Development of Diagnostic Microscopic and Chemical Markers of Some Euphorbia Latexes

The latexes of the three Euphorbia species, namely E. antiquorum L., E. nerifolia L., and E. tirucalli L., are highly valued in the Indian system of medicine as purgatives, in addition to their specific and distinct therapeutic activities. In order to distinguish these latexes and develop their diagnostic microscopic and chemical markers, we performed extensive chemical and microscopic studies. The three latexes differ significantly in their microscopic features by exhibiting characteristic starch grain patterns. Although amoebic structures were found to be characteristic of E. antiquorum, dumb-bell and oval structures are characteristic of E. nerifolia and E. tirucalli, respectively. In addition, these latexes showed bone-shaped structures as a common feature, but these differed considerably in their length （10-60, 30-55, and 50-70 μm in length in E. antiquorum, E. nerifolia, and E. tirucalli, respectively）. The chemical markers nerifoliene and euphol were found to be common to both E. antiquorum and E. nerifolia, whereas euphol is the only marker for E. tirucalli. A reverse-phase high-performance thin-layer chromatographic （HPTLC） method was developed to distinguish these three latexes and to generate their standard fingerprinting patterns. Most significantly, the markers nerifoliene and euphol could be resolved by RP-18 F254s precoated aluminium plates and the latexes have been quantitatively estimated with respect to these markers. The developed microscopic, chemical and HPTLC patterns can be used to distinguish the three latexes.     

Age, growth and reproductive strategy of the snakehead, Ophicephalus striatus Bloch, from Sri Lanka

A total of 281 snakehead-lula, Ophicephalus striatus , collected between November 1982 and June 1983 from inundated rice fields and swamps in south-western Sri Lanka were analysed. Age determination by length frequencies and scale annuli revealed six age groups. An asymptotic length of 520 mm was estimated by the von Bertalanffy growth model.
The ova were assigned to four developmental stages and a maturity scale was developed for the females. Fast growing 2-year-old fish attain sexual maturity. The ovum size frequencies and occurrence of mature and spent fish indicate that this fish spawns during the south-west monsoon season. Fecundity estimates ranged from 1688 to 7146 ova. Total length and weight are equally useful for predicting fecundity.     

Temperature preference and tolerance of hybrid carp (female grass carp,Ctenopharyngodon idella x male bighead,Aristichthys nobilis)

Synopsis This study examined the effects of various pH values on sperm motility times of white suckers,Catostomus commersoni, from two artificially acidified lakes in the Experimental Lakes Area (ELA), northwestern Ontario. White sucker sperm were active (motile) in water at all pH values tested (3.0–7.0). The maximum sperm motility time was 76.9 seconds and the minimum time was 51.9 seconds. Sperm motility times of fish from Lake 302N were similar to those of fish from Lake 223 at all pH values except pH 5.0 and 5.5. At these two pH values, sperm motility times of Lake 223 fish were longer than those of Lake 302N fish. In both lakes sperm motility at ambient lake pH levels (Lake 223 + 5.1, Lake 302N + 6.3) were similar to those at pH 7.0. Motility times of all fish tested were within the range of time during which fertilization normally occurs, indicating that reproductive failures in Lake 223 were probably not caused by impairment of sperm motility times.     

Laboratory diagnosis of melioidosis: Past,present and future

Melioidosis is an emerging, potentially fatal disease caused by Burkholderia pseudomallei, which requires prolonged antibiotic treatment to prevent disease relapse. However, difficulties in laboratory diagnosis of melioidosis may delay treatment and affect disease outcomes. Isolation of B. pseudomallei from clinical specimens has been improved with the use of selective media. However, even with positive cultures, identification of B. pseudomallei can be difficult in clinical microbiology laboratories, especially in non-endemic areas where clinical suspicion is low. Commercial identification systems may fail to distinguish between B. pseudomallei and closely related species such as Burkholderia thailandensis. Genotypic identification of suspected isolates can be achieved by sequencing of gene targets such as groEL which offer higher discriminative power than 16S rRNA. Specific PCR-based identification of B. pseudomallei has also been developed using B. pseudomallei-specific gene targets such as Type III secretion system and Tat-domain protein. Matrix-assisted laser desorption ionization time-of-flight mass spectrometry, a revolutionary technique for pathogen identification, has been shown to be potentially useful for rapid identification of B. pseudomallei, although existing databases require optimization by adding reference spectra for B. pseudomallei. Despite these advances in bacterial identification, diagnostic problems encountered in culture-negative cases remain largely unresolved. Although various serological tests have been developed, they are generally unstandardized “in house” assays and have low sensitivities and specificities. Although specific PCR assays have been applied to direct clinical and environmental specimens, the sensitivities for diagnosis remain to be evaluated. Metabolomics is an uprising tool for studying infectious diseases and may offer a novel approach for exploring potential diagnostic biomarkers. The metabolomics profiles of B. pseudomallei culture supernatants can be potentially distinguished from those of related bacterial species including B. thailandensis. Further studies using bacterial cultures and direct patient samples are required to evaluate the potential of metabolomics for improving diagnosis of melioidosis.