Kortyna, M. L. | bioRxiv Science

bioRxiv2026

The Tangled History and Taxonomy of an Iconic Chorus Frog Complex Clarified using Genomic Analyses

Species represent a fundamental unit of biodiversity in evolutionary biology, but the nature of the speciation continuum and inadequate sampling of organisms with broad distributions provide substantial challenges to species delimitation. The Pacific Treefrog complex (Pseudacris regilla sensu lato) is an iconic but systematically poorly understood group of chorus frogs inhabiting a vast portion of western North America. Current studies tentatively recognize three species in this complex (P. hypochondriaca, P. regilla, P. sierra), but disagreement remains among morphological, mitochondrial, and nuclear genetic data. In this study, we used thorough geographic sampling and thousands of nuclear loci, along with an integrative, multi-method approach to clarify the phylogenetic relationships and divergence history of P. regilla s.l. lineages and recommend a new taxonomic arrangement for the group. Pseudacris regilla and P. sierra fall firmly within the "gray zone" of speciation, composing a combined "north" lineage. Based on the degree of congruence in inferences from our analyses and evidence for isolating mechanisms, we propose a two species taxonomy for this complex, recognizing the "north" lineage as P. regilla and retaining P. hypochondriaca as a species. Our study shows how extensive geographic sampling, high-throughput sequencing, and multiple analytical approaches can resolve systematic uncertainties in challenging species complexes.

evolutionary biology↗

bioRxiv2025

The host protein cyclophilin A inhibits HIV-1 nuclear entry by decreasing capsid elasticity

Binding of the host protein cyclophilin A (CypA) to the HIV-1 capsid exerts a variety of effects on infection, including enhancement of reverse transcription, stabilization of the capsid, and promotion of nuclear entry. For several HIV-1 mutants, CypA binding inhibits nuclear entry by an unknown mechanism. We recently demonstrated that HIV-1 cores are elastic and that HIV-1 mutants with inelastic capsids are impaired for nuclear entry and infection of nondividing cells. Here we show that CypA prevents infection of nondividing cells by such mutants and inhibits their entry into the nucleus. CypA binding to mutant cores further reduced their elasticity in vitro, and this effect was reversed by suppressor mutations that restored nuclear entry. We suggest that HIV-1 nuclear entry involves temporal modulation of capsid elasticity by host proteins prior to and during traversal of the nuclear pore.

microbiology↗