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One of the earliest studies publishing sequencing data (Illumina) from two SARS-Cov2 patients in Wuhan failed to identify potentially pathogenic bacteria using the program Metaphlan2, when they clearly exist.

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  • One of the earliest studies publishing sequencing data (Illumina) from two SARS-Cov2 patients in Wuhan failed to identify potentially pathogenic bacteria using the program Metaphlan2, when they clearly exist.


    Chakraborty, S. (2020, March 30). One of the earliest studies publishing sequencing data (Illumina) from two SARS-Cov2 patients in Wuhan failed to identify potentially pathogenic bacteria using the program Metaphlan2, when they clearly exist. https://doi.org/10.31219/osf.io/wcg4k

    Abstract

    It is increasingly being evident that bacterial coinfection is playing an important role in SARS-Cov2 [1–4], explaining hydroxychloroquine and azithromycin working in clinical trials [5]. Previously, I have analyzed the metagenomes in patients from China [6,7], San Diego [8] and Brazil [9] - showing many bacterial species (sometimes many unknowns), and Prevotella immune-suppression genes taking over [6]. Failure to identify pathogenic bacteria using Metaphlan2 One of the earliest studies publishing sequencing data (Illumina) from two SARS-Cov patients in Wuhan [10] wrote ‘bacterial pathogen identification was carried out by using the Metaphlan2 program, which revealed Capnocytophaga sp and Veillonella sp in sample 2 and none in sample 1, and both bacteria identified were not known for their pathogenicity. Collectively, coronavirus is likely to be the main microbial pathogen’ [10]. This is clearly wrong - Capnocytophaga and Lautropia are there, and also so many other pathogenic species (Table 1). Sequences and full list of bacterial species are in SIstudy3MNGS. And Capnocytophaga, found in the saliva of humans, dogs and cats can be pathogenic [11]. Another observation is that bacteria will high counts are mostly anaerobic.
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