Flavobacterium mekongense sp. nov., isolated from the Mekong River in Thailand.

IF 2 3区 生物学 Q4 MICROBIOLOGY
Chitwadee Phithakrotchanakoon, Supattra Kitikhun, Paopit Siriarchawatana, Piyanat Charoenyingcharoen, Sukanya Jeennor, Thanyakorn Nilsakha, Amonwan Chanpet, Thanat Vorajinda, Sermsiri Mayteeworakoon, Pattaraporn Yukphan, Supawadee Ingsriswang
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引用次数: 0

Abstract

Two Gram-stain-negative, aerobic, non-motile, non-gliding, rod-shaped bacterial strains, designated as TBRC 19031T and TBRC 19032, were isolated from water samples collected from the Mekong River, Thailand. Strain TBRC 19031T was obtained from Chiang Saen in the upstream section near the borders with China and Myanmar, while TBRC 19032 originated from Khong Chiam, in the downstream section where the river exits Thailand. Colonies of both strains were circular, smooth and deep yellow on Reasoner's 2A agar and did not produce flexirubin-type pigments. Phylogenetic analysis with 16S rRNA gene sequences placed both strains within the genus Flavobacterium, showing the highest sequence similarity to Flavobacterium cheonhonense ARSA-15T (98.29% for TBRC 19031T and 98.22% for TBRC 19032). However, whole-genome comparisons between the strains and F. cheonhonense ARSA-15T revealed average nt identity (89.39% and 89.29%), average aa identity (92.84% and 92.95%) and digital DNA-DNA hybridization (35.00% and 34.70%). The predominant fatty acids were iso-C15:1, iso-C15:0 and iso-C15:0 3-OH, and menaquinone MK-6 was the major respiratory quinone. The major polar lipids of both strains included phosphatidylethanolamine, steryl ester and diacylglycerol. The genome sizes were 3.02 and 3.04 Mbp, with G+C contents of 38.3% and 38.2% for TBRC 19031T and TBRC 19032, respectively. Comparative genomic analyses revealed the absence of genes involved in sulphate reduction and denitrification pathways and the presence of a gene encoding phosphatidylinositol synthase, distinguishing them from other Flavobacterium within the clade. Ecological profiling using public metagenomic datasets showed that both strains were associated with lotic freshwater environments. This study not only introduces Flavobacterium mekongense sp. nov. as a new species but also provides broader insights into the ecology, metabolism and environmental distribution of freshwater Flavobacterium. The genomic features identified here offer promising leads for future studies in microbial ecology, comparative genomics and functional gene mining in aquatic ecosystems. The type strain is TBRC 19031T (TBRC 19031T=NBRC 117006T).

泰国湄公河黄杆菌。
从泰国湄公河水样中分离到2株革兰氏染色阴性、需氧、非运动、非滑行的杆状细菌,编号为TBRC 19031T和TBRC 19032。菌株TBRC 19031T来自靠近中国和缅甸边境的上游河段清盛,而菌株TBRC 19032来自泰国流出的下游河段香江。两株菌落在Reasoner’s 2A琼脂上呈圆形、光滑、深黄色,不产生柔红素型色素。采用16S rRNA基因序列进行系统发育分析,结果表明该菌株与黄杆菌属(Flavobacterium cheonhonense ARSA-15T)的序列相似性最高(与TBRC 19031T和TBRC 19032的序列相似性分别为98.29%和98.22%)。全基因组比较结果显示,该菌株与天牛瘟杆菌ARSA-15T的nt同源性分别为89.39%和89.29%,aa同源性分别为92.84%和92.95%,数字DNA-DNA杂交性分别为35.00%和34.70%。主要脂肪酸为iso-C15:1、iso-C15:0和iso-C15:0 3-OH,呼吸醌类以甲基萘醌MK-6为主。两种菌株的主要极性脂质为磷脂酰乙醇胺、甾酯和二酰基甘油。TBRC 19031T和TBRC 19032的基因组大小分别为3.02和3.04 Mbp, G+C含量分别为38.3%和38.2%。比较基因组分析显示,与硫酸盐还原和反硝化途径相关的基因缺失,而编码磷脂酰肌醇合成酶的基因存在,将它们与该分支中的其他黄杆菌区分出来。利用公共宏基因组数据集进行的生态分析表明,这两种菌株都与淡水环境有关。本研究不仅介绍了mekongense Flavobacterium sp. nov.作为一个新物种,而且对淡水黄杆菌的生态学、代谢和环境分布提供了更广泛的认识。这些基因组特征为水生生态系统中微生物生态学、比较基因组学和功能基因挖掘的未来研究提供了有希望的线索。型应变为TBRC 19031T (TBRC 19031T=NBRC 117006T)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.20
自引率
21.40%
发文量
426
审稿时长
1 months
期刊介绍: Published by the Microbiology Society and owned by the International Committee on Systematics of Prokaryotes (ICSP), a committee of the Bacteriology and Applied Microbiology Division of the International Union of Microbiological Societies, International Journal of Systematic and Evolutionary Microbiology is the leading forum for the publication of novel microbial taxa and the ICSP’s official journal of record for prokaryotic names. The journal welcomes high-quality research on all aspects of microbial evolution, phylogenetics and systematics, encouraging submissions on all prokaryotes, yeasts, microfungi, protozoa and microalgae across the full breadth of systematics including: Identification, characterisation and culture preservation Microbial evolution and biodiversity Molecular environmental work with strong taxonomic or evolutionary content Nomenclature Taxonomy and phylogenetics.
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