ABSTRACT
Aim: The study was conducted to screen the tuberose genotypes for nematode resistance and to establish histopathological, biochemical and nutritional changes in resistant/tolerant genotype against root knot nematode, Meloidogyne incognita. Methodology: Twenty seven tuberose genotypes comprising of two types viz., single (18 genotypes) and double (9 genotypes) were evaluated for root knot nematode resistance. Tuberose bulbs of uniform size were surface sterilized and planted in 9 inch plastic pots and inoculated with nematode juveniles (J2) 15 days after planting. Gall Index was recorded on a 0-5 scale after 120 days of inoculation. Histopathological, biochemical (total phenols, peroxidase, polyphenol oxidase and phenylalanine ammonia lyase) and nutrient estimation studies were conducted on the roots of resistant/tolerant genotypes against root knot nematode, Meloidogyne incognita. Results: Among the twenty seven tuberose genotypes screened for nematode resistance, Suarna Rekha was categorized as resistant genotype and Arka Shirngar, IIHR-2, IIHR-4, Variegated, IIHR-12, GK-T-C4, Calcutta Double, Bidhan Rajani-2 and Bidhan Rajani-3 were categorized as tolerant genotypes. Histological characterization of resistant/tolerant genotypes revealed that giant cell formation was disrupted with higher number of phenolic cells and cells with lignified cell wall that prevented the successful establishment of nematode feeding site. The resistant and tolerant genotypes significantly recorded higher accumulation of phenols and defence enzymes viz., polyphenol oxidase (PPO), peroxidase (PO) and phenyl alanine ammonia lyase (PAL) and macro and micro nutrients as compared to susceptible genotypes. Interpretation: Screening of tuberose genotypes for root knot nematode resistance in this study has led to the identification of several nematode resistant/ tolerant genotypes. This would serve as a valuable information for the breeders to utilize resistant/ tolerant genotypes as parents in their breeding programmes.
ABSTRACT
Neurofibromatosis (NF) with sphenoid wing dysplasia is a rare clinical entity. Herewith, we present a case of NF with sphenoid wing dysplasia which presented with pulsatile progressive proptosis. Other ocular symptoms or visual disturbances were absent. Diagnosis of the condition was not easy and the management was a challenging task which needed multidisciplinary approach as there were ocular, neurological, orthopedic, and dermatological manifestations. With neurosurgical intervention, reconstruction of the sphenoid wing was possible. Proptosis was corrected without any disturbance of vision.