Search

Simple Summary: Interspecific competition occurs when two or more species require similar resources. Competition could be avoided by selecting a habitat with fewer competitors. While this behavior is well known, the identification mechanism is poorly understood. Mosquitoes select larval habitats during oviposition, and high competitor densities reduce larval survival. In this study, we show that ovipositing mosquito females can detect and avoid pools containing crowding signals originating from interspecific larvae. Furthermore, when larvae were not crowded, the habitat was found to be attractive to conspecifics. These findings increase our understanding of signals affecting mosquito oviposition, competitor recognition, and habitat selection under competition conditions. Numerous species of animals alter their behavior in response to increasing competition. To do so, they must possess the ability to detect the presence and density of interspecific competitors. We studied the role of semiochemicals released by increasing densities of larval Culiseta longiareolata Macquart on female oviposition habitat selection in two field experiments. Similarly to C. longiareolata larvae, subordinate Culex laticinctus Edwards are periphyton grazers who dwell in rain-filled pools in the Mediterranean region. We show that C. laticinctus females oviposited significantly less in mesocosm pools that were treated with crowding signals originating from C. longiareolata larvae. In the second experiment, we placed a similar number of larvae directly inside the 50 L mesocosms. These low-density mesocosms did not affect C. laticinctus oviposition but were attractive to conspecific oviposition. These results increase our understanding of the female ability to detect species-specific signals, indicating increased larval competition. [ABSTRACT FROM AUTHOR]

Bacterial adhesion to tissue is the starting point for many pathogenic processes and beneficial interactions. The dynamics and speed of adhesion (minutes) make high-resolution temporal kinetic data important, but this capability is absent from the current toolset. We present a high-throughput method with a second-to-minute kinetic resolution, testing the adhesion of Pseudomonas aeruginosa PAO1 wild-type, flagella-, pili-, and quorum-sensing mutants to human embryonic kidney (HEK293) cells. Adhesion rates were in good correlation with HEK293 confluence, and the ways in which various bacterial mutations modified adhesion patterns are in agreement with the published literature. This simple assay can facilitate drug screening and treatment development as well as provide a better understanding of the interactions of pathogenic and probiotic bacteria with tissues, allowing the design of interventions and prevention treatments. [ABSTRACT FROM AUTHOR]