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Sharan, M.

Publications and source records attributed to Sharan, M..

2 recordsLinked to original sources

Extinction of innate floral preferences in the pollinator Eristalis tenax

Innate behaviors allow solitary animals to complete essential tasks in the absence of social learning. However, we know little about the degree to which ecologically relevant innate preferences can change. The hoverfly Eristalis tenax, a solitary generalist pollinator, is an ideal model for studying innate behavior in a naturalistic context because its survival depends on the innate ability to identify flowers. Innate behavior in E. tenax has previously been considered inalterable, but we hypothesized that E. tenax can modulate their innate behavior after training in a multimodal sensory context, in contrast to the prior work that employed unimodal sensory cues. To test this, we examined if E. tenax can extinguish an innate proboscis extension response (PER) to a multimodal floral object after undergoing aversive conditioning with quinine, and if flies can acquire PER to an innately unattractive object using sucrose as reinforcement. Finally, we assessed long-term memory retention. Here, we report a complete extinction of the proboscis extension response (PER) to an innately attractive floral object following aversive training. E. tenax can also acquire PER to an innately unattractive object after appetitive training. Flies can retain these memories for days after training, and aversive memories last longer than appetitive memories. Our results contrast with literature stating that innate preferences cannot be extinguished in E. tenax. This could be because our study uses multimodal objects instead of the unimodal stimuli used in previous work. Ultimately, these findings improve our understanding of how animals navigate the uncertainties of dynamic objects in the natural world.

animal behavior and cognition↗

Conserved SQ and QS motifs in bacterial effectors suggest pathogen interplay with the ATM kinase family during infection

Understanding how bacteria hijack eukaryotic cells during infection is vital to develop better strategies to counter the pathologies that they cause. ATM kinase family members phosphorylate eukaryotic protein substrates on Ser or Thr residues followed by Gln. The kinases are active under oxidative stress conditions and/or the presence of ds-DNA breaks. While examining the protein sequences of well-known bacterial effector proteins such as CagA and Tir, we noticed that they often show conserved (S/TQ) motifs, even though the evidence for effector phosphorylation by ATM has not been reported. We undertook a bioinformatics analysis to examine effectors for their potential to mimic the eukaryotic substrates of the ATM kinase. The candidates we found could interfere with the hosts intracellular signaling network upon interaction, which might give an advantage to the pathogen inside the host. Further, the putative phosphorylation sites should be accessible, conserved across species and, in the vicinity to the phosphorylation sites, positively charged residues should be depleted. We also noticed that the reverse motif (QT/S) is often also conserved and located close to (S/TQ) sites, indicating its potential biological role in ATM kinase function. Our findings could suggest a mechanism of infection whereby many pathogens inactivate/modulate the host ATM signaling pathway.

bioinformatics↗