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First record of Pseudomonas syringae pv.
viburni in the UK
D.E. Stead*, H. Stanford, A. Aspin and S.A. Weller
Central Science Laboratory, Sand Hutton, York, YO41 1LZ, United
Kingdom
*d.stead@csl.gov.uk
Accepted for publication 10/10/05
Various Pseudomonas syringae pathovars cause leaf spots and
cankers of hardy nursery stock species in the UK, including P.s. pv.
syringae on lilac, P.s. pv. berberidis on Berberis
spp. and P.s. pv. philadelphi on Philadelphus spp.
(Roberts, 1997). Leaf spots on some other hosts are attributed to P.s.
pv. syringae or to P. syringae pv. undetermined.
Occasionally Central Science Laboratory has received samples of Viburnum
spp. with watersoaked leaf spots from which P. syringae has been
isolated; one was from Viburnum tinus in 1986. The isolate, a
typical LOPAT group 1 member of P. syringae (Lelliott &
Stead, 1987), was placed in the National Collection of Plant Pathogenic
Bacteria (NCPPB) as NCPPB 3450 and was listed under P.s. pv. viburni
with a ‘b’ ranking; denoting authenticity not verified. More
recently, plants of Viburnum sargentii with typical bacterial
leaf spots were received from a Lincolnshire nursery and from which
LOPAT 1 strains were isolated. Host tests confirmed pathogenicity on Viburnum
sargentii. Virulence was weaker on Viburnum opulus var.
‘Sterile’. Two isolates from V. sargentii on the same
nursery, taken at different times (CSL 4205 and 4206), were acceded to
the NCPPB as NCPPB 4265 and NCPPB 4266 respectively.

Figure 1: BOX-PCR fingerprints showing unique pattern within P.s.pv.
viburni
Fatty acid profiles obtained were typical of P. syringae.
REP-PCR based on primers from the repetitive enterobacterial consensus
sequence and BOX-PCR, based on primers from the BOX A subunit were
carried out (Stead et al., 2000). Fingerprints were compared with
those of reference strains of all validly-named P. syringae pathovars
held in the NCPPB, including P.s . pv. viburni (NCPPB
1921, the only authentic strain). UPGMA dendrograms of both assays
showed that NCPPB 3450 did not have the profile of P.s. pv. viburni
but was very similar to that of P.s. pv. maculicola and P.s
pv. tomato. However, NCPPB 4265 and NCPPB 4266 had profiles very
similar to that of the P.s. pv. viburni type strain and
were different from all other reference strains. A subset of BOX-PCR
fingerprints of strains of P. syringae pathovars known to occur
in the UK is shown in Fig 1. Bradbury (1986) lists the known
distribution as USA and Spain, with the Spanish strains coming from a
rot of tobacco. This is the first authentic record of P.s. pv. viburni
in the UK. The precise taxonomic position of NCPPB 3450 remains
uncertain.
Acknowledgement
This work was funded by DEFRA Plant Health Division Project PH0154.
References
Bradbury JF, 1986. Guide to Plant Pathogenic Bacteria.
Wallingford, UK: CAB International.
Lelliott RA, Stead DE, 1987. Methods for the Diagnosis of
Bacterial Diseases of Plants. Oxford, UK: Blackwell Scientific
Publications.
Roberts S, 1997. Top of the spots: bacterial diseases of hardy
nursery stock. HDC Project News (December 1997) 49, 4-6.
Stead DE, Elphinstone JG, Weller SA, Smith NC, Hennessy J, 2000.
Modern methods for characterising, identifying and detecting bacteria
associated with plants. Acta Horticulturae 530, 45-59.
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