Biology subjects

Lawrence, S.

Publications and source records attributed to Lawrence, S..

3 recordsLinked to original sources

bioRxiv2022

Patterns of secondary invasion in the understory of exotic, invasive timber stands

Current climate and land cover change threaten global mountaintops with increased spread of invasive species. Long-established plantations of exotic and invasive trees on these mountaintops can alter their surroundings, further increasing invader-facilitated or secondary invasion. Identifying the ecological conditions that promote such specific associations can help develop better management interventions. The Western Ghatss Shola Sky Islands (>1400m MSL) host vast stretches of exotic and invasive tree plantations that sustain colonisation of other invasive woody, herbaceous and fern species in their understories. Here we analysed vegetation and landscape variables from 232 systematically-placed plots in randomly selected grids using NMDS and Phi Coefficient approaches, to examine patterns of association (positive interactions) between secondary understory invasive species with specific exotic and invasive overstory species. We also conducted GLMM with zero inflation to determine the influence of environmental variables where such associations occur. We find that secondary invasion of multiple species under the canopy of other exotic invasives is widespread across the Shola Sky Islands. Stands of Eucalyptus host the colonisation of 70% of non-native invasive species surveyed across the Shola Sky Islands. In particular, Lantana camara invasion is strongly associated with Eucalyptus stands. We also found that climatic variables affect the colonisation of understorey woody invasive species, while invasion by exotic herbaceous species is associated with the density of road networks.. Canopy cover impacts all invasives negatively, while incidence of fire was negatively associated with invasion by Lantana spp and the Pteridium spp. While the restoration of natural habitats largely targets the highly invasive Acacia, less invasive Eucalyptus and Pine are often not included. Our study suggests that retaining such exotic species in natural habitats, particularly protected areas, can hinder ongoing restoration efforts by facilitating further invasions by multiple woody and herbaceous species.

ecology↗

bioRxiv2021

A tyrosine-based trafficking signal in the simian immunodeficiency virus envelope cytoplasmic domain is strongly selected for in pathogenic SIV infection

The HIV/SIV envelope glycoprotein (Env) cytoplasmic domain contains a highly conserved Tyr-dependent trafficking signal that mediates both clathrin-dependent endocytosis and polarized sorting of Env. Despite extensive characterization, the role of these functions in viral infection and pathogenesis is unclear. An SIV molecular clone (SIVmac239) in which the Tyr-based signal is inactivated by deletion of Gly-720 and Tyr-721 (SIVmac239{Delta}GY) replicates to high levels acutely in pigtail macaques (PTM) but is rapidly controlled. We previously reported that rhesus macaques and PTM can progress to AIDS following SIVmac239{Delta}GY infection in association with novel amino acid changes in the Env cytoplasmic domain. These included an R722G flanking the {Delta}GY deletion and a nine nucleotide deletion that encodes amino acids 734-736 ({Delta}QTH) and overlaps with the rev and tat open reading frames. We show that molecular clones containing these mutations reconstitute signals for both endocytosis and polarized sorting. In one PTM, a novel genotype was selected, which generated a new signal for polarized sorting but not endocytosis. This mutation by itself was sufficient to maintain high viral loads for several months when introduced into naive PTMs. These findings reveal, for the first time, strong selection pressure for Env endocytosis and, in particular, for polarized sorting during pathogenic SIV infection in vivo.

cell biology↗

bioRxiv2021

Single-molecule super-resolution imaging of T-cell plasma membrane CD4 redistribution upon HIV-1 binding

The first step of cellular entry for the human immunodeficiency virus type-1 (HIV-1) occurs through the binding of its envelope protein (Env) with the plasma membrane receptor CD4 and co-receptor CCR5 or CXCR4 on susceptible cells, primarily CD4+ T cells and macrophages. Although there is considerable knowledge of the molecular interactions between Env and host cell receptors that lead to successful fusion, the precise way in which HIV-1 receptors redistribute to sites of virus binding at the nanoscale remains unknown. Here, we quantitatively examine changes in the nanoscale organisation of CD4 on the surface of CD4+ T cells following HIV-1 binding. Using single-molecule super-resolution imaging, we show that CD4 molecules are distributed mostly as either individual molecules or small clusters of up to 4 molecules. Following virus binding, we observe a local 3-to-10-fold increase in cluster diameter and molecule number for virus-associated CD4 clusters. Moreover, a similar but smaller magnitude reorganisation of CD4 was also observed with recombinant gp120. For the first time, our results quantify the nanoscale CD4 reorganisation triggered by HIV-1 on host cells. Our quantitative approach provides a robust methodology for characterising the nanoscale organisation of plasma membrane receptors in general with the potential to link spatial organisation to function.

biophysics↗