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Comparison of mitochondrial DNA sequences of seven morphospecies of black flies (Diptera: Simuliidae).

Universal primers constructed from the 16S ribosomal RNA gene in the Drosophila yakuba mitochondrial genome were successfully used to amplify, via the polymerase chain reaction, the homologous region of mitochondrial DNA from seven black fly morphospecies. Amplification was achieved from single larval salivary glands and from single adults preserved in Carnoy's fixative (ethanol - acetic acid, 3:1), allowing DNA sequences and polytene chromosome banding pattern data to be gathered from the same individuals. Nucleotide sequences of the amplified DNA segment (347 base pairs) were obtained from all the species examined. As in Drosophila, the nucleotide base composition of the sequenced segment from black flies had a high adenine (A) and thymine (T) content (A + T on average comprised 77% of all nucleotides.). Nucleotide differences among the seven species were observed at 59 positions (55 nucleotide substitutions and 4 deletions). There were more transversion differences than transition differences both among and within genera; the proportion of transversions was higher between genera than within genera. Most transversion differences were A----T type, comprising 79% of all transversion differences and 50% of all sequence differences. Phylogenetic inference based strictly on transversion differences confirmed traditional generic and tribal groupings, i.e., Prosimulium fuscum (Syme & Davies) is close to Prosimulium magnum (Dyar & Shannon); Simulium decorum (Walker), Simulium venustum s.l. (Say), and Simulium vittatum s.l. (Zetterstedt) are close to each other; Stegopterna mutata (Malloch) and Cnephia dacotensis (Dyar & Shannon), which belong to the tribe Cnephiini, are grouped together.

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Entomopathogenic fungi of the order Entomophthorales (Zygomycotina) in adult black fly populations (Diptera: Simuliidae) in Quebec.

Infections by insect-pathogenic fungi of the order Entomophthorales in two adult black fly populations were studied in the Réserve Faunique du Saint-Maurice (Quebec). Entomophaga near limoniae infected Simulium verecundum/rostratum in June whereas Erynia curvispora predominantly parasitized Simulium decorum from the 2nd week of July to September and Erynia conica attacked the Simulium venustum complex, Simulium verecundum/rostratum, and the Simulium vittatum complex from May to September. The fungi did not infect the adult stage of Prosimulium species. Possible evidence of host specificity for Erynia conica is discussed.

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The cytotaxonomy and morphotaxonomy of Simulium mengense (Diptera: Simuliidae).

Human onchocerciasis is hyper-endemic in south-western Cameroon and the island of Bioko. The vector on the island is the endemic 'Bioko' form of Simulium yahense. On the mainland, S. damnosum s.s., S. squamosum and S. mengense are recorded around Mount Cameroon but their contribution to transmission in the area is unclear. As elimination of onchocerciasis, through vector eradication, is a possibility on the island, it is important to be able to identify vector flies which might migrate to Bioko from the mainland. The morphologies of S. damnosum s.s. and S. squamosum are already well known. New cytotaxonomic and morphotaxonomic descriptions of S. mengense, a species which is less well known, are presented. Simulium mengense can be distinguished from the other cytospecies in the area by the presence of tufts of hair-like setae on the larval thorax, the presence of hairs on the subcostal vein of the adult female, and by the scutal pattern of the adult male. Although Vajime and Dunbar described seven fixed inversions in S. mengense, in 1977, nine were observed in the present study. Of the nine, three were the same as Vajime and Dunbar's but the other six were either missed or misinterpreted by them.

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A molecular marker for the identification of Simulium squamosum (Diptera: Simuliidae).

All except one of the important groups of West African vectors of Onchocerca volvulus that lie within the Simulium damnosum complex can be distinguished from each other using morphological characteristics. The exception is S. squamosum, which overlaps with other species, and this results in significant levels of misidentification. Variation in the untranscribed H3-H4 histone intergenic spacer region of flies of the S. damnosum complex has now been investigated. Although a CAA/CAG microsatellite was found to be hyper-variable and unsuitable for species diagnosis, a 10-bp indel seemed to vary in a species-specific manner. This indel was apparently absent from S. squamosum but present in all of the other species tested (S. damnosum s.s., S. sirbanum, S yahense, S. sanctipauli and S. leonense/konkourense). It should now be possible to identify individual, adult, female S. squamosum from the absence of the indel, using a PCR-based amplification and agarose- or polyacrylamide-gel electrophoresis, thus removing the major barrier to the routine identification of unknown samples.

Africa, Western↗

Cytotaxonomic description of Simulium kaffaense, a new member of the S. damnosum complex (Diptera: Simuliidae) from south-western Ethiopia.

Although Ethiopia is one of the countries worst affected by human onchocerciasis, the exact taxonomic identity of the blackflies acting as the main vectors in the endemic areas has never been determined. A cytotaxonomic analysis of Simulium damnosum s.l. collected from three endemic sites in south-western Ethiopia has now revealed the existence of the 'Kisiwani' form (a non-anthropophilic cytoform that is common in East Africa) and a newly recognized species, Simulium kaffaense. Simulium kaffaense sp. nov. is differentiated from other members of the S. damnosum complex by six fixed inversions and dozens of 'new' floating inversions. The rearing of egg batches from some of the biting adult females, to larvae or adults, indicated that the human-biting blackflies were all S. kaffaense. As S. kaffaense is not only highly anthropophilic but also, apparently, the only anthropophilic member of the S. damnosum complex present, it is likely to be the main (if not the only) vector of Onchocerca volvulus in the study area. The presence of inversion 1S-1 and a complex inversion possibly involving 1L-3 indicates that S. kaffaense either belongs or is close to the 'Nile' phylogenetic group of S. damnosum s. l. The karyotype frequencies of the inversions in the collections from the three study sites indicate that at least two forms of S. kaffaense, here designated 'Bebeka' and 'Jimma', were caught. The taxonomy and medical importance of S. kaffaense are discussed.

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Incrimination of Simulium thyolense (Diptera: Simuliidae) as the anthropophilic blackfly in the Thyolo focus of human onchocerciasis in Malawi.

The sibling species of the Simulium damnosum complex that are potential vectors in the foci of human onchocerciasis found in southern Malawi (the southern-most foci in Africa) were identified, using a combination of cytotaxonomic and molecular techniques. Simulium thyolense was found to be the most abundant species within the foci (representing 91% of the larvae collected), whilst S. kilibanum and cytoforms of the 'Ketaketa' subcomplex were the dominant members of the complex found outside of the foci. As all 188 biting female flies collected from the Thyolo, Mwanza and Mulanje foci were identified as S. thyolense, this species is probably the only significant vector of Onchocerca volvulus in the area, and the other Simulium species collected are assumed to be zoophilic. The results confirm the diagnostic value of the size of the amplicon(s) produced in PCR based on the sequences coding for the internal-transcribed-spacer region of the nuclear ribosomal DNA (ITS-1 rDNA), with a characteristic 340bp amplicon for S. thyolense. Chromosomal polymorphisms within S. thyolense indicate some degree of geographical isolation of the 'Thyolo-Mulanje' focus from the Mwanza focus.

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Descriptions of members of the Simulium damnosum complex (Diptera: Simuliidae) from southern Africa, Ethiopia and Tanzania.

This paper presents cytotaxonomic details of five populations of the Simulium damnosum complex from South Africa, Swaziland and Ethiopia. The 'Nkusi SW' and 'Pienaars' forms are newly designated members of the complex from South Africa, but the taxonomic rank of an isolate indistinguishable chromosomally from the 'Nkusi' cytoform remains unclear. From Ethiopia two cytoforms were identified, one of which shares two diagnostic chromosome inversions with the cytoform 'Kisiwani' from Tanzania. The second form belongs to S. kaffaense, and is the suspected local vector of Onchocerca volvulus. In addition, a re-analysis of the cytoform 'Kibwezi' from north-eastern Tanzania provided further insights into its population subdivision, and its genetic and morphological characteristics. Cytotaxonomic similarities between 'Kibwezi', S. mengense and S. pandanophilum, along with their biogeography, indicate a relict status of each of these taxa.

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[New synonyms and corrections in Simulium with the revalidation of S. pruinosum Lutz, 1904 (Culicomorpha, Simuliidae)].

The following synonyms are proposed: Simulium antunesi (Lane & Porto, 1940), Simulium mauense Nunes de Mello, 1974 and Simulium nilesi Rambajam, 1979 are synonyms of Simulium perflavum Roubaud, 1906; Simulium sucamense Nunes de Mello, 1974 and Simulium santaelenae Ramírez-Pérez & Peterson, 1981 are synonyms of Simulium (Psilopelmia) iracouboense Floch & Abonnenc, 1946; Simulium major Lane & Porto, 1940 are synonym of Simulium (Hemicnetha) rubrithorax Lutz, 1909. The recent use of the miswriting name Grenierella to the subgenus Grenieriella Vargas & Nájera, 1951 is mentioned. Simulium (Grenieriella) pruinosum Lutz, 1910 is revalidated and Simulium nigrimanum Macquart, 1838 should be considered species inquirendae.

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[3 new species of Simulium Latreille of the Neotropical region: Simulium (Hemicnetha) cristalinum sp.n., (Grenieriella) wygodzinskyorum sp.n. and sumapazense sp.n. (Diptera, Simuliidae)].

Three new species are described and illustrated: Simulium (Hemicnetha) cristalinum from Roraima, Brazil, (female, male, pupa and larva) belonging to the brachycladum group; (Grenieriella) wygodzinskyorum from Junín, Perú (female, male, pupa and larva) belonging to the lahillei group and of the sumapazense from Cundinamarca, Colombia, the pupa, and part of the male are described.

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[Susceptibility of populations of Simulium (Chirostilbia) pertinax Kollar, 1832 (Culicomorpha, Simuliidae) to eemephos and to Bacillus thuringiensis var. israelensis-based formulation].

The use of wooden troughs on stream beds, artificially colonized by blackfly larvae, is proposed for larvicide evaluations. Mortality was recorded 3 or 4 hours after treatment. Larval susceptibility was also evaluated utilizing the LT50 criterion. In there field assays Simulium (C.) pertinax populations from the litoral of S. Paulo and Rio de Janeiro States were shown to be resistant to temephos, even when subjected to high concentrations. Vectobac 12 AS, a Bacillus thuringiensis var. israelensis product, was shown to be more potent against late instar larvae and efficient in concentrations higher than 7,200 ITU/l (10 min). The LT50 to 3,744 ITU/l (10 min) was calculated as 70.9 min.

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Identification of vector species (Diptera:Simuliidae) of human onchocerciasis in the amazonia focus of Brazil and Venezuela.

The taxonomic status of three Amazonian simuliid species, Simulium guianese Wise, S. oyapockense Floch & Abonnenc and S. yarzabali Ramirez Perez is reviewed. Simulium cuasisanguineum Ramirez Perez, Yarzabal & Peterson is synonymized with S. oyapockense, and S. yarzabali is revalidated from its synonymy with S. incrustatum Lutz. The role of these three species in the transmission of human onchocerciasis and mansonelliasis in Amazonia is reviewed.

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Cytological and isoenzyme analysis of the Bucay and Quevedo cytotypes of the Onchocerciasis vector Simulium exiguum (Diptera: Simuliidae) in Ecuador.

Four cytotypes of Simulium exiguum occur in Ecuador, where this morphospecies is the primary vector of onchocerciasis. In this paper, we give the first full description of the banding pattern of the larval polytene chromosomes of the Quevedo cytotype and assess its degree of genetic separation from the Bucay cytotype. Both cytotypes differ from the chromosomal standard sequence (of the Cayapa cytotype) by the fixed inversions IIL-5 and IIL-6. The Quevedo cytotype additionally differs from the standard and Bucay cytotypes by possessing a differentiated X chromosome, which is indicated by the inversion IIS-A. As the degree of reproductive isolation between the Bucay and Quevedo cytotypes has not yet been established, they must be regarded as intraspecific variants of the same species. In fact, isoenzyme characterizations showed that the Bucay and Quevedo cytotypes are differentiated only to the extent expected of incipient species or geographical populations. Moreover, the sibling species status previously given to the Bucay cytotype needs be reassessed, there being inadequate analysis from areas in Ecuador where Bucay occurs in sympatry with the standard Cayapa cytotype. No isoenzyme electromorphs were discovered that identified all or most adult females of any one (cytotypepure) collection.

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