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Biology subjects

Tata, M.

Publications and source records attributed to Tata, M..

2 recordsLinked to original sources

Parkinson Disease vs Aging Features Impairments in Formation and Release of a Power Grip in Real and Pantomimed String-Pulling

Parkinson disease (PD) impairs skilled reaching tasks but less is known about its effects on rhythmic bimanual actions. We used a bimanual hand-over-hand string-pulling task that requires repeated reach, grasp, pull, push and release movements. We predicted that participants with PD would show impairment in making the rotary skilled hand movement of retrieving the string, analogous to impairments observed in single handed target reaching. Nine participants with PD (mean UPDRS-III: 24.6), 16 older adults, and 10 young adults successfully performed a real string-pulling task and then pantomimed the action. Video analyses combined optical-flow estimation of whole-body movement speed, markerless 2D pose estimation of upper-limb kinematics, and expert frame-by-frame scoring of hand and finger shaping. Machine-learning classification then identified the discriminative information carried by these multilevel movement components. Participants with PD showed lower movement speed, a smaller hand workspace, and reduced hand and finger shaping, with older adults showing intermediate values. All participants grasped the real string with a power grip, but participants with PD showed reduced rotary movements of the arm and the wrists and absent of arpeggio-like sequential finger movement during grasp and release. During pantomime, participants with PD moved faster and made larger hand movements, while grasp-related hand opening and finger sequencing was reduced or absent. The findings suggest that PD is expressed across this multicomponent movement manifold, and that the movement organization changes with task demands: real string pulling requires formation and release of a power grip, whereas pantomime does not place demands on grasping ability.

neuroscience↗

PspA-mediated aggregation protects Streptococcus pneumoniae against desiccation on fomites

Streptococcus pneumoniae (Spn) resides in the nasopharynx where it can disseminate to cause disease. One key Spn virulence factor is pneumococcal surface protein A (PspA), which promotes survival by blocking the antimicrobial peptide lactoferricin. PspA has also been shown to mediate attachment to dying epithelial cells in the lower airway due to its binding of cell surface-bound mammalian (m)GAPDH. Importantly, the role of PspA during colonization is not well understood. Wildtype Spn was present in nasal lavage elutes collected from asymptomatically colonized mice at levels [~]10-fold higher that its isogenic PspA-deficient mutant ({Delta}pspA). Wildtype Spn also formed aggregates in mucosal secretions composed of sloughed epithelial cells and hundreds of pneumococci, whereas {Delta}pspA did not. Spn within the center of these aggregates better survived prolonged desiccation on fomites than individual pneumococci and were capable of infecting naive mice, indicating PspA-mediated aggregation conferred a survival/transmission advantage. Incubation of Spn in saline containing mGAPDH also enhanced tolerance to desiccation, but only for wildtype Spn. mGAPDH was sufficient to cause low-level aggregation of wildtype Spn but not {Delta}pspA. In strain WU2, the subdomain of PspA responsible for binding GAPDH (aa230-281) is ensconced within the lactoferrin (LF)-binding domain (aa167-288). We observed that LF inhibited GAPDH-mediated aggregation and desiccation tolerance. Using surface plasmon resonance, we determined that Spn forms multimeric complexes of PspA-GAPDH-LF on its surface and that LF dislodges GAPDH. Our findings have important implications regarding pneumococcal colonization/transmission processes and ongoing PspA-focused immunization efforts for this deadly pathogen. IMPORTANCEStreptococcus pneumoniae (Spn) is a dangerous human pathogen capable of causing pneumonia and invasive disease. The virulence factor pneumococcal surface protein A (PspA) has been studied for nearly four decades with well-established roles in pneumococcal evasion of C-reactive protein and neutralization of lactoferricin. Herein, we show that mammalian (m)GAPDH in mucosal secretions promotes aggregation of pneumococci in a PspA-dependent fashion, whereas lactoferrin counters this effect. PspA-mediated GAPDH-dependent bacterial aggregation protected Spn in nasal lavage elutes and grown in vitro from desiccation on fomites. Furthermore, surviving pneumococci within these aggregates retained their ability to colonize naive hosts after desiccation. We report that Spn binds to and forms protein complexes on its surface composed of PspA, mGAPDH, and lactoferrin. Changes in the levels of these proteins therefore most likely have critical implications on Spn colonization, survival on fomites, and transmission.

microbiology↗