ABSTRACT
The risk of malaria recurrence increases due to the main vector, Anopheles pharoensis. The physiological age of the mosquito population is needed to expect malaria vector dynamics. The number of completed gonotrophic cycles is of great importance in determining the physiological age of females. A technique has been described that focuses on the number of dilatations remaining in the ovarioles after each oviposition to determine how many blood meals have been taken. At each gonotrophic cycle, the chances of infection of the vectors are repeated. The histological changes that occur immediately in the ovarioles and ovulation itself were studied. Under the influence of the contractions of the ovarian muscles, the eggs begin to move over the distal end of the ovariole into the inner oviduct. The terminal pedicle is markedly dilated near the diameter of the eggs. After the expulsion of the mature eggs, ovariole dilations were found at the point of their development in the terminal pedicle due to the accumulation of nurse cell remnants and follicular epithelium. The results were used to develop epidemiological localization and to evaluate the effectiveness of antimalaria interventions. The ovarian inspection often provides a technique to distinguish nulliparous from parous female anophelines. In addition, this study can provide basic entomological knowledge on the physiological age of mosquitoes by considering the histological changes in the ovaries, which allow the evaluation of vector management strategies in the field.
Subject(s)
Anopheles , Malaria , Animals , Anopheles/physiology , Female , Histological Techniques , Mosquito Vectors , OvipositionABSTRACT
BACKGROUND: Rodentolepis nana (syn. Hymenolepis nana), the most common cyclophyllid tapeworm infecting rodents, is a well-studied gastrointestinal parasite in mice and belongs to the family Hymenolepididae. METHODS: The present study focuses on the molecular analysis for the nuclear genes (ITS-1, 18 S, and 28 S rDNA) used for the accurate recognition of the recovered Rodentolepis species. RESULTS: The annotated partial ITS-1, 18 S, and 28 S rDNA gene regions were deposited in GenBank (gbÇ MW310394.1, gbÇ MW327585.1, and gbÇ MW324479.1, respectively) and further used in the maximum likelihood method (ML) to clarify their genetic relationships at the species level. The interrogation sequence of R. nana was aligned and belonged to the family Hymenolepididae, in the same group as all Hymenolepis species, which were distinct from Cyclophyllidea cestodes, especially species belonging to Anoplocephalidae and Taeniidae. Sequence data support the paraphyly of Hymenolepis species. CONCLUSIONS: The phylogeny supports the availability of the ITS-1, 18 S, and 28 S rDNA genes as reliable genetic markers for evolutionary relationships.
