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Robison, A.

Publications and source records attributed to Robison, A..

3 recordsLinked to original sources

Small- and large-scale patches shape benthic microbial community structure and function in streams at the subcontinental scale

Streams and rivers process dissolved and particulate matter as water moves along the land-to-ocean continuum, making important contributions to global biogeochemical cycles. Yet, predicting stream and river microbial metabolism associated with biogeochemical transformations at broad spatial scales remains challenging. Here, we used data from the National Ecological Observatory Network program to investigate whether ecological relationships among microbial community structure and function and environmental conditions observed at small scales hold at the subcontinental scale. We found that microbial communities were best explained by site-specific conditions. However, when field replicates were averaged, stream physico-chemical characteristics such as pH and temperature emerged as driving factors. This indicates that water quality acted as an environmental filter on microbial communities at the subcontinental scale, but was masked by small-scale patches that created high spatial heterogeneity. Our findings underscore the importance of considering multiple spatial scales to fully understand benthic microbial communities role in stream biogeochemistry. SCIENTIFIC SIGNIFICANCE STATEMENTMicrobial communities in streams process materials as water flows toward the ocean. As microbial communities are influenced by environmental conditions, it remains challenging to predict stream microbial metabolism at large spatial scales. In this study, we used the National Ecological Observatory Network (NEON) public database to investigate the drivers of microbial community structure and functions in stream sediments across the USA. This unique dataset revealed high variability in microbial communities among streams that were best explained by local conditions, then by water quality and streambed habitat type. However, stream physico-chemical characteristics emerged as strong predictors of microbial communities when field replicates were averaged and considered as single, large microbial communities. These findings indicate multiple spatial scales must be considered to fully understand benthic microbial communities.

ecology↗

Select autosomal dominant DFNA11 deafness mutations activate Myo7A in epithelial cells

Myosin-7A (Myo7A) is a motor protein crucial for the organization and function of stereocilia, specialized actin-rich protrusions on the surface of inner ear hair cells that mediate hearing. Mutations in Myo7A cause several forms of genetic hearing loss, including autosomal dominant DFNA11 deafness. Despite its importance, the structural elements of Myo7A that control its motor activity within cells are not well understood. In this study, we used cultured kidney epithelial cells to screen for mutations that activate the motor-dependent targeting of Myo7A to the tips of apical microvilli on these cells. Our findings reveal that Myo7A is regulated by specific IQ motifs within its lever arm, and that this regulation can function at least partially independent of its tail sequence. Importantly, we demonstrate that many of the DFNA11 deafness mutations reported in patients activate Myo7A targeting, providing a potential explanation for the autosomal dominant genetics of this form of deafness.

cell biology↗

Effects of inactivation method on SARS-CoV-2 virion proteins and structure

The risk posed by Severe Acute Respiratory Syndrome Coronavirus -2 (SARS-CoV-2) dictates that live-virus research is conducted in a biosafety level 3 (BSL3) facility. Working with SARS-CoV-2 at lower biosafety levels can expedite research yet requires the virus to be fully inactivated. In this study, we validated and compared two protocols for inactivating SARS-CoV-2: heat treatment and ultraviolet irradiation. The two methods were optimized to render the virus completely incapable of infection while limiting destructive effects of inactivation. We observed that 15 minutes of incubation at 65{degrees}C completely inactivates high titer viral stocks. Complete inactivation was also achieved with minimal amounts of UV power (70,000 J/cm2), which is 100-fold less power than comparable studies. Once validated, the two methods were then compared for viral RNA quantification, virion purification, and antibody recognition. We observed that UV irradiation resulted in a 2-log reduction of detectable genomes compared to heat inactivation. Protein yield following virion enrichment was equivalent for all inactivation conditions, but the resulting viral proteins and virions were negatively impacted by inactivation method and time. We outline the strengths and weaknesses of each method so that investigators might choose the one which best meets their research goals.

microbiology↗