Les OBP sont des petites protéines solubles qui se lient avec des molécules odorantes et phéromonales. Le rôle des OBPs n’est pas complètement compris. Une hypothèse suggère que l’OBP solubilise et transporte les ligands aux récepteurs olfactifs et la liaison entre les molécules odorantes et l’OBP est non spécifique. Une autre hypothèse suggère que le complexe formé est une liaison spécifique entre une molécule odorante donnée et une OBP spécifique. Ce travail de thèse montre que les OBPs sont impliquées dans la première étape de la discrimination des odeurs. Dans un premier temps, nous avons montré l’implication de la Phe35 et la Tyr 82 dans la sortie du ligand par l’OBP. Dans un second temps, nous avons mis en évidence la présence de différentes isoformes d’OBP et de VEG qui diffèrent par les modifications post-traductionnelles (phosphorylation et GlcNAcylation) a la fois sur les protéines natives extraites de la muqueuse respiratoire et sur les protéines recombinantes produites par P.pastoris et CHO. Ces isoformes sont capables de discriminer des molécules odorantes et phéromonales. Les OBPs ne sont pas des transporteurs passifs car elles assurent un fin codage des molécules odorantes ou phéromonales avant l’interaction de ce complexe avec un récepteur spécifique. / OBPs are small soluble proteins that bind with odorant molecules and pheromones. The role of OBP is not completely understood. A hypothesis suggests that OBP solubilize and transport the ligands to olfactory receptors and the binding between odorant molecule and OBP is unspecific. An other hypothesis suggest that the complex formed is the specific binding between a given odorant molecule and a specific OBP. This work of thesis show that OBP are involved in the first step of odorant discrimination. Initially, we have showed the involvement of the Phe35 and Tyr 82 in the uptake of ligands by OBP. Second, we have given rise to the presence of various isoform of OBP and VEG that differ by post-translational modifications (phosphorylation and GlcNAcylation) both on natives proteins extract of respiratory mucosa and on recombinants proteins produce by P. pastoris and CHO. These isoforms are able to discriminate of odorant molecules and pheromones. OBPs are not passives carriers because they ensure a fine coding of odorant molecules and pheromones before interaction of this complex with specific receptor.

This PhD project aimed to investigate the possibility of using Odorant Binding Proteins (OBPs) as sensing layers of chemical sensors, for the detection of organic compounds in both vapour and liquid phases. OBPs are small soluble proteins present in high concentrations in the olfactory system of vertebrates and insects. OBPs are attractive in the biosensor field since they can bind odorants and pheromones in a reversible way. They are resistant to high temperatures and protease activity and they can be easily expressed in large amounts. OBPs belonging to different species of mammals and insects were utilised for developing biosensors relied on different transduction mechanisms. Recombinant OBPs were grafted on the gold electrode of transducers by using Self-assembled monolayers (SAMs) of alkanethiols. The efficiency of the immobilisation method was proved by using electrochemical techniques. Quartz crystal microbalances (QCMs), screen-printed electrodes (SPEs) and interdigitated electrodes (IDEs) were employed for developing three types of OBP-based biosensors. I. QCMs functionalised with OBPs were tested against pheromones (i.e. bombykol and bombykal) and volatile compounds found in foodstuffs (i.e. pyrazine derivatives and geosmin) in vapour phase. The QCM based biosensors showed a good degree of selectivity and a detection limit of the order of parts per billion, in air. II. In liquid phase, impedimetric biosensors based on SPEs also showed a good selectivity and sensitivity being able to detect analyte concentrations of the order of 10-9 M. III. OBPs immobilised on the gold electrodes of IDEs were instead tested against S-(+) carvone vapour, proving that the binding activity of the proteins was preserved in vapour phase and can be quantified as variation of capacitance. The developed OBP biosensors showed good selectivity, sensitivity and stability over time in both liquid and vapour phase. The responses of the sensors were reversible, allowing to the device to be used several times. Moreover, the biosensors were label-free, hence the interaction between OBPs and ligand was directly detected without using auxiliary probes/species. With these findings, we envisage the use of our biosensors in several applications, including monitoring of the quality of food along the transportation and storage, controlling of pests and useful insects in agriculture, or as analytical devices for studying the dynamics in binding processes.

The initial step in odor recognition by the nose is the binding of odorant molecules to receptor sites embedded in the dendritic membranes of olfactory receptor cells. Despite considerable interest and experimentation into the nature of these receptor sites, little is known of their specificity to different types of odorant molecules. This lack of knowledge partially stems from the fact that the nature of receptor proteins is most effectively studied when specific and irreversible inhibitors are available for use as chemical probes, yet no such agents have been discovered for use in the olfactory system. A series of alkylating agents and other chemically active odorants were tested to determine whether they might react with specific odorant receptors and modify olfactory responses. Electroolfactogram (EOG) recordings were obtained before, during, and after treatment of the olfactory mucosae of grass frogs (Rana pipiens) with a chemically active odorant.

Philosophiae Doctor - PhD / Tsetse flies are the biological vectors of human and animal trypanosomiasis and hence representant medical and veterinary importance. The sense of smell plays a significant role in tsetse and its ecological interaction, such as finding blood meal source, resting, and larvicidal sites and for mating. Tsetse olfactory behaviour can be exploited for their management; however, olfactory studies in tsetse flies are still fragmentary. Here in my PhD thesis, using scanning electron microscopy, electrophysiology, behaviour, bioinformatics and molecular biology techniques, I have investigated tsetse flies (Glossina fuscipes fuscipes) olfaction using behaviourally well studied odorants, tsetse repellent by comparing with attractant odour. Insect olfaction is mediated by olfactory sensory neurons (OSNs), located in olfactory sensilla, which are cuticular structures exposed to the environment through pore and create a platform for chemical communication.

The development of an inexpensive, portable, stable, sensitive and selective biosensor for detection of odorants is a daunting task. Here, we hypothesized the development of a detector layer composed of the protein groups; the olfactory receptors (ORs) and the odorant binding proteins (OBPs), known to bind odorants in animal sensing. We report the design of 13 OR gene-vector constructs, and their subsequent transformation into Escherichia (E.) coli (BL21 (DE3)-STAR-pLysS) strain. Moreover, we report the expression of several ORs into an in vitro wheat germ extract using three separate detergent mixes for protein solubilization.   In addition, we describe the design of an odorant binding protein from the Aenopheles gambiae mosquito PEST strain (OBP-PEST) gene-vector construct under an IPTG (Isopropyl β-D-1-thiogalactopyranoside) inducible promoter. OBP-PEST was heterologously expressed in E.coli with an 8 amino acid long sequence (WSPQFEK) attached C-terminally, via a thrombin cleavage site and a flexible linker (GSSG). The WSPQFEK sequence, commonly referred to as a Strep-tag, enabled subsequent affinity chromatography purification of the protein, via binding to an engineered Streptavidin equivalent. Surprisingly, the OBP-PEST was found to contain a signal sequence leading to its truncation and secretion when expressed in E.coli.   Biophysical analyses were established using Circular Dichroism (CD) for the analysis of two lipocalins: Beta-lactoglobulin (BLG) and OBP-PEST. We studied the solubility, refoldability and the conformational transitions of BLG, as a result of change in solvent, pH and temperature. The secondary structure of OBP-PEST and its thermal stability was investigated.   In conclusion, this thesis work has enabled biophysical analyses of OBP-PEST and future analogs of interest to the development of a stable protein detector layer. Although further experiments are needed to fully characterize the biophysical properties, and to find odorant substrates of OBP-PEST, it was found to be a suitable alternative to ORs in a biosensor detector layer application. More importantly, an inherent OBP-PEST signal sequence was found to mediate protein secretion when expressed heterologously in E.coli. To the best of our knowledge this is the first lipocalin discovered to be secreted upon heterologous expression in E.coli.   We hypothesize that this signal peptide could be used as a means for targeted secretion and, hence, efficient protein purification.

Insect Odorant-Binding Proteins (OBPs) are small, water-soluble molecules that solubilize hydrophobic odorant molecules in the sensillum lymph and transport them to their cognate receptors in the olfactory receptor neurons. With the availability of the genome sequence of the African malaria mosquito, Anopheles gambiae, there has been a profound interest in the characterization and functional analyses of Obp genes in order to understand the molecular basis of mosquito host-seeking behavior. However, no direct evidence has been found for specific functions of any mosquito OBPs. In this study, I describe the comparative genomics and expression analyses on two mosquito Obp genes (Obp1 and Obp7) as well as efforts to determine their functions. Both of these Obp genes were identified in Anopheles stephensi and only Obp7 gene was identified in Anopheles quadriannulatus by screening bacterial artificial chromosome (BAC) libraries of these species. Comparative analyses revealed several interesting features including segments of conserved non-coding sequences (CNSs) that contain potential regulatory elements relevant to olfactory tissue development and blood-feeding. The expression profiles of these genes were examined in detail in the Asian malaria mosquito An. stephensi. Obp1 and Obp7 transcripts were significantly higher in females than male mosquitoes and they were predominantly found in the antenna, which is the primary olfactory organ of mosquitoes. Twenty-four hours after a blood meal, mRNA levels of these two genes were significantly reduced in the maxillary palp and proboscis, referred to as secondary olfactory organs of mosquitoes. These findings collectively indicate that Obp1 and Obp7 genes in An. stephensi likely function in female olfactory response and may be involved in behaviors related to blood-feeding. To investigate the function of these Obp genes more directly, a Sindbis virus based expression system is established to knockdown the two Obp gene orthologs in Aedes aegypti. The effective knockdown of Obp1 and Obp7 genes (8 and 100-fold, respectively) is accomplished in female mosquito olfactory tissues. The potential for a systematic analysis of the molecular players involved in mosquito olfaction using this newly developed technique is discussed. Such analysis will provide the foundation for interfering with mosquito host-seeking behavior for the prevention of disease transmission. / Ph. D.

No description available.

<p dir="ltr">Given the relatively poor visual acuity of compound eyes, many insects have developed alternative means for navigating their environment. For example, insects often rely on chemosensation to find food, mates, and inter- and intraspecific communication. Eusocial insects in particular have developed complex systems of pheromone communication to organize their colonies, enabling them to partition labor for foraging, brood care, and colony defense tasks to different portions of the colony. A variety of genes coding for proteins are involved in detecting these chemicals, including gustatory receptors, ionotropic receptors, and odorant receptors (ORs). Eusocial insects, and especially ants, have evolved an expanded clade of ORs in their genome, likely due to an increased reliance on pheromones compared to other insects. The ability to recognize nestmates from non-nestmates is one of the vital functions performed by these ORs, which detect hydrocarbons present on the cuticle to distinguish friend from foe. However, research into the details of nestmate recognition has been stymied due to difficulties in manipulating OR genes. Despite advances in genetic sequencing and manipulation technologies, strict reproductive divisions within most ant lineages make generating transgenic ants nearly impossible, and so we have been left with limited options to further investigate these receptors. To narrow down the ORs that could be involved in nestmate recognition in the Argentine ant (Mayr, 1868), I took a multi-pronged approach of generating tissue transcriptomes to identify ORs that are selectively upregulated in the antennae, as well as conducting a phylostratigraphic analysis to identify which OR genes arose more recently in the Argentine ant genome. While conducting these analyses, it became necessary to reannotate the set of Argentine ant OR genes, due to current published annotations not containing the full breadth of <i>L. humile</i> ORs. Finally, I orally administered fluorescently-labelled dsRNA to workers, and tracked the extent to which ingested dsRNA is capable of traversing the tissues of ant workers, to investigate whether RNAi is a viable method for investigating gene function for genes showing tissue-selective expression. I discovered a subset of OR genes that are highly expressed in the antennae and confirmed that dsRNA is able to reach the antennae and knock down OR gene expression through ingestion, meaning that RNA interference is a viable method for the practical study of ant OR genes and can be used to further explore how individual ORs regulate nestmate recognition.</p>

Olfactory transduction mechanisms are best studied when specific blocking agents are available with which to modify cellular responses to odorant stimulation. This study is an electrophysiological investigation of functional group-specific olfactory acceptor mechanisms using ethylbromo acetate (EtBrAc), a World War I war gas which inhibits olfactory responses to odorant stimulation. The major findings of this investigation show that (1) vaporous EtBrAc is found to be a quick and effective inhibitor of electroolfactogram (EOG) responses to odorant stimulation, (2) isoamyl acetate is shown to protect EOG responses to a wide variety of odorants, inclusive of itself, from the inhibition effect of EtBrAc treatment, and (3) amine acceptor sites exist which are resistant to the inhibitory effects fo EtBrAc treatment.

Rhipicephalus micropulus, conhecido como carrapato dos bovinos, é um dos parasitas mais importantes para a pecuária, pois causa enormes prejuízos ao produtor. Esses prejuízos se estendem desde a ação espoliativa que o carrapato exerce nos seus hospedeiros até a transmissão de uma diversidade de patógenos. Os carrapatos utilizam vários estímulos térmicos, sonoros, visuais, gustativos, táteis e olfativos na fase de busca pelo hospedeiro. Essas substâncias são conhecidas como semioquímicos e podem atuar em indivíduos de uma mesma espécie como os ferormônios ou entre indivíduos de espécies diferentes como os alomônios e cairomônios. Nos bovinos, já se sabe que uma de suas lipocalinas pode atrair insetos, porém não é sabido se essa atração ocorre para R. microplus. Já é sabido que o carrapato consegue distinguir odores liberados entre bovinos das raças Nelore e Holandês Preto e Branco (HPB), sendo mais atraído para bovinos da raça Holandês. A lipocalina por ser uma proteína globular e estar associada com o transporte de pequenas moléculas hidrofóbicas, tais como odorantes e esteroides, e pode favorecer a atração do R. microplus, uma vez que essa proteína bovina pode ligar a odorantes e desempenhar um papel fundamental na liberação de odores para o ambiente, que por sua vez pode atrair, ou não, o R. microplus. Existem diferentes níveis de infestação de carrapatos entre bovinos das raças Nelore e Holandês, bem como entre os sexos da mesma raça. Além disso, o período do ciclo de vida do bovino também pode influenciar na susceptibilidade a infestação, por exemplo, as vacas no período de lactação são consideradas mais susceptíveis ao parasito. Assim, o objetivo do presente estudo foi avaliar o papel da lipocalina bovina na resistência e suscetibilidade ao carrapato, através da quantificação dessa proteína em líquidos corporais dos bovinos, tais como soro, saliva, urina, suor, secreção nasal e biopsia de pele obtidos de bovinos que apresentam fenótipos contrastantes de infestações, a saber: hospedeiros macho (touros) e fêmea (vacas em lactação) das raças resistentes (Bos indicus) e suscetíveis (Bos taurus). Os resultados deste trabalho tem demonstrado que a lipocalina bovina está presente em todos os fluídos investigados, exceto a urina, como observado por Western blot. Com os resultados deste trabalho podemos concluir que a bcOBP apresenta 9 diferença significativa nos fluidos de saliva e secreção nasal de touros e vacas em lactação da raça HPB quando comparados com touros e vacas em lactação da raça Nelore. Em amostras de biópsia de pele também ocorreu uma maior marcação da bcOBP na raça susceptível (HPB), demonstrando que a bcOBP possivelmente esta auxiliando na susceptibilidade destes bovinos ao carrapato, através do transporte de um maior número de odorantes que estariam atraindo um maior número de carrapatos. Ao analisar os fluidos entre bovinos da mesma raça, porém de sexo diferente, observou-se uma maior quantidade de bcOBP em vacas no período de lactação HPB nos fluidos de saliva e secreção nasal, visto que as vacas estão no período de lactação e são mais susceptíveis a infestações. Consequentemente, a bcOBP poderia estar colaborando para a sua maior susceptibilidade quando comparadas com touros HPB, e o mesmo ocorreu para biopsia de pele. Porém no fluído soro o aumento foi significativo para touro HPB quando comparado às vacas em lactação da raça HPB. Acredita-se que esse fenômeno ocorra devido ao período de lactação nas fêmeas uma vez que a produção da lipocalina bovina esta intimamente relacionada com a produção do leite. Os resultados deste trabalho demonstram que possivelmente a bcOBP na raça HPB está carreando odorantes para o ambiente os quais estariam atraindo mais carrapatos, e auxiliando na susceptibilidade destes bovinos. / Rhipicephalus micropulus, known as bovine tick, is one of the most important parasites for livestock, as they cause enormous damage to the producer. These demages extend from the spoliation action that the tick exerts on the skin of its hosts until the transmission of a diversity of pathogens. Ticks use various thermal, sound, visual, gustatory, tactile and olfactory stimuli in the search phase to the host. These substances are known as semiochemicals and can act within individuals of the same species as the pheromones or among individuals of different species such as alomones and cairomones. In the cattle, it is known that the lipocalin protein may attract insects, but this attraction is not known to influence the R. microplus. It is known that the tick can distinguish released odors between Nelore and Holstein cattle, being more attracted to cattle of the Holstein breed. Lipocalin, being a globular protein and associated with the transport of small hydrophobic molecules, such as odorants and steroids, can favor the attraction of R. microplus, since this bovine protein can bind to odorants and play a key role in the release of odors into the environment, which in turn may or may not attract R. microplus. There are different levels of tick infestation among cattle of the Nelore and Holstein breeds, as well as between the sexes of the same breed. In addition, the life cycle period of the bovine can also influence the susceptibility to infestation. For example, cows in the lactation period are considered more susceptible to the parasite. Thus, the objective of the present study was to evaluate the role of bovine lipocalin in the resistance and susceptibility to tick by quantifying that protein in bovine body fluids such as serum, saliva and urine, sweat, nasal secretions and skin biopsies obtained from resistant (Bos indicus) and susceptible (Bos taurus) cattle breeds. The results of this work have demonstrated that bovine lipocalin is present in all investigated fluids except urine, as observed by Western Blot. With the results of this work we can conclude that bcOBP presents a significant difference in fluids saliva and nasal secretion of bulls and cows in lactation breed HPB when compared to bulls and lactating cows of the Nelore breed. In skin biopsy specimens, there was also a greater labeling of bcOBP in the susceptible strain (HPB), which could then aid in the susceptibility of these cattle to the 11 tick, by transporting a larger number of odorants that would be attracting a greater number of ticks. When analyzing the fluids between bovines of the same breed, but of different sex, a greater amount of bcOBP was observed in cows during the period of HPB lactation in the fluids saliva and nasal secretion, since the cows are in the lactation period and are more susceptible to infestations. Consequently, bcOBP could be contributing to its greater susceptibility when compared to HPB bulls, and the same was done for skin biopsy. However, in the fluid serum, the increase was significant for the bull when compared to the lactating cows of the HPB race. It is believed that this phenomenon occurs due to the lactation period in females since the production of bovine lipocalin is closely related to milk production. The results of this work demonstrate that possibly Lipocalin in Holstein cattle is carrying odorants to the environment which would be attracting more ticks, and enhancing in the susceptibility of these cattle.