Eggplant (Solanum melongena L.) is an important vegetable cultivated in Mexico and the state of Sinaloa is the largest producer of eggplants with 90% of the country's total production. In… Click to show full abstract
Eggplant (Solanum melongena L.) is an important vegetable cultivated in Mexico and the state of Sinaloa is the largest producer of eggplants with 90% of the country's total production. In April 2022, eggplants cv. Barcelona exhibiting root-knot, stunted growth, and yellowing were detected in a greenhouse in Culiacán, Sinaloa, Mexico. Disease incidence was approximately 10% (1000 plants evaluated). Ten soil samples were collected from the greenhouse. An average of 400 root-knot nematode second-stage juveniles (J2s) were extracted from 100 g of soil for each sample. Roots were washed with tap water and dissected. Females and egg masses were obtained by dissecting galls. Microscopic examination of the perineal pattern of mature females (n= 10) was round to ovoid, with rounded and high dorsal arch. Females (n= 20) were globular to pear-shaped, body length of 645 to 739 µm, body width of 470 to 559 μm; the stylet was dorsally curved, 15.1 to 16.2 μm long, and with rounded stylet knobs; neck length of 195 to 202 µm and the distance from the base of the stylet to the dorsal gland orifice (DGO) was 4.2 to 5.8 µm. Second-stage juveniles were vermiform, annulated, and tapering at both ends. Morphological characteristics of the females and J2s were consistent with those reported for Meloidogyne enterolobii (Yang and Eisenback 1983). For molecular identification, total DNA was extracted from individual females according to the extraction protocol described by Hu et al. (2011), and the ribosomal intergenic spacer 2 (IGS2) was amplified by PCR using the specific primers Me-F/Me-R for M. enterolobii (Long et al. 2006). PCR amplification generated a 236-bp fragment for the analyzed sample and the amplicon was sequenced. The sequence was deposited in GenBank under the accession number OP004802. BLASTn searches showed 100% identity with available sequences of M. enterolobii from the USA (MH800967) and China (KP411228, MT742011). A phylogenetic tree including published IGS2 sequences for Meloidogyne spp. was constructed based on Maximum Likelihood method. The phylogenetic analysis placed the sequence MeCUB in the same clade with Meloidogyne enterolobii. Pathogenicity tests were performed under greenhouse conditions by inoculating 5000 eggs of a pure population of M. enterolobii on 10 healthy eggplants cv. Barcelona (30-day-old) grown in pots with sterilized soil. Five uninoculated eggplants were used as control. Plants were maintained at 26 to 34°C in a greenhouse for 35 days. Stunted growth and root-galling symptoms appeared on inoculated plants after 21 days, whereas control plants remained symptomless. Nematode reproduction factor (final population density/initial population density) was 0.93 and 2.28 at 28 and 35 days after inoculation, respectively. The nematode on the inoculated roots was morphologically identical to that observed on naturally infected roots in the field. The pathogenicity test was carried out twice with similar results. Meloidogyne enterolobii has been previously reported on eggplants in Puerto Rico (Rammah and Hirschmann 1988). To our knowledge, this is the first report of M. enterolobii causing root-knot of eggplant in Mexico. This nematode is widely distributed in Sinaloa affecting other vegetable crops such as tomato (Martínez-Gallardo et al. 2015), chili (Carrillo-Fasio et al. 2020), and cucumber (Gómez-González et al. 2020), so future studies are required to evaluate integrated management strategies.
               
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