First Report of Pectobacterium parmentieri Causing Blackleg on Potato in Inner Mongolia, China

Blackleg on potato plants ( ) is caused by spp. and spp. (Charkowski, 2018) worldwide. From June to August in both 2018 and 2019, cases of blackleg were investigated in potato-producing areas in Hulunbuir, Ulanqab, and Hohhot in Inner Mongolia, China. The total surveyed field area was about 200 hectares. The plants showed typical blackleg symptoms, such as black and stunted stems or curled leaves (Fig. S1), and the number of infected plants were counted. The disease showed an incidence of around 8%. Five diseased plants were collected from a 10 ha potato field with approximately 75,000 potato plants (cv. mainly Favorita and Xisen) per hectare. Two-centimeter-long samples of symptomatic stems were removed from the selected plants using a sterile scalpel. The surfaces of the samples were disinfected with 75% ethanol for 2 min. They were then rinsed with sterile distilled water and soaked in 5 ml sterile distilled water for 30 min. Aliquots of three tenfold dilutions of this solution were plated onto the crystal violet pectate agar (CVP) plate and incubated for 3 days at 28°C (Ge ., 2018). A single bacterial colony that showed pitting on CVP plates (Fig. S2) was picked with a toothpick, streaked onto nutritional agar (She ., 2013) to obtain pure colonies. Amplification of a 1.4-kb segment containing 16S rRNA gene was performed on the pure colonies using the universal primer set 27F/1492R (Monciardini ., 2002). The amplicons were sequenced and submitted to the GenBank Nucleotide Basic Local Alignment Search Tool analysis. The 16S rRNA gene sequences of four isolates (GenBank accession numbers: MN626412, MN626449, MN625916, and MT235556) showed more than 99% sequence identity to type strain RNS 08-42-1A (NR_153752.1) (Fig. S3). Six housekeeping genes (MT427753-MT427756), (MT427757-MT427760), (MT427761-MT427764), (MT427765-MT427768), (MT427769-MT427772), and (MT427773-MT427776) of these four isolates were amplified and sequenced (Ma ., 2007, Waleron ., 2008). All sequences showed 99% to 100% sequence identity with strains. Phylogenetic trees (Fig. S4) were constructed by multi-locus sequence analysis (MLSA) using MEGA 6.0 software (Tamura ., 2013). The samples were tested against Koch's postulates on potato seedlings (cv. Favorita) by injecting 100 μl bacterial suspension (10 CFU/ml) or sterile phosphate buffered solution into the stems 2 cm above the base (Ge ., 2018). The seedlings were incubated at 21°C and 80% humidity (She ., 2013). Three to 5 days after in