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The influence of temperature on the development and survival of Toxocara canis larvae was investigated under laboratory conditions, in water at 15, 20, 25, 30 and 35°C and at room temperature 22°C ± 1°C. T. canis eggs were able to develop to the larvated stage at all the tested temperatures. Development rate increased with temperature. Linear regression of development rate against temperature predicted a lower development threshold of 11.8°C. Eggs survived cooling to 1 and −2°C for 6 weeks, and could develop to the infective, larvated stage when transferred to higher temperatures, but their development rates were then retarded compared with non-chilled eggs. Larvated eggs remained viable after 7 weeks of incubation across the tested temperature range, with the highest percentage viability (47%) obtained at 25°C. Development of eggs to the infective larval stage required, on average, 121 degree days between 20°C and 30°C. Results provide a basis for predicting variation in the infectivity of eggs in the environment over time in different climates. [ABSTRACT FROM AUTHOR]

In the present study, the potential of RNA interference (RNAi) as a gene silencing tool and the resultant effects on Ascaris suum larval development was examined by targeting a gene (represented by the EST 06G09) specifically expressed in the infective larvae of A. suum. BALB/c mice were infected with RNAi-treated larvae. The results showed that the target gene was silenced after soaking for 72 h, and the survival rate of the RNAi-treated larvae was reduced by 17.25% ( P < 0.01). A significant difference ( P < 0.05) was detected in the numbers of larvae collected from the livers and lungs of infected mice 4 days after infection with untreated larvae (164.29 ± 21.51) and RNAi-treated larvae (71.43 ± 14.35). Significant differences ( P < 0.01) were also found in the body length and width between untreated larvae (480 ± 105.77 μm for length and 23.93 ± 3.72 μm for width) and RNAi-treated larvae (400.57 ± 71.31 μm for length and 20.20 ± 2.43 μm for width). These results show that the gene represented by EST 06G09 may play a role in the development of A. suum larvae. [ABSTRACT FROM AUTHOR]

Efficacy of extracts of Ageratum conyzoides, Argemone mexicana, and Azadirachta indica were tested against Culex quinquefasciatus larvae. Petroleum ether extracts of A. conyzoides and A. mexicana with LC50 values 425.60 and 267.90 ppm and 140.15 and 137.70 ppm after a period of 24 and 48 h, respectively, were found effective. However, the methanol extract of A. indica with LC50 values 21.95 and 11.30 ppm after 24 and 48 h of exposure, respectively, was the most competent larvicide. The methanol extract of A. indica, being the most potent extract was therefore studied for its impact on the developmental scenario of the mosquito. It had a significant effect on the life cycle of the vector, C. quinquefasciatus. Hatching was delayed and its rate was reduced compared to control. Larval and pupal development was arrested resulting in decreased pupal transformation and adult emergence. Larval and pupal periods were prolonged with appearance of larval–pupal and pupal–adult intermediates, with an overall increase in the developmental period. Disrupted egg shells, dechitinized body walls, and distorted intestines were observed, indicating clearly the anti-juvenile potential of the extract. The growth index was considerably reduced. [ABSTRACT FROM AUTHOR]

Abstract  Research on the infection of snails by trematodes has been conducted in Europe for over a hundred years. The initial poor knowledge of the intra-molluscan stages of these parasites together with the difficulty of classifying them constituted a serious obstacle to the undertaking of integrated parasitological and malacological efforts to gain a better understanding of the phenomenon. The compilation of morphological and anatomical results of research on trematode larvae resulted in the publication of keys to designate species of parasites, but was not sufficient to encourage malacologists to collaborate with parasitologists. This paper undertakes to collect data published over the last hundred years on the natural infection of European populations of freshwater snails by trematode larvae. The aim of this undertaking is to make researchers of malacofauna and, above all, experts on freshwater snails aware of the scale of the problem of molluscs being exploited as intermediate hosts of trematodes and, consequently, to encourage parasitologists and malacologists to collaborate on this phenomenon that is crucial for both parasites and hosts. [ABSTRACT FROM AUTHOR]

Abstract  In the present study, larvae of Ascaris suum and Trichuris muris were investigated by light and electron microscopy after incubation in a hatching medium containing 89% phosphate-buffered saline (pH 7.4), 10% RPMI-1640 and 1% sodiumhypochlorite at 40 and 37°C, respectively. The larvae were obtained from fertilised eggs of the worms during defined phases of development (A. suum, 36th–50th day of development; T. muris, once a week from week 16 to 20). Light and electron micrographs of the larvae gave evidence that the third larval stage of A. suum is probably the infectious stage. The first moult of the larvae had already taken place before the 36th day of incubation starting at day 1. After 36 days of incubation, only the second larval stage was found within eggs. Some of these larvae were coated by a separated sheath so that a second moult of the larvae is reasonable. On the other hand, no sheathed larvae of T. muris were found in the eggs incubated for 20 weeks in distilled water. No signs of moult were seen for 20 weeks neither on light nor on the electron micrographs. Therefore, in T. muris, the first larval stage is the infectious stage, which was proven by means of re-infections of mice 16, 18 or 20 weeks after incubation of the eggs. [ABSTRACT FROM AUTHOR]

Abstract  The Stomacher® is very widely used in food and medical research for extracting tissues. To determine whether nematode larvae were disrupted by the Stomacher®, L3 larvae of Haemonchus contortus were homogenised for up to 40 min at full power but no larval disruption occurred. Therefore, tissue from the mucosa and submucosa of the caecum of horses collected from a licenced abattoir was treated to determine whether inhibited cyathostomin larvae could be extracted. The optimum time on full power for a 10-g sample was 20 min, and in three out of five caecal samples from different horses, significantly more larvae were recovered than with 6 h pepsin HCl digestion. It is concluded that the Stomacher® provides a simple fast method of extracting inhibited nematode larvae from gastrointestinal tissues in the horse that could replace digestion with pepsin HCl. [ABSTRACT FROM AUTHOR]

Abstract  The present work was aimed at evaluating the in vitro efficacy of thymol on engorged and unengorged larvae of Rhipicephalus sanguineus. In order to perform the study, unengorged larvae were interleaved on filter paper (2 × 2 cm) recently sprayed with thymol in the following concentrations: 0.25%, 0.5%, 1.0%, 1.5%, and 2.0%. For each concentration, ten repetitions of 50 larvae each were performed. A control group was established (water + DMSO) together with a positive control group (Amitraz), with ten repetitions each. Mortality was evaluated after 24 h. For the test with engorged larvae, the same thymol concentrations were used with the larvae being immersed for 5 min and mortality evaluated after 15 days. The values found for thymol efficacy for unengorged larvae were of 21.3%, 17.4%, 19.1%, 32.1%, 37.7% and for engorged larvae 3.0%, 0.0%, 3.0%, 97.0%, and 100.0% in concentrations of 0.25%, 0.5%, 1.0%, 1.5%, and 2.0% respectively. We have concluded that thymol had a deleterious effect on larvae of R. sanguineus, especially on engorged larvae for which 100% mortality was found in higher concentration. [ABSTRACT FROM AUTHOR]