Nota sobre Lutzomyia (Lutzomyia) Cruzi (mangabeira, 1938), com a descrição da fêmea (Diptera, Psychodidae, Phlebotominae)

Depois de examinar o tipo de Lutzomyia (Lutzomyia) cruzi (Mangabeira, 1938), depositado na coleção do Instituto Oswaldo Cruz (Rio de Janeiro), sob o número 941, e 74 espécimens machos da mesma espécie, a maioria da localidade tipo (Camapuan, Estado de Mato Grosso do Sul), os Autores verificaram que o tufo basal do basistilo é composto de apenas quatro cerdas foliáceas, e não seis, como descrito por Mangabeira, devido á superposição dos dois basistilos no holótipo. Além disso é feita uma descrição da fêmea, até agora não conhecida, e a redescrição do macho, baseada no holótipo.

Simulium hirtipupa Lutz, 1910 (Diptera: Simuliidae): descrição dos adultos e larva e redescrição da pupa

Com a "Segunda contribuição para o conhecimento das espécies brasileiras do genero Silulium", Lutz (1910) descreve 18 espécies novas, porém dedica somente um breve parágrafo a S. hirtipupa, mencionando exclusivamente caracteres específicos para a pupa, aliás insuficiente. Descrevemos aqui, pela primeira vez, os adultos e a larva, redescrevemos a pupa e elegemos um neótipo para a espécie.

Redescrição do macho e descrição da fêmea de Lutzomyia (Helcocyrtomyia) Peresi (Mangabeira, 1942) (Diptera: Psychodidae, Phlebotominae)

Os autores redescrevem o macho e descrevem a fêmea de Lutzomyia (Helcocyrtomyia) peresi (Mangabeira, 1942).

Descrição de uma nova espécie do subgênero Helcocyrtomyia, Lutzomyia Pusilla sp. n. (Diptera, Psychodidae, Phlebotominae)

Estudando o material de Helcocyrtomyia depositado na coleção de flebotomíneos do Centro de Pesquisas René rachou, os autores verificaram a ocorrência de uma nova espécie, Lutzomyia pusilla sp. n., que até o momento era confundida com lutzomyia peresi (Mangabeira, 1942).

Descrição de uma nova espécie do subgênero Helcocyrtomyia, Lutzomyia capixaba sp.n. (Diptera, Psychodidae, Phlebotominae)

Os autores descrevem uma nova espécie, Lutzomyia capixaba sp.n., pertencente ao grupo dos flebotomíneos de cinco espinhos do subgênero Helcocyrtomyia Barreto, 1962.

Redescrição do macho e descrição da fêmea de Lutzomyia (Helcocyrtomyia) ferreirana (Barretto, Martins & Pellegrino, 1958) (Diptera, Psychodidae, Phlebotominae)

Os autores após examinarem um grande número de exemplares pertencentes ao grupo dos flebotomíneos de cinco espinhos do subgênero Helcocyrtomyia Barretto, 1962, verificaram a correlação dos sexos de Lutzomyia ferreirana que até o presente momento não estava definida.

Classificação de Phaonia Robineau-Desvoidy (Diptera, Muscidae) da região neotropical: I. Considerações sobre a sinonímia de Bigotomyia Malloch, com descrição de uma espécie nova

Some considerations about the synonym of Bigotomyia Malloch, 1922 and Phaonia R.-D, 1830 are made. A new species, P. hugonis sp. n. is described from Peru and Equador.

Estudo sobre os Ceratopogonídeos de Minas Gerais: I - Descrição dos machos de Heteromyia chaquensis Duret & Lane, 1955 e Dasyhelea paulistana Forattini & Rabello, 1957 (Diptera, Ceratopogonidae)

This paper describes some results of a systematic survey of the Ceratopogonidae midges of the State of Minas Gerais, Brazil. Three species, Stilobezzia punctulata Lane, 1947, Heteromyia chaquensis Duret & Lane, 1955 and Dasyhelea paulistana Forattini & Rabello, 1957 were identified from a small lake, "Lagoinha" or "Olhos d'Água", near to the main lake of Lagoa Santa. The first descriptions of the males of Heteromyia chaquensis and Dasyhelea paulistana are presented.

Descrição da fêmea, genitália do macho e larva de Ocyptamos sativus (Curran, 1941) (Diptera: Syrphidae)

The female, male genital apparatus and larva of Ocyptamus sativus are described. A short report of the predatory habits of this species is made.

Notas sobre Limnophorinae (Diptera, Muscidae) com descrição de uma espécie nova no Brasil

This work deals with two genera of Limnophorinae. Heliographa longiseta sp. n., and female genitalia of the Heliographa altaneira Albuquerque, 1954, and genital complex of the Spilogona golbachi Snyder, 1957 are studied. New occurrence for Spilogona argentifrontata and Spilogona pubiceps (Stein, 1911) are stated.

Notas sobre os flebótomos dos estados do Ceará e Piauí, com a descrição da fêmea de Lutzomyia samueli (Deane, 1955) (Diptera, Psychodidae, Phlebotominae)

The authors present the list of the species caught in the National Parks of Ubajara and Sete Cidades, in the counties of Ubajara (CE) and Piracuruca (PI), respectively, and described the Lutzomyia (Helcocyrtomyia) samueli (Deane, 1955) female, which up to now had been known by the male.

Descrição dos Ovos e dos Estádios Ninfais de Triatoma jurbergi Carcavallo, Galvão & Lent, 1998 Vistos Através de Microscopia Óptica e Eletrônica de Varredura (Hemiptera, Reduviidae)

Eggs and nymphs of Triatoma jurbergi were described using optical microscopy and scanning electron microscopy. T. jurbergi is a wild species, found in State of Mato Grosso (15ºS and 300 m.a.s.l), Brazil. Eggs showed the operculum and surface with pentagonal and hexagonal cells, with small fractures and punctuations randomly distributed. Differences were found in the five nymphal stages of T. jurbergi, that allow their to be distinguished from the similar species T. guazu. The diagnostic characters most useful for differentiation were the general color of the insect, abdomen shape and its length.

Early white matter alterations in men predisposed to FXTAS revealed by MT imaging.

Introduction: The Fragile X - associated Tremor Ataxia Syndrome (FXTAS) is a recently described, and under-diagnosed, late onset (≈ 60y) neurodegenerative disorder affecting male carriers of a premutation in the Fragile X Mental Retardation 1 (FMR1) gene. The premutation is an CGG (Cytosine-Guanine-Guanine) expansion (55 to 200 CGG repeats) in the proximal region of the FMR1 gene. Patients with FXTAS primarily present with cerebellar ataxia and intention tremor. Neuroradiological features of FXTAS include prominent white matter disease in the periventricular, subcortical, middle cerebellar peduncles and deep white matter of the cerebellum on T2-weighted or FLAIR MR imaging (Jacquemmont 2007, Loesch 2007, Brunberg 2002, Cohen 2006). We hypothesize that a significant white matter alteration is present in younger individuals many years prior to clinical symptoms and/or the presence of visible lesions on conventional MR sequences and might be detectable by magnetization transfer (MT) imaging. Methods: Eleven asymptomatic premutation carriers (mean age = 55 years) and seven intra-familial controls participated to the study. A standardized neurological examination was performed on all participants and a neuropsychological evaluation was carried out before MR scanning performed on a 3T Siemens Trio. The protocol included a sagittal T1-weighted 3D gradient-echo sequence (MPRAGE, 160 slices, 1 mm^3 isotropic voxels) and a gradient-echo MTI (FA 30, TE 15, matrix size 256*256, pixel size 1*1 mm, 36 slices (thickness 2mm), MT pulse duration 7.68 ms, FA 500, frequency offset 1.5 kHz). MTI was performed by acquiring consecutively two set of images; first with and then without the MT saturation pulse. MT images were coregistered to the T1 acquisition. The MTR for every intracranial voxel was calculated as follows: MTR = (M0 - MS)/M0*100%, creating a MTR map for each subject. As first analysis, the whole white matter (WM) was used to mask the MTR image in order to create an histogram of the MTR distribution in the whole tissue class over the two groups examined. Then, for each subject, we performed a segmentation and parcellation of the brain by means of Freesurfer software, starting from the high resolution T1-weighted anatomical acquisition. Cortical parcellations was used to assign a label to the underlying white matter by the construction of a Voronoi diagram in the WM voxels of the MR volume based on distance to the nearest cortical parcellation label. This procedure allowed us to subdivide the cerebral WM in 78 ROIs according to the cortical parcellation (see example in Fig 1). The cerebellum, by the same procedure, was subdivided in 5 ROIs (2 per each hemisphere and one corresponding to the brainstem). For each subject, we calculated the mean value of MTR within each ROI and averaged over controls and patients. Significant differences between the two groups were tested using a two sample T-test (p<0.01). Results: Neurological examination showed that no patient met the clinical criteria of Fragile X Tremor and Ataxia Syndrome yet. Nonetheless, premutation carriers showed some subtle neurological signs of the disorder. In fact, premutation carriers showed a significant increase of tremor (CRST, T-test p=0.007) and increase of ataxia (ICARS, p=0.004) when compared to controls. The neuropsychological evaluation was normal in both groups. To obtain general characterizations of myelination for each subject and premutation carriers, we first computed the distribution of MTR values across the total white matter volume and averaged for each group. We tested the equality of the two distributions with the non parametric Kolmogorov-Smirnov test and we rejected the null-hypothesis at a p=0.03 (fig. 2). As expected, when comparing the asymptomatic permutation carriers with control subjects, the peak value and peak position of the MTR values within the whole WM were decreased and the width of the distribution curve was increased (p<0.01). These three changes point to an alteration of the global myelin status of the premutation carriers. Subsequently, to analyze the regional myelination and white matter integrity of the same group, we performed a ROI analysis of MTR data. The ROI-based analysis showed a decrease of mean MTR value in premutation carriers compared to controls in bilateral orbito-frontal and inferior frontal WM, entorhinal and cingulum regions and cerebellum (Fig 3). The detection of these differences in these regions failed with other conventional MR techniques. Conclusions: These preliminary data confirm that in premutation carriers, there are indeed alterations in "normal appearing white matter" (NAWM) and these alterations are visible with the MT technique. These results indicate that MT imaging may be a relevant approach to detect both global and local alterations within NAWM in "asymptomatic" carriers of premutations in the Fragile X Mental Retardation 1 (FMR1) gene. The sensitivity of MT in the detection of these alterations might point towards a specific physiopathological mechanism linked to an underlying myelin disorder. ROI-based analyses show that the frontal, parahippocampal and cerebellar regions are already significantly affected before the onset of symptoms. A larger sample will allow us to determine the minimum CGG expansion and age associated with these subclinical white matter alterations.

Cell proliferation and interferon-gamma response to recombinant MBP-3, NarL, MT-10.3, and 16kDa Mycobacterium tuberculosis antigens in Brazilian tuberculosis patients

Human pulmonary tuberculosis (TB) is a worldwide public health problem. In resistant individuals, control of the infection mainly requires development of a Th1 cell immune response with production of cytokines, of which interferon-gamma (IFN-gamma)plays an important role. Several antigens from Mycobacterium tuberculosis complex has been described for use in vaccine development or for diagnostic purposes, however little evaluation has been done in endemic area for TB. The proliferative and IFN-gamma human T cell immune responses, to four recombinant proteins (MBP-3, NarL, MT-10.3, 16 kDa) and PPD, of 38 Brazilian TB patients (6 untreated and 32 treated) and 67 controls (38 positive and 29 negative tuberculin skin test - TST) were compared. The highest reactivity mean rate was obtained with PPD followed by 16 kDa in TB patients. While most of the patients (87%) and controls (> 64%) respond to the PPD, 16kDa was more specifically recognized (> 21%) although less sensitive (54%). When TB patients were divided according to treatment status, opposite to PPD, higher average level of IFN-gamma was induced by 16kDa in untreated (505 pg/ml) compared to treated TB patients and TST+ (269.8 pg/ml x 221.6pg/ml, respectively), although the difference was not significant. These data show that in contrast with the other recombinant proteins, the stimulatory potency of 16kDa to induce proliferative and INF-gamma response was more effective and is more recognized by active TB untreated patients, eliciting in control individuals a more selective immune response than PPD.