BackgroundAnaplasma phagocytophilum is an emerging pathogen of humans, dogs and other animals, and it is transmitted by ixodid ticks. The objective of the current study was a) detect A. phagocytophilum in dogs and ixodid ticks using real-time Polymerase Chain Reaction (qPCR); and b) Determine important variables associated to host, environment and potential tick vectors that are related to the presence of A. phagocytophilum in dogs domiciled in Rio de Janeiro, Brazil.MethodsWe tested blood samples from 398 dogs and samples from 235 ticks, including 194 Rhipicephalus sanguineus sensu lato, 15 Amblyomma cajennense, 8 Amblyomma ovale and 18 pools of Amblyomma sp. nymphs. A semi-structured questionnaire was applied by interviewing each dog owner. Deoxyribonucleic acid obtained from ticks and dog buffy coat samples were amplified by qPCR (msp2 gene). The sequencing of 16S rRNA and groESL heat shock operon genes and a phylogenetic analysis was performed. The multiple logistic regression model was created as a function of testing positive dogs for A. phagocytophilum.ResultsAmong the 398 blood samples from dogs, 6.03% were positive for A. phagocytophilum. Anaplasma phagocytophilum was detected in one A. cajennense female tick and in five R. sanguineus sensu lato ticks (four males and one female). The partial sequences of the 16S rRNA, and groESL genes obtained were highly similar to strains of A. phagocytophilum isolated from wild birds from Brazil and human pathogenic strains. The tick species collected in positive dogs were R. sanguineus sensu lato and A. cajennense, with A.cajennense being predominant. Tick infestation history (OR = 2.86, CI = 1.98-14.87), dog size (OR = 2.41, IC: 1.51-12.67), the access to forest areas (OR = 3:51, CI: 1.52-16.32), hygiene conditions of the environment in which the dogs lived (OR = 4.35, CI: 1.86-18.63) and Amblyomma sp. infestation (OR = 6.12; CI: 2.11-28.15) were associated with A. phagocytophilum infection in dogs.ConclusionsThis is the first report of A. phagocytophilum in ixodid ticks from Brazil. The detection of A. phagocitophylum in A. cajennense, an aggressive feeder on a wide variety of hosts, including humans, is considered a public health concern.

Anaplasma phagocytophilum was detected in dogs from Brazil in the municipalities of Seropédica and Itaguaí, Rio de Janeiro state, by real-time polymerase chain reaction (PCR) using SYBR Green to detect the amplification. Of 253 samples, 18 (7.11%) were positive, with a threshold cycle (Ct) ranging from 31 to 35 cycles. The PCR product from a positive sample was cloned and sequenced. The sequence obtained demonstrated 100% identity with other A. phagocytophilum sequences published in the GenBank database. The analytical sensitivity of RT-PCR using SYBR Green system was able to detect 3 plasmid copies when defined numbers of plasmid copies containing 122 base pairs from the msp2 gene were used. The assay was considered specific when DNA from bacteria (Anaplasma platys, Anaplasma marginale, Ehrlichia canis, Neorickettsia risticii, Rickettsia rickettsii) closely related to A. phagocytophilum was placed in the reaction. These results demonstrate that the canine granulocytic anaplasmosis agent is present in regions in which dogs could be a source of infection for tick vectors. The current study reports the detection of A. phagocytophilum, a zoonotic agent responsible for Human granulocytic anaplasmosis, in Brazilian dogs.

The technique is so simple that it can be performed by the parents themselves, allowing continuation of the treatment at home.

The aim of this research was to monitor the presence of females of Aedes aegypti (Linnaeus, 1762) on the Seropédica municipality, Rio de Janeiro State, from 2010 to 2013. For this purpose, the Intelligent Dengue Monitoring (IM-Dengue) and Intelligent Virus Monitoring (IM-Virus) developed by Universidade Federal de Minas Gerais (Ecovec – Minas Gerais, Brazil), were used. IM-Dengue is a tool that allows achieving a weekly overview of A. aegypti infestation, while IM-Virus is another tool that allows detecting dengue virus directly from the mosquito, by Real Time-PCR. Both tools were developed for diagnosis in a prepathogenesis period of the disease, before infection occurrence. Traps were distributed in 19 locations inside the municipality and the bugs were collected weekly during the years of the research. As a result, the presence of 163 females of A. aegypti was recorded over the period; there was no circulation of the virus in the municipality. In one of the 19 study sites, a high degree of disease transmission risk was verified. The study concluded that the municipality, as a whole, showed no risk of disease transmission throughout the field research period.

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Muitos vegetais são consumidos crus em saladas. Desse modo, se não forem devidamente higienizados, poderão veicular patógenos. No Brasil, a alface (Lactuca sativa) é uma das hortaliças mais consumidas. Em função disso, este estudo teve como objetivo avaliar o nível de contaminação por parasitas em amostras de alfaces comercializadas in natura e de alfaces prontas para consumo, servidas cruas em restaurantes do tipo self-service do município do Rio de Janeiro. No período de julho a outubro de 2010 foram coletadas 90 amostras, sendo 60 comercializadas in natura (30 da variedade lisa e 30 da crespa) e 30 da variedade crespa servidas em restaurantes. As amostras foram analisadas na Subgerência de Parasitologia da Unidade de Diagnóstico, Vigilância, Fiscalização Sanitária e Medicina Veterinária Jorge Vaitsman, sendo utilizada a técnica de Dennis, Stone e Swanson. De 90 amostras, 70% estavam contaminadas por parasitas. Estatisticamente, não houve diferença significativa entre alfaces lisas e crespas in natura, mas houve diferença estatística significativa entre alfaces crespas in natura e servidas em restaurantes. Os parasitas encontrados foram: ovos e larvas de Strongyloides sp., ovos de ancilostomídeos, larvas de estrongilídeos, ovos de Hymenolepis sp., oocistos de coccídeos, cistos de Entamoeba sp. e oocistos de Isospora sp. Os resultados revelam a importância do fortalecimento do sistema de Vigilância Sanitária e da orientação de produtores de hortaliças, manipuladores de alimentos e da população em geral sobre a importância da aquisição de hortaliças de proveniência confiável, assim como da necessidade de boa lavagem e desinfecção das folhas de alface antes do consumo. Palavras-chave: Parasitas. Alface. Saúde Pública. Vigilância Sanitária. AbstractMany raw vegetables are eaten in salads. Thus, they can carry pathogens when no properly sanitized. In Brazil, lettuce (Lactuca sativa) is one of the main vegetable components of salads. Therefore, this study aimed to evaluate the occurrence of parasites contaminating lettuce samples commercialized in natura as well as raw lettuce served in self-service restaurants in Rio de Janeiro municipality.

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The current study investigated the biology of nymphs of the first and second instars of Argas (Persicargas) miniatus. Nymphs were deprived of food for 15, 30 or 60 days and held at 27 ± 1 ºC and 80 ± 10% relative humidity (controlled conditions) or at room conditions of temperature and relative humidity. Nymphs of first instar deprived of food for 15 or 30 days molted to second and third instars in both controlled and room conditions. Nymphs of the first instar deprived of food for 60 days had 28 and 37% mortality in controlled and room conditions, respectively; and survivors did not attach to the host. Nymphs of the second instar, deprived of food for 60 days, molted either to the third instar or to males after feeding on Gallus gallus, and the nymphs of the third instar developed to adults (42.42% males and 36.36% females when nymphs were held in controlled temperature and humidity conditions, and 40.54% males and 48.65% females when nymphs were held in room conditions). The remainder of the nymphs molted to the fourth instar and then molted to females. In conclusion, the nymphal starvation period of 60 days determined the number of nymph instars in the life cycle of A. miniatus under the experimental conditions studied.