RESUMO: O objetivo do presente estudo foi detectar ovos de helmintos e oocistos de protozoários em amostras de fezes de aves da ordem Passeriformes no estado do Pará, Brasil. Amostras de fezes foram coletadas individualmente de 403 aves Passeriformes oriundas de apreensão e mantidas em cativeiro no estado do Pará. As amostras foram processadas usando a técnica de dupla centrifugação em solução saturada de sacarose e as amostras positivas para oocistos de coccídios foram submetidas à esporulação em dicromato de potássio 2,0%. Ovos de helmintos e/ou oocistos de protozoários foram observados em 43,18% (174/403) das amostras fecais examinadas. Oocistos de coccídios foram detectados em 93,68% (163/174) das amostras positivas, enquanto que ovos de helmintos foram observados em 10,34% (18/174). A esporulação de oocistos ocorreu em 43,56% (71/163) das amostras, e somente oocistos de Isospora spp. foram detectados. Ovos de nematódeos das Superfamílias Trichostrongyloidea (4,60%; 8/174), Ascaridoidea (0,57%; 1/174) e Trichuroidea (0,57%; 1/174) foram diagnosticados nas amostras positivas. Ovos de Cestoda foram diagnosticados em 2,87% (5/174), enquanto que ovos de Trematoda foram detectados em 2,30% (4/174) das amostras positivas. Aves Passeriformes oriundas de apreensão e mantidas em cativeiro nas áreas visitadas estavam parasitadas por helmintos e protozoários, predominando a infecção por coccídios do gênero Isospora.

ABSTRACT: The objective of this study was to detect helminth eggs and protozoan oocysts in samples of feces from birds of the order Passeriformes in Para State, Brazil. Fecal samples were collected individually from 403 passerine birds seized and kept in captivity in Para State. Samples were processed by the double centrifugation technique in saturated sucrose solution and the coccidial oocyst-positive samples were submitted to sporulation in potassium dichromate 2.0%. Helminth eggs and/or protozoan oocysts were observed in 43.18% (174/403) of the fecal samples examined. Coccidial oocysts were detected in 93.68% (163/174) of the positive samples, whereas helminth eggs were observed in 10.34% (18/174) of the positive samples. Oocyst sporulation occurred in 43.56% (71/163) of the samples, and only Isospora spp. oocysts were detected. Nematode eggs of the superfamilies Trichostrongyloidea (4.60%; 8/174), Ascaridoidea (0.57%; 1/174), and Trichuroidea (0.57%; 1/174) were diagnosed in the positive samples. Cestoda eggs were diagnosed in 2.87% (5/174), whereas Trematoda eggs were detected in 2.30% (4/174) of positive samples. Passerine birds seized and kept in captivity in the visited local presented parasitism by intestinal helminths and protozoan, with a predominance of infection with coccidia of the gender Isospora.

Os efeitos da localização do alvo e da incerteza quanto à posição do alvo em movimentos de alcance foram investigados. Dez adultos permaneceram em pé em frente a um monitor sensível ao toque. Eles foram instruídos a pressionar com o dedo indicador direito um interruptor e tocar o centro do alvo apresentado no monitor após ele acender, movendo o membro superior rapidamente. O alvo foi mostrado ipsi ou contralateralmente e os participantes tinham ou não certeza sobre a posição do alvo. O tempo de reação (TR) e movimento (TM) e o erro radial (ER) foram avaliados. Os resultados revelaram menor TR (≈35 ms) e ER (≈0,19 cm) para a condição de certeza e maiores TR (≈8 ms) e TM (≈18 ms) para os moimentos ao alvo contralateral. Concluindo, esses achados mostraram que os efeitos da incerteza da localização e a posição final do alvo podem ser aplicados para movimentos de alcance na posição ereta.

The effects of target location and uncertainty of target position on reaching movements while standing were investigated. Ten healthy, right-handed adults stood facing a 17'' touchscreen. They were instructed to press with their right index fingertip a push bottom and touch the center of the target displayed on the screen after it was lighted on, moving quickly their arm. The target was shown either ipsi- or contralateral to the right arm and either in a certain or uncertain position. Reaction time (RT), movement time (MT), and radial error (RE) were assessed. Results revealed shorter RT (≈ 35 ms) and smaller RE (≈ 0.19 cm) for certain than for uncertain condition and slightly longer RT (≈ 8 ms) and MT (≈ 18 ms) for reaches towards the contralateral target. In conclusion, the findings of this study showing the effect of uncertainty of target location as well as target position are also applied to arm reaching in standing position.

Los efectos de la ubicación de la diana y la incertidumbre acerca de la posición de la diana en los movimientos de alcance fueron investigados. Diez adultos sanos y diestros estaban frente a una pantalla táctil de 17''. Se les instruyó para presionar un interruptor con el dedo índice derecho y tocar el centro de la diana que aparece en la pantalla después de haber sido iluminado, moviéndo rápidamente su miembro superior. La diana fue mostrada ya sea ipsi o contralateralmente y los participantes tenían o no certidumbre sobre la posición de la misma. El tiempo de reacción (TR), el tiempo de movimiento (TM), y el error radial (ER) fueron evaluados. Los resultados revelaron ser más cortos TR (≈ 35 ms) y RE menor (≈ 0,19cm) en la condición de certeza y mayores TR (≈ 8 ms) y TM (≈ 18 ms) en los movimientos hacia la meta contralateral. En conclusión, los hallazgos de este estudio que muestra los efectos de la incertidumbre de la ubicación de la diana, así como la posición de la diana se aplican también a movimientos de alcance en la posición erecta.

CA88 is the first long nuclear repetitive DNA sequence identified in the blood fluke, Schistosoma mansoni. The assembled S. mansoni sequence, which contains the CA88 repeat, has 8,887 nucleotides and at least three repeat units of approximately 360 bp. In addition, CA88 also possesses an internal CA microsatellite, identified as SmBr18. Both PCR and BLAST analysis have been used to analyse and confirm the CA88 sequence in other S. mansoni sequences in the public database. PCR-acquired nuclear repetitive DNA sequence profiles from nine Schistosoma species were used to classify this organism into four genotypes. Included among the nine species analysed were five sequences of both African and Asian lineages that are known to infect humans. Within these genotypes, three of them refer to recognised species groups. A panel of four microsatellite loci, including SmBr18 and three previously published loci, has been used to characterise the nine Schistosoma species. Each species has been identified and classified based on its CA88 DNA fingerprint profile. Furthermore, microsatellite sequences and intra-specific variation have also been observed within the nine Schistosoma species sequences. Taken together, these results support the use of these markers in studying the population dynamics of Schistosoma isolates from endemic areas and also provide new methods for investigating the relationships between different populations of parasites. In addition, these data also indicate that Schistosoma magrebowiei is not a sister taxon to Schistosoma mattheei, prompting a new designation to a basal clade.

The identification and description of signal transduction molecules and mechanisms are essential to elucidate Schistosoma mansoni host-parasite interactions and parasite biology. This mini review focuses on recent advancements in the study of signalling molecules and transduction mechanisms in S. mansoni, drawing special attention to the recently identified and characterised protein tyrosine kinases of S. mansoni.

Sulfonamides are drugs extensively used in the management of AIDS patients. However, the use of sulfonamides is often associated with the development of allergic reactions, provoking the substitution of the drug (by another that may be less effective); alternatively attempts are made to desensitize the patient. OBJECTIVE: Compare two drug regimens (full vs. escalating doses) for the oral desensitization of AIDS patients allergic to sulfonamides. MATERIAL AND METHODS: AIDS patients with previous allergic reactions to sulfonamides and requiring prophylaxis against Pneumocistis carinii, central nervous system toxoplasmosis and diarrhea caused by Isospora belli were randomly assigned to a group receiving a routine dose of cothrimoxazole, or another that received escalating doses of an oral suspension of the same drug, initiating with 75mg/day of sulfamethoxazole that was doubled every 48 hours till the full dose was reached, if no allergic reaction occurred. Patients were monitored for at least 6 months after enrollment in the trial. The major end-point was the ability to maintain prophylactic treatment after that period of time. Plasma viral load (PVL) and CD4/CD8 counts were measured at baseline. Liver enzymes and hematological parameters were measured at baseline and after 1, 3 and 6 months. RESULTS: Eighteen patients were enrolled in the study (15 men and 3 women), with ages ranging from 30 to 57 years (mean 39.9). The mean CD4 counts were slightly higher for patients receiving a full dose; there was also a trend towards higher baseline CD8 counts among patients developing new reactions. The mean PVL was similar among the patients in both desensitization groups. The incidence of new allergic reactions was identical (40%) in the two groups. All adverse reactions were mild and no significant increase in liver enzymes were observed. CONCLUSON: Dose regimen is not a predictor of the development of new allergic reactions amongst patients challenged with sulfonamides after an initial allergic reaction.