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Aguiar Martins, K.

Publications and source records attributed to Aguiar Martins, K..

2 recordsLinked to original sources

New insights on the Feeding Site and Salivation by Lutzomyia longipalpis (Diptera: Psychodidae) During Blood Ingestion on Host Skin

Phlebotomine sand flies are major vectors of Leishmania parasites, yet the mechanisms underlying their blood-feeding behavior remain poorly understood. In Lutzomyia longipalpis, the primary vector of Leishmania infantum in the Americas, feeding occurs via telmophagy, a pool-feeding method which is known by involving dermal laceration, salivation, and the creation of a blood pool. While the biochemical effects of sand fly saliva on host hemostasis, inflammation, and immunity are well studied, the dynamics of mouthpart movements and saliva at the feeding site remain to be systematically explored. Using intravital microscopy, fluorescent saliva labelling and image analysis, we characterized the mechanical actions of mouthparts and the spatial-temporal patterns of salivation during feeding on mammalian skin. Our recordings indicate that the labrum and hypopharynx are the most prominent mouthparts during feeding and exhibit scissor-like movements during probing. At specific moments, these structures close forcefully, generating small blood splashes in multiple directions. Feeding occurred in two distinct phases: an initial probing phase, often distinguished by ineffective blood intake, and a subsequent engorgement phase that was initiated exclusively upon the activation of small dermal "feeder vessels."Acridine Orange labelling showed abundant early salivation that penetrated progressively deeper into the dermis and remained detectable for over an hour, reflecting both the tissue damage and enzymatic effects. The analysis of images demonstrated the sequential salivation events, highlighting an initial high-frequency phase followed by a more gradual pattern during engorgement. These findings provide the first real-time, detailed view of the coordinated interactions between mouthpart mechanics, targeted salivation, and host microvascular responses in Lu. longipalpis. This study redefines sand fly telmophagy as a non-passive and coordinated process integrating mouthpart mechanics, salivation, and modulation of host vasculature. This work advances our understanding of sand fly vector-host interactions and underscores the potential of salivary molecules as targets for transmission-blocking strategies. Author SummaryPhlebotomine sand flies are the main vectors of Leishmania infantum, the parasite responsible for visceral leishmaniasis in the Americas. Although sand flies are traditionally classified as "pool feeders," meaning they lacerate the skin and feed from small pools of blood, the mechanics of how they obtain blood and deliver saliva into host skin have remained poorly understood. In this study, we used image analysis, intravital microscopy and fluorescent labeling of saliva to visualize, in real time, the feeding behavior of Lutzomyia longipalpis on mammalian skin. We show that blood feeding is not a passive process based solely on blood pooling. Instead, it involves coordinated movements of the mouthparts, modulation of host microvessels with the saliva contribution, and the recruitment of small dermal "feeder vessels" that supply blood directly to the insect. Our findings reveal that sand fly feeding is a highly orchestrated interaction between vector and host, integrating mechanical tissue disruption, salivary secretion, and vascular responses. These processes likely create a favorable microenvironment for Leishmania establishment and transmission. By providing a detailed characterization of mouthpart and salivation dynamics, this study advances our understanding of sand fly biology and highlights salivary components and feeding-site events as potential targets for transmission-blocking strategies.

microbiology↗

TRPtracker: a community database for monitoring praziquantel sensitivity at TRPMPZQ variants

The anthelmintic praziquantel (PZQ) has been used for decades as the clinical therapy for schistosomiasis, and remains the only available drug. As a cheap and effective drug therapy for all human disease-causing Schistosoma species, usage of PZQ underpins mass drug administration strategies aimed at eliminating schistosomiasis as a public health problem by 2030. Concern over the potential emergence of resistance to PZQ is therefore warranted, as it would constitute a major threat to this approach. In terms of molecular adaptations conferring PZQ resistance, variation in the sequence and/or expression of the drug target is an obvious mechanism and should be a priority for surveillance efforts. The target of PZQ is a transient receptor potential ion channel, TRPMPZQ, which is established as a locus that regulates schistosome sensitivity to PZQ. Here, we describe the establishment of a community resource, TRPtracker, which coalesces data on TRPMPZQ natural variants together with measurements of individual variant sensitivity to PZQ. A compendium of laboratory-generated mutants in TRPMPZQ is also compiled in TRPtracker to map regions within TRPMPZQ critical for PZQ sensitivity. Aggregation of data from multiple research groups into TRPtracker permits rapid community-wide exchange of data, cataloguing which TRPMPZQ variants have been functionally profiled, where geographically these variants have been found, their frequency within populations and their potential impact on PZQ sensitivity.

microbiology↗