Biology subjects

Neuhaus, E. B.

Publications and source records attributed to Neuhaus, E. B..

3 recordsLinked to original sources

bioRxiv2026

A chromosome-level genome of the franciscana dolphin, Pontoporia blainvillei

The franciscana dolphin (Pontoporia blainvillei) is a small coastal cetacean endemic to the southwestern Atlantic Ocean and one of the most threatened marine mammals worldwide. It faces severe threats from bycatch, habitat degradation, and pollution. Classified as "Vulnerable" by the IUCN and "Critically Endangered" in Brazil, the species restricted range, strong fidelity to shallow waters, and low reproductive rate increase its extinction risk. Here, we present the first chromosome-level genome assembly for the franciscana dolphin, generated using PacBio HiFi long-read sequencing and Hi-C chromatin conformation capture. The final assembly totaled 3.13 Gb across 22 chromosomes (1500 scaffolds), consistent with the estimated karyotype of 2n = 44, with scaffold N50 of 111.18 Mb, high BUSCO completeness (99.42%), and a consensus quality value of 65.76. This high-quality genomic resource fills an important phylogenetic gap within Cetacea, enabling comparative and conservation studies. It provides an essential foundation for population genomics research to assess genetic diversity, structure, and connectivity, thereby supporting evidence-based conservation strategies for this endangered species.

genomics↗

bioRxiv2019

Mitigating Pandemic Risk with Influenza A Virus Field Surveillance at a Swine-Human Interface

Working overnight at a large swine exhibition, we identified an influenza A virus (IAV) outbreak in swine, nanopore-sequenced 13 IAV genomes from samples collected, and in real-time, determined that these viruses posed a novel risk to humans due to genetic mismatches between the viruses and current pre-pandemic candidate vaccine viruses (CVV). We developed and used a portable IAV sequencing and analysis platform called Mia (Mobile Influenza Analysis) to complete and characterize full-length consensus genomes approximately 18 hours after unpacking the mobile lab. Swine are important animal IAV reservoirs that have given rise to pandemic viruses via zoonotic transmission. Genomic analyses of IAV in swine are critical to understanding pandemic risk of viruses in this reservoir, and characterization of viruses circulating in exhibition swine enables rapid comparison to current seasonal influenza vaccines and CVVs. The Mia system rapidly identified three genetically distinct swine IAV lineages from three subtypes: A(H1N1), A(H3N2) and A(H1N2). Additional analysis of the HA protein sequences of the A(H1N2) viruses identified >30 amino acid differences between the HA1 portion of the hemagglutinin of these viruses and the most closely related pre-2009 CVV. All virus sequences were emailed to colleagues at CDC who initiated development of a synthetically derived CVV designed to provide an optimal antigenic match with the viruses detected in the exhibition. In subsequent months, this virus caused 13 infections in humans, and was the dominant variant virus in the US detected in 2018. Had this virus caused a severe outbreak or pandemic, our proactive surveillance efforts and CVV derivation would have provided an approximate 8 week time advantage for vaccine manufacturing. This is the first report of the use of field-derived nanopore sequencing data to initiate a real-time, actionable public health countermeasure.

microbiology↗

bioRxiv2018

Complete genome direct RNA sequencing of influenza A virus

For the first time, a complete genome of an RNA virus has been sequenced in its original form. Previously, RNA was sequenced by the chemical degradation of radiolabelled RNA, a difficult method that produced only short sequences. Instead, RNA has usually been sequenced indirectly by copying it into cDNA, which is often amplified to dsDNA by PCR and subsequently analyzed using a variety of DNA sequencing methods. We designed an adapter to short highly conserved termini of the influenza virus genome to target the (-) sense RNA into a protein nanopore on the Oxford Nanopore MinION sequencing platform. Utilizing this method and total RNA extracted from the allantoic fluid of infected chicken eggs, we demonstrate successful sequencing of the complete influenza virus genome with 100% nucleotide coverage, 99% consensus identity, and 99% of reads mapped to influenza. By utilizing the same methodology we can redesign the adapter in order to expand the targets to include viral mRNA and (+) sense cRNA, which are essential to the viral life cycle. This has the potential to identify and quantify splice variants and base modifications, which are not practically measurable with current methods.

genomics↗