Milliron X

Milliron X

Rachel Palinski

19 Sep 2024
Thomas A. Christensen II Rachel Palinski Bob Gentry

Bovine papillomavirus (BPV) is a major cause of reproductive failure in cattle. In bulls, penile papillomas caused by BPV may cause reluctance to breed, and is always a cause to fail an animal on a breeding soundness exam. Historically, it has been thought that BPV was transmitted via direct contact and could be controlled by managing clinically presenting animals in the herd, but more recent evidence suggests alternative modes of transmission. BPV has been found repeatably in clinically healthy animals, and in non-cutaneous secretions including milk, blood, urine and semen. Currently, no commercially available BPV vaccine uses isolated viral particles and naturally occurring virus does not produce cross-protective immunity. In order to develop a proper vaccine for penile papillomas further studies are required to understand the epidemiology of BPV in herds. While vulvar, cutaneous, and mammary papillomas have been genotyped in recent years, this information is not available for penile papillomas. In this study there were 31 submissions, collected from 7 states, NE, KS, NY, TX, AL, MO and SD (14 different cattle operations) Samples were collected between August of 2022 and April 2024. Twenty-two submissions were penile papillomas and with pooling of samples represented over 50 penile papillomas. Samples were metagenomically sequenced at the Kansas State Veterinary Diagnostic Lab, and the genotype of each sample was determined using the phylogenetic analysis. The clade of each sample was determined by aligning consensus sequences of the L1 gene (used for both for phylogeny and as a vaccine target) using MAFFT and a maximum-likelihood phylogeny generated in Mega X. Analysis found that all penile papilloma submissions were composed of BPV type 2, with one sample showing co-infection with BPV type 1. Conversely, cutaneous and teat papillomas had BPV genotypes that were more variable with genotypes of 1,2,7,12,14,29 and 40. These results indicate that BPV type 2 and type 1 provide a unified target for bovine penile papilloma vaccine development.

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05 Mar 2024
Thomas A. Christensen II Steven Stancic Andrea Lu Dana Mitzel William Wilson Rachel Palinski

Viral populations within an infected host are composed of viral particles with a spectrum of genetic mutations rather than a unified genome. This phenomenon is referred to as viral “quasispecies,” and has been useful for the understanding of viral transmission and early detection of new viral variants. Next generation sequencing (NGS) has enabled the study of these quasispecies for many viral species, notably Influenza A and B, Human Immunodeficiency Virus (HIV), Foot and Mouth Disease Virus (FMDV), and Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV2), and established protocols and computer analysis tools have been developed for these species. Some of the most important viruses, such as emerging and exotic disease agents, however, do not have replicatable protocols or software tools capable of producing valid output from their sequence data. Here, we present Yet Another Viral Subspecies Analysis Pipeline (YAVSAP). YAVSAP is a fully automated bioinformatic pipeline built from the ground up to identify and analyze viral quasispecies of any arbitrary virus in human and veterinary samples. YAVSAP provides reference-based genome mapping of both long- and short-read sequencing reads to any reference genome that the user chooses, identifies subconsensus variants and haplotypes, and assesses the phylogenies of all viral sequences found within a sample. YAVSAP is written in Nextflow and conforms to the nf-core initiative’s standards, which allows it to run on low-end computers, high performance computing (HPC) clusters, or anything in between with zero configuration. YAVSAP has been tested on viruses of interest to veterinary medicine and public health, including Japanese Encephalitis Virus (JEV), Influenza D Virus (IDV), Bovine Coronavirus (BCoV), SARS CoV2, and Rift Valley Fever Virus (RVFV), and can correctly identify consensus genomes and quasispecies within samples containing each of these viruses. This tool provides a means for biologists with little bioinformatic experience to analyze deep sequence data while correcting for many of the pitfalls associated with previous and current analysis platforms. YAVSAP is open source software and is publicly available at https://github.com/ksumngs/yavsap.

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27 Apr 2022
Tyler Doerksen Thomas A. Christensen II Andrea Lu Lance Noll Jianfa Bai Jamie Henningson Rachel Palinski

Enteric disease is the predominant cause of morbidity and mortality in young mammals including pigs. Viral species involved in porcine enteric disease complex (PEDC) include rotaviruses, coronaviruses, picornaviruses, astroviruses and pestiviruses among others. The virome of three groups of swine samples submitted to the Kansas State University Veterinary Diagnostic Laboratory for routine testing were assessed, namely, a Rotavirus A positive (RVA) group, a Rotavirus co-infection (RV) group and a Rotavirus Negative (RV Neg) group. All groups were designated by qRT-PCR results testing for Porcine Rotavirus A, B, C and H such that samples positive for RVA only went in the RVA group, samples positive for >1 rotavirus went in the RV group and samples negative for all were grouped in the RVNeg group. All of the animals had clinical enteric disease resulting in scours and swollen joints/lameness, enlarged heart and/or a cough. All samples were metagenomic sequenced and analyzed for viral species composition that identified 14 viral species and eight bacterial viruses/phages. Sapovirus and Escherichia coli phages were found at a high prevalence in RVA and RV samples but were found at low or no prevalence in the RV Neg samples. Picobirnavirus was identified at a high proportion and prevalence in RV Neg and RV samples but at a low prevalence in the RVA group. A sequence analysis of the possible host of Picobirnaviruses revealed fungi as the most likely host. Non-rotaviral diversity was highest in RVA samples followed by RV then RV Neg samples. Various sequences were extracted from the sample reads and a phylogenetic update was provided showing a high prevalence of G9 and P[23] RVA genotypes. These data are important for pathogen surveillance and control measures

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