Seeking the identification ofA. cantonensis has already been found in Southeast Asia, South Pacific, Africa, India, Caribbean, Australia, North America (Pien & Pien 1999), Jamaica (Lindo et al. 2002) and Haiti (Raccurt et al. 2003).Eosinophilic meningitis is a rare clinical entity that is defined by the presence of 10 or more eosinophils/ ml in the cerebrospinal fluid (CSF) or a CSF eosinophilia of at least 10% of the total CSF leukocyte count (Kuberski 1979). The most common cause is invasion of the central nervous system by helminthic parasites, inciting an inflammatory response that eventually kills the parasites. Clinical manifestations, which develop in humans at two to 35 days after larvae ingestion, may include headache, nuchal rigidity and visual disturbances (Koo et al. 1988). Cerebral angiostrongyliasis usually has an incubation period of about two weeks, although it may vary from 12 to 28 days (Dooley & Neafie 1976). Paresthesias of the extremities, trunk or face, are the most distinctive neurological findings and can persist for weeks to months after the other symptoms are resolved. Occasionally, infective larvae can migrate to the eye, causing retinal detachment or intraocular hemorrhage, but most patients recover completely (Alicata 1962, Sawanyawisuth et al. 2007. In Brazil, a clinical case of eosinophilic meningoencephalitis that resulted in death ten days after ingestion of three Achatina fulica snails was reported in a regional meeting in 2006 (AVS Moll, G Zanini and C Graeff-Teixeira, unpublished observations).In January 2007, two male individuals aged 21 and 39 years were admitted to the local hospital of Cariacica, state of Espírito Santo (ES), Brazil, with eosinophilic meningitis and history of ingestion of raw terrestrial slugs. By that time, a male child aged one year and eight months from the city of Vila Velha, ES, had also been admitted to the hospital with similar symptoms.A number of 270 mollusc specimens and feces from Rattus norvergicus were collected with a grasping tool, in peridomiciliary areas of the patients' houses by health agents of the Central Laboratory of the ES (LACEN-ES). The materials were sent to the Laboratory of Intestinal Helminthiasis of Instituto René Rachou-Fiocruz for mollusc morphological identification and molecular characterization of nematode larvae. The gastropods were identified as: Sarasinula marginata (Semper, 1885) (Veronicellidae), 45 specimens, Subulina octona (Bruguière, 1792) (Subulinidae), 157 specimens, A. fulica (Bowdich, 1822) (Achatinidae), 45 specimens, and Bradybaena similaris (Férussac, 1821) (Bradybaenidae), 23 specimens.
Short interfering RNAs (siRNA) guide degradation of target RNA by the RNA-induced silencing complex (RISC). The use of siRNA in animals is limited partially due to the short half-life of siRNAs in tissues. Chemically modified siRNAs are necessary that maintain mRNA degradation activity, but are more stable to nucleases. In this study, we utilized alternating 2′-O-methyl and 2′-deoxy-2′-fluoro (OMe/F) chemically modified siRNA targeting PTEN and Eg5. OMe/F-modified siRNA consistently reduced mRNA and protein levels with equal or greater potency and efficacy than unmodified siRNA. We showed that modified siRNAs use the RISC mechanism and lead to cleavage of target mRNA at the same position as unmodified siRNA. We further demonstrated that siRNAs can compete with each other, where highly potent siRNAs can compete with less potent siRNAs, thus limiting the ability of siRNAs with lower potency to mediate mRNA degradation. In contrast, a siRNA with low potency cannot compete with a highly efficient siRNA. We established a correlation between siRNA potency and ability to compete with other siRNAs. Thus, siRNAs that are more potent inhibitors for mRNA destruction have the potential to out-compete less potent siRNAs indicating that the amount of a cellular component, perhaps RISC, limits siRNA activity.
Hematological and coagulation profiles were studied in crossbred dogs experimentally infected with Angiostrongylus vasorum. Two groups of five dogs were experimentally inoculated with 50 and 100 third stage infective larvae (L(3)) of A. vasorum per kilogram of body weight. A third group of five uninfected animals was used as control. One sample of 10 ml of blood was collected from each animal on the 10, 20, 30, and 45 days after inoculation (dai) and at 30-day intervals thereafter for the remainder of the 210-day experimental period. The blood sample was used for the complete hemogram and platelet count, as well as measurements of prothrombin time, partial thromboplastin time and factors V and VIII. Anemia was observed in infected dogs, 6 weeks after the infection. The eosinophils presented peaks in four periods after infection. Thrombocytopenia became accentuated on the 72 dai. Decreased prothrombin time activity and increased partial thromboplastin time were observed at the 6 and 9 weeks after infection and decreased of factors VIII and V activities occurred from 4 to 6 weeks after infection. It may be conclude that infection by A. vasorum in dogs may cause a discrete anemia during the acute phase which is probably regenerative. In addition, important hemostatic alterations due to the infection suggest a chronic intravascular consumption coagulopathy.
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