Accepted for/Published in: JMIR Public Health and Surveillance
Date Submitted: Aug 15, 2020
Date Accepted: Sep 23, 2020
Warning: This is an author submission that is not peer-reviewed or edited. Preprints - unless they show as "accepted" - should not be relied on to guide clinical practice or health-related behavior and should not be reported in news media as established information.
Letter to the Editor: Errors in tracing coronavirus SARS-CoV-2 transmission using a maximum likelihood tree
ABSTRACT
Tracing and quarantining symptomatic and asymptomatic individuals infected by the novel coronavirus SARS-CoV-2 is an important approach in controlling the current epidemic. Tracing the source of an infection can be achieved by conventional interviews, by mobile telephone tracking, or by phylogenetic tracing of the virus genomes itself, as we have proposed (reference 1) In a recent critique (reference 2) (see also our reply in reference 3), Mavian and colleagues have disputed our phylogenetic tracing approach and conclude: “it is not possible with the present data to decide which branching pattern (and, therefore, which phylogeographic reconstruction) most likely represents actual dissemination routes among European countries.” Their underlying reanalysis is however based on a trivial oversight. They analyse genomes collected worldwide in early March 2020 and initially confirm the B-subclade that we had identified, which links a German sequence to an Italian sequence and thence to further Finnish, Mexican, Swiss, and German sequences. However, they then claim “in a new tree inferred just one week later, when more than 135 new full genome sequences were made available on GISAID, the direct link between Germany and Italy […] disappeared due to additional clustering of [five] previously unsampled sequences from Portugal, Brazil, Wales, and [two from] the Netherlands”. Upon request, Dr Mavian provided us with a file of these five new sequences. Comparing these five in our coronavirus sequence alignment table (freely available at www.fluxus-engineering.com), it transpires that these five sequences are identical to each other and to the pre-existing Italian sequence. Mavian and colleagues appear not to have noticed the identity as they fail to mention it, and instead they present a “maximum likelihood” tree which misleadingly shows these five new sequences and the pre-existing Italian sequence to be separated by apparently deep branches, even though all six are identical. Mavian and colleagues appear to have relied on their computer program without investigating their entered sequences. Moreover, Mavian and colleagues have not presented the documented patient travel histories of the five new viral sequences. We present these now, using freely available GISAID information and contemporary reports, and find that the Welshman (references 4, 5), both Dutch (reference 6), and the Brazilian (reference 7) all had visited Italy a few days before falling ill. The Portuguese (reference 8) had visited Spain. Thus, in four of the five new cases, the patient’s travel history to Italy confirms the viral sequence matches to the pre-existing Italian sequence. It is therefore unfounded for Mavian and colleagues to claim that the data cannot reveal branching patterns or likely dissemination routes among European countries.”
Citation
Request queued. Please wait while the file is being generated. It may take some time.
Copyright
© The authors. All rights reserved. This is a privileged document currently under peer-review/community review (or an accepted/rejected manuscript). Authors have provided JMIR Publications with an exclusive license to publish this preprint on it's website for review and ahead-of-print citation purposes only. While the final peer-reviewed paper may be licensed under a cc-by license on publication, at this stage authors and publisher expressively prohibit redistribution of this draft paper other than for review purposes.