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1.
Trop Med Int Health ; 12(11): 1354-60, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18045262

RESUMO

BACKGROUND AND METHOD: Variation in wing length among natural populations of Aedes (Stegomyia) aegypti (L.) (Diptera: Culicidae) is associated with different vectorial capacities. Geometric morphometrics allowed us to use a more powerful estimator of wing size ('centroid size'), as well as to visualize the variation of wing shape, to describe the effects of density or food variation at larval stage on 20 anatomical landmarks of the wing of A. aegypti. RESULTS: Almost perfect correlations between (centroid) size and larval density or size and larval food were observed in both sexes: a negative correlation with increasing density and a positive one with increasing amount of food. The allometric component of shape change was always highly significant, with stronger contribution of size to shape under food effects. Within each experiment, either food or density effects, and excluding extreme conditions, allometric trends were similar among replicates and sexes. However, they differed between the two experiments, suggesting different axes of wing growth. CONCLUSION: Aedes aegypti size is highly sensible to food concentration or population density acting at larval stages. As larger individuals could be better vectors, and because of the stronger effect of food concentration on size, vector control activities should pay more attention in eliminating containers with rich organic matter. Furthermore, as a simple reduction in larval density could significantly increase the size of the survivors, turning them into potentially better vectors, the control activities should try to obtain a complete elimination of the domestic populations.


Assuntos
Aedes/anatomia & histologia , Alimentos , Asas de Animais/anatomia & histologia , Animais , Feminino , Larva/fisiologia , Masculino , Densidade Demográfica
2.
Ann Trop Med Parasitol ; 97(6): 587-92, 2003 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-14511557

RESUMO

In concurrent infections in vivo, the blood stages of Plasmodium vivax suppress those of Plasmodium falciparum. To see if the paroxysm (i.e. the periodic febrile episode) of P. vivax infection contributes to this suppression, sera from a P. vivax-infected volunteer were added to cultures of whole blood taken from cases of P. falciparum malaria. The crude 'rate' of schizont generation from the ring forms, measured as the percentage of all asexual parasites that were schizonts after incubation for 24 h, was similar whether the cultures contained serum samples collected during paroxysms or those collected, from the same volunteer, at other times (19.1% v. 18.9%; P=0.842). After a random-effect linear regression was used to adjust for disparities between the P. falciparum isolates, however, the degree of schizont maturation, measured as the mean number of nuclei per schizont, was significantly lower for the cultures with 'paroxysm serum' than for those with 'non-paroxysm serum' (4.8 v. 5.3; P=0.002). The proportion of schizonts considered mature was also significantly lower when 'paroxysm serum' was used (3.7% v. 6.3%: P=0.03). This appears to be the first in-vitro study in which sera collected during a paroxysm of P. vivax have been shown to inhibit the maturation of P. falciparum schizonts. The role of this mechanism in intra- and inter-specific competition is discussed.


Assuntos
Febre/parasitologia , Malária Vivax/sangue , Plasmodium falciparum/fisiologia , Plasmodium vivax , Adolescente , Adulto , Animais , Feminino , Febre/sangue , Humanos , Modelos Lineares , Masculino , Parasitemia , Parasitologia/métodos
3.
Artigo em Inglês | MEDLINE | ID: mdl-2576970

RESUMO

Early observations suggested that the female sound was a possible cause of mating. Attempts had been made for introduction of female wing beat sound for removal male mosquitoes from the population for the control purpose. The traps emitted female wing beat sound, were set on black clothes as a swarm marker, could collect a large number of male Cx. tritaeniorhynchus in Japan. Those traps were later improved with introduction of two attractants, hamster and dry ice. Consequently, two systems were adopted for efficiency trapping of males and females. A cylinder trap with 350 Hz of wing beat frequency was introduced for male Cx. tritaeniorhynchus collection, while the cage trap with 530 Hz was for female collection. The traps were set every other days after sun set for three weeks in a paddy field. Although there was no decrease of population density, the reduction of parous rate was evident. For future effective control, it may suggest the need to distribute more wing beat sound traps to cover all larva breeding paddy field and near by blood sources. On the other hand, other control methods should be integrated.


Assuntos
Culicidae/fisiologia , Encefalite Japonesa/transmissão , Insetos Vetores/fisiologia , Controle de Mosquitos/métodos , Animais , Culicidae/microbiologia , Vírus da Encefalite Japonesa (Espécie) , Humanos , Insetos Vetores/microbiologia , Controle Biológico de Vetores , Densidade Demográfica , Som
4.
Artigo em Inglês | MEDLINE | ID: mdl-3238486

RESUMO

The population genetic studies on the Anopheles minimus complex revealed that An. minimus is a species complex evident by IK value were less than 0.0534 and 0.4163 for the morphotaxonomy and isozyme studies. There are two sibling species in the An. minimus species complex. The first is the typical minimus and its variations described by Harrison. Esterase-2 alleles 100 and 102 are predominant with a few other alleles of 96 and 104. It is exophagic and zoophilic. It is widely distributed in all provinces where minimus breeds. The second of the two sibling species is An. minimus species C, with 2 pale spots on the humeral dark band and Est-2 allele 98. It is found most frequently in Pu Toei District of Kanchanaburi Province, Thailand. An. minimus probably species B showing M1 + 2 wing vein entirely dark is found in China.


Assuntos
Anopheles/genética , Genética Populacional , Malária/transmissão , Animais , Anopheles/classificação , Humanos , Insetos Vetores/classificação , Insetos Vetores/genética , Malária/epidemiologia , Especificidade da Espécie , Tailândia
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