Thrips Settling, Oviposition and IYSV Distribution on Onion Foliage

Thrips tabaci Lindeman (Thysanoptera: Thripidae) adult and larval settling and oviposition on onion (Allium cepa L.) foliage were investigated in relation to leaf position and leaf length at prebulb plant growth stages under controlled conditions. In the laboratory, four and six adult females of T. tabaci were released on onion plants at three-leaf stage and six- to eight-leaf stage, respectively, and thrips egg, nymph, and adult count data were collected on each of the three inner most leaves at every 2-cm leaf segment. Thrips settling and oviposition parameters were quantified during the light period on the above ground portion of onion plants from the distal end of the bulb or leaf sheath “neck” through the tips of the foliage. Results from studies confirmed that distribution of thrips adults, nymphs, and eggs were skewed toward the base of the plant. The settling distributions of thrips adults and nymphs differed slightly from the egg distribution in that oviposition occurred all the way to the tip of the leaf while adults and nymphs were typically not observed near the tip. In a field study, the foliage was divided into three equal partitions, i.e., top, middle, basal thirds, and thrips adults by species, primarily Frankliniella fusca (Hinds) and T. tabaci, were collected from each partition to determine if there was a similar bias of all adult thrips toward the base of the plant. The results suggested that adults of different species appear to segregate along leaf length. Finally, thrips oviposition on 2-cm segments and Iris yellow spot virus positive leaf segments were quantified in the field, irrespective of thrips species. Both variables demonstrated a very similar pattern of bias toward the base of the plant and were significantly correlated

Evolutionary and Experimental Assessment of Novel Markers for Detection of Xanthomonas euvesicatoria in Plant Samples

BACKGROUND: Bacterial spot-causing xanthomonads (BSX) are quarantine phytopathogenic bacteria responsible for heavy losses in tomato and pepper production. Despite the research on improved plant spraying methods and resistant cultivars, the use of healthy plant material is still considered as the most effective bacterial spot control measure. Therefore, rapid and efficient detection methods are crucial for an early detection of these phytopathogens. METHODOLOGY: In this work, we selected and validated novel DNA markers for reliable detection of the BSX Xanthomonas euvesicatoria (Xeu). Xeu-specific DNA regions were selected using two online applications, CUPID and Insignia. Furthermore, to facilitate the selection of putative DNA markers, a customized C program was designed to retrieve the regions outputted by both databases. The in silico validation was further extended in order to provide an insight on the origin of these Xeu-specific regions by assessing chromosomal location, GC content, codon usage and synteny analyses. Primer-pairs were designed for amplification of those regions and the PCR validation assays showed that most primers allowed for positive amplification with different Xeu strains. The obtained amplicons were labeled and used as probes in dot blot assays, which allowed testing the probes against a collection of 12 non-BSX Xanthomonas and 23 other phytopathogenic bacteria. These assays confirmed the specificity of the selected DNA markers. Finally, we designed and tested a duplex PCR assay and an inverted dot blot platform for culture-independent detection of Xeu in infected plants. SIGNIFICANCE: This study details a selection strategy able to provide a large number of Xeu-specific DNA markers. As demonstrated, the selected markers can detect Xeu in infected plants both by PCR and by hybridization-based assays coupled with automatic data analysis. Furthermore, this work is a contribution to implement more efficient DNA-based methods of bacterial diagnostics

In vitro assay evaluating fungicide activity against Colletotrichumgloeosporioides, causal agent of twister disease of onion

Twister disease of onion has become epidemic in coastal tract and other onion growing districts of Karnataka which caused heavy loss and its causal agents are C. gloeosporioides and F. oxysporum . Efforts were made to screen fungicides to know their efficacy of different fungicides at different concentrations under In vitro by poisoned food technique. Among the four non-systemic fungicides evaluated against C. gloeosporioides maximum inhibition was observed in chlorothalonil (42.60%). Among the seven systemic fungicides against F. oxysporum evaluated, hundred per cent inhibition of mycelial growth of C. gloeosporioides at all tested concentrations was observed in propiconazole, hexaconazole, tebuconazole and tricyclazole. Among the seven combi product fungicides evaluated carbendazim 12 per cent + iprodione 63 per cent (Quintal) inhibited maximum mycelial growth (95.43%). In vitro evaluation of fungicides revealed that among the four non-systemic fungicides evaluated, maximum inhibition of mycelial growth of F.oxysporum was observed in copper oxychloride (64.84%). Among six systemic fungicides evaluated, maximum inhibition of mycelial growth of F. oxysporum was observed in propiconazole (93.52%). Among the six combiproduct fungicides evaluated, hundred per cent inhibition of mycelial growth was observed in Saaf, Sprint and Vitavax power at all tested concentrations