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      Streptococcus canis sequence type 43 may be associated with treatment failure in dogs with corneal ulceration

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          Abstract

          OBJECTIVE

          To profile Streptococcus canis isolates obtained from corneal ulcers in dogs.

          ANIMALS

          10 dogs.

          PROCEDURES

          Medical records were searched to identify dogs diagnosed with ulcerative keratitis by a veterinary ophthalmologist and having a positive corneal culture for S canis during the year 2020. For each case, clinical findings and outcome were determined, antimicrobial resistance and sensitivity panels were summarized, whole genome sequencing was performed, and isolates were typed using multi-locus sequence typing and genome-based proteome phylogenetic analysis.

          RESULTS

          10 S canis isolates were included from dogs diagnosed with ulcerative keratitis. Dogs were either treated surgically via keratectomy and conjunctival grafting (n = 6) or treated medically (4). Three of 10 corneas failed to heal and required enucleation (2/6 conjunctival grafts and 1/4 medically managed corneal ulcers). All three corneal ulcers that failed to heal were associated with S canis sequence type (ST) 43. Sequence types identified from successfully treated cases included ST8 (n = 1), ST50 (1), ST2 (2), ST27 (1), and ST15 (1). One ST43 isolate was obtained from a dog that healed following a conjunctival graft, however this was the only dog that received an oral antibiotic in addition to topical antibiotics.

          CLINICAL RELEVANCE

          Based on this small dataset, S canis ST43 may be associated with increased virulence and contribute to conjunctival graft failure and progressive corneal collagenolysis. The postoperative administration of an oral antimicrobial may protect against conjunctival graft rejection in dogs specifically due to S canis ST43.

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          Most cited references45

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          SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing.

          The lion's share of bacteria in various environments cannot be cloned in the laboratory and thus cannot be sequenced using existing technologies. A major goal of single-cell genomics is to complement gene-centric metagenomic data with whole-genome assemblies of uncultivated organisms. Assembly of single-cell data is challenging because of highly non-uniform read coverage as well as elevated levels of sequencing errors and chimeric reads. We describe SPAdes, a new assembler for both single-cell and standard (multicell) assembly, and demonstrate that it improves on the recently released E+V-SC assembler (specialized for single-cell data) and on popular assemblers Velvet and SoapDeNovo (for multicell data). SPAdes generates single-cell assemblies, providing information about genomes of uncultivatable bacteria that vastly exceeds what may be obtained via traditional metagenomics studies. SPAdes is available online ( http://bioinf.spbau.ru/spades ). It is distributed as open source software.
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            Prokka: rapid prokaryotic genome annotation.

            T Seemann (2014)
            The multiplex capability and high yield of current day DNA-sequencing instruments has made bacterial whole genome sequencing a routine affair. The subsequent de novo assembly of reads into contigs has been well addressed. The final step of annotating all relevant genomic features on those contigs can be achieved slowly using existing web- and email-based systems, but these are not applicable for sensitive data or integrating into computational pipelines. Here we introduce Prokka, a command line software tool to fully annotate a draft bacterial genome in about 10 min on a typical desktop computer. It produces standards-compliant output files for further analysis or viewing in genome browsers. Prokka is implemented in Perl and is freely available under an open source GPLv2 license from http://vicbioinformatics.com/. © The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
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              CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

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                Author and article information

                Journal
                Journal of the American Veterinary Medical Association
                javma
                American Veterinary Medical Association (AVMA)
                0003-1488
                July 15 2022
                July 15 2022
                : 1-7
                Affiliations
                [1 ]Small Animal Clinical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Canada
                [2 ]Large Animal Clinical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Canada
                [3 ]Population Health Sciences, Faculty of Veterinary Medicine, Utrecht University, Netherlands
                Article
                10.2460/javma.22.03.0153
                35943931
                41241fac-0982-4fe7-bf2b-c52f1a0ae0ab
                © 2022
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