P. allii has been reported on wild plants of A. vineale in Bulgaria, Portugal, Spain, Sweden, the UK and USA, but not on cultivated varieties (Farr & Rossmann, 2014). Kirk and Cooper (2009) list 32 records of P. allii and two of P. porri on A. vineale in Britain and Ireland. Only one of these (P. allii) was on an unnamed ornamental variety (growing in the National Botanic Garden of Wales, April 2009) and symptoms were reported on the leaves, not the stems. To our knowledge this is the first report of P. porri sensu lato on A. vineale ‘Hair’ in the world.

A field experiment conducted by Koike and Smith (2001) suggested that invasive A. vineale has the potential to act as a source of overwintering inoculum of P. porri (as P. allii) for commercial crops of garlic (A. sativum) and onion (Allium cepa). Although not investigated, cultivated ornamental varieties of A. vineale are not only at risk of infection themselves, but could also act as an inoculum source of P. porri for other commercial crops of Allium spp. in the UK.

Figure1+
Figure 1: Stem lesions of Puccinia porri on Allium vineale 'Hair', collected June 2014.
Figure 1: Stem lesions of Puccinia porri on Allium vineale 'Hair', collected June 2014.
Figure2+
Figure 2: Stem lesions of Puccinia porri on desiccated Allium vineale 'Hair', collected August 2014.
Figure 2: Stem lesions of Puccinia porri on desiccated Allium vineale 'Hair', collected August 2014.
Figure3+
Figure 3: Teliospores of Puccinia porri obtained from stem lesions of Allium vineale 'Hair'. (Bar = 50 µm)
Figure 3: Teliospores of Puccinia porri obtained from stem lesions of Allium vineale 'Hair'. (Bar = 50 µm)
Figure4+
Figure 4: Molecular Phylogenetic analysis of the ITS region (using complete sequences of ITS 1, 5.8S and ITS 2) by Maximum Likelihood method. Figures are branch support shown as % of trees. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. Gaps and missing data were eliminated and 1089 positions were in the final dataset. Evolutionary analyses were conducted in MEGA6.
Figure 4: Molecular Phylogenetic analysis of the ITS region (using complete sequences of ITS 1, 5.8S and ITS 2) by Maximum Likelihood method. Figures are branch support shown as % of trees. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. Gaps and missing data were eliminated and 1089 positions were in the final dataset. Evolutionary analyses were conducted in MEGA6.

Acknowledgements

We thank A.M. Ainsworth, RBG, Kew and S. Helfer, RBG, Edinburgh for their input on taxonomy and preservation of infected material.


References

  1. Anikster Y, Szabo LJ, Eilam T, Manisterski J, Koike ST, Bushnell WR, 2004. Morphology, life cycle biology, and DNA sequence analysis of rust fungi on garlic and chives from California. Phytopathology, 94, 569-577. [http://dx.doi.org/10.1094/PHYTO.2004.94.6.569]
  2. Farr DF, Rossman AY, 2014. Fungal Databases, Systematic Mycology and Microbiology Laboratory, ARS, USDA. Retrieved August 18, 2014, from http://nt.ars-grin.gov/fungaldatabases/
  3. Kirk P, Cooper J, 2009. The Fungal Records Database of Britain and Ireland. British Mycological Society. Retrieved August 18, 2014, from http://www.fieldmycology.net/FRDBI/FRDBI.asp
  4. Koike ST, Smith RF, 2001. First report of rust caused by Puccinia allii on wild garlic in California. Plant Disease 85, 1290. [http://dx.doi.org/10.1094/PDIS.2001.85.12.1290D]
  5. Maier W, Begerow D, Weiß M, Oberwinkler F, 2003. Phylogeny of the rust fungi: an approach using nuclear large subunit ribosomal DNA sequences. Canadian Journal of Botany, 81, 12-23. [http://dx.doi.org/10.1139/b02-113]
  6. McNabb RFR, 1966. Additions to the rust fungi of New Zealand - 4. New Zealand Journal of Botany, 4, 86-94. [http://dx.doi.org/10.1080/0028825X.1966.10443956]

To cite this report: Sansford C, Beal EJ, Denton G, Denton JO, 2015. First report of the rust Puccinia porri on cultivated Allium vineale 'Hair'. New Disease Reports 31, 4. [http://dx.doi.org/10.5197/j.2044-0588.2015.031.004]

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