Fifteen bifidobacterial strains were obtained from faeces of Rousettus aegyptiacus; after grouping them by RAPD PCR only eight were selected and characterized. Analysis of 16S rRNA and of five housekeeping (hsp60, rpoB, clpC, dnaJ, dna G) genes revealed that these eight strains were classified into five clusters: Cluster I (RST 8 and RST 16T), Cluster II (RST 9T and RST 27), Cluster III (RST 7 and RST 11), Cluster IV (RST 19), Cluster V (RST 17) were closest to Bifidobacterium avesanii DSM 100685T (96.3%), Bifidobacterium callitrichos DSM 23973T (99.2% and 99.7%), Bifidobacterium tissieri DSM 100201T (99.7 and 99.2%), Bifidobacterium reuteri DSM 23975 T (98.9%) and Bifidobacterium myosotis DSM 100196T (99.3%), respectively. Strains in Cluster I and strain RST 9 in Cluster II could not be placed within any recognized species while the other ones were identified as known species. The average nucleotide identity values between two novel strains, RST 16T and RST 9T and their closest relatives were lower than 79% and 89%, respectively. In silico DNA–DNA hybridization values for those closest relatives were 32.5 and 42.1%, respectively. Phenotypic and genotypic tests demonstrated that strains in Cluster I and RST 9T in Cluster II represent two novel species for which the names Bifidobacterium vespertilionis sp. nov. (RST 16T = BCRC 81138T = NBRC 113380T = DSM 106025T ; RST 8 = BCRC 81135 = NBRC 113377) and Bifidobacterium rousetti sp. nov. (RST 9T = BCRC 81136T = NBRC 113378T = DSM 106027T) are proposed.

Characterization of Bifidobacterium species in feaces of the Egyptian fruit bat: Description of B. vespertilionis sp. nov. and B. rousetti sp. nov / Modesto M.; Satti M.; Watanabe K.; Puglisi E.; Morelli L.; Huang C.-H.; Liou J.-S.; Miyashita M.; Tamura T.; Saito S.; Mori K.; Huang L.; Sciavilla P.; Sandri C.; Spiezio C.; Vitali F.; Cavalieri D.; Perpetuini G.; Tofalo R.; Bonetti A.; Arita M.; Mattarelli P.. - In: SYSTEMATIC AND APPLIED MICROBIOLOGY. - ISSN 0723-2020. - ELETTRONICO. - 42:6(2019), pp. 126017.126017-126017.126026. [10.1016/j.syapm.2019.126017]

Characterization of Bifidobacterium species in feaces of the Egyptian fruit bat: Description of B. vespertilionis sp. nov. and B. rousetti sp. nov

Modesto M.;Sandri C.;Bonetti A.;Mattarelli P.
2019

Abstract

Fifteen bifidobacterial strains were obtained from faeces of Rousettus aegyptiacus; after grouping them by RAPD PCR only eight were selected and characterized. Analysis of 16S rRNA and of five housekeeping (hsp60, rpoB, clpC, dnaJ, dna G) genes revealed that these eight strains were classified into five clusters: Cluster I (RST 8 and RST 16T), Cluster II (RST 9T and RST 27), Cluster III (RST 7 and RST 11), Cluster IV (RST 19), Cluster V (RST 17) were closest to Bifidobacterium avesanii DSM 100685T (96.3%), Bifidobacterium callitrichos DSM 23973T (99.2% and 99.7%), Bifidobacterium tissieri DSM 100201T (99.7 and 99.2%), Bifidobacterium reuteri DSM 23975 T (98.9%) and Bifidobacterium myosotis DSM 100196T (99.3%), respectively. Strains in Cluster I and strain RST 9 in Cluster II could not be placed within any recognized species while the other ones were identified as known species. The average nucleotide identity values between two novel strains, RST 16T and RST 9T and their closest relatives were lower than 79% and 89%, respectively. In silico DNA–DNA hybridization values for those closest relatives were 32.5 and 42.1%, respectively. Phenotypic and genotypic tests demonstrated that strains in Cluster I and RST 9T in Cluster II represent two novel species for which the names Bifidobacterium vespertilionis sp. nov. (RST 16T = BCRC 81138T = NBRC 113380T = DSM 106025T ; RST 8 = BCRC 81135 = NBRC 113377) and Bifidobacterium rousetti sp. nov. (RST 9T = BCRC 81136T = NBRC 113378T = DSM 106027T) are proposed.
2019
Characterization of Bifidobacterium species in feaces of the Egyptian fruit bat: Description of B. vespertilionis sp. nov. and B. rousetti sp. nov / Modesto M.; Satti M.; Watanabe K.; Puglisi E.; Morelli L.; Huang C.-H.; Liou J.-S.; Miyashita M.; Tamura T.; Saito S.; Mori K.; Huang L.; Sciavilla P.; Sandri C.; Spiezio C.; Vitali F.; Cavalieri D.; Perpetuini G.; Tofalo R.; Bonetti A.; Arita M.; Mattarelli P.. - In: SYSTEMATIC AND APPLIED MICROBIOLOGY. - ISSN 0723-2020. - ELETTRONICO. - 42:6(2019), pp. 126017.126017-126017.126026. [10.1016/j.syapm.2019.126017]
Modesto M.; Satti M.; Watanabe K.; Puglisi E.; Morelli L.; Huang C.-H.; Liou J.-S.; Miyashita M.; Tamura T.; Saito S.; Mori K.; Huang L.; Sciavilla P.; Sandri C.; Spiezio C.; Vitali F.; Cavalieri D.; Perpetuini G.; Tofalo R.; Bonetti A.; Arita M.; Mattarelli P.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/722929
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