Evaluation of SP1001 (Pelargonic Acid) in Combination with Glyphosate on Cattail and Alligatorweed

Cattail (Typha latifolia L.) is a common and troublesome weed in shallow, freshwater environments throughout the United States. Alligatorweed (Alternanthera philoxeroides (Mart.)Griseb.), in spite of the introduction and success of several insects as biological controls, remains a troublesome we4ed in a a number of locations in the Southeast where there are frequent human disturbances (e.g., insecticide spraying, mechaniceal removal, etc.) and/or weather conditions that affect the life cycle of the insects (Kay1992, Vogt et al. 1992). Both of these weeds routinely are managed by foliar applications of the herbicide, glyphosate [N-(phosphonomethyl)glycine]. Regrowth and reinfestation of previously treated areas usually necessitates additional herbicide application during subsequent years. A new product that could enhance the activity of glyphosate on these weeds would be useful in their management. In 1997, SePRO Corp. initiated t4esting of an experimental compound, SP1001, to determine its efficacy either as a herbicide or as an adjuvant to boost the activity of glyphosate for use in aquatic sites. The objective of this study was to evaluate the potential for using SP1001 as an adjuvant to replace surfactants customarily used during application of glyphosate for control of cattail and alligatorweed.

Development and evaluation of the polymerase chain reaction (PCR) method for diagnosis of spring viremia of carp virus (SVCV)

Aquaculture has been expanded rapidly to become a major commercial and food-producing sector worldwide in recent decade. In parallel, viral diseases rapidly spread among farms causing enormous economic losses. The accurate detection of pathogens at early stages of infection is a key point for disease control in aquaculture. Spring Viraemia of Carp Virus (SVCV) is a very severe pathogen of carp fishes in different parts of the world and is categorized as a reportable listed disease in the annual published list of World Organization for animal Health (OIE). The objective of this study was to develop and evaluate RT- PCR test for detecting SVC virus and also the sensitivity and specificity of this test. A semi nested RT- PCR was designed using combination of three primers: two external (SVCF , SVCR) and one internal (SVCS) primers which based on conserved region of G gen. The specificity of designed primers (only external ones) by examination on Viral Hemorrhagic Septicemia Virus (VHSV) and Infectious Hematopoietic Necrosis Virus (IHNV) was confirmed. For optimizing of the PCR test, primer concentration, primer annealing temperature, cycle number and Mgcl2 concentration were surveyed. Also for validity test, prevention of false negative and Assurance of its accuracy, a competitive internal control (mimic) designed and its suitable concentration was defined. Evaluation of the sensitivity of designed test were conducted first by comparing the different commercially available RNA isolation guidelines, two guidelines: isotiocyanate phenol–chloroform based protocols (RNX–Plus Iran, Iq2000 kit Taiwan ) and two column based protocols (Cinna pure RNA Iran , high pure viral RNA kit, Roche Germany ). The results indicated that the column based protocols (Roche method and Cinna pure), yield 36.77 ng/μl and 16/47 ng/μl RNA concentration respectively, which were significantly higher than other protocols(P<0.05). Then for evaluation of extracted RNA sensitivity, Serial dilution of SVCV strain 56.70 grown in EPC (1.9×105 TCID50/ml) was examined To compare sensitivity. Extracted RNA from serial dilution with stone's primers and commercial IQ-2000 kit were examined simultaneously. The result indicated that designed semi- nested RT- PCR was able to recognize SVC virus to 10-4 dilution and stone's primer recognize to 10-3 dilution whereas Iq-2000 commercial kit did not recognized in any dilution. In high virus titer in designed test two DNA band (462 bp and 266 bp) produced, and by decreasing virus titer 462 bp was omitted. In low virus titer or lack of virus, just DNA band (mimic) 729 bp can propagate. After designing and optimizing PCR test, a total of 400 suspected cultured Cyprinus carpio with high mortality from 4 aquaculture zone of Khuzestan province were collected and tested for SVCV during 2012- 2013 using developed PCR method and IQ- 2000. The results indicated that SVC virus was not observed in samples using both methods.