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. 2020 Aug 2;9(8):631. doi: 10.3390/pathogens9080631

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© 2020 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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(a) Nucleotide sequence alignment of the ompB gene of sample B188 against the homologous reference sequence of R. parkeri (KY113111) indicating 100% homology. Reference sequence was obtained based on highest percentage homology that the test sequence has with R. parkeri which was obtained through Nucleotide BLAST tool in the GenBank. The dots represent nucleotide similarity of the query sequence with the reference strain. (b) Amino acid sequence alignment of the ompB gene of sample B188 against the homologous reference sequence of R. parkeri (KY113111) indicating 100% homology. Reference sequence was obtained based on highest percentage homology that the test sequence has with R. parkeri which was obtained through Nucleotide BLAST tool in the GenBank. The dots represent amino acid similarity of the query sequence with the reference strain. (c) The degree of homology between test sequence A188 and Candidatus Rickettsia (EU272186.1) reference strain: Nucleotide sequence alignment of the ompA gene of sample A188 against the homologous reference sequence of Candidatus Rickettsia sp. (EU272186.1) indicating 95% homology. The dots represent nucleotide similarity of the query sequence with the reference strain. (d) Amino acid alignment of the ompA gene of sample A188 against the homologous reference sequence of Candidatus Rickettsia sp. (EU272186.1) indicating 95% homology. The dots represent amino acid similarity of the query sequence with the reference strain.