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Rogers, M. E.

Publications and source records attributed to Rogers, M. E..

4 recordsLinked to original sources

Exploiting nectar and blood feeding cues and phagostimulants to optimise Attractive Targeted Sugar Baits against a sand fly vector of leishmaniasis.

BackgroundLeishmaniasis presents a major public health problem for a large number of countries requiring effective integrated management of the vector, sand flies, for sustained control. Such strategies need to be economically and environmentally sustainable and adaptable to the behaviour of local vectors. One such tool is Attractive Targeted Sugar Baits (ATSB) that exploit the necessity of sand flies to acquire sugars between bloodmeals. Here we explored the kinetics and cues for sugar and blood feeding to improve the efficacy of ATSBs against sand flies. MethodsA fluorescent assay was developed to quantify sugarmeals to assess the feeding efficiency of colony-reared female Lutzomyia longipalpis sand flies. ResultsSand flies showed a range of preferences for different sugars presented on cotton wool and could be manipulated to deposit them into the crop and/or midgut. We found that the combination of 10% sucrose and 10% fructose allowed flies to obtain the largest sugarmeals taken to the crop. Sugarmeals were taken to both the crop and midgut when it contained 200 mM bovine serum albumin (BSA) as a source of protein and 1 mM adenosine triphosphate (ATP) as a phagostimulant. Using this combination, the efficacy of the ingested insecticide fipronil was significantly increased; reducing the 50% lethal concentration from 584 {micro}M to 1.65 {micro}M in a sugarmeal that promoted the simultaneous uptake of the insecticide into the midgut as well as the crop. ConclusionsIn this study we highlight the potential of understanding the cues used by vectors to sugar feed and blood feed. By incorporating blood feeding phagostimulants, such as BSA and ATP, in ATSB we vastly improve their killing efficiency against sand flies. This demonstrates a new approach to target these disease vectors. Author SummaryMany insect vectors of disease use sugars, such as nectar, as fuel to enable them to obtain blood, that in turn sustains parasite transmission. In most blood feeding Diptera sugars are diverted to the crop where it is stored and released into the midgut for energy whereas blood is taken directly to the midgut where it is digested to provide nutrients for egg development. For sand flies the cues required to switch between sugar and blood feeding programmes are unknown but if they were they could be exploited to improve Attractive Targeted Sugar Baits (ATSB) as a means of poisoning sand flies when they sugar feed. In this study we find that the sand fly, Lutzomyia longipalpis, uses a combination of physical cues (biting/piercing vs sucking) and meal composition to allow them to efficiently feed on nectar and blood. We show that they sense protein and adenosine triphosphate (ATP) to direct blood to the midgut and we demonstrate that this can be turned to our advantage to improve the lethality of ATSB. We show that inclusion of bovine serum albumin as a source of protein and the phagostimulant ATP can trick sand flies to blood feed on sugar and direct the insecticide fipronil to the midgut where it was 355-fold more potent than in sugar alone. These results show the potential of phagostimulants to improve the efficacy and selectivity of ATSB towards blood feeding arthropods, including sand flies, and highlights the value of understanding the feeding programmes of disease vectors in general.

zoology↗

Insights into the salivary N-glycome of Lutzomyia longipalpis, vector of visceral leishmaniasis

During Leishmania transmission sand flies inoculate parasites and saliva into the skin of vertebrates. Saliva has anti-haemostatic and anti-inflammatory activities that evolved to facilitate bloodfeeding, but also modulate the hosts immune responses. Sand fly salivary proteins have been extensively studied, but the nature and biological roles of protein-linked glycans remain overlooked. Here, we characterised the profile of N-glycans from the salivary glycoproteins of Lutzomyia longipalpis, vector of visceral leishmaniasis in the Americas. In silico predictions suggest half of Lu. longipalpis salivary proteins may be N-glycosylated. SDS-PAGE coupled to LC-MS analysis of sand fly saliva, before and after enzymatic deglycosylation, revealed several candidate glycoproteins. To determine the diversity of N-glycan structures in sand fly saliva, enzymatically released sugars were fluorescently tagged and analysed by HPLC, combined with highly sensitive LC-MS/MS, MALDI-TOF-MS, and exoglycosidase treatments. We found that the N-glycan composition of Lu. longipalpis saliva mostly consists of oligomannose sugars, with Man5GlcNAc2 being the most abundant, and a few hybrid-type species. Interestingly, some glycans appear modified with a group of 144 Da, whose identity has yet to be confirmed. Our work presents the first detailed structural analysis of sand fly salivary glycans.

biochemistry↗

Probing behavior of Diaphorina citri (Hemiptera: Liviidae) on Valencia orange influenced by sex, color, and size

Candidatus Liberibacter asiaticus is vectored by the psyllid Diaphorina citri Kuwayama (Hemiptera: Liviidae) and putatively causes Huanglongbing disease in citrus. Huanglongbing has reduced yields by 68% relative to pre-disease yields in Florida. Disease management is partly through vector control. Understanding vector biology is essential in this endeavor. Our goal was to document differences in probing behavior linked to sex. Based on both a literature review and our results we conclude that there is either no effect of sex or that identifying such an effect requires a sample size at least four times larger than standard methodologies. Including both color and sex in statistical models did not improve model performance. Both sex and color are correlated with body size, and body size has not been considered in previous studies on sex in D. citri. An effect of body size was found wherein larger psyllids took longer to reach ingestion behaviors and larger individuals spent more time ingesting phloem, but these relationships explained little of the variability in these data. We suggest that the effects of sex can be ignored when running EPG experiments on healthy psyllids.

animal behavior and cognition↗

ODORANT RECEPTOR INHIBITION IS FUNDAMENTAL TO ODOR ENCODING

Most natural odors are complex mixtures of many volatile components, competing to bind odorant receptors (ORs) expressed in olfactory sensory neurons (OSNs) of the nose. To date surprisingly little is known about how OR antagonism shapes neuronal representations in the periphery of the olfactory system. Here, we investigated its prevalence, the degree to which it disrupts OR ensemble activity, and its conservation across related ORs. Calcium imaging microscopy of dissociated OSNs revealed significant inhibition, often complete attenuation, of responses to indole, a commonly occurring volatile associated with both floral and fecal odors, by a set of 36 tested odorants. To confirm an OR mechanism for the observed inhibition, we performed single-cell transcriptomics on OSNs that exhibited specific response profiles to a diagnostic panel of odorants and identified the receptor Olfr743 which, when tested in vitro, recapitulated ex vivo responses. We screened ten ORs from the Olfr743 clade with 800 perfumery-related odorants spanning a range of chemical scaffolds and functional groups, over half of which (430) antagonized at least one of the ten ORs. Furthermore, OR activity outcomes were divergent rather than redundant, even for the most closely related paralogs. OR activity fitted a mathematical model of competitive receptor binding and suggests that normalization of OSN ensemble responses to odorant mixtures is the rule rather than the exception. In summary, we observed OR antagonism, inverse agonism and partial agonism occurring frequently and in a combinatorial manner. Thus, extensive receptor-mediated computation of mixture information appears to occur in the olfactory epithelium prior to transmission of odor information to the olfactory bulb.

neuroscience↗