Genetic Control of Mosquitoes: population suppression strategies / Controle genético de mosquitos: estratégias de supressão de populações

Over the last two decades, morbidity and mortality from malaria and dengue fever among other pathogens are an increasing Public Health problem. The increase in the geographic distribution of vectors is accompanied by the emergence of viruses and diseases in new areas. There are insufficient specific therapeutic drugs available and there are no reliable vaccines for malaria or dengue, although some progress has been achieved, there is still a long way between its development and actual field use. Most mosquito control measures have failed to achieve their goals, mostly because of the mosquito's great reproductive capacity and genomic flexibility. Chemical control is increasingly restricted due to potential human toxicity, mortality in no target organisms, insecticide resistance, and other environmental impacts. Other strategies for mosquito control are desperately needed. The Sterile Insect Technique (SIT) is a species-specific and environmentally benign method for insect population suppression, it is based on mass rearing, radiation mediated sterilization, and release of a large number of male insects. Releasing of Insects carrying a dominant lethal gene (RIDL) offers a solution to many of the drawbacks of traditional SIT that have limited its application in mosquitoes while maintaining its environmentally friendly and species-specific utility. The self-limiting nature of sterile mosquitoes tends to make the issues related to field use of these somewhat less challenging than for self-spreading systems characteristic of population replacement strategies. They also are closer to field use, so might be appropriate to consider first. The prospect of genetic control methods against mosquito vectored human diseases is rapidly becoming a reality, many decisions will need to be made on a national, regional and international level regarding the biosafety, social, cultural and ethical aspects of the use and deployment of these vector control methods.

Ao longo das duas últimas décadas, morbidade e mortalidade da malária e dengue e outros patógenos tem se tornado cada vez mais um problema de Saúde Pública. O aumento na distribuição geográfica de seus respectivos vetores é acompanhada pela emergência de doenças em novas áreas. Não estão disponíveis drogas específicas suficientes e não há vacinas específicas para imunizar as populações alvo. As medidas de controle de mosquitos atuais falharam em atingir os objetivos propostos, principalmente devido à grande capacidade reprodutiva dos mosquitos e alta flexibilidade genômica. O controle químico se torna cada vez mais restrito devido a sua potencial toxicidade aos seres humanos, mortalidade de organismos não alvos, resistência a inseticida além de outros impactos ambientais. Novas estratégias de controle são necessárias. A técnica do inseto estéril (SIT) é um método de supressão populacional espécie específico e ambientalmente amigável, baseia-se na criação em massa, esterilização mediante irradiação e liberação de um grande número de insetos machos. Liberar insetos carregando um gene letal dominante (RIDL) oferece uma solução a muitas limitações impostas pela técnica do inseto estéril (SIT) que limitaram sua aplicação em mosquitos e ainda assim mantém suas características de ambientalmente amigável e espécie específica. A natureza auto-limitante de mosquitos estéreis tende a deixar alguns empecilhos para uso no campo, de certa forma, menos desafiadores quando comparados a sistemas auto-propagação, característicos de estratégias de substituição de população. Sistemas auto-limitantes estão mais próximos para uso no campo, portanto pode ser apropriado considerá-lo primeiro. A perspectiva de métodos de controle genéticos contra mosquitos vetores de doenças que acometem humanos está rapidamente se tornando uma realidade, muitas decisões terão de ser tomadas em âmbito nacional, regional e internacional com relação a aspectos étnicos, sociais, culturais e de biossegurança para o uso e liberação destes métodos de controle de vetores.

Chronic ethanol consumption in mice does not induce DNA damage in somatic or germ cells, evaluated by the bone marrow micronucleous assay and the dominant lethal mutation assay

Although alcohol is known to be a carcinogen for humans, ethanol-genotoxicity studies are incomplete. Ethanol seems not to be a bacterial mutagen, but the results are conflicting in rodent assays. We investigate the genotoxicity in the bone marrow micronucleus (MN) test and in the dominant lethal mutation (DLM) assay using two long-term ethanol exposure protocols. In the MN test, mice consumed three doses (5, 10 and 15% v/v) for 32 weeks. MN induction was compared to two control groups of 5- and 38-week-old mice (the ages of the treated mice when the treatment was initiated and when they were killed, respectively). For the three groups treated with ethanol there was no significant increase in MN induction as compared to the first control group, but observed MN frequencies were significantly lower than in the 38-week-old control group. This suggests a protective effect against genotoxic damage caused by aging, probably due to ethanol action as a hydroxyl radical scavenger. In the DLM assay, male mice drank ethanol at 15% or 30% (v/v) for 20 weeks. In both groups the number of dead implants was similar to the control, but there was a significant reduction in total implants, indicating a pre-implantation loss.

DNA repair and synthetic lethality / 国际口腔科学杂志·英文版

Tumors often have DNA repair defects, suggesting additional inhibition of other DNA repair pathways in tumors may lead to synthetic lethality. Accumulating data demonstrate that DNA repair-defective tumors, in particular homologous recombination (HR), are highly sensitive to DNA-damaging agents. Thus, HR-defective tumors exhibit potential vulnerability to the synthetic lethality approach, which may lead to new therapeutic strategies. It is well known that poly (adenosine diphosphate (ADP)-ribose) polymerase (PARP) inhibitors show the synthetically lethal effect in tumors defective in BRCA1 or BRCA2 genes encoded proteins that are required for efficient HR. In this review, we summarize the strategies of targeting DNA repair pathways and other DNA metabolic functions to cause synthetic lethality in HR-defective tumor cells.

Bacterial containment system regulated by the concentration of salicylate / 生物工程学报

Use of genetically engineered microorganisms (GEMs) for pollution abatement has been limited because of the risks associated with their uncontrolled release in environment. In this study, a pollutant-dependent bacterial containment system was constructed in E. coli JM109. The system consisted of two plasmids containing a killing element and a regulatory element respectively. The survival of strains can be regulated by the concentration of salicylate in environment. In the presence of salicylate, the expression of the suicide gene gef was inhibited with the synthesis of LacI protein, leading to the normal proliferation of the strain. While in the absence of salicylate, the expression of the regulatory element was cancelled, and the expression of the suicide gene gefled to a high rate of cell killing. This containment system can be used as a model during the construction of genetically engineered strains for bioremediation.

Drosophila simulans Lethal hybrid rescue mutation (Lhr) rescues inviable hybrids by restoring X chromosomal dosage compensation and causes fluctuating asymmetry of development.

The Drosophila simulans Lhr rescues lethal hybrids from the cross of D. melanogaster and D. simulans. We describe here, the phenotypes of Lhr dependent rescue hybrids and demonstrate the effects of Lhr on functional morphology of the salivary chromosomes in the hybrids. Our results reveal that the phenotypes of the 'Lhr dependent rescued' hybrids were largely dependent on the genetic background and the dominance in species and hybrids, and not on Lhr. Cytological examination reveal that while the salivary chromosome of 'larval lethal' male carrying melanogaster X chromosome was unusually thin and contracted, in 'rescued' hybrid males (C(mel)X(mel)Y(sim); A(mel)A(sim)) the X chromosome showed typical pale staining, enlarged diameter and incorporated higher rate of (3)H-uridine in presence of one dose Lhr in the genome. In hybrid males carrying simulans X chromosome (C(mel)X(sim)Y(mel); A(mel)A(sim)), enlarged width of the polytene X chromosome was noted in most of the nuclei, in Lhr background, and transcribed at higher rate than that of the single X chromosome of male. In hybrid females (both viable, e.g., C(mel)X(mel)X(sim); A(mel)A(sim) and rescued, e.g., C(mel)X(mel)X(mel); A(mel)A(sim)), the functional morphology of the X chromosomes were comparable to that of diploid autosomes in presence of one dose of Lhr. In hybrid metafemales (C(mel)X(mel)X(mel)X(sim); A(mel)A(sim)), two dose of melanogaster X chromosomes and one dose of simulans X chromosome were transcribed almost at 'female' rate in hybrid genetic background in presence of one dose of Lhr. In rescued hybrid males, the melanogaster-derived X chromosome appeared to complete its replication faster than autosomes. These results together have been interpreted to have suggested that Lhr suppresses the lethality of hybrids by regulating functional activities of the X chromosome(s) for dosage compensation.

Use of a synthetic lethal screen to identify genes related to TIF51A in Saccharomyces cerevisiae

The putative eukaryotic translation initiation factor 5A (eIF5A) is an essential protein for cell viability and the only cellular protein known to contain the unusual amino acid residue hypusine. eIF5A has been implicated in translation initiation, cell proliferation, nucleocytoplasmic transport, mRNA decay, and actin polarization, but the precise biological function of this protein is not clear. However, eIF5A was recently shown to be directly involved with the translational machinery. A screen for synthetic lethal mutations was carried out with one of the temperature-sensitive alleles of TIF51A (tif51A-3) to identify factors that functionally interact with eIF5A and revealed the essential gene YPT1. This gene encodes a small GTPase, a member of the rab family involved with secretion, acting in the vesicular trafficking between endoplasmatic reticulum and the Golgi. Thus, the synthetic lethality between TIF51A and YPT1 may reveal the connection between translation and the polarized distribution of membrane components, suggesting that these proteins work together in the cell to guarantee proper protein synthesis and secretion necessary for correct bud formation during G1/S transition. Future studies will investigate the functional interaction between eIF5A and Ypt1 in order to clarify this involvement of eIF5A with vesicular trafficking.

A cytological study of the O5 chromosomal inversion of Drosophila subobscura (Diptera, Drosophilidae)

The O5 chromosomal inversion has been a cornerstone for understanding different aspects of the American colonization by Drosophila subobscura. To obtain more information of this evolutionary event it is important to know the pattern of bands of this inversion in detail. Comparing this pattern with that of D. melanogaster it is possible to predict which genes are located inside or close to the O5 inversion and use them as genetic markers. In this study, the complete band pattern of the O5 inversion is presented. Furthermore, the most important genes located inside it have been predicted. Finally, a constriction located close to the proximal breakage point of the O5 inversion has been observed many times and its possible genetic significance is discussed

Ubiquitous overexpression of a transgene encoding the extracellular portion of the Drosophila Roughest-Irregular Chiasm C protein induces early embryonic lethality

The cell adhesion molecule Rst-irreC is a transmembrane glycoprotein of the immunoglobulin superfamily involved in several important developmental processes in Drosophila, including axonal pathfinding in the optic lobe and programmed cell death and pigment cell differentiation in the pupal retina. As an initial step towards the "in vivo" functional analysis of this protein we have generated transgenic fly stocks carrying a truncated cDNA construct encoding only the extracellular domain of Rst-IrreC under the transcriptional control of the heat shock inducible promoter hsp70. We show that heat-shocking embryos bearing the transgene during the first 8hs of development lead to a 3-4 fold reduction in their viability compared to wild type controls. The embryonic lethality can already be produced by applying the heat pulse in the first 3hs of embryonic development, does not seem to be suppressed in the absence of wildtype product and is progressively reduced as the heat treatment is applied later in embryogenesis. These results are compatible with the hypothesis of the lethal phenotype being primarily due to heterophilic interactions between Rst-IrreC extracellular domain and an yet unknown ligand.

Síndrome hidroletal, Informe de una paciente en la maternidad Isidro Ayora (Quito-Ecuador) / Hidrolethalus syndrome. a case report

Introducción. El síndrome hidroletal es una rara entidad autosómica recesiva caracterizada principalmente por polihidramnios, hidrocefalia, letalidad y polidactilia. La gran mayoría de estos casos han sido descritos en Finlandia con escasos reportes de dicho problema en otros países. Caso clínico. Se reporta un caso con características compatibles con síndrome hidroletal en una pareja no consanguínea, sin ancestros europeos en cuyo caso el recién nacido no fallece a las pocas horas.Conclusión. Este sería el primer caso de síndrome hidroletal reportado en Latinoamérica y su presentación ligeramente diferente podría ser una variante alélica de su similar finlandés.

Contribución genética a la mortalidad embrionaria en 2 poblaciones de roedores no consanguíneos / Genetic contribution to embrionary mortality in 2 population of non-consanguineous rodents

Se calcularon los porcientos de genes letales recesivos que en estado homocigótico, provocan mortalidad embrionaria tomando como base poblaciones de ratas y ratones no consanguíneos. El aporte de los genes letales recesivos se halló por la diferencia de la mortalidad embrionaria entre 2 grupos con diferentes variantes de apareamiento: sistema rotatorio y cruzamiento consanguíneo. Se comparó al efecto el número de cuerpos lúteos, fetos vivos y reabsorciones en 200 ratones y 160 ratas en los días 15 y 17 del embarazo. Solamente en las ratas se encontraron diferencias significativas entre ambos sistemas debido al efecto de los genes letales recesivos. La mortalidad embrionaria después de la implantación y en general fue de 5,05 y 4,25 por ciento respectivamente

Analysis of sex distribution within families in a large Latin American sample

Uma amostra de 59.496 indivíduos latino-americanos pertencentes a 28.545 irmandades foi tomada de um grande Estudo Colaborativo de Malformaçöes Congênitas (ECLAMC). Recém-nascidos com malformaçöes congênitas e seus respectivos controles foram excluídos da amostra com a finalidade de evitar vieses associados com malformaçöes. Alguns modelos estatísticos foram aplicados, admitindo-se que os efeitos de Poisson e de Markovian näo säo importantes na determinaçäo da distribuiçäo geral das irmandades na populaçäo. O modelo geral foi o binomial duplo com excesso unicaudal. Este modelo pode ser simplificado para o binomial duplo, o binomial simples com excesso unicaudal ou o binomial simples. As primeiras três distribuiçöes ajustaram-se aos dados. Os mesmos modelos foram aplicados a vários estudos realizados em diferentes países e em épocas diferentes, os quais apresentaram resultados semelhantes. O modelo mais parcimonioso que se ajustou à maioria dos conjuntos de dados foi o binomial duplo, sugerindo que cerca de 9 por cento dos casais segregam letais recessivos ligados ao X, uma vez que as duas proporçöes de segregaçäo do modelo estäo próximas da previsäo genética.

The Malaysian experience in the typing of genetic variants of alpha-1-antitrypsin.

It is known that alpha1-antitrypsin deficiency is associated with emphysema in adults and liver cirrhosis in neonates. The phenotypes PiZZ and PiSZ are considered to be high risk groups. alpha1-antitrypsin deficiency is one of the most common lethal congenital disorders in Europe and the USA, occurring in approximately 1 in 2,000 caucasians of North European descent. Studies in Malaysia have found that the phenotypes PiZ and PiS are present in our population. Out of 950 samples analyzed, it was found that 10 samples were shown to be apparently Z homozygous phenotype. The phenotype is determined by high resolution isoelectrofocusing on an ultra-thin polyacrylamide gel embedded with narrow range Pi phamarlyte. The isoelectrofocused bands are confirmed by immunofixation and the plasma alpha1-antitrypsin levels determined by electroimmunoassay. The abnormal phenotypes are further confirmed by polymerase chain reaction using allele specific oligonucleotides.

The MEX.156 sex-limited lethal x chromosome of Drosophila melanogaster: moment of action

O presente trabalho teve por objetivo estimar o momento de açäo do letal Mex.156, limitado ao sexo feminino, do cromossomo X de Drosophila melanogaster

Immunologic and neuroendocrine interactions in pregnancy.

The neuroendocrine system helps in the success of the fetal graft by suppressing maternal cellular immune response against the foreign paternal histocompatibility (HLA) antigens. In addition, placenta absorbs the antibodies directed against the paternal HLA antigens, thus inhibiting the humoral rejection of the fetal graft. In contrast, neuropeptides released in the maternal blood stream under adverse mental states may stimulate lymphocyte blastogenesis and natural killer (NK) cell activity resulting in premature loss of the fetus. Further, homozygosity of a lethal gene which is in linkage disequilibrium with HLA genes may have a role in some unexplained fetal deaths.