Bruguierivorax albus gen. nov. sp. nov. Isolated from Mangrove Sediment and Proposal of Bruguierivoracaceae fam. nov

A novel Gram-negative, motile, aerobic rod-shaped bacterium designated BGMRC 2031T was isolated from mangrove sediment collected from Guangxi Province, China. Optimal growth occurred at 28 °C and pH 7.0–8.0 in the presence of 1% (w/v) NaCl. Alignment based on 16S rRNA gene sequences indicated that strain BGMRC 2031T is most closely related to Sodalis praecaptivus HS1T (95.6%, sequence similarity), followed by Biostraticola tofi DSM 19580T (95.5%), Sodalis glossinidius DSM 16929T (95.4%), and Brenneria goodwinii FRB141T (94.9%) sequence similarity. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain BGMRC 2031T formed a distinct branch in a robust cluster and revealed that strain BGMRC 2031T, genera Biostraticola and Sodalis, formed a novel family-level clade in the order Enterobacterales. The novel strain showed an average nucleotide similarity of 74.7%, 74.2%, and 73.1% for S. praecaptivus HS1T, S. glossinidius DSM 16929T, and B. tofi DSM 19580T, respectively. The genomes of the BGMRC 2031T shared the presence of a riboflavin synthesis gene cluster. The menaquinones of strain BGMRC 2031T were MK-8 and Q-8, which were similar to those of genus Biostraticola. The major fatty acids (> 10%) were C16:0 (19.9%), summed feature 2 (iso-C16:1 and/or C14:0 3-OH, 18.10%), summed feature 3 (C16:1ω7c and/or C16:1ω6c, 15.3%), C12:0 (13.9%), C17:0 cyclo (11.4%), and C14:0 (10.4%). The main polar lipids were phosphatidyl methylethanolamine, phosphatidyl glycerol, diphosphatidyl glycerol, phosphatidyl inositol, one unidentified phospholipid, and one unknown polar lipid. The G+C content of strain BGMRC 2031T was 55.4%. Strain BGMRC 2031T could extend the mean lifespan and maximum lifespan of Caenorhabditis elegans by 4.5% and 12.5%, respectively. Overall, the results of this study indicate that BGMRC 2031T is a novel species in a new genus, for which the name Bruguierivorax albus gen. nov. sp. nov. is proposed, and the type of strain is designated as BGMRC 2031T (= NBRC 111907T = KCTC 52119T). In addition, a novel family, Bruguierivoracaceae fam. nov., is proposed to accommodate the genera Bruguierivorax, Biostraticola, and Sodalis.


Introduction
The order Enterobacterales is a large group within the class Gammaproteobacteria which was revised in 2016 by Adeolu et al. [1]. This order is characterized by its non-sporeforming, rod-shaped bacteria, as well as its Gram-negative and facultatively anaerobic characteristics [1]. At the time of its revision, the Enterobacterales comprised seven families according to the EzTaxon database, Enterobacteriaceae, Erwiniaceae, Pectobacteriaceae, Yersiniaceae, Hafniaceae, Morganellaceae, and Budviciaceae [1].
The genera Biostraticola and Sodalis were first proposed by Verbarg et al. [2] and Dale et al. [3], respectively. In 2016, Biostraticola and Sodalis were affiliated to two families, Enterobacteriaceae and Pectobacteriaceae, respectively, based on their genome phylogeny and taxonomy [1]. At the time of writing, the genus Biostraticola The GenBank accession numbers for the 16S rRNA gene sequence and draft genome sequence of Bruguierivorax albus BGMRC 2031 T are MN059649 and SZPQ00000000, respectively. Transmission electron micrographs of cells of strain BGMRC 2031 T , polar lipids of strain BGMRC 2031 T and Biostraticola tofi DSM 19580 T , Maximum-Likelihood tree, and Minimum Evolution tree are available as supplementary figures in Current microbiology Online. contained a single species, B. tofi, while Sodalis contained two validly named species (S. praecaptivus [4] and S. glossinidius [3]) and two candidatus species (Candidatus S. melophagi [5] and Candidatus S. baculum [6]). Two Candidatus strains were live in symbiosis with various groups of insects and, respectively, symbiose relationships with Melophagus ovinus and Hemipteran insects. To date, the majority of Sodalis members have been found in several insect groups, and S. praecaptivus has been found in human hand wounds [4,6]. The strain S. lignotolerans 159R was isolated from an anaerobic lignin degrading consortium.
In our study of microbial biodiversity in medicinal mangrove plants, strain BGMRC 2031 T was isolated from a Bruguiera gymnorrhiza rhizosphere soil sample. Comparative 16S rRNA gene sequence analysis showed that strain BGMRC 2031 T was closely related to species in the genera Biostraticola (95.5%) and Sodalis (95.4-95.6%). However, strain BGMRC 2031 T could not be assigned to any species of the genera Biostraticola or Sodalis because of its low sequence similarity with the two type strains (≤ 95.6%). Therefore, the present study is conducted to report the taxonomic characterization of the new isolate, BGMRC 2031 T .

Bacterial Strain and Culture Conditions
Strain BGMRC 2031 T was isolated from sediment of Bruguiera gymnorrhiza roots collected from Guangxi Province, China (21° 55′ N, 108° 50′ E). Samples were immediately stored in sterile plastic bags at 4 °C, then transported to the laboratory within 12 h. Soil (2 g) was added to 20 mL of sterilized seawater, then shaken at 37 °C for 1 h. Next, 1 mL of the suspension was transferred to 9 mL sterilized sea water and serially diluted to 10 -2 , 10 -3 , 10 -4 , and 10 -5 . The serial dilutions of the samples (200 μL) were subsequently plated onto R2A medium (0.5 g yeast extract powder, 0.5 g peptone, 0.5 g casein hydrolysate, 0.5 g glucose, 0.5 g starch, 0.3 g K 2 HPO 4 , 0.024 g MgSO 4 , 0.3 g sodium pyruvate, 15.0 g agar, 1 L seawater, pH 7.2), then incubated at 28 °C for 1 week. Single colony was selected and purified on modified Yeast Malt Extract (ISP2) (2.0 g yeast extract, 2.0 g malt extract, 2.0 g D-( +)-glucose anhydrous, 15.0 g agar powder and 1 L seawater) at 28 °C. Strain BGMRC 2031 T was isolated using the preceding method, then preserved in 20% (v/v) glycerol suspensions at -80 °C. The reference strain, B. tofi DSM 19580 T , was obtained from the Leibniz Institut DSMZ-German Collection of Microorganisms and Cell Cultures GmbH.

Morphological and Physiological Characteristics
Morphological and physiological characteristics were observed on modified ISP2 medium unless stated. Growth and colony morphology were observed after 2 days incubation at 28 °C. Cell morphology was observed using a scanning electron microscope (FEI Quanta 250 Environmental Scanning Electron Microscope), and the flagellum of the strain was observed via transmission electron microscopy (Hitachi Transmission Electron Microscope HT7700) after growth on ISP2 at 28 °C for 2 days. Cell motility determination was conducted by observing the development of turbidity in a tube using ISP2 semisolid medium containing 0.4% agar [7]. Gram staining was determined on ISP2 plates following the protocols described by Gerhardt et al. [8]. Oxidase activity was examined using 1% (w/v) N, N, N', N'-tetramethyl-p-phenylenediamine reagent. Catalase activity was assessed using 3% (w/v) H 2 O 2 solution [9]. Growth at various concentrations of NaCl (0%-15%, w/v, with an interval of 1.0%), was tested on ISP2 agar (Difco) at 28 °C. The temperature range was determined by incubating cells in ISP2 medium broth at 4 °C, 10 °C, 15 °C, 20 °C, 25 °C, 28 °C, 37 °C, 40 °C, and 45 °C for 2 weeks. The pH range for growth (pH 4.0-12.0 at intervals of 1 pH unit) was tested in ISP2 broth at 28 °C using the buffer system developed by Xu et al. [10]. Cultural characteristics were determined by observing growth of the strain at 28 °C for 2 weeks on ISP2, ISP3, ISP4, ISP5, and ISP7 agar plates, lysogeny broth (LB agar), R2A agar, and tryptic soy agar. ISCC-NBS color charts [11] were used to assess colony colors. Biochemical tests, including H 2 S production, hydrolysis of cellulose, gelatin, starch, Tweens 20, 40, and 80, were performed using the methods described by Tindall [12]. Coagulation and peptonisation of milk were evaluated as described by Gonzalez [13]. Carbohydrate metabolism was determined using API ZYM and API 20E strips (BioMérieux, Marcyl'Etoile, France) according to the manufacturer's instructions. Anaerobic fermentation was evaluated using the API 50CH system (BioMérieux). The incubation temperature for all API kits was 28 °C, and results were observed after 48 h.

Chemotaxonomic Characterization
Cell biomass for the chemotaxonomic characterization was obtained from ISP2 medium after incubation at 28 °C for 3 days. Polar lipids were extracted as described by Kamekura [14] and identified by two-dimensional thinlayer chromatography (TLC) on silica gel 60 GF 254 plates (Merck KGaA, Darmstadt Germany) that had been sprayed with ethanolic molybdophosphoric acid, molybdenum 1 3 blue, and ninhydrin after two-dimensional TLC [15]. Respiratory quinones were extracted and analyzed using reverse-phase HPLC [16,17]. Cellular fatty acid composition was analyzed by gas chromatography (G6890N; Agilent Technologies, Savage, MD, USA) and identified using the Sherlock Microbial Identification System (version 6.0) according to the manufacturer's instructions and as previously described [18].

Phylogenetic Analyses
PCR amplification of strain BGMRC 2031 T with the universal primers 27F and 1492R and subsequent 16S rRNA gene sequencing [19] were conducted as described by Li et al. [20]. The purified DNA product was cloned into the pEASY-T1 vector and transformed into Escherichia coli DH5α using the pEASY-T1 cloning kit. The 16S rRNA gene sequence was compared with that of recognized species using EzBioCloud (http://www.ezbio cloud .net) [21]. Multiple alignments of the sequence data were conducted using CLUSTAL X 1.83 [22]. Phylogenetic analyses were conducted based on the neighbor-joining [23], maximumlikelihood [24], and maximum-parsimony [25] algorithms using the MEGA software (version 7.0) [26]. Kimura's twoparameter model was used to calculate evolutionary distance matrices of the neighbor-joining method [27]. The topology of the phylogenetic tree was evaluated by bootstrap analysis with 1000 replicates [28].

Genomic Characterization
To further distinguish strain BGMRC 2031 T from its closely related species, whole-genome sequencing was conducted by BGI (Wuhan, China) using the Illumina Hiseq 4000 system (Illumina, San Diego, CA, USA) according to the manufacturer's suggested protocols. The draft genome was assembled using SOAP de novo version 2.04, and the short oligonucleotides of the obtained results were further optimized using SOAP aligner 2.21 [29,30]. The obtained genome sequences were annotated by using the NCBI Prokaryotic Genome Annotation Pipeline and deposited at DDBJ/ENA/ GenBank. Genomes were annotated using the Rapid Annotation Subsystems Technology (RAST) servers [31]. Genomic information of B. tofi DSM 19580 T (SMCR00000000), S. praecaptivus HS T (CP006569.1), S. glossinidius DSM 16929 T (GCA_000010085.1), and Candidatus S. baculum HBA(LT897836) was downloaded from GenBank and was used to evaluate genomic relatedness with strain BGMRC 2031 T . The average nucleotide identity (ANI) was calculated using the ANI calculator tool from EzBioCloud [32]. The estimated genome sequence-based digital DNA-DNA hybridization values were calculated using formula 2 from the online Genome-to-Genome Calculator (http://ggdc. dsmz.de/ggdc.php) as described by Meier-Kolthoff et al. [33].

Effects on Lifespan of Caenorhabditis elegans
The antiaging activities of crude extract of strain BGMRC 2031 T were investigated as previously described [34]. Briefly, the strain was fermented in ISP2 liquid medium at 28 °C and 180 rpm for 7 days. The fermentation liquor was then extracted with ethyl acetate, after which it was concentrated and desiccated to yield crude extract [35]. Wild-type C. elegans strains (N2) were purchased from the Caenorhabditis Genetic Center (CGC) at the University of Minnesota (Minneapolis, MN, USA). Synchronized worms can eliminate variation in results due to age differences [34]; therefore, adult worms were seeded with E. coli OP50 on nematode growth medium (NGM) plates and incubated for about 2 days at 20 °C. Next, M9 buffer (0.3% KH 2 PO 4 , 0.6% Na 2 HPO 4 , 0.5% NaCl, 1 mM MgSO 4 ) was poured onto the plate and gently swirled it to dislodge the worms. Alkaline hypochlorite (20%) was subsequently used to completely lyse the adult worms, after which synchronized eggs were collected. The synchronized eggs were grown in M9 buffer overnight at 20 °C, then put on NGM plates at the L4 stage. Synchronized L4 larvae were subsequently used to analyze the life span of worms at 20 °C. Forty L4 stage larvae were randomly transferred onto fresh NGM plates seeded with dead E. coli OP50 (day 0 of lifespan), then treated with 100 μL, 0.1% (v/v) DMSO (blank control) or 500 μg·mL −1 BGMRC 2031 T crude extract. The BGMRC 2031 T crude extracts were dissolved in dimethyl sulfoxide, and the final concentration of DMSO was less than 0.1%. During the lifespan experiments, media were exchanged every 2 days, and survival of the animals was measured daily based on touch-provoked movement. All lifespan experiments were repeated at least two independent times.

Morphological and Physiological Characteristics
Colonies of strain BGMRC 2031 T were round, flat, and white with diameters of 0.5-1.0 mm after cultivation for 2 days on ISP2 at 28 °C. Cells of BGMRC 2031 T were Gram-negative and motile. Scanning electron microscopy showed that the cells were short rods of about 0.4-0.6 × 1.0-1.6 μm (Fig. S3). No growth was observed under anaerobic conditions. Strain BGMRC 2031 T growth occurred at 15 °C-37 °C (optimum, 28 °C) and pH 5.0-9.0 (optimum, pH 7.0-8.0) in the presence of 0%-6% (w/v) NaCl (optimum, 0-1%) ( Table 1). Growth occurred on ISP2, LB, and R2A agar plates, but not ISP3, ISP4, ISP5, ISP7, or trypticase soy yeast agar plates. The strain was positive for catalase activities and negative for oxidase. Milk coagulation and peptonisation were positive, and hydrolysis of gelatin, nitrate reduction, cellulose, starch, and Tween 20, 40, and 80 were negative. The differences in the physiological and biochemical characteristics of strain BGMRC 2031 T and its closest related type strains are listed in Table 1 and Tables S1 and S2. Strain BGMRC 2031 T and the other related species were motile and catalase positive; however, strain S. glossinidius DSM 16929 T was non-motile and catalase negative. Strain BGMRC 2031 T was VP, valine arylamidase, cystine arylamidase, trypsin, 2-ketogluconate, and 5-ketogluconate positive, as well as positive for milk coagulation, peptonisation and fermentation of d-mannose, d-adonitol, d-glucose, dulcitol, d-sorbitol, l-fucose, d-arabinitol, and l-arabinitol. However, the strain was negative for esterase (C4) and esterase lipase (C8), as well as fermentation of d-cellobiose. These characteristics enable strain BGMRC 2031 T to be clearly distinguished from its closest phylogenetic relatives.
An overview of some characteristics of the respective gene content of the strain BGMRC 2031 T , B. tofi, S. praecaptivus, S. glossinidius, Candidatus S. baculum, and S. lignotolerans 159R was given in Table 4. The genomes of

Effects on Lifespan of Caenorhabditis elegans
The mean survival times (% vs DMSO) of the worms pretreated with strain BGMRC 2031 T and blank control are shown in Fig S5. The lifespan of worms treated with BGMRC 2031 T extract did not differ significantly from that of the worms treated with the blank control (0.1% DMSO), which extended the mean lifespan and maximum lifespan by 4.5% and 12.5%, respectively. In summary, the unique phenotypic characteristics, principal fatty acid composition (C 16:0 and iso-C 16:1 and/or C 14:0 3-OH) and polar lipid composition, as well as the similar respiratory quinone composition and DNA G+C content indicated that strain BGMRC 2031 T may represent a novel species in a new genus of a novel family. Low 16S rRNA gene similarities (≤ 95.6%), ANI values (≤ 74.7%) and DDH values (≤ 21.1%) coupled with phenotypic and chemotaxonomic characteristics support that strain BGMRC 2031 T represents a novel taxon. Additionally, phylogenetic analyses indicated strain BGMRC 2031 T together with the genera Biostraticola and Sodalis represent a novel family within the order Enterobacterales of class Gammaproteobacteria.
The major fatty acids of family Bruguierivoracaceae are C 16:0 and feature 3 (C 16:1 ω7c and/or C 16:1 ω6c). Major respiratory quinones are MK-8 and Q-8. The 16S rRNA genebased and phylogenomic analysis showed that the genus Bruguierivorax, Biostraticola and Sodalis forms a separate phylogenetic clade. The family Bruguierivoracaceae contains the type genus Sodalis [3] and the genera Biostraticola [2] and Bruguierivorax. These bacteria are motile rod-shaped, catalase positive, and oxidase negative, and do not produce hydrogen disulfide. Members of this family produce acid from N-acetylglucosamine and are negative for orthinine decarboxylase lysine decarboxylase. The family Bruguierivoracaceae belongs to the order Enterobacterales of the class Gammaproteobacteria.
Cells are Gram-negative, aerobic, motile, rod-shaped, catalase positive, and oxidase negative. Acid is produced from 2-ketogluconate, dulcitol, d-adonitol and d-mannose. The major respiratory quinones are MK-8 and Q-8. The major polar lipids are phosphatidyl methyl ethanolamine, phosphatidyl glycerol, diphosphatidyl glycerol, phosphatidyl inositol, one unidentified phospholipid and one unknown polar lipid. The type species is Bruguierivorax albus.

Description of Bruguierivorax albus sp. nov.
Bruguierivorax albus (al'bus. L. masc. adj. albus white, referring to the color of the colonies).
Cells are usually 0.4-0.6 μm wide and 1.0-1.6 μm long. After 2 days of incubation on ISP2 agar at 28 °C, colonies are circular, smooth, white and round and 0.5-1.5 mm in diameter. Noval strain grew well on ISP2 agar, LB agar and R2A agar, but no growth occurred on ISP3, ISP4, ISP5, ISP7, nutrient agar or trypticase soy yeast agar plates. Optimum growth occurred at 28 °C, at pH 7.0-8.0 and in the presence of 0-1% (w/v) NaCl. The strain was negative for gelatin hydrolysis, nitrate reduction, hydrolysis of cellulose, starch, and Tween 20, 40, and 80 tests, while it was positive for milk coagulation and peptonisation tests. The strain was positive for O-nitrophenyl-β-D-galactopyranoside, VP, glucose fermentation, mannitol fermentation, sorbitol fermentation, amygdalin, rhamnose, and NO 2 . The alkaline phosphatase, leucine arylamidase, valine arylamidase, cystine arylamidase, trypsin, acid phosphatase, naphthol-AS-BI-phosphohydrolase and β-galactosidase activities were positive of new strain. New strain produced acid from d-arabinitol, l-arabinitol, d-adonitol, 5-ketogluconate, 2-ketogluconate, d-glucose, d-arabinose, l-arabinose, d-mannitol, dulcitol, d-mannose, d-ribose, d-trehalose, l-fucose, d-fructose, d-sorbitol, d-galactose, l-rhamnose, d-mannose, gluconate, d-xylose and N-acetyl-D-glucosamine. The major fatty acids of new strain were C 16:0 , summed feature 2 (iso-C 16:1 and/or C 14:0 3-OH), summed feature 3 (C 16:1 ω7c and/or C 16:1 ω6c), C 12:0 , C 17:0 cyclo, and C 14:0 .   Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creat iveco mmons .org/licen ses/by/4.0/.