bioRxiv ScienceSearch

Biology subjects

Shrotri, S.

Publications and source records attributed to Shrotri, S..

3 recordsLinked to original sources

The genome trilogy of Anopheles stephensi, an urban malaria vector, reveals structure of a locus associated with adaptation to environmental heterogeneity

BackgroundAnopheles stephensi is the most menacing malaria vector to watch for in newly urbanizing parts of the world. The fitness is reported to be a direct consequence of the vector adapting to laying eggs in over-head water tanks with street-side water puddles polluted by oil and sewage. Large frequent inversions of malaria vectors are implicated in adaptation. ResultsWe report the assembly of a strain of An. stephensi of the type-form, collected from a construction site from Chennai (IndCh) in 2016. The genome completes the trilogy with respect to a 16 Mbp inversion (2Rb) in An. stephensi associated with adaptation to environmental heterogeneity. Comparative genome analysis revealed breakpoint structure and allowed extraction of 22,650 segregating SNPs for typing this inversion. Using whole genome sequencing of 82 individual mosquitoes, we conclude that one third of both wild and laboratory populations maintain heterozygous genotype of 2Rb. The large number of SNPs are tailored to assign inversion genotype directly from 1740 exonic SNPs 80% of which are expressed in various developmental stages. ConclusionsThe genome trilogy approach accelerates study of fine structure and typing of important inversions in malaria vectors putting the genome resources for the much understudied An. stephensi, on par with the extensively studied malaria vector, Anopheles gambiae. We argue that the IndCh genome is relevant for field translation work compared to those reported earlier by showing that individuals from diverse populations cluster with IndCh pointing to significant commerce between cities, perhaps, allowing for survival of the fittest strain.

genomics

When to be a male? Role of resource-limitation and pollinators in determining gender in an andromonoecious spiderwort.

The evolution and maintenance of sexual systems in plants is often driven by resource allocation and pollinator preferences, and very little is known about their role in determining floral sex expression in plants. In annual, entomophilous plants three major constraints can be identified towards optimal reproduction: 1) nutrient resources available from the environment, 2) nutrient resources allocated towards reproduction, i.e., fruits vs. flowers, and 3) pollinator visitations.Andromonoecy is a sexual system where plants bear both staminate and hermaphrodite flowers on the same inflorescence. The optimal resource allocation hypothesis suggests that under nutrient constraints, plants will produce more male flowers since they are energetically cheaper to produce over the more expensive hermaphrodite flowers. We test this hypothesis in the andromonoecious Murdannia simplex (Commelinaceae) by quantifying male and hermaphrodite flowers in a natural population and contrasting the distribution of the two sexes in plants from two resource conditions (stream population vs. plateau population). We next carried out choice experiments to test pollinator preference towards a specific sex.We found that in M. simplex, production of hermaphrodite flowers is resource-dependent and under resource constraints fewer numbers of flowers were produced and most of them were males. We failed to observe pollinator preference towards either sex but Amegilla spp. and Apis cerana showed higher visitation towards the most abundant sex within a trial, suggesting frequency-dependent visitation. Thus, we conclude that environmentally driven resource constraints play a bigger role in driving floral sex expression in Murdannia over direct pollinator-driven constraints.Competing Interest StatementThe authors have declared no competing interest.View Full Text

ecology

Comprehensive Transcriptomic Analysis of COVID-19 Blood, Lung, and Airway

AbstractSARS-CoV2 is a previously uncharacterized coronavirus and causative agent of the COVID-19 pandemic. The host response to SARS-CoV2 has not yet been fully delineated, hampering a precise approach to therapy. To address this, we carried out a comprehensive analysis of gene expression data from the blood, lung, and airway of COVID-19 patients. Our results indicate that COVID-19 pathogenesis is driven by populations of myeloid-lineage cells with highly inflammatory but distinct transcriptional signatures in each compartment. The relative absence of cytotoxic cells in the lung suggests a model in which delayed clearance of the virus may permit exaggerated myeloid cell activation that contributes to disease pathogenesis by the production of inflammatory mediators. The gene expression profiles also identify potential therapeutic targets that could be modified with available drugs. The data suggest that transcriptomic profiling can provide an understanding of the pathogenesis of COVID-19 in individual patients. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=168 HEIGHT=200 SRC="FIGDIR/small/121889v1_ufig1.gif" ALT="Figure 1"> View larger version (52K): org.highwire.dtl.DTLVardef@7dccedorg.highwire.dtl.DTLVardef@1190e1forg.highwire.dtl.DTLVardef@1ee2e67org.highwire.dtl.DTLVardef@289f72_HPS_FORMAT_FIGEXP M_FIG C_FIG

immunology