182 research outputs found

    Quiescent X-ray variability in the neutron star Be/X-ray transient GRO J1750-27

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    The Be/X-ray transient GRO J1750-27 exhibited a type-II (giant) outburst in 2015. After the source transited to quiescence, we triggered our multi-year Chandra monitoring programme to study its quiescent behaviour. The programme was designed to follow the cooling of a potentially heated neutron-star crust due to accretion of matter during the preceding outburst, similar to what we potentially have observed before in two other Be/X-ray transients, namely 4U 0115+63 and V 0332+53. However, unlike for these other two systems, we do not find any strong evidence that the neutron-star crust in GRO J1750-27 was indeed heated during the accretion phase. We detected the source at a rather low X-ray luminosity (~10^33 erg/s) during only three of our five observations. When the source was not detected it had very low-luminosity upper limits (<10^32 erg/s; depending on assumed spectral model). We interpret these detections and the variability observed as emission likely due to very low-level accretion onto the neutron star. We also discuss why the neutron-star crust in GRO J1750-27 might not have been heated while the ones in 4U 0115+63 and V 0332+53 possibly were.Comment: 13 pages, 6 figures, 5 tables. Accepted for A&

    Bilateral vestibulopathy and age:experimental considerations for testing dynamic visual acuity on a treadmill

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    Introduction: Bilateral vestibulopathy (BVP) can affect visual acuity in dynamic conditions, like walking. This can be assessed by testing Dynamic Visual Acuity (DVA) on a treadmill at different walking speeds. Apart from BVP, age itself might influence DVA and the ability to complete the test. The objective of this study was to investigate whether DVA tested while walking, and the drop-out rate (the inability to complete all walking speeds of the test) are significantly influenced by age in BVP-patients and healthy subjects. Methods: Forty-four BVP-patients (20 male, mean age 59 years) and 63 healthy subjects (27 male, mean age 46 years) performed the DVA test on a treadmill at 0 (static condition), 2, 4 and 6 km/h (dynamic conditions). The dynamic visual acuity loss was calculated as the difference between visual acuity in the static condition and visual acuity in each walking condition. The dependency of the drop-out rate and dynamic visual acuity loss on BVP and age was investigated at all walking speeds, as well as the dependency of dynamic visual acuity loss on speed. Results: Age and BVP significantly increased the drop-out rate (p ≤ 0.038). A significantly higher dynamic visual acuity loss was found at all speeds in BVP-patients compared to healthy subjects (p < 0.001). Age showed no effect on dynamic visual acuity loss in both groups. In BVP-patients, increasing walking speeds resulted in higher dynamic visual acuity loss (p ≤ 0.036). Conclusion DVA tested while walking on a treadmill, is one of the few “close to reality” functional outcome measures of vestibular function in the vertical plane. It is able to demonstrate significant loss of DVA in bilateral vestibulopathy patients. However, since bilateral vestibulopathy and age significantly increase the drop-out rate at faster walking speeds, it is recommended to use age-matched controls. Furthermore, it could be considered to use an individual “preferred” walking speed and to limit maximum walking speed in older subjects when testing DVA on a treadmill

    A highly polymorphic effector protein promotes fungal virulence through suppression of plant-associated Actinobacteria

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    Plant pathogens secrete effector proteins to support host colonization through a wide range of molecular mechanisms, while plant immune systems evolved receptors to recognize effectors or their activities to mount immune responses to halt pathogens. Importantly, plants do not act as single organisms, but rather as holobionts that actively shape their microbiota as a determinant of health. The soil-borne fungal pathogen Verticillium dahliae was recently demonstrated to exploit the VdAve1 effector to manipulate the host microbiota to promote vascular wilt disease in the absence of the corresponding immune receptor Ve1. We identify a multiallelic V. dahliae gene displaying c. 65% sequence similarity to VdAve1, named VdAve1-like (VdAve1L), which shows extreme sequence variation, including alleles that encode dysfunctional proteins, indicative of selection pressure to overcome host recognition. We show that the orphan cell surface receptor Ve2, encoded at the Ve locus, does not recognize VdAve1L. Additionally, we demonstrate that the full-length variant VdAve1L2 possesses antimicrobial activity, like VdAve1, yet with a divergent activity spectrum, that is exploited by V. dahliae to mediate tomato colonization through the direct suppression of antagonistic Actinobacteria in the host microbiota. Our findings open up strategies for more targeted biocontrol against microbial plant pathogens
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