The genus Clostridium encompasses phylogenetically diverse, obligately anaerobic, Gram-positive, spore-forming bacteria, yet taxonomic resolution for several members remains limited by the conservatism of the 16S rRNA gene. We reassessed four closely related species pairs: Clostridium baratii and Clostridium nitritogenes; Clostridium thermopalmarium and Clostridium colicanis; Clostridium botulinum and Clostridium combesii; and Clostridium estertheticum subsp. estertheticum and Clostridium estertheticum subsp. laramiense. A polyphasic framework was applied, integrating 16S rRNA and core-genome phylogenies, whole-genome relatedness metrics (digital DNA-DNA hybridization, average nucleotide identity and average amino acid identity), phenotypic characterization and carbohydrate-active enzyme profiling. Concordant genomic and phenotypic evidence supported the synonymization of C. nitritogenes (Prévot 1940) Bernard et al. 2018 with C. baratii (Prévot 1938) Holdeman and Moore 1970, C. colicanis Greetham et al. 2003 with C. thermopalmarium Soh et al. 1991 and C. estertheticum subsp. laramiense (Kalchayanand et al. 1993) Spring et al. 2003 with C. estertheticum subsp. estertheticum (Collins et al. 1993) Spring et al. 2003. By contrast, despite high genomic relatedness, C. botulinum (van Ermengem 1896) Bergey et al. 1923 and C. combesii (Prévot and Laplanche 1947) Bernard et al. 2018 displayed reproducible phenotypic and functional distinctions consistent with subspecies status. We, therefore, propose C. botulinum subsp. combesii comb. nov., alongside C. botulinum subsp. botulinum comb. nov., thereby refining genome-based classification within the genus.
梭状芽孢杆菌属包括系统发育多样化,专门厌氧,革兰氏阳性,孢子形成细菌,但对一些成员的分类分辨率仍然受到16S rRNA基因保守性的限制。我们重新评估了四个密切相关的物种对:巴拉氏梭菌和硝化梭菌;热铝梭状芽胞杆菌和结肠梭状芽胞杆菌;肉毒梭菌和复合梭菌;和酯梭菌亚种。酯酸梭菌和酯酸梭菌亚种。laramiense。采用多相框架,整合16S rRNA和核心基因组系统发育、全基因组亲缘性指标(数字DNA-DNA杂交、平均核苷酸识别和平均氨基酸识别)、表型表征和碳水化合物活性酶谱。一致的基因组和表型证据支持C. nitritogenes (pr vot 1940) Bernard et al. 2018与C. baratii (pr vot 1938) Holdeman and Moore 1970, C. colicanis Greetham等人2003与C. thermopalmarium Soh等人1991和C. estertheticum subsp同属。Spring等人,2003年与C. estertheticum亚种。estertheticum (Collins et al. 1993) Spring et al. 2003。相比之下,尽管具有高度的基因组相关性,C. botulinum (van Ermengem 1896) Bergey et al. 1923和C. combesii (pr vot and Laplanche 1947) Bernard et al. 2018显示出与亚种状态一致的可复制表型和功能差异。因此,我们提出肉毒杆菌亚杆菌。combesii梳子。11月,与肉毒杆菌一起。肉毒梳子。11月,从而完善了属内基于基因组的分类。
{"title":"Genome-based phylogenomic reassessment of <i>Clostridium</i> with proposals for species synonymization and new subspecies.","authors":"Guendouz Dif, Noureddine Bouras, Nadjette Djemouai, Imane Dif, Abdelghani Zitouni","doi":"10.1099/ijsem.0.007048","DOIUrl":"https://doi.org/10.1099/ijsem.0.007048","url":null,"abstract":"<p><p>The genus <i>Clostridium</i> encompasses phylogenetically diverse, obligately anaerobic, Gram-positive, spore-forming bacteria, yet taxonomic resolution for several members remains limited by the conservatism of the 16S rRNA gene. We reassessed four closely related species pairs: <i>Clostridium baratii</i> and <i>Clostridium nitritogenes</i>; <i>Clostridium thermopalmarium</i> and <i>Clostridium colicanis</i>; <i>Clostridium botulinum</i> and <i>Clostridium combesii</i>; and <i>Clostridium estertheticum</i> subsp. <i>estertheticum</i> and <i>Clostridium estertheticum</i> subsp. <i>laramiense</i>. A polyphasic framework was applied, integrating 16S rRNA and core-genome phylogenies, whole-genome relatedness metrics (digital DNA-DNA hybridization, average nucleotide identity and average amino acid identity), phenotypic characterization and carbohydrate-active enzyme profiling. Concordant genomic and phenotypic evidence supported the synonymization of <i>C. nitritogenes</i> (Prévot 1940) Bernard <i>et al</i>. 2018 with <i>C. baratii</i> (Prévot 1938) Holdeman and Moore 1970, <i>C. colicanis</i> Greetham <i>et al</i>. 2003 with <i>C. thermopalmarium</i> Soh <i>et al</i>. 1991 and <i>C. estertheticum</i> subsp. <i>laramiense</i> (Kalchayanand <i>et al</i>. 1993) Spring <i>et al</i>. 2003 with <i>C. estertheticum</i> subsp. <i>estertheticum</i> (Collins <i>et al</i>. 1993) Spring <i>et al</i>. 2003. By contrast, despite high genomic relatedness, <i>C. botulinum</i> (van Ermengem 1896) Bergey <i>et al</i>. 1923 and <i>C. combesii</i> (Prévot and Laplanche 1947) Bernard <i>et al</i>. 2018 displayed reproducible phenotypic and functional distinctions consistent with subspecies status. We, therefore, propose <i>C. botulinum</i> subsp. <i>combesii</i> comb. nov., alongside <i>C. botulinum</i> subsp. <i>botulinum</i> comb. nov., thereby refining genome-based classification within the genus.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146105512","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Anna Muratova, Artur Akhremchuk, Katsiaryna Akhremchuk, Olesya Evdokimova, Darya Guliayeva, Volha Akulava, Vladislav Miamin, Leonid Valentovich
Three strains of Gram-negative, cold-adapted, aerobic bacteria were isolated on the coast of the Alasheyev Bight in the area of the Vecherniy region, the Thala Hills Oasis, Enderby Land, East Antarctica. Strains TMP9T and TMP25 were isolated from temporary meltwater ponds, while strain G.S.17T was obtained from a sample of green snow. Strains TMP9T and TMP25 were motile rods, catalase-negative and oxidase-positive, while G.S.17T was rod-shaped and exhibited motility, but was catalase- and oxidase-positive. TMP9T and TMP25 grew at 4-25 °C, pH 5.5-9.0 and tolerated up to 4.5% NaCl. G.S.17T grew at 4-28 °C, pH 5.0-8.5 and NaCl concentration up to 3.0%. The 16S rRNA gene sequence analysis placed all strains within the genus Pseudomonas: strains TMP9T and TMP25 are closely related to Pseudomonas peli DSM 17833Т (99.5% identity), and the strain G.S.17T exhibits the highest similarity to Pseudomonas rossensis P2663T (99.1% identity). Whole-genome comparisons using average nucleotide identity suggested that strains TMP9T and TMP25 represent a novel species within the genus Pseudomonas, which is most closely related to Pseudomonas guineae LMG 24016T (83.3%). Strain G.S.17T also represents a novel species within the genus Pseudomonas and is most closely related to Pseudomonas caspiana FBF102T (80.5%). The predominant cellular fatty acids of strains TMP9T, TMP25 and G.S.17T were cis-9-hexadecenoic, hexadecanoic and trans-9-octadecenoic acids. Physiological and biochemical tests, as well as genomic analysis results, clearly differentiated strains TMP9T, TMP25 and G.S.17T from type strains of closely related species. Thus, according to the data obtained, two novel species within the genus Pseudomonas are proposed: Pseudomonas vesperimontis sp. nov. (type strain TMP9T=BIM B-1560T=VKM B-3887T) and Pseudomonas viridinivis sp. nov. (type strain G.S.17T=BIM B-1635T=VKM B-3888T).
{"title":"<i>Pseudomonas vesperimontis</i> sp. nov. and <i>Pseudomonas viridinivis</i> sp. nov., isolated from temporary meltwater ponds and green snow in the Thala Hills Oasis, Antarctica.","authors":"Anna Muratova, Artur Akhremchuk, Katsiaryna Akhremchuk, Olesya Evdokimova, Darya Guliayeva, Volha Akulava, Vladislav Miamin, Leonid Valentovich","doi":"10.1099/ijsem.0.006999","DOIUrl":"https://doi.org/10.1099/ijsem.0.006999","url":null,"abstract":"<p><p>Three strains of Gram-negative, cold-adapted, aerobic bacteria were isolated on the coast of the Alasheyev Bight in the area of the Vecherniy region, the Thala Hills Oasis, Enderby Land, East Antarctica. Strains TMP9<sup>T</sup> and TMP25 were isolated from temporary meltwater ponds, while strain G.S.17<sup>T</sup> was obtained from a sample of green snow. Strains TMP9<sup>T</sup> and TMP25 were motile rods, catalase-negative and oxidase-positive, while G.S.17<sup>T</sup> was rod-shaped and exhibited motility, but was catalase- and oxidase-positive. TMP9<sup>T</sup> and TMP25 grew at 4-25 °C, pH 5.5-9.0 and tolerated up to 4.5% NaCl. G.S.17<sup>T</sup> grew at 4-28 °C, pH 5.0-8.5 and NaCl concentration up to 3.0%. The 16S rRNA gene sequence analysis placed all strains within the genus <i>Pseudomonas</i>: strains TMP9<sup>T</sup> and TMP25 are closely related to <i>Pseudomonas peli</i> DSM 17833<sup>Т</sup> (99.5% identity), and the strain G.S.17<sup>T</sup> exhibits the highest similarity to <i>Pseudomonas rossensis</i> P2663<sup>T</sup> (99.1% identity). Whole-genome comparisons using average nucleotide identity suggested that strains TMP9<sup>T</sup> and TMP25 represent a novel species within the genus <i>Pseudomonas</i>, which is most closely related to <i>Pseudomonas guineae</i> LMG 24016<sup>T</sup> (83.3%). Strain G.S.17<sup>T</sup> also represents a novel species within the genus <i>Pseudomonas</i> and is most closely related to <i>Pseudomonas caspiana</i> FBF102<sup>T</sup> (80.5%). The predominant cellular fatty acids of strains TMP9<sup>T</sup>, TMP25 and G.S.17<sup>T</sup> were cis-9-hexadecenoic, hexadecanoic and trans-9-octadecenoic acids. Physiological and biochemical tests, as well as genomic analysis results, clearly differentiated strains TMP9<sup>T</sup>, TMP25 and G.S.17<sup>T</sup> from type strains of closely related species. Thus, according to the data obtained, two novel species within the genus <i>Pseudomonas</i> are proposed: <i>Pseudomonas vesperimontis</i> sp. nov. (type strain TMP9<sup>T</sup>=BIM B-1560<sup>T</sup>=VKM B-3887<sup>T</sup>) and <i>Pseudomonas viridinivis</i> sp. nov. (type strain G.S.17<sup>T</sup>=BIM B-1635<sup>T</sup>=VKM B-3888<sup>T</sup>).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146149597","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zi-Xuan Liu, Rui Wang, You-Jun Liao, Dorji Phurbu, Ai-Hua Li
Two bacterial strains, designated E22-M8T and B22-R8T, were isolated from water sample collected from LungmuCo lake in Xizang of China. The 16S rRNA gene analysis revealed that strain E22-M8T was most closely related to members of the genus Pseudidiomarina, exhibiting the highest sequence similarity of 97.38 and 97.39% to Pseudidiomarina halophila BH195T and Pseudidiomarina terrestris 1APP75-27aT, respectively. While strain B22-R8T showed the highest similarity to species of the genera Terrihabitans and Flaviflagellibacter: 97.69, 96.80 and 96.66% to 'Terrihabitans rhizophilus' PJ23T, Terrihabitans soli IZ6T and Flaviflagellibacter deserti SYSU D60017T. For strain E22-M8T, the digital DNA-DNA hybridization (dDDH) values with its closest relatives P. halophila BH195T and P. terrestris 1APP75-27aT were 25.7 and 20.1%, respectively; the average nucleotide identity (ANI) values were 83.5 and 78%; and the average amino acid identity (AAI) values were 90.4 and 86.4%, all below the recognized species delineation thresholds. For strain B22-R8T, the corresponding dDDH, ANI and AAI values with its closest relatives 'T. rhizophilus' PJ23T, T. soli IZ6T and F. deserti SYSU D60017T also fell below the respective species thresholds. Biochemically and physiologically, both strains exhibited distinct traits that further supported their novelty. Based on comprehensive polyphasic analyses, strain E22-M8T (=CGMCC 1.19205T=KCTC 92346T) is proposed as a novel species named Pseudidiomarina xizangensis sp. nov., and strain B22-R8T (=CGMCC 1.19187T=KCTC 92343T) as a novel species designated Terrihabitans aquatilis sp. nov.
{"title":"<i>Pseudidiomarina xizangensis</i> sp. nov. and <i>Terrihabitans aquatilis</i> sp. nov., isolated from LungmuCo lake in Xizang, with the reclassification of <i>Flaviflagellibacter deserti</i> as <i>Terrihabitans deserti</i> comb. nov.","authors":"Zi-Xuan Liu, Rui Wang, You-Jun Liao, Dorji Phurbu, Ai-Hua Li","doi":"10.1099/ijsem.0.007073","DOIUrl":"https://doi.org/10.1099/ijsem.0.007073","url":null,"abstract":"<p><p>Two bacterial strains, designated E22-M8<sup>T</sup> and B22-R8<sup>T</sup>, were isolated from water sample collected from LungmuCo lake in Xizang of China. The 16S rRNA gene analysis revealed that strain E22-M8<sup>T</sup> was most closely related to members of the genus <i>Pseudidiomarina</i>, exhibiting the highest sequence similarity of 97.38 and 97.39% to <i>Pseudidiomarina halophila</i> BH195<sup>T</sup> and <i>Pseudidiomarina terrestris</i> 1APP75-27a<sup>T</sup>, respectively. While strain B22-R8<sup>T</sup> showed the highest similarity to species of the genera <i>Terrihabitans</i> and <i>Flaviflagellibacter</i>: 97.69, 96.80 and 96.66% to '<i>Terrihabitans rhizophilus</i>' PJ23<sup>T</sup>, <i>Terrihabitans soli</i> IZ6<sup>T</sup> and <i>Flaviflagellibacter deserti</i> SYSU D60017<sup>T</sup>. For strain E22-M8<sup>T</sup>, the digital DNA-DNA hybridization (dDDH) values with its closest relatives <i>P. halophila</i> BH195<sup>T</sup> and <i>P. terrestris</i> 1APP75-27a<sup>T</sup> were 25.7 and 20.1%, respectively; the average nucleotide identity (ANI) values were 83.5 and 78%; and the average amino acid identity (AAI) values were 90.4 and 86.4%, all below the recognized species delineation thresholds. For strain B22-R8<sup>T</sup>, the corresponding dDDH, ANI and AAI values with its closest relatives '<i>T. rhizophilus</i>' PJ23<sup>T</sup>, <i>T. soli</i> IZ6<sup>T</sup> and <i>F. deserti</i> SYSU D60017<sup>T</sup> also fell below the respective species thresholds. Biochemically and physiologically, both strains exhibited distinct traits that further supported their novelty. Based on comprehensive polyphasic analyses, strain E22-M8<sup>T</sup> (=CGMCC 1.19205<sup>T</sup>=KCTC 92346<sup>T</sup>) is proposed as a novel species named <i>Pseudidiomarina xizangensis</i> sp. nov., and strain B22-R8<sup>T</sup> (=CGMCC 1.19187<sup>T</sup>=KCTC 92343<sup>T</sup>) as a novel species designated <i>Terrihabitans aquatilis</i> sp. nov.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146157191","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sunho Park, Hyunji Lee, Subin Yook, Chunghwan Baek, Jisu Kim, Seunghui Kwak, Taeho Na, Taegun Seo
The novel strains CHS3-5T and M-2T were isolated from seawater collected near Suaeda japonica colonies on Seongmodo Island, Republic of Korea. Strain CHS3-5T was Gram-stain-negative, motile with flagella, rod-shaped, strictly aerobic and formed circular, convex, ivory-coloured colonies, while strain M-2T was Gram-stain-negative, motile by gliding, rod-shaped, strictly aerobic and formed circular, raised, dark yellow colonies. Based on 16S rRNA and draft genome analyses, strains CHS3-5T and M-2T were identified as members of the Oceanimonas and Arenibacter genera, respectively. Strain CHS3-5T grew at temperatures of 10-40 °C, pH 4.0-10.0 and in the presence of 2.0-11.0% NaCl, with optimal growth at 30 °C, pH 7.0 and 3.0% NaCl. Strain M-2T grew at temperatures of 15-40 °C, pH 6.0-9.0 and in the presence of 2.0-4.0% NaCl, with optimal growth at 30 °C, pH 7.0 and 3.0% NaCl. Both novel strains showed low genomic relatedness to their respective type species. The average nucleotide identity and digital DNA-DNA hybridization values were 84.5-85.7% and 26.5-34.7% for strain CHS3-5T and 76.6-85.9% and 18.6-30.3% for strain M-2T, respectively, supporting their classification as novel species. We propose the names Oceanimonas aquatica sp. nov. (type strain CHS3-5T=KACC 23248T=TBRC 17651T) and Arenibacter flavimaris sp. nov. (type strain M-2T=KACC 23249T=TBRC 17650T) for these strains.
{"title":"<i>Oceanimonas aquatica</i> sp. nov. and <i>Arenibacter flavimaris</i> sp. nov., isolated from seawater.","authors":"Sunho Park, Hyunji Lee, Subin Yook, Chunghwan Baek, Jisu Kim, Seunghui Kwak, Taeho Na, Taegun Seo","doi":"10.1099/ijsem.0.007054","DOIUrl":"https://doi.org/10.1099/ijsem.0.007054","url":null,"abstract":"<p><p>The novel strains CHS3-5<sup>T</sup> and M-2<sup>T</sup> were isolated from seawater collected near <i>Suaeda japonica</i> colonies on Seongmodo Island, Republic of Korea. Strain CHS3-5<sup>T</sup> was Gram-stain-negative, motile with flagella, rod-shaped, strictly aerobic and formed circular, convex, ivory-coloured colonies, while strain M-2<sup>T</sup> was Gram-stain-negative, motile by gliding, rod-shaped, strictly aerobic and formed circular, raised, dark yellow colonies. Based on 16S rRNA and draft genome analyses, strains CHS3-5<sup>T</sup> and M-2<sup>T</sup> were identified as members of the <i>Oceanimonas</i> and <i>Arenibacter</i> genera, respectively. Strain CHS3-5<sup>T</sup> grew at temperatures of 10-40 °C, pH 4.0-10.0 and in the presence of 2.0-11.0% NaCl, with optimal growth at 30 °C, pH 7.0 and 3.0% NaCl. Strain M-2<sup>T</sup> grew at temperatures of 15-40 °C, pH 6.0-9.0 and in the presence of 2.0-4.0% NaCl, with optimal growth at 30 °C, pH 7.0 and 3.0% NaCl. Both novel strains showed low genomic relatedness to their respective type species. The average nucleotide identity and digital DNA-DNA hybridization values were 84.5-85.7% and 26.5-34.7% for strain CHS3-5<sup>T</sup> and 76.6-85.9% and 18.6-30.3% for strain M-2<sup>T</sup>, respectively, supporting their classification as novel species. We propose the names <i>Oceanimonas aquatica</i> sp. nov. (type strain CHS3-5<sup>T</sup>=KACC 23248<sup>T</sup>=TBRC 17651<sup>T</sup>) and <i>Arenibacter flavimaris</i> sp. nov. (type strain M-2<sup>T</sup>=KACC 23249<sup>T</sup>=TBRC 17650<sup>T</sup>) for these strains.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146118821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Two aerobic, Gram-stain-negative, motile, rod-shaped bacteria, designated as strains TEGAF015T and KACHI17T, were isolated from surface lake and river waters in Japan. Strains TEGAF015T and KACHI17T had cell dimensions of ~0.4-0.6×1.3-2.9 µm and 0.4-0.5×2.5-4.8 µm (width×length), respectively. Strain KACHI17T was positive for casein hydrolysis, whereas strain TEGAF015T was negative. Phylogenetic analyses based on the 16S rRNA gene (1,290 bp) and 120 ubiquitous single-copy protein-encoding genes (5,035 aa) revealed that TEGAF015T and KACHI17T formed clusters closely related to Sediminibacterium salmoneum NJ-44T and Sediminibacterium goheungense HME7863T, respectively. However, the average nucleotide identity by orthology, average amino acid identity and digital DNA-DNA hybridization values confirmed that the isolates represent distinct species from closest phylogenetic relatives. The major cellular fatty acids identified in both strains included iso-C15:0, iso-C15:1 G, anteiso-C15:0 and iso-C17:0 3-OH. Additionally, TEGAF015T contained anteiso-C15:1 A, iso-C15:0 3-OH and iso-C16:0 3-OH. Phosphatidylethanolamine was identified as the major polar lipid of strains TEGAF015T and KACHI17T, which also contained menaquinone-7 as the predominant respiratory quinone and had DNA G+C contents of 38.5 and 40.0 mol%, respectively. Genome sequencing of the two isolates revealed genome sizes of 3.06 and 3.14 Mbp, respectively. Furthermore, both isolates were capable of converting dissolved organic nitrogen into ammonium during growth. These results indicated that strains TEGAF015T and KACHI17T represent two distinct novel species within the genus Sediminibacterium. The proposed names are Sediminibacterium planctonicum sp. nov. (type strain TEGAF015T=JCM 16661T=NCIMB 15525T) and Sediminibacterium longum sp. nov. (type strain KACHI17T=JCM 36264T=LMG 33984T).
{"title":"<i>Sediminibacterium planctonicum</i> sp. nov. and <i>Sediminibacterium longum</i> sp. nov., isolated from surface lake and river water.","authors":"Keiji Watanabe, Rina Kurokawa, Yusuke Ogata, Chie Shindo, Shusuke Takemine, Yuichi Ishii, Wataru Suda","doi":"10.1099/ijsem.0.007060","DOIUrl":"https://doi.org/10.1099/ijsem.0.007060","url":null,"abstract":"<p><p>Two aerobic, Gram-stain-negative, motile, rod-shaped bacteria, designated as strains TEGAF015<sup>T</sup> and KACHI17<sup>T</sup>, were isolated from surface lake and river waters in Japan. Strains TEGAF015<sup>T</sup> and KACHI17<sup>T</sup> had cell dimensions of ~0.4-0.6×1.3-2.9 µm and 0.4-0.5×2.5-4.8 µm (width×length), respectively. Strain KACHI17<sup>T</sup> was positive for casein hydrolysis, whereas strain TEGAF015<sup>T</sup> was negative. Phylogenetic analyses based on the 16S rRNA gene (1,290 bp) and 120 ubiquitous single-copy protein-encoding genes (5,035 aa) revealed that TEGAF015<sup>T</sup> and KACHI17<sup>T</sup> formed clusters closely related to <i>Sediminibacterium salmoneum</i> NJ-44<sup>T</sup> and <i>Sediminibacterium goheungense</i> HME7863<sup>T</sup>, respectively. However, the average nucleotide identity by orthology, average amino acid identity and digital DNA-DNA hybridization values confirmed that the isolates represent distinct species from closest phylogenetic relatives. The major cellular fatty acids identified in both strains included iso-C<sub>15:0</sub>, iso-C<sub>15:1</sub> G, anteiso-C<sub>15:0</sub> and iso-C<sub>17:0</sub> 3-OH. Additionally, TEGAF015<sup>T</sup> contained anteiso-C<sub>15:1</sub> A, iso-C<sub>15:0</sub> 3-OH and iso-C<sub>16:0</sub> 3-OH. Phosphatidylethanolamine was identified as the major polar lipid of strains TEGAF015<sup>T</sup> and KACHI17<sup>T</sup>, which also contained menaquinone-7 as the predominant respiratory quinone and had DNA G+C contents of 38.5 and 40.0 mol%, respectively. Genome sequencing of the two isolates revealed genome sizes of 3.06 and 3.14 Mbp, respectively. Furthermore, both isolates were capable of converting dissolved organic nitrogen into ammonium during growth. These results indicated that strains TEGAF015<sup>T</sup> and KACHI17<sup>T</sup> represent two distinct novel species within the genus <i>Sediminibacterium</i>. The proposed names are <i>Sediminibacterium planctonicum</i> sp. nov. (type strain TEGAF015<sup>T</sup>=JCM 16661<sup>T</sup>=NCIMB 15525<sup>T</sup>) and <i>Sediminibacterium longum</i> sp. nov. (type strain KACHI17<sup>T</sup>=JCM 36264<sup>T</sup>=LMG 33984<sup>T</sup>).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146124871","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The prokaryotic generic names Brachymonas Hiraishi et al. 1995 and Bosea Das et al. 1996 are illegitimate because they are later homonyms of the genus names Brachymonas Grassé 1952 (Protozoa, Polymastigidae) and Bosea He and Qian 1979 (a fossil dinoflagellate) [Principle 2 and Rule 51b(4) of the International Code of Nomenclature of Prokaryotes (ICNP)]. We therefore propose the replacement names Allobrachymonas gen. nov., Allobrachymonas chironomi comb. nov., Allobrachymonas denitrificans comb. nov., Allobrachymonas wangyanguii comb. nov., Allobosea gen. nov., Allobosea beijingensis comb. nov., Allobosea caraganae comb. nov., Allobosea eneae comb. nov., Allobosea lathyri comb. nov., Allobosea lupini comb. nov., Allobosea massiliensis comb. nov., Allobosea minatitlanensis comb. nov., Allobosea psychrotolerans comb. nov., Allobosea robiniae comb. nov., Allobosea rubneri comb. nov., Allobosea spartocytisi comb. nov., Allobosea thiooxidans comb. nov., Allobosea vaviloviae comb. nov., Allobosea vestrisii comb. nov. and Alloboseaceae fam. nov.
原核生物的属名Brachymonas Hiraishi et al. 1995和Bosea Das et al. 1996是非法的,因为它们后来与属名Brachymonas grass1952(原生动物,多鞭毛虫科)和Bosea He and Qian 1979(一种鞭毛化石)同义[国际原核生物命名规则(ICNP)原则2和规则51b(4)]。因此,我们建议将其命名为Allobrachymonas gen. nov., Allobrachymonas chironomi comb。11月,异长单胞菌反硝化菌梳。11月,异长臂单胞菌王艳桂梳。11月11日,北京异花楸属植物。11月,锦鸡儿花鸡冠。2011年11月,白桦桦齿梳。11月,异叶螨梳子。11月11日,白花海星梳。11月,马西利异花虱梳子。11月,米纳特兰白齿海梳。11月,异花苜蓿耐寒植物梳。11月,枇杷草梳子。11月,海白莲梳子。11月,异花苜蓿(Allobosea spartocytisi)。11月,硫代氧化酶梳。11月,异花苜蓿梳子。11月,白花海棠梳。11 .和异球藻科。11月。
{"title":"Proposal of <i>Allobrachymonas</i> gen. nov. and three new combinations as replacement names for the illegitimate prokaryotic genus name <i>Brachymonas</i>, proposal of <i>Allobosea</i> gen. nov. and 12 new combinations as replacement names for the illegitimate prokaryotic genus name <i>Bosea</i> and proposal of <i>Alloboseaceae</i> fam. nov. as a replacement name for the illegitimate family name <i>Boseaceae</i>.","authors":"Umakant Bhoopati Deshmukh, Aharon Oren","doi":"10.1099/ijsem.0.007072","DOIUrl":"10.1099/ijsem.0.007072","url":null,"abstract":"<p><p>The prokaryotic generic names <i>Brachymonas</i> Hiraishi <i>et al</i>. 1995 and <i>Bosea</i> Das <i>et al</i>. 1996 are illegitimate because they are later homonyms of the genus names <i>Brachymonas</i> Grassé 1952 (Protozoa, Polymastigidae) and <i>Bosea</i> He and Qian 1979 (a fossil dinoflagellate) [Principle 2 and Rule 51b(4) of the International Code of Nomenclature of Prokaryotes (ICNP)]. We therefore propose the replacement names <i>Allobrachymonas</i> gen. nov., <i>Allobrachymonas chironomi</i> comb. nov., <i>Allobrachymonas denitrificans</i> comb. nov., <i>Allobrachymonas wangyanguii</i> comb. nov., <i>Allobosea</i> gen. nov., <i>Allobosea beijingensis</i> comb. nov., <i>Allobosea caraganae</i> comb. nov., <i>Allobosea eneae</i> comb. nov., <i>Allobosea lathyri</i> comb. nov., <i>Allobosea lupini</i> comb. nov., <i>Allobosea massiliensis</i> comb. nov., <i>Allobosea minatitlanensis</i> comb. nov., <i>Allobosea psychrotolerans</i> comb. nov., <i>Allobosea robiniae</i> comb. nov., <i>Allobosea rubneri</i> comb. nov., <i>Allobosea spartocytisi</i> comb. nov., <i>Allobosea thiooxidans</i> comb. nov., <i>Allobosea vaviloviae</i> comb. nov., <i>Allobosea vestrisii</i> comb. nov. and <i>Alloboseaceae</i> fam. nov.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12882080/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146131987","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Umakant Bhoopati Deshmukh, Marko Kostovski, Aharon Oren
The prokaryotic genus names Baileyella Wylensek et al. 2021, Lucifera Sánchez-Andrea et al. 2019, and Microvenator Wang et al. 2022 are illegitimate because they are later homonyms of Baileyella Özdikmen 2009 (a fossil member of the Gonyaulacaceae, Gonyaulacales, Dinophyceae), Lucifera Baker 2010 (Keroplaridae, Diptera) and Microvenator Ostrom 1970 (a fossil member of the Caetagnatidae, Saurichia, Reptilia), respectively [Principle 2 and Rule 51b(5) of the International Code of Nomenclature of Prokaryotes (ICNP)]. We therefore propose the replacement names Allobaileyella gen. nov., Allobaileyella intestinalis comb. nov., Allolucifera gen. nov., Allolucifera butyrica comb. nov., Allomicrovenator gen. nov., Allomicrovenator marinus comb. nov. and Allomicrovenatoraceae fam. nov.
原核属名称Baileyella Wylensek et al. 2021, Lucifera Sánchez-Andrea et al. 2019和Microvenator Wang et al. 2022是非法的,因为它们后来与Baileyella Özdikmen 2009 (Gonyaulacaceae, Gonyaulacales, Dinophyceae的化石成员),Lucifera Baker 2010 (kerplaridae,双翅目)和Microvenator Ostrom 1970 (Caetagnatidae, Saurichia, Reptilia)的化石成员同音。分别[《国际原核生物命名规则》(ICNP)原则2和规则51b(5)]。因此,我们建议将其命名为Allobaileyella gen. nov., Allobaileyella intestine inalis comb。11月,异绿虫gen. 11月,异绿虫butyrica梳子。11月,Allomicrovenator gen. 11月,Allomicrovenator marinus comb.。11 .和异花苜蓿科。11月。
{"title":"Proposal of <i>Allobaileyella</i> gen. nov., <i>Allobaileyella intestinalis</i> comb. nov., <i>Allolucifera</i> gen. nov., <i>Allolucifera butyrica</i> comb. nov., <i>Allomicrovenator</i> gen. nov., <i>Allomicrovenator marinus</i> comb. nov. and <i>Allomicrovenatoraceae</i> fam. nov. as replacement names for <i>Baileyella</i>, <i>Baileyella intestinalis</i>, <i>Lucifera</i>, <i>Lucifera butyrica</i>, <i>Microvenator</i>, <i>Microvenator marinus</i> and <i>Microvenatoraceae</i>, respectively.","authors":"Umakant Bhoopati Deshmukh, Marko Kostovski, Aharon Oren","doi":"10.1099/ijsem.0.007061","DOIUrl":"10.1099/ijsem.0.007061","url":null,"abstract":"<p><p>The prokaryotic genus names <i>Baileyella</i> Wylensek <i>et al</i>. 2021, <i>Lucifera</i> Sánchez-Andrea <i>et al</i>. 2019, and <i>Microvenator</i> Wang <i>et al</i>. 2022 are illegitimate because they are later homonyms of <i>Baileyella</i> Özdikmen 2009 (a fossil member of the Gonyaulacaceae, Gonyaulacales, Dinophyceae), <i>Lucifera</i> Baker 2010 (Keroplaridae, Diptera) and <i>Microvenator</i> Ostrom 1970 (a fossil member of the Caetagnatidae, Saurichia, Reptilia), respectively [Principle 2 and Rule 51b(5) of the International Code of Nomenclature of Prokaryotes (ICNP)]. We therefore propose the replacement names <i>Allobaileyella</i> gen. nov., <i>Allobaileyella intestinalis</i> comb. nov., <i>Allolucifera</i> gen. nov., <i>Allolucifera butyrica</i> comb. nov., <i>Allomicrovenator</i> gen. nov., <i>Allomicrovenator marinus</i> comb. nov. and <i>Allomicrovenatoraceae</i> fam. nov.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12872784/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146118808","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
During a survey for natural-rubber-degrading actinobacteria associated with soils from Hevea brasiliensis plantations in Thailand, two strains, ABSL1-1T and ABSL49-1T, were isolated using mineral salts medium with natural rubber as the sole carbon source. Polyphasic taxonomy placed both strains within the genus Gordonia. Strain ABSL1-1T showed the highest 16S rRNA gene sequence similarity to Gordonia otitidis NBRC 100426T (98.5%) and Gordonia soli NBRC 108243T (98.3%), while ABSL49-1T showed the highest similarity to Gordonia polyisoprenivorans DSM 44302T (98.4%). The digital DNA-DNA hybridization (dDDH) and average nucleotide identity based on blast values between ABSL1-1T and closely related type strains were 20.1-20.9%, and 74.1-76.5%, respectively, while those for ABSL49-1T and closely related type strains were 20.6-22.9%, and 74.3-79.1%, respectively. The cell-wall peptidoglycan of both strains contained meso-diaminopimelic acid and the whole-cell sugars comprised ribose, arabinose, galactose and glucose. Both strains contained MK-9(H2) as the major menaquinone and phosphatidylethanolamine, diphosphatidylglycerol, phosphatidylglycerol, phosphatidylinositol and phosphatidylinositol mannoside were detected as the polar lipids. The predominant fatty acids of ABSL1-1T were C16:0, and C18:1ω9c, while those for ABSL49-1T were C16:0, C18:1ω9c, summed feature 3 (C16:1ω7c/C16:1ω6c) and C18:0 10-methyl. The G+C contents of the genomic DNA of strains ABSL1-1T and ABSL49-1T were 67.0 mol% and 66.0 mol%, respectively. Based on the results of a polyphasic taxonomic analysis, strains ABSL1-1ᵀ and ABSL49-1ᵀ represent the type strains of two novel species of the genus Gordonia, for which the names Gordonia heveisoli sp. nov. (type strain ABSL1-1ᵀ=TBRC 15892ᵀ=NBRC 116252ᵀ) and Gordonia gummivorans sp. nov. (type strain ABSL49-1ᵀ=TBRC 15624ᵀ=NBRC 115559ᵀ) are proposed.
{"title":"<i>Gordonia heveisoli</i> sp. nov. and <i>Gordonia gummivorans</i> sp. nov., two natural rubber-degrading actinobacteria isolated from soil in <i>Hevea brasiliensis</i> plantations.","authors":"Chanwit Suriyachadkun, Wipaporn Ngaemthao, Tawanmol Pujchakarn, Papichaya Kwantong, Nitcha Chamroensaksri, Chomnutcha Boonmee, Thanawadee Leejarkpai, Nattawut Boonyuen","doi":"10.1099/ijsem.0.007055","DOIUrl":"https://doi.org/10.1099/ijsem.0.007055","url":null,"abstract":"<p><p>During a survey for natural-rubber-degrading actinobacteria associated with soils from <i>Hevea brasiliensis</i> plantations in Thailand, two strains, ABSL1-1<sup>T</sup> and ABSL49-1<sup>T</sup>, were isolated using mineral salts medium with natural rubber as the sole carbon source. Polyphasic taxonomy placed both strains within the genus <i>Gordonia</i>. Strain ABSL1-1<sup>T</sup> showed the highest 16S rRNA gene sequence similarity to <i>Gordonia otitidis</i> NBRC 100426<sup>T</sup> (98.5%) and <i>Gordonia soli</i> NBRC 108243<sup>T</sup> (98.3%), while ABSL49-1<sup>T</sup> showed the highest similarity to <i>Gordonia polyisoprenivorans</i> DSM 44302<sup>T</sup> (98.4%). The digital DNA-DNA hybridization (dDDH) and average nucleotide identity based on blast values between ABSL1-1<sup>T</sup> and closely related type strains were 20.1-20.9%, and 74.1-76.5%, respectively, while those for ABSL49-1<sup>T</sup> and closely related type strains were 20.6-22.9%, and 74.3-79.1%, respectively. The cell-wall peptidoglycan of both strains contained <i>meso</i>-diaminopimelic acid and the whole-cell sugars comprised ribose, arabinose, galactose and glucose. Both strains contained MK-9(H<sub>2</sub>) as the major menaquinone and phosphatidylethanolamine, diphosphatidylglycerol, phosphatidylglycerol, phosphatidylinositol and phosphatidylinositol mannoside were detected as the polar lipids. The predominant fatty acids of ABSL1-1<sup>T</sup> were C<sub>16:0</sub>, and C<sub>18:1</sub> <i> </i>ω<i>9c</i>, while those for ABSL49-1<sup>T</sup> were C<sub>16:0</sub>, C<sub>18:1</sub> <i> </i>ω<i>9c</i>, summed feature 3 (C<sub>16:1</sub> <i> </i>ω<i>7</i>c/<sub>C16:1</sub> <i> </i>ω<i>6c</i>) and C<sub>18:0</sub> 10-methyl. The G+C contents of the genomic DNA of strains ABSL1-1<sup>T</sup> and ABSL49-1<sup>T</sup> were 67.0 mol% and 66.0 mol%, respectively. Based on the results of a polyphasic taxonomic analysis, strains ABSL1-1ᵀ and ABSL49-1ᵀ represent the type strains of two novel species of the genus <i>Gordonia</i>, for which the names <i>Gordonia heveisoli</i> sp. nov. (type strain ABSL1-1ᵀ=TBRC 15892ᵀ=NBRC 116252ᵀ) and <i>Gordonia gummivorans</i> sp. nov. (type strain ABSL49-1ᵀ=TBRC 15624ᵀ=NBRC 115559ᵀ) are proposed.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146124932","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Seunghwan Kim, Daseul Lee, Jun Heo, Hyorim Choi, Yunhee Choi, Yiseul Kim
Two bacterial strains, designated M3-11T and M6-14T, were isolated from paddy field soils in the Republic of Korea. Cells were aerobic, Gram-stain-negative, rod-shaped and non-flagellated but motile. The strains exhibited optimal growth at 28 °C and pH 7.0 and in the absence of NaCl. Phylogenetic analysis based on 16S rRNA gene sequences indicated that strains M3-11T and M6-14T were placed within the genus Flavobacterium, showing the highest similarity to Flavobacterium zhairuonense A5.7T (97.98%) and Flavobacterium nitrogenifigens NXU-44T (98.23 %), respectively. The genomic similarity between two strains and their closely related strains was 39.3 and 51.1 % for digital DNA-DNA hybridization and 90.0 and 93.2 % for orthologous average nucleotide identity, both of which were lower than the thresholds recommended for species delineation. The respiratory quinone was menaquinone-6, and the major polar lipids were phosphatidylethanolamine and aminolipid. The major fatty acids (>10 %) were iso-C15 : 0 and summed feature 3. The phenotypic, chemotaxonomic and genotypic data obtained in this study showed that strains M3-11T and M6-14T represent novel species of the genus Flavobacterium, for which the names Flavobacterium oryzagri sp. nov. (type strain M3-11T=KACC 22761T=JCM 35942T) and Flavobacterium oryzicola sp. nov. (type strain M6-14T=KACC 22763T=JCM 35943T) are proposed.
{"title":"<i>Flavobacterium oryzagri</i> sp. nov. and <i>Flavobacterium oryzicola</i> sp. nov., isolated from paddy soil.","authors":"Seunghwan Kim, Daseul Lee, Jun Heo, Hyorim Choi, Yunhee Choi, Yiseul Kim","doi":"10.1099/ijsem.0.007063","DOIUrl":"10.1099/ijsem.0.007063","url":null,"abstract":"<p><p>Two bacterial strains, designated M3-11<sup>T</sup> and M6-14<sup>T</sup>, were isolated from paddy field soils in the Republic of Korea. Cells were aerobic, Gram-stain-negative, rod-shaped and non-flagellated but motile. The strains exhibited optimal growth at 28 °C and pH 7.0 and in the absence of NaCl. Phylogenetic analysis based on 16S rRNA gene sequences indicated that strains M3-11<sup>T</sup> and M6-14<sup>T</sup> were placed within the genus <i>Flavobacterium</i>, showing the highest similarity to <i>Flavobacterium zhairuonense</i> A5.7<sup>T</sup> (97.98%) and <i>Flavobacterium nitrogenifigens</i> NXU-44<sup>T</sup> (98.23 %), respectively. The genomic similarity between two strains and their closely related strains was 39.3 and 51.1 % for digital DNA-DNA hybridization and 90.0 and 93.2 % for orthologous average nucleotide identity, both of which were lower than the thresholds recommended for species delineation. The respiratory quinone was menaquinone-6, and the major polar lipids were phosphatidylethanolamine and aminolipid. The major fatty acids (>10 %) were iso-C<sub>15 : 0</sub> and summed feature 3. The phenotypic, chemotaxonomic and genotypic data obtained in this study showed that strains M3-11<sup>T</sup> and M6-14<sup>T</sup> represent novel species of the genus <i>Flavobacterium</i>, for which the names <i>Flavobacterium oryzagri</i> sp. nov. (type strain M3-11<sup>T</sup>=KACC 22761<sup>T</sup>=JCM 35942<sup>T</sup>) and <i>Flavobacterium oryzicola</i> sp. nov. (type strain M6-14<sup>T</sup>=KACC 22763<sup>T</sup>=JCM 35943<sup>T</sup>) are proposed.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142286","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nine isolates from the gingiva of cheetahs kept in captivity were subjected to genotypic and phenotypic characterization. Sequencing of the 16S rRNA gene documented the highest identity of three representative strains to the type strain of Pasteurella multocida subsp. septica with 95.82%. The highest digital DNA-DNA hybridization predicted from the whole-genome sequence of strain 22721-9-1T was to Haemophilus felis with 25.0%. The highest average nucleotide identity of strain 22721-9-1T was also to H. felis with 74.36%, confirming a separate taxonomic status at species level. The phylogenetic comparison of concatenated conserved protein sequences showed a unique position of the taxon investigated, which qualifies for the status of a new genus, since the highest identity was found to Lonepinella koalarum with 83%, well below the upper threshold among genera of 91%. A new genus with one species, Reella acinonychis, is proposed. Production of indole and acid from sucrose and dulcitol separate the genus from most of the other genera of the Pasteurellaceae. Matrix-assisted laser desorption/ionization-time of flight MS analysis of the isolates clustered them close together and clearly separated them from other Pasteurellaceae species, allowing clear discrimination and making this the method of choice for identification. The G+C content of the type strain 22721-9-1T (=DSM 118580T=CCUG 77953T) is 38.53 mol%, calculated from the whole genome.
{"title":"Classification of <i>Reella acinonychis</i> gen. nov., sp. nov., within <i>Pasteurellaceae</i>.","authors":"Henrik Christensen, Peter Kuhnert, Magne Bisgaard","doi":"10.1099/ijsem.0.007067","DOIUrl":"https://doi.org/10.1099/ijsem.0.007067","url":null,"abstract":"<p><p>Nine isolates from the gingiva of cheetahs kept in captivity were subjected to genotypic and phenotypic characterization. Sequencing of the 16S rRNA gene documented the highest identity of three representative strains to the type strain of <i>Pasteurella multocida</i> subsp. <i>septica</i> with 95.82%. The highest digital DNA-DNA hybridization predicted from the whole-genome sequence of strain 22721-9-1<sup>T</sup> was to <i>Haemophilus felis</i> with 25.0%. The highest average nucleotide identity of strain 22721-9-1<sup>T</sup> was also to <i>H. felis</i> with 74.36%, confirming a separate taxonomic status at species level. The phylogenetic comparison of concatenated conserved protein sequences showed a unique position of the taxon investigated, which qualifies for the status of a new genus, since the highest identity was found to <i>Lonepinella koalarum</i> with 83%, well below the upper threshold among genera of 91%. A new genus with one species, <i>Reella acinonychis</i>, is proposed. Production of indole and acid from sucrose and dulcitol separate the genus from most of the other genera of the <i>Pasteurellaceae</i>. Matrix-assisted laser desorption/ionization-time of flight MS analysis of the isolates clustered them close together and clearly separated them from other <i>Pasteurellaceae</i> species, allowing clear discrimination and making this the method of choice for identification. The G+C content of the type strain 22721-9-1<sup>T</sup> (=DSM 118580<sup>T</sup>=CCUG 77953<sup>T</sup>) is 38.53 mol%, calculated from the whole genome.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"76 2","pages":""},"PeriodicalIF":2.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146149643","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}