Abstract:Microfilariae of Wuchereria bancrofti and Brugia pahangi were killed by the chewing action of the cibarial and pharyngeal armatures and other papillae and spines in the fore-gut of mosquitoes. The proportion of ingested microfilariae that were killed was largely dependent on the presence and shape of the cibarial armature. Anopheles farauti No. 1 and Anopheles gambiae species A and B have well developed cibarial armatures and killed 36 to 96% of the ingested microfilariae. Culex pipiens fatigans has a poorly d… Show more
“…Gorirossi (1950) described epipharyngeal and hypostomal teeth in B. bacoti; their presence explains this early destruction of microfilariae. Similar events are also described in some other filaria-vector pairs (Coluzzi and Trabucchi, 1968;Bain et al, 1974;Omar and Garms, 1975;McGreevy et al, 1978;Buse and Kulhow, 1979).…”
The mites, Bdellonyssus bacoti, are engorged on rodents having 800 to 60,000 microfilariae/10 mm3 blood. Quantitation of L. galizai larval development shows that an additional blood meal improves development and that high microfilaremiae do not result in a proportional increase in the number of infective larvae.The first important stage of transmission regulation occurs during ingestion of microfilariae: the numbers of ingested microfilariae are lower than expected in cases of high microfilaremia. This phe nomenon cannot be ascribed to the mite vector that engorges a constant blood meal whatever the level of microfilaremia. Contrarily, one finds that microfilarial density in the small peripheral blood vessels (blood drawn from incision of the dorsal skin) increases less than in large blood vessels (retro-orbital sinus). A similar observation was reported by Dickerson et al. (1989) work ing with Wuchereria bancrofti. We assume that in both cases, the high microfilaremiae cause the small blood vessels accessible to the vector to become saturated with parasites.Although regulation during engorging is not the sole factor to monitor the infection in B. bacoti (another one operates during larval development of L. galizai), demonstrating its existence seems to us fundamental: it points out the concept that sub-ingestion, as well as over-ingestion, shows the inequalities of microfilarial densities in the host which seem to be dependent on mechanical factors such as the diameter of blood vessels and the size of micro filariae.R ésumé : La filaire Litomosoides galizai chez l'acarien vecteur; distribution des microfilaires chez l'hôte et régulation de la transmission.Le vecteur, Bdellonyssus bacoti, est gorgé sur des rongeurs ayant 800 à 60.000 microfilaires/10 mm3. L'analyse quantitative du déve loppement larvaire de L. galizai montre que celui-ci est meilleur quand le vecteur prend un repas de sang surnuméraire, et que les fortes microfilarémies n'entraînent pas une augmentation pro portionnelle du nombre de larves infectantes.Une première et importante phase de régulation s'effectue lors de l'ingestion des microfilaires : celles-ci sont sous-ingérées quand les microfilarémies sont fortes. Ce phénomène ne peut être imputé au vecteur, qui prend un volume de sang constant quelle que soit la microfilarémie. Par contre, on constate que la densité microfilarienne du sang périphérique, prélevé après incision de la peau du dos, augmente moins que celle du sang profond, prélevé au sinus rétro-orbital. Un phénomène analogue est observé par Dickerson et al., 1989 avec Wuchereria bancrofti. Nous supposons que, dans les deux cas, les fortes microfilarémies entraînent une saturation en parasites dans les petits vaisseaux accessibles au vecteur.Bien que la régulation lors de l'ingestion ne soit pas la seule à contrôler l'infection chez B. bacoti (une autre a lieu durant le développement larvaire de L. galizai), sa mise en évidence nous paraît fondamentale; elle appuie la notion que la sous-ingestion, de même que la sur-ingestion, refl...
“…Gorirossi (1950) described epipharyngeal and hypostomal teeth in B. bacoti; their presence explains this early destruction of microfilariae. Similar events are also described in some other filaria-vector pairs (Coluzzi and Trabucchi, 1968;Bain et al, 1974;Omar and Garms, 1975;McGreevy et al, 1978;Buse and Kulhow, 1979).…”
The mites, Bdellonyssus bacoti, are engorged on rodents having 800 to 60,000 microfilariae/10 mm3 blood. Quantitation of L. galizai larval development shows that an additional blood meal improves development and that high microfilaremiae do not result in a proportional increase in the number of infective larvae.The first important stage of transmission regulation occurs during ingestion of microfilariae: the numbers of ingested microfilariae are lower than expected in cases of high microfilaremia. This phe nomenon cannot be ascribed to the mite vector that engorges a constant blood meal whatever the level of microfilaremia. Contrarily, one finds that microfilarial density in the small peripheral blood vessels (blood drawn from incision of the dorsal skin) increases less than in large blood vessels (retro-orbital sinus). A similar observation was reported by Dickerson et al. (1989) work ing with Wuchereria bancrofti. We assume that in both cases, the high microfilaremiae cause the small blood vessels accessible to the vector to become saturated with parasites.Although regulation during engorging is not the sole factor to monitor the infection in B. bacoti (another one operates during larval development of L. galizai), demonstrating its existence seems to us fundamental: it points out the concept that sub-ingestion, as well as over-ingestion, shows the inequalities of microfilarial densities in the host which seem to be dependent on mechanical factors such as the diameter of blood vessels and the size of micro filariae.R ésumé : La filaire Litomosoides galizai chez l'acarien vecteur; distribution des microfilaires chez l'hôte et régulation de la transmission.Le vecteur, Bdellonyssus bacoti, est gorgé sur des rongeurs ayant 800 à 60.000 microfilaires/10 mm3. L'analyse quantitative du déve loppement larvaire de L. galizai montre que celui-ci est meilleur quand le vecteur prend un repas de sang surnuméraire, et que les fortes microfilarémies n'entraînent pas une augmentation pro portionnelle du nombre de larves infectantes.Une première et importante phase de régulation s'effectue lors de l'ingestion des microfilaires : celles-ci sont sous-ingérées quand les microfilarémies sont fortes. Ce phénomène ne peut être imputé au vecteur, qui prend un volume de sang constant quelle que soit la microfilarémie. Par contre, on constate que la densité microfilarienne du sang périphérique, prélevé après incision de la peau du dos, augmente moins que celle du sang profond, prélevé au sinus rétro-orbital. Un phénomène analogue est observé par Dickerson et al., 1989 avec Wuchereria bancrofti. Nous supposons que, dans les deux cas, les fortes microfilarémies entraînent une saturation en parasites dans les petits vaisseaux accessibles au vecteur.Bien que la régulation lors de l'ingestion ne soit pas la seule à contrôler l'infection chez B. bacoti (une autre a lieu durant le développement larvaire de L. galizai), sa mise en évidence nous paraît fondamentale; elle appuie la notion que la sous-ingestion, de même que la sur-ingestion, refl...
“…Mosquitoes are able to control the infection by D. immitis through mechanisms that reduce parasite burden by destroying or preventing the development of the nematode, i.e., well developed cibarial armature that inflict larval damage (Bryan et al 1974, McGreevy et al 1978, trapping of larvae in the coagulated bloodmeal in the mosquito's midgut (Kartman 1953), oxyhaemoglobin crystals formed by bloodmeal coagulation in the midgut that hinder the movement of mf and kill them (Nayar & Sauerman 1975, Lowrie 1991, lysis of larval cuticle by host cells (Talluri & Cancrini 1994), and encapsulation and/or melanization of the parasite in the Malpighian tubules. This last defense reaction is an important mechanism of refractoriness to D. immitis developed by mosquitoes in the genus Aedes (Lindemann 1977, Christensen 1981, Christensen et al 1989.…”
“…Thus, melanization can act as an important mechanism for vector survival by limiting the number of larvae that complete development and thereby guaranteeing its own survival (Christensen 1981, Christensen & Forton 1986, Christensen & Tracy 1989. In addition, some mosquito species have well developed cibarial armature, the teeth of which, when numerous and/or developed, injuring ingested microfilariae and reducing their survival potential (McGreevy et al 1978, Coluzzi et al 1982.…”
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