RESUMO
A dog naturally infected with Dipetalonema dracunculoides and having a microfilaremia of 6050 microfilariae per mm3 of blood was used as source of infection. Experimentally cultivated nymphs of Rhipicephalus sanguineus were fed on the donor dog. Once engorged, ninety-three nymphs were removed and kept at 30 degrees C and RH 90% until they moulted to the adult stage. To study the development of microfilariae in the vector, ten ticks were dissected at Day 37 post-infection. Adult infected ticks were fed on two uninfected dogs. The observed pre-patent periods were 69 and 76 days. Trans-stadial transmission of Dipetalonema dracunculoides by Rhipicephalus sanguineus was demonstrated.
Assuntos
Vetores Aracnídeos/parasitologia , Infecções por Dipetalonema/veterinária , Dipetalonema/crescimento & desenvolvimento , Doenças do Cão/transmissão , Carrapatos/parasitologia , Animais , Infecções por Dipetalonema/transmissão , Cães , Feminino , Masculino , Microfilárias/crescimento & desenvolvimento , Ninfa/parasitologia , Organismos Livres de Patógenos EspecíficosRESUMO
This paper reports the development of the canid filarial worm, Dipetalonema dracunculoides, in the brown dog tick, Rhipicephalus sanguineus by determining whether development is similar within larval, nymphal and adult stages of infected ticks. This study demonstrates that only infected nymphal ticks can support the complete development of the filarial worm. Infected larval ticks are not suitable intermediate hosts, nor are infected adults. Development depends on some stage-specific property of the vector, and the maturation to the infective stage is stimulated during the course of the nymphal-adult moult.
Assuntos
Dipetalonema/crescimento & desenvolvimento , Carrapatos/parasitologia , Animais , Dipetalonema/anatomia & histologia , Insetos Vetores , Larva , Carrapatos/crescimento & desenvolvimentoRESUMO
In order to clarify the importance of humoral antibody in host resistance to ticks, in the present work we studied the immunological response of rabbits infested with larvae, nymphs or adults of Rhipicephalus sanguineus, using extracts of eggs (EE), larvae (LE), nymphs (NE), male salivary glands (MSGE), male midguts (MME), female salivary glands (FSGE) and female midguts (FME). When serum from rabbits infested with larvae or nymphs was tested using enzyme-linked immunosorbent assay, no reactions were observed with any of the extracts including the homologous LE or NE. In sera from rabbits infested with adult ticks, the reactions were observed in both homologous (MSGE, MME, FSGE and FME) and heterologous (EE, LE and NE) system. However, differences were seen regarding the type of antigen used. When the experiment was carried out using extracts from adults higher responses were found. With FSGE and FME antigens, antibody levels were systematically higher than those observed when MSGE and MME were used.
Assuntos
Anticorpos/sangue , Infestações por Carrapato/imunologia , Carrapatos/imunologia , Animais , Ensaio de Imunoadsorção Enzimática , Feminino , Larva/imunologia , Masculino , CoelhosRESUMO
We carried out an SDS-PAGE analysis of antigens of Rhipicephalus sanguineus using extracts of eggs (EE), larvae (LE), nymphs (NE), male salivary glands (MSGE), male midguts (MME), female salivary glands (FSGE) and female midguts (FME). Under non-reducing conditions a common band of about 205 kDa was observed. EE, LE and NE extracts showed groups of bands between 150 and 75 kDa. A protein pattern was observed in FSGE extract with a group of bands between 75 and 50 kDa and four bands between 15 and 6.5 kDa. In this case an apparently exclusive band of molecular weight about 25 kDa was observed. Under reducing conditions similarities between LE and NE extracts increased, separating from the EE pattern. On the other hand, we have determined the presence of stage-specific and common antigens on EE, LE, NE, MSGE, MME, FSGE and FME extracts of R.sanguineus by means of immunoblots using polyclonal sera of rabbits infested with larvae, nymphs or adults of this tick. EE extract was only recognized by the anti-larva sera. Higher reactivity was observed when the extracts were tested with anti-adult sera. In these experiments a very prominent band of molecular weight about 45 kDa was detected. This band was not observed under reducing conditions. Higher reactivity with anti-adult sera was observed against FSGE extract.