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At least 145 records · Page 8Linked to original sources

Analysis of sister chromatid exchange, micronucleus and chromosomal aberration frequencies in rodents exposed to mosquito coil smoke by inhalation route.

Mosquito coil smoke emitting from a mosquito repellent, was tested for its mutagenic effect in bone marrow cells from mouse and rat after 4 h acute inhalation exposure. Coil smoke with suspended particulate concentrations of 99-129 mg/m3, significantly elevated the frequencies of sister chromatid exchanges in bone marrow cells and micronuclei in polychromatic erythrocytes. Analysis of chromosomal aberrations in metaphases also revealed a significantly higher incidence of chromosomal aberration frequency in exposed rats and mice.

Administration, Inhalation↗

Gambicin: a novel immune responsive antimicrobial peptide from the malaria vector Anopheles gambiae.

A novel mosquito antimicrobial peptide, gambicin, and the corresponding gene were isolated in parallel through differential display-PCR, an expressed sequence tag (EST) project, and characterization of an antimicrobial activity in a mosquito cell line by reverse-phase chromatography. The 616-bp gambicin ORF encodes an 81-residue protein that is processed and secreted as a 61-aa mature peptide containing eight cysteines engaged in four disulfide bridges. Gambicin lacks sequence homology with other known proteins. Like other Anopheles gambiae antimicrobial peptide genes, gambicin is induced by natural or experimental infection in the midgut, fatbody, and hemocyte-like cell lines. Within the midgut, gambicin is predominantly expressed in the anterior part. Both local and systemic gambicin expression is induced during early and late stages of natural malaria infection. In vitro experiments showed that the 6.8-kDa mature peptide can kill both Gram-positive and Gram-negative bacteria, has a morphogenic effect on a filamentous fungus, and is marginally lethal to Plasmodium berghei ookinetes. An oxidized form of gambicin isolated from the cell line medium was more active against bacteria than the nonoxidized form from the same medium.

Amino Acid Sequence↗

Progress in the map-based cloning of the Anopheles gambiae genes responsible for the encapsulation of malarial parasites.

A genetically selected strain of the mosquito Anopheles gambiae, the major vector of malaria in sub-Saharan Africa, is able to encapsulate and kill Plasmodium ookinetes after they have penetrated the midgut cells and come to rest between the midgut epithelial cells and the surrounding basal lamina. The genetic basis of this phenotype has now been examined by high-resolution mapping using microsatellite loci. Results of this mapping indicate that three genes contribute to this phenotype, with one gene on the left arm of chromosome 2 accounting for the most of the effect. These genes, called Pen1, Pen2, and Pen3 (for Plasmodium encapsulation genes 1, 2 and 3) have also been physically localized to relatively small and well defined regions of the polytene chromosome complement. Strategies for cloning these genes by genetic and physical mapping methods are discussed.

Africa South of the Sahara↗

KLP-18, a Klp2 kinesin, is required for assembly of acentrosomal meiotic spindles in Caenorhabditis elegans.

The proper segregation of chromosomes during meiosis or mitosis requires the assembly of well organized spindles. In many organisms, meiotic spindles lack centrosomes. The formation of such acentrosomal spindles seems to involve first assembly or capture of microtubules (MTs) in a random pattern around the meiotic chromosomes and then parallel bundling and bipolar organization by the action of MT motors and other proteins. Here, we describe the structure, distribution, and function of KLP-18, a Caenorhabditis elegans Klp2 kinesin. Previous reports of Klp2 kinesins agree that it concentrates in spindles, but do not provide a clear view of its function. During prometaphase, metaphase, and anaphase, KLP-18 concentrates toward the poles in both meiotic and mitotic spindles. Depletion of KLP-18 by RNA-mediated interference prevents parallel bundling/bipolar organization of the MTs that accumulate around female meiotic chromosomes. Hence, meiotic chromosome segregation fails, leading to haploid or aneuploid embryos. Subsequent assembly and function of centrosomal mitotic spindles is normal except when aberrant maternal chromatin is present. This suggests that although KLP-18 is critical for organizing chromosome-derived MTs into a parallel bipolar spindle, the order inherent in centrosome-derived astral MT arrays greatly reduces or eliminates the need for KLP-18 organizing activity in mitotic spindles.

Animals↗

Chromosome key to the larvae of the Simulium metallicum complex (Diptera: Simuliidae) from Latin America.

A key based on larval salivary gland polytene chromosome inversions is presented for 11 members (species A-K) of the Simulium metallicum Bellardi complex from Latin America. Most members (B, D, E, G, H, I, J, and K) can be distinguished from the cytological standard, sibling A, solely on the basis of fixed inversion differences. A suite of characters (sex-linked inversions as well as polymorphisms) must be examined to separate cytotypes C and F from A.

Animals↗

Isolation and characterization of a retroelement from B chromosome (PSR) in the parasitic wasp Nasonia vitripennis.

Molecular characterization of the paternal-sex-ratio (PSR) chromosome in Nasonia vitripennis (Hymenoptera: Pteromalidae) has led to the isolation of a dispersed repetitive element. The element is a LTR-containing retrotransposon which has been named NATE (NAsonia Transposable Element). NATE has direct terminal repeats and has an internal amino acid sequence similar to reverse transcriptases of other retroelements. Phylogenetic analysis indicates NATE is a member of the Gypsy/Ty3 group of retrotransposons, and represents the first isolated from Hymenoptera. Five closely related copies of NATE were isolated from the PSR chromosome, but cross-hybridizing elements were not detected on the autosomes of N. vitripennis. Strongly cross-hybridizing elements were, however, detected in two other Nasonia species. This observed distribution of NATE is interesting, because the supernumerary PSR chromosome may be derived from the genome of a sibling species of N. vitripennis.

Amino Acid Sequence↗

Cytological approaches to simuliid biosystematics in relation to the epidemiology and control of human onchocerciasis.

This paper presents an overview of advances in cytological research on the biosystematics of vector simuliid complexes in the areas of identification, age grading, and the evolution of resistance in relation to the epidemiology and control of human onchocerciasis. Systematic theory is discussed and relevant examples are given to show its application in predicting and resolving current problems in species identification for New World and Old World vector complexes. These complexes include Simulium damnosum s.l. and S. neavei s.l. from Africa and S. exiguum s.l., S. metallicum s.l., S. ochraceum s.l., and S. oyapockense s.l. from Latin America. The evolution of resistance in S. damnosum s.l. and the need for future molecular research as part of resistance management strategies are discussed.

Africa↗

Studies on x-ray induced chromosomal translocations in Anopheles albimanus. III. Effect of the release of translocation males on the dynamics of cage populations.

Anopheles albimanus males carrying an Y-autosome translocation were continuously released into a cage population at a ratio of 1:5 in favor of translocation males. The release caused a significant decrease in the absolute density of cage populations. Virtually complete replacement of wild type Y chromosome by translocated Y chromosome was observed after four generations. The results obtained from the cage experiments encourage actual field trials for the control of this vector species.

Animals↗

[Lagoonal and coastal malaria at Cotonou: entomological findings].

Nowadays, malaria control is planned according to the epidemiological context. Various aspects of malaria have been described in sub-Saharan Africa. We report here entomological data from the coastal area of Benin, West Africa, which has many lakes and lagoons. We carried out a longitudinal study in which we investigated the dynamics of populations of malaria vectors in various zones, the frequency of inoculation in these zones, the infestation rate of the Anopheles gambiae mosquitoes collected, the effect of urbanization on malaria transmission, the effects of inundation and of salinity at mosquito breeding sites. A total of 3, 342 identifications were made on a chromosomal basis. Two species of the Anopheles gambiae complex were detected in the coastal and lagoon areas of Benin: An. melas and An. gambiae ss. The density of the populations of these species was highly dependent on the level of urbanization. In traditional villages on the lagoons (such as Agbalilamè, Djegbadji and Kétonou), the density of An. melas (86. 2%) was much higher than that in more urbanized areas (such as Ladji and Abomey-Calavi) (4.9%). We checked for chromosome polymorphism. We detected a 2Rn1 inversion in An. melas, similar to the 2Rn inversion found in mosquitoes in Gambia and Guinea-Bissau. The frequency of the n1 inversion and the density of An. melas populations were correlated and both seemed to depend on a single factor, salinity. The epidemiological situation with respect to malaria was very heterogeneous in the lagoon area of Benin. In the city of Cotonou, transmission was seasonal, sporozoite indices and the frequency of inoculation were high, in contrast to what would normally be expected in an urban area. In communities built on the beach, the level of transmission was markedly lower: about 5 infected bites per person per year versus 29 infected bites per person in the center of the city. In the traditional fishing villages, a paradoxical situation was observed in which the mosquitoes were very aggressive towards humans (4,502 bites per person per year) but the frequency of transmission was low (d = 0. 27%, CS+ = 0.57%). This was largely due to the high density in this area of An. melas, a poor malaria vector. If traditional villages become more urbanized, more freshwater breeding sites are created and the An. gambiae population increases, leading to an increase in malaria transmission. This is the reason for the higher level of malaria transmission at Ladji and Abomey-Calavi (h = 47 infected bites per person per year) than at Agbailamè, Djegbadji and Kétonou (h = 12.1 infected bites per person per year)

Animals↗

Heterogeneities of the malaria vectorial system in tropical Africa and their significance in malaria epidemiology and control.

The most important units of the malaria vectorial system in tropical Africa are included in the Linnaean taxon Anopheles gambiae, which has been split into six sibling species recognized by the application of genetic techniques. More recent studies have shown further complexities involving chromosomal inversion polymorphism in some vector populations as well as incipient speciation processes. The significance for field research in malaria of the splitting of a morphological taxon into genetically defined units and subunits is discussed.

Anopheles↗

Chromosomal evidence for sibling species of the malaria vector Anopheles (Cellia) culicifacies Giles.

The ovarian polytene chromosomes of adult Anopheles culicifacies from natural populations in Pakistan, India and Sri Lanka, and from four laboratory colonies (one from Pakistan and three from India) are compared with the published cytological map for this taxon. Two types of X-chromosome exist. One of these is identical with the published map; the other differs by two inversions. No autosome arm rearrangements are detected. A photomap is presented which documents the X-chromosome inversions. Both types of Xs are found in a natural population near New Delhi in the apparent absence of heterozygotes. This is interpreted as evidence for biologically distinct species within the taxon An. culicifacies Giles. The formal taxonomic and practical implications are briefly discussed.

Animals↗

Genetic and cytogenetic analysis of the olive fruit fly Bactrocera oleae (Diptera: Tephritidae).

The genetic and cytogenetic characteristics of one of the major agricultural pests, the olive fruit fly Bactmcera oleae, are presented here. The mitotic metaphase complement of this insect consists of six pairs of chromosomes including one pair of heteromorphic sex chromosomes, with the male being the heterogametic sex. The analysis of the polytene complements of three larval tissues, the fat body, the salivary glands and the Malpighian tubules of this pest has shown (a) a total number of five long chromosomes (10 polytene arms) that correspond to the five autosomes of the mitotic nuclei and a heterochromatic mass corresponding to the sex chromosomes, (b) the constancy of the banding pattern of the three somatic tissues, (c) the absence of a typical chromocenter as an accumulation of heterochromatin, (d) the existence of reverse tandem duplications, and (e) the presence of toroid tips of the chromosome arms. The in situ hybridization of genes or DNA sequences to the salivary gland polytene chromosomes of B. oleae provided molecular markers for all five autosomes and permitted the establishment of chromosomal homologies among B. olea, B. tryoni and Ceratitis capitata. The heat shock response of B. oleae, as revealed by heat-inducible puffing and protein pattern, shows a higher thermotolerance than Drosophila melanogaster.

Animals↗