RÉSUMÉ
Quatro colônias desenvolvidas em laboratório, de duas formas cariotípicas de Anopheles aconitus i.e. forma B (cepa Chiang Mai e Phet Buri) e C (Cepa Chiang Mai e Mae Hong Son), foram infectadas experimentalmente com Plasmodium falciparum e P. vivax usando técnica de alimentação com membrana artificial e dissecados oito e 12 dias após alimentação da média de oocistos e esporozoitos, respectivamente. Os resultados revelaram que An. aconitus formas B e C foram suscetíveis ao P. falciparum e P. vivax isto é, forma B (cepa Chiang Mai e Phet Buri/P. falciparum e P. vivax) e forma C (cepa Chiang Mai e Mae Hong Son/P. vivax). Análises estatísticas comparativas das taxas de oocistos, número médio de oocistos por intestino médio infectado e taxas de esporozoitos entre todas as cepas de An. aconitus formas B e C ao grupo interno de vetores controles, An. minimus A e C, não exibiram nenhuma diferença significante, confirmando o alto potencial vetor das duas espécies de Plamodium. Os cristais semelhantes a esporozoitos encontrados no lobo médio das glândulas salivares que poderiam ser um fator enganoso na identificação de esporozoitos verdadeiros nas glândulas salivares foram encontrados em ambos An. aconitus formas B e C.
Sujet(s)
Animaux , Femelle , Humains , Anopheles/parasitologie , Vecteurs insectes/parasitologie , Plasmodium falciparum/physiologie , Plasmodium vivax/physiologie , Anopheles/génétique , Interactions hôte-parasite , Plasmodium falciparum/croissance et développement , Plasmodium vivax/croissance et développement , ThaïlandeRÉSUMÉ
Four laboratory-raised colonies of two karyotypic forms of Anopheles aconitus, i.e., Form B (Chiang Mai and Phet Buri strains) and C (Chiang Mai and Mae Hong Son strains), were experimentally infected with Plasmodium falciparum and P. vivax using an artificial membrane feeding technique and dissected eight and 12 days after feeding for oocyst and sporozoite rates, respectively. The results revealed that An. aconitus Form B and C were susceptible to P. falciparum and P. vivax, i.e., Form B (Chiang Mai and Phet Buri strains/P. falciparum and P. vivax) and Form C (Chiang Mai and Mae Hong Son strains/P. vivax). Comparative statistical analyses of the oocyst rates, average number of oocysts per infected midgut and sporozoite rates among all strains of An. aconitus Form B and C to the ingroup control vectors, An. minimus A and C, exhibited mostly no significant differences, confirming the high potential vector of the two Plasmodium species. The sporozoite-like crystals found in the median lobe of the salivary glands, which could be a misleading factor in the identification of true sporozoites in salivary glands were found in both An. aconitus Form B and C.
Sujet(s)
Anopheles/parasitologie , Vecteurs insectes/parasitologie , Plasmodium falciparum/physiologie , Plasmodium vivax/physiologie , Animaux , Anopheles/génétique , Femelle , Interactions hôte-parasite , Humains , Plasmodium falciparum/croissance et développement , Plasmodium vivax/croissance et développement , ThaïlandeRÉSUMÉ
Comparative morphometric and morphological studies of eggs under scanning electron microscope (SEM) were undertaken in the three strains of two karyotypic forms of Anopheles aconitus, i.e., Form B (Chiang Mai and Phet Buri strains) and Form C (Chiang Mai and Mae Hong Son strains). Morphometric examination revealed the intraspecific variation with respect to the float width [36.77 +/- 2.30 microm (Form C: Chiang Mai strain) = 38.49 +/- 2.78 microm (Form B: Chiang Mai strain) = 39.06 +/- 2.37 microm (Form B: Phet Buri strain) > 32.40 +/- 3.52 microm (Form C: Mae Hong Son strain)] and number of posterior tubercles on deck [2.40 +/- 0.52 (Form B: Phet Buri strain) = 2.70 +/- 0.82 (Form B: Chiang Mai strain) < 3.10 +/- 0.32 (Form C: Chiang Mai strain) = 3.20 +/- 0.42 (Form C: Mae Hong Son strain)], whereas the surface topography of eggs among the three strains of two karyotypic forms were morphologically similar.
Sujet(s)
Anopheles/génétique , Ovule/ultrastructure , Animaux , Anopheles/ultrastructure , Biométrie , Femelle , Caryotypage , Mâle , Microscopie électronique à balayageRÉSUMÉ
Estudos comparativos morfométricos e morfológicos de ovos à microscopia eletrônica de varredura (SEM) foram efetuados nas três linhagens de duas formas cariotípicas de Anopheles aconitus, isto é, Forma B (linhagens Chiang Mai e Phet Buri) e Forma C (linhagens Chiang Mai e Mae Hong Son). Exame morfométrico revelou a variação intraespecífica com respeito à largura de superfície [36,77 ± 2,30 µm (Forma C: linhagem Chiang Mai) = 38,49 ± 2,78 µm (Forma B: linhagem Chiang Mai) = 39,06 ± 2,37 µm (Forma B: linhagem Phet Buri) > 32,40 ± 3,52 µm (Forma C: linhagem Mae Hong Son)] e número de tubérculos posteriores sobre a superfície livre [2,40 ± 0,52 (Forma B: linhagem Phet Buri) = 2,70 ± 0,82 (Forma B: linhagem Chiang Mai) < 3,10 ± 0,32 (Forma C: linhagem Chiang Mai) = 3,20 ± 0,42 (Forma C: linhagem Mae Hong Son)] embora a topografia de superfície dos ovos entre as três linhagens de duas formas cariotípicas tenham sido morfologicamente semelhantes.
Sujet(s)
Animaux , Mâle , Femelle , Anopheles , Ovule , Biométrie , Caryotypage , Microscopie électronique à balayageRÉSUMÉ
Blood-feeding and autogenous sub-colonies were selected from a laboratory, stock colony of Aedes togoi, which was originally collected from Koh Nom Sao, Chanthaburi province, Southeast Thailand. Comparative biology and filarial susceptibility between the two sub-colonies (blood-feeding: F11, F13; autogeny: F38, F40) were investigated to evaluate their viability and vectorial capacity. The results of comparison on biology revealed intraspecific differences, i.e., the average egg deposition/gravid female (F11/F38; F13/F40), embryonation rate (F13/F40), hatchability rate (F11/F38; F13/F40), egg width (F11/F38), wing length of females (F13/F40), and wing length and width of males (F11/F38) in the blood-feeding sub-colony were significantly greater than that in the autogenous sub-colony; and egg length (F11/F38) and width (F13/F40), and mean longevity of adult females (F11/F38) and males (F13/F40) in the blood-feeding sub-colony were significantly less than that in the autogenous sub-colony. The results of comparison on filarial susceptibility demonstrated that both sub-colonies yielded similar susceptibilities to Brugia malayi [blood-feeding/autogeny = 56.7% (F11)/53.3%(F38), 60%(F13)/83.3%(F40)] and Dirofilaria immitis [blood-feeding/autogeny = 85.7%(F11)/75%(F38), 45%(F13)/29.4%(F40)], suggesting autogenous Ae. togoi sub-colony was an efficient laboratory vector in study of filariasis.
Sujet(s)
Aedes/parasitologie , Brugia malayi/physiologie , Dirofilaria immitis/physiologie , Comportement alimentaire , Vecteurs insectes/parasitologie , Aedes/anatomie et histologie , Aedes/physiologie , Animaux , Cricetinae , Femelle , Interactions hôte-parasite , Vecteurs insectes/anatomie et histologie , Vecteurs insectes/physiologie , Longévité , Mâle , OvipositionRÉSUMÉ
Blood-feeding and autogenous sub-colonies were selected from a laboratory, stock colony of Aedes togoi, which was originally collected from Koh Nom Sao, Chanthaburi province, Southeast Thailand. Comparative biology and filarial susceptibility between the two sub-colonies (blood-feeding: F11, F13; autogeny: F38, F40) were investigated to evaluate their viability and vectorial capacity. The results of comparison on biology revealed intraspecific differences, i.e., the average egg deposition/gravid female (F11/F38; F13/F40), embryonation rate (F13/F40), hatchability rate (F11/F38; F13/F40), egg width (F11/F38), wing length of females (F13/F40), and wing length and width of males (F11/F38) in the blood-feeding sub-colony were significantly greater than that in the autogenous sub-colony; and egg length (F11/F38) and width (F13/F40), and mean longevity of adult females (F11/F38) and males (F13/F40) in the blood-feeding sub-colony were significantly less than that in the autogenous sub-colony. The results of comparison on filarial susceptibility demonstrated that both sub-colonies yielded similar susceptibilities to Brugia malayi [blood-feeding/autogeny = 56.7 percent (F11)/53.3 percent(F38), 60 percent(F13)/83.3 percent(F40)] and Dirofilaria immitis [blood-feeding/autogeny = 85.7 percent(F11)/75 percent(F38), 45 percent(F13)/29.4 percent(F40)], suggesting autogenous Ae. togoi sub-colony was an efficient laboratory vector in study of filariasis