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Younger, M. A.

Publications and source records attributed to Younger, M. A..

6 recordsLinked to original sources

Recurrent connectivity supports carbon dioxide sensitivity in Aedes aegypti mosquitoes

The mosquito Aedes aegyptis human host-seeking behavior depends on the integration of multiple sensory cues. One of these cues, carbon dioxide (CO2), gates odorant and heat pathways and activates host-seeking behavior. The neuronal circuits underlying processing of CO2 information remain unclear. We used automated serial-section transmission electron microscopy (EM) to image and reconstruct the circuitry of the glomeruli that are innervated by the Ae. aegypti maxillary palp, including the glomerulus that responds to CO2. Notably, CO2-sensitive olfactory sensory neurons (OSNs) make high levels of recurrent synaptic connections with one another, while making a low density of feedforward synapses. At some of these contacts between CO2 OSNs, we observe ribbon- like presynaptic structures, which may further enhance recurrent signaling. We compared both feedforward and recurrent connectivity with all olfactory glomeruli in Drosophila melanogaster, and we found more recurrent connections between the Ae. aegypti CO2-responsive OSNs than in any D. melanogaster glomeruli. We developed a computational circuit model that demonstrates recurrent synapses are necessary for robust CO2 detection under normal physiological conditions. Together, elevated levels of recurrent connectivity and ribbon-like structures may amplify sensory information detected by CO2-sensitive OSNs to support mosquito activation and sensitization by CO2, even in the presence of high levels of other odorants in the environment. We propose that this circuit organization supports the salience of CO2 as a mosquito host cue. One Sentence SummaryConnectomic analysis of carbon dioxide circuitry in the disease-vector mosquito Aedes aegypti.

neuroscience↗

When non-canonical olfaction is optimal

The early olfactory system is canonically described by a "one-receptor-to-one-neuron" model: each olfactory sensory neuron (OSN) expresses a single type of olfactory receptor. Although the olfactory systems of many model organisms approximately follow this canonical organization, a number of exceptions are known. In particular, Aedes aegypti mosquitoes co-express multiple types of olfactory receptors in many OSNs. Why do some olfactory systems follow the canonical organization while others violate it? We approach this question from the normative perspective of efficient coding. We find that the canonical and non-canonical organizations optimally encode odor signals in different types of olfactory environment. Non-canonical olfaction is beneficial when relevant sources emit correlated odorants and the environment contains odorants from ethologically irrelevant odor sources. Our theory explains previous observations of receptor co-expression and provides a framework from which to understand the structure of early olfactory systems.

neuroscience↗

Global genomics of Aedes aegypti unveils widespread and novel persistent infectious viruses capable of triggering a small RNA response

The mosquito Aedes aegypti is a prominent vector for arboviruses, but the breadth of mosquito viruses that infects this specie is not fully understood. In the broadest global survey to date of over 200 Ae. aegypti small RNA samples, we detected viral small interfering RNAs (siRNAs) and Piwi interacting RNAs (piRNAs) arising from mosquito viruses. We confirmed that most academic laboratory colonies of Ae. aegypti lack persisting viruses, yet two commercial strains were infected by a novel tombus-like virus. Ae. aegypti from North to South American locations were also teeming with multiple insect viruses, with Anphevirus and a bunyavirus displaying geographical boundaries from the viral small RNA patterns. Asian Ae. aegypti small RNA patterns indicate infections by similar mosquito viruses from the Americas and reveal the first wild example of dengue virus infection generating viral small RNAs. African Ae. aegypti also contained various viral small RNAs including novel viruses only found in these African substrains. Intriguingly, viral long RNA patterns can differ from small RNA patterns, indicative of viral transcripts evading the mosquitoes RNA interference (RNAi) machinery. To determine whether the viruses we discovered via small RNA sequencing were replicating and transmissible, we infected C6/36 and Aag2 cells with Ae. aegypti homogenates. Through blind passaging, we generated cell lines stably infected by these mosquito viruses which then generated abundant viral siRNAs and piRNAs that resemble the native mosquito viral small RNA patterns. This mosquito small RNA genomics approach augments surveillance approaches for emerging infectious diseases.

genomics↗

Non-canonical odor coding ensures unbreakable mosquito attraction to humans

Female Aedes aegypti mosquitoes are a persistent human foe, transmitting arboviruses including dengue and yellow fever when they bite us to obtain a blood meal. Mosquitoes are intensely attracted to human-emitted body odor, heat, and carbon dioxide, which they detect using three different large multi-gene families encoding odor-gated ion channels. Genetic mutations that cause profound disruptions to the olfactory system have modest effects on human attraction, suggesting significant redundancy in odor coding. The canonical view is that olfactory sensory neurons each express a single chemosensory receptor that defines its ligand selectivity. Using immunostaining, RNA in situ hybridization, and single nucleus RNA sequencing, we discovered that Aedes aegypti uses an entirely different organizational principle, with many neurons co-expressing multiple chemosensory receptor genes. In vivo electrophysiology demonstrates that the broad ligand-sensitivity of mosquito olfactory neurons is due to this non-canonical co-expression. The redundancy afforded by an olfactory system in which many neurons co-express multiple receptors with different chemical sensitivity may greatly increase the robustness of the mosquito olfactory system and explain our longstanding inability to engineer new compounds that disrupt the detection of human body odor by mosquitoes.

neuroscience↗

Chemical signatures of human odour generate a unique neural code in the brain of Aedes aegypti mosquitoes

A globally invasive form of the mosquito Aedes aegypti specializes in biting humans, making it an efficient vector of dengue, yellow fever, Zika, and chikungunya viruses. Host-seeking females strongly prefer human odour over the odour of non-human animals, but exactly how they distinguish the two is not known. Vertebrate odours are complex blends of volatile chemicals with many shared components, making discrimination an interesting sensory coding challenge. Here we show that human and animal odour blends evoke activity in unique combinations of olfactory glomeruli within the Aedes aegypti antennal lobe. Human blends consistently activate a universal glomerulus, which is equally responsive to diverse animal and nectar-related blends, and a more selective human-sensitive glomerulus. This dual signal robustly distinguishes humans from animals across concentrations, individual humans, and diverse animal species. Remarkably, the human-sensitive glomerulus is narrowly tuned to the long-chain aldehydes decanal and undecanal, which we show are consistently enriched in (though not specific to) human odour and which likely originate from unique human skin lipids. We propose a model of host-odour coding wherein normalization of activity in the human-sensitive glomerulus by that in the broadly-tuned universal glomerulus generates a robust discriminatory signal of the relative concentration of long-chain aldehydes in a host odour blend. Our work demonstrates how animal brains may distil complex odour stimuli of innate biological relevance into simple neural codes and reveals novel targets for the design of next-generation mosquito-control strategies.

neuroscience↗

The ion channel ppk301 controls freshwater egg-laying in the mosquito Aedes aegypti

Aedes aegypti mosquitoes are deadly vectors of arboviral pathogens including Zika, dengue, and yellow fever, and breed in containers of freshwater associated with human habitation1,2. Female Ae. aegypti lay eggs near freshwater because larval and pupal stages are aquatic3. They use volatile cues to locate water at a distance4, while at close-range they contact water to evaluate its suitability for egg-laying4-7. High salinity is lethal to mosquito offspring and therefore correctly laying eggs in freshwater is a crucial parenting decision made by female mosquitoes. Here we show that the DEG/ENaC channel8-10 ppk301 is required for mosquitoes to exploit freshwater egg-laying substrates. When ppk301 mutant females contact water, they do not lay eggs as readily as wild-type animals and are more likely to make aberrant decisions between freshwater and saltwater at concentrations that impair offspring survival. We used a CRISPR-Cas9-based genetic knock-in strategy combined with the Q-binary transactivator system11 to build genetic tools for labelling and imaging neurons in the mosquito. We found that ppk301 is expressed in sensory neurons in legs and proboscis, appendages that directly contact water, and that ppk301-expressing neurons project to central taste centres. Using in vivo calcium imaging with the genetically-encoded calcium sensor GCaMP6s12, we found that ppk301-expressing cells respond to water but, unexpectedly, also to salt. This suggests that ppk301 is instructive for egg-laying at low salt concentrations but that a ppk301-independent pathway is responsible for inhibiting egg-laying at high salt concentrations. Water is a key resource for insect survival and understanding how mosquitoes interact with water to control different behaviours is an opportunity to study the evolution of chemosensory systems. The new genetic tools described here will enable direct study of not only egg-laying, but also other behaviours in mosquitoes that influence disease transmission and enable comparative studies of insect biology more broadly.

neuroscience↗