<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(11)</volume><submitter>Queiroz-Ferreira MS</submitter><pubmed_abstract>Sida mottle virus (SiMoV) and Sida micrantha mosaic virus (SiMMV) are major Brazilian begomoviruses (&lt;i>Geminiviridae&lt;/i>). However, the range of DNA-A identity of isolates of these viruses (81-100%) is not in agreement with the current criteria for &lt;i>Begomovirus&lt;/i> species demarcation (&lt;91%). To clarify this putative classification problem, we performed a comprehensive set of molecular analyses with all 53 publicly available isolates (with complete DNA-A genomes) designated as either SiMoV or SiMMV (including novel isolates obtained herein from nationwide metagenomics-based studies). Two well-defined phylogenetic clusters were identified. The SiMMV complex (&lt;i>n&lt;/i> = 47) comprises a wide range of strains (with a continuum variation of 88.8-100% identity) infecting members of five botanical families (Malvaceae, Solanaceae, Fabaceae, Oxalidaceae, and Passifloraceae). The SiMoV group now comprises eight isolates (90-100% identity) restricted to Malvaceae hosts, including one former reference SiMMV isolate (gb|NC_077711) and SP77 (gb|FN557522; erroneously named as "true SiMMV"). Iteron analyses of metagenomics-derived information allowed for the discovery of the missing DNA-B cognate of SiMoV (93.5% intergenic region identity), confirming its bipartite nature. Henceforth, the correct identification of SiMoV and SiMMV isolates will be a crucial element for effective classical and biotech resistance breeding of the viral host species.</pubmed_abstract><journal>Viruses</journal><pagination>1796</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11599112</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Reexamination of the Sida Micrantha Mosaic Virus and Sida Mottle Virus Complexes: Classification Status, Diversity, Cognate DNA-B Components, and Host Spectrum.</pubmed_title><pmcid>PMC11599112</pmcid><pubmed_authors>Reis A</pubmed_authors><pubmed_authors>Queiroz-Ferreira MS</pubmed_authors><pubmed_authors>de Noronha Fonseca ME</pubmed_authors><pubmed_authors>Pereira-Carvalho RC</pubmed_authors><pubmed_authors>Melo FFS</pubmed_authors><pubmed_authors>Boiteux LS</pubmed_authors><pubmed_authors>Dos Reis LNA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reexamination of the Sida Micrantha Mosaic Virus and Sida Mottle Virus Complexes: Classification Status, Diversity, Cognate DNA-B Components, and Host Spectrum.</name><description>Sida mottle virus (SiMoV) and Sida micrantha mosaic virus (SiMMV) are major Brazilian begomoviruses (&lt;i>Geminiviridae&lt;/i>). However, the range of DNA-A identity of isolates of these viruses (81-100%) is not in agreement with the current criteria for &lt;i>Begomovirus&lt;/i> species demarcation (&lt;91%). To clarify this putative classification problem, we performed a comprehensive set of molecular analyses with all 53 publicly available isolates (with complete DNA-A genomes) designated as either SiMoV or SiMMV (including novel isolates obtained herein from nationwide metagenomics-based studies). Two well-defined phylogenetic clusters were identified. The SiMMV complex (&lt;i>n&lt;/i> = 47) comprises a wide range of strains (with a continuum variation of 88.8-100% identity) infecting members of five botanical families (Malvaceae, Solanaceae, Fabaceae, Oxalidaceae, and Passifloraceae). The SiMoV group now comprises eight isolates (90-100% identity) restricted to Malvaceae hosts, including one former reference SiMMV isolate (gb|NC_077711) and SP77 (gb|FN557522; erroneously named as "true SiMMV"). Iteron analyses of metagenomics-derived information allowed for the discovery of the missing DNA-B cognate of SiMoV (93.5% intergenic region identity), confirming its bipartite nature. Henceforth, the correct identification of SiMoV and SiMMV isolates will be a crucial element for effective classical and biotech resistance breeding of the viral host species.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-06-29T08:16:04.371Z</modification><creation>2025-04-04T00:46:33.227Z</creation></dates><accession>S-EPMC11599112</accession><cross_references><pubmed>39599910</pubmed><doi>10.3390/v16111796</doi></cross_references></HashMap>