Access to instant test results would enable the growers to implement timely orchard management practices. The commonly utilized bacterial gene used for laboratory based diagnostics of

Las is a fragment of the 16S rDNA gene (Li et al., 2006). We have developed LAMP primer sequences for the phage related region of the Las genome. If Las positives are found, the crude extracts used in LAMP assays can be re-evaluated in diagnostic laboratories by qPCR for the 16S rDNA region. Utilization of two different genomic regions will be beneficial in detecting potential contaminations. The LAMP assay developed here is about 100 times more sensitive than standard qPCR Trametinib molecular weight technique and hence likely to detect the bacterium in low-titer situations (Fig. 3). While testing a large number of plant DNA samples of different varieties, we observed that it was easier to discriminate between weak positives Selleck Pifithrin�� and negatives in LAMP assays rather than in qPCR assays where samples with Ct values of 34 or above are generally considered inconclusive. Very high levels of sensitivity of LAMP reactions have been reported in many other systems. In the filarial parasite

Loa loa associated with a tropical human disease Loiasis, it has been shown that LAMP assay can detect 0.5 ag of the worm genomic DNA; compared to the qPCR test that detects 0.1 pg, LAMP was considered 200,000 times more sensitive ( Fernandez-Soto et al., 2014). In our analysis, the increased sensitivity observed in LAMP compared to qPCR may be because Urease of two reasons: a) qPCR is generally conducted in a duplex format to detect plant gene (‘Cox’) or psyllid gene (‘wingless’) in addition to the bacterial gene (16S rDNA). When the bacterial titer is low, amplification of the internal control genes may deplete the reagents required for the amplification of the bacterial target gene and this may negatively affect the Ct value calculated in qPCR assays; b) when target concentration is low, the PCR inhibitors present in the extract may negatively affect qPCR Ct values. Such an effect seems to be less of a problem with LAMP reactions. When the qPCR

assays were conducted for only Las (without housekeeping gene) and the bacterial titers were low, the sensitivity of qPCR appeared to be lower than LAMP. The Liberibacter genomic region chosen by our study seems to be specific to Las and is not reported from other bacteria. Psyllids are known to harbor several endosymbiotic bacteria like Wolbachia (alpha proteobacterial group) and Candidatus Carsonella (gamma proteobacteria) ( Saha et al., 2012). The LAMP reaction was always negative with known Las-free ACP and B. cockerelli indicating that the primers did not amplify DNA from the endosymbiont populations. If the LAMP technology is extended in the future to test plant root samples that are reported to have the bacterium earlier than the canopy ( Johnson et al.