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      Phylogenetic inference of pneumococcal transmission from cross-sectional data, a pilot study

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          Abstract

          Background: Inference on pneumococcal transmission has mostly relied on longitudinal studies which are costly and resource intensive. Therefore, we conducted a pilot study to test the ability to infer who infected whom from cross-sectional pneumococcal sequences using phylogenetic inference.

          Methods: Five suspected transmission pairs, for which there was epidemiological evidence of who infected whom, were selected from a household study. For each pair, Streptococcus pneumoniae full genomes were sequenced from nasopharyngeal swabs collected on the same day. The within-host genetic diversity of the pneumococcal population was used to infer the transmission direction and then cross-validated with the direction suggested by the epidemiological records.

          Results: The pneumococcal genomes clustered into the five households from which the samples were taken. The proportion of concordantly inferred transmission direction generally increased with increasing minimum genome fragment size and single nucleotide polymorphisms. We observed a larger proportion of unique polymorphic sites in the source bacterial population compared to that of the recipient in four of the five pairs, as expected in the case of a transmission bottleneck. The only pair that did not exhibit this effect was also the pair that had consistent discordant transmission direction compared to the epidemiological records suggesting potential misdirection as a result of false-negative sampling.

          Conclusions: This pilot provided support for further studies to test if the direction of pneumococcal transmission can be reliably inferred from cross-sectional samples if sequenced with sufficient depth and fragment length.

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          Most cited references47

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          Trimmomatic: a flexible trimmer for Illumina sequence data

          Motivation: Although many next-generation sequencing (NGS) read preprocessing tools already existed, we could not find any tool or combination of tools that met our requirements in terms of flexibility, correct handling of paired-end data and high performance. We have developed Trimmomatic as a more flexible and efficient preprocessing tool, which could correctly handle paired-end data. Results: The value of NGS read preprocessing is demonstrated for both reference-based and reference-free tasks. Trimmomatic is shown to produce output that is at least competitive with, and in many cases superior to, that produced by other tools, in all scenarios tested. Availability and implementation: Trimmomatic is licensed under GPL V3. It is cross-platform (Java 1.5+ required) and available at http://www.usadellab.org/cms/index.php?page=trimmomatic Contact: usadel@bio1.rwth-aachen.de Supplementary information: Supplementary data are available at Bioinformatics online.
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            The Sequence Alignment/Map format and SAMtools

            Summary: The Sequence Alignment/Map (SAM) format is a generic alignment format for storing read alignments against reference sequences, supporting short and long reads (up to 128 Mbp) produced by different sequencing platforms. It is flexible in style, compact in size, efficient in random access and is the format in which alignments from the 1000 Genomes Project are released. SAMtools implements various utilities for post-processing alignments in the SAM format, such as indexing, variant caller and alignment viewer, and thus provides universal tools for processing read alignments. Availability: http://samtools.sourceforge.net Contact: rd@sanger.ac.uk
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              RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies

              Motivation: Phylogenies are increasingly used in all fields of medical and biological research. Moreover, because of the next-generation sequencing revolution, datasets used for conducting phylogenetic analyses grow at an unprecedented pace. RAxML (Randomized Axelerated Maximum Likelihood) is a popular program for phylogenetic analyses of large datasets under maximum likelihood. Since the last RAxML paper in 2006, it has been continuously maintained and extended to accommodate the increasingly growing input datasets and to serve the needs of the user community. Results: I present some of the most notable new features and extensions of RAxML, such as a substantial extension of substitution models and supported data types, the introduction of SSE3, AVX and AVX2 vector intrinsics, techniques for reducing the memory requirements of the code and a plethora of operations for conducting post-analyses on sets of trees. In addition, an up-to-date 50-page user manual covering all new RAxML options is available. Availability and implementation: The code is available under GNU GPL at https://github.com/stamatak/standard-RAxML. Contact: alexandros.stamatakis@h-its.org Supplementary information: Supplementary data are available at Bioinformatics online.
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                Author and article information

                Contributors
                Role: Formal AnalysisRole: InvestigationRole: MethodologyRole: SoftwareRole: ValidationRole: VisualizationRole: Writing – Original Draft PreparationRole: Writing – Review & Editing
                Role: Data CurationRole: Writing – Review & Editing
                Role: ResourcesRole: SoftwareRole: Writing – Review & Editing
                Role: Data CurationRole: Writing – Review & Editing
                Role: ResourcesRole: SoftwareRole: Writing – Review & Editing
                Role: Data CurationRole: Writing – Review & Editing
                Role: ConceptualizationRole: Writing – Review & Editing
                Role: ConceptualizationRole: Writing – Review & Editing
                Role: SupervisionRole: Writing – Review & Editing
                Role: SupervisionRole: Writing – Review & Editing
                Role: ConceptualizationRole: Writing – Review & Editing
                Role: ConceptualizationRole: Funding AcquisitionRole: Project AdministrationRole: Writing – Review & Editing
                Role: ConceptualizationRole: Funding AcquisitionRole: MethodologyRole: SupervisionRole: Writing – Original Draft PreparationRole: Writing – Review & Editing
                Role: ConceptualizationRole: Funding AcquisitionRole: MethodologyRole: SupervisionRole: Writing – Original Draft PreparationRole: Writing – Review & Editing
                Journal
                Wellcome Open Res
                Wellcome Open Res
                Wellcome Open Research
                F1000 Research Limited (London, UK )
                2398-502X
                6 October 2023
                2023
                : 8
                : 427
                Affiliations
                [1 ]Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK
                [2 ]School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan
                [3 ]Vaccine Preventable Bacteria Section, UK Health Security Agency, London, UK
                [4 ]Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK
                [5 ]Immunisation & Countermeasures Division, UK Health Security Agency, London, UK
                [6 ]Department of Paediatric Infectious Diseases, Nagasaki University, Nagasaki, Japan
                [1 ]University of Calgary, Calgary, Canada
                [1 ]University of Alberta, Edmonton, Alberta, Canada
                [1 ]Burnett School of Biomedical Sciences, University of Central Florida, Orlando, Florida, USA
                Author notes

                *Contributed equally

                Competing interests: C.L.S, D.L, and N.K.F received grant funding from Pfizer and GSK for investigator-led research projects into carriage and disease caused by S. pneumoniae in England.

                Competing interests: No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Author information
                https://orcid.org/0000-0001-8412-8674
                https://orcid.org/0000-0002-2699-9057
                https://orcid.org/0000-0002-1382-1137
                https://orcid.org/0000-0002-5808-2606
                Article
                10.12688/wellcomeopenres.19219.1
                11024593
                38638914
                8795f46a-0f7d-405f-8781-3c5ce7d9016e
                Copyright: © 2023 Hackman J et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 3 August 2023
                Funding
                Funded by: Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT)
                Funded by: Wellcome Trust
                Award ID: 208812
                Funded by: WISE scheme
                Funded by: EU grant
                Award ID: QLG4-CT-2000-00640
                Funded by: National Institute for Health Research Health Protection Research Unit
                Award ID: NIHR200929
                This study was supported by the Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT) and the WISE scheme and EU grant QLG4-CT-2000-00640. SF is funded by a Sir Henry Dale Fellowship through the Wellcome Trust and the Royal Society (208812/Z/17/Z). EM receives support from the National Institute for Health Research (NIHR) Health Protection Research Unit in Immunisation at the London School of Hygiene and Tropical Medicine in partnership with the UKHSA (Grant Reference NIHR200929). The funders had no input in the study design, data analysis, or manuscript draft.
                The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Articles

                within-host diversity,phylogenetic,transmission direction,streptococcus pneumoniae,pneumococcus

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