The opportunistic pathogen Pseudomonas aeruginosa exploits bacterial biotin synthesis pathway to benefit its infectivity

Pseudomonas aeruginosa is an opportunistic pathogen that predominantly causes nosocomial and community-acquired lung infections. As a member of ESKAPE pathogens, carbapenem-resistant P. aeruginosa (CRPA) compromises the limited therapeutic options, raising an urgent demand for the development of lead compounds against previously-unrecognized drug targets. Biotin is an important cofactor, of which the de novo synthesis is an attractive antimicrobial target in certain recalcitrant infections. Here we report genetic and biochemical definition of P. aeruginosa BioH (PA0502) that functions as a gatekeeper enzyme allowing the product pimeloyl-ACP to exit from fatty acid synthesis cycle and to enter the late stage of biotin synthesis pathway. In relative to Escherichia coli, P. aeruginosa physiologically requires 3-fold higher level of cytosolic biotin, which can be attributed to the occurrence of multiple biotinylated enzymes. The BioH protein enables the in vitro reconstitution of biotin synthesis. The repertoire of biotin abundance is assigned to different mouse tissues and/or organ contents, and the plasma biotin level of mouse is around 6-fold higher than that of human. Removal of bioH renders P. aeruginosa biotin auxotrophic and impairs its intra-phagosome persistence. Based on a model of CD-1 mice mimicking the human environment, lung challenge combined with systemic infection suggested that BioH is necessary for the full virulence of P. aeruginosa. As expected, the biotin synthesis inhibitor MAC13772 is capable of dampening the viability of CRPA. Notably, MAC13772 interferes the production of pyocyanin, an important virulence factor of P. aeruginosa. Our data expands our understanding of P. aeruginosa biotin synthesis relevant to bacterial infectivity. In particular, this study represents the first example of an extracellular pathogen P. aeruginosa that exploits biotin cofactor as a fitness determinant, raising the possibility of biotin synthesis as an anti-CRPA target.


Introduction
Emergence and spread of antimicrobial resistance (AMR) become a serious challenge of global health concern. Before 2014, 700,000 peoples per year died of global AMR infections, and annual 10 million of deaths is estimated to be associated with drug-resistant infections unless AMR is tackled [1]. The Gram-negative bacterium, Pseudomonas aeruginosa, is a ubiquitous opportunistic pathogen that frequently causes nosocomial and community-acquired infections. In fact, P. aeruginosa is a predominant causative of chronic lung infections in cystic fibrosis (CF) patients, with infection in up to 70% of adult CF patients [2][3][4]. It is also noted that rapid dissemination of carbapenem-resistant P. aeruginosa (CRPA) is a major threat in clinic settings, compromising the limited therapeutic options [5,6]. Therefore, P. aeruginosa is included by the World Health Organization (WHO) into an 'ESKAPE' panel of pathogens, which are critically prioritized to tackle AMR [1]. The successful infection of P. aeruginosa largely relies on the production of virulence-associated components (e.g., pyocyanin [7] and biofilms [8,9]) and its regulatory networks including two-component systems [10,11] and quorum sensing [9,12]. Essentially, P. aeruginosa dictates certain metabolic fluxes to circumvent host immune defenses and antimicrobial killing, and thus benefits its colonization and proliferation during infections [13,14]. In light that the complex interplay of bacterial metabolisms occurs at infection sites, deep understanding of P. aeruginosa metabolic states [exemplified with biotin [15][16][17][18] and lipoic acid [19,20]] might offer alternative strategies to prevent and intervene the severe infections caused by this extracellular pathogen [14,21].
The water-soluble B vitamin cofactor, biotin is widely-distributed in all the three domains of life [22,23]. As a sulfur-containing, seven-carbon fatty acid derivative, this covalently-linked coenzyme plays critical roles in the CO 2 transfer between carboxylation and decarboxylation reactions involved in central metabolisms, including fatty acid biosynthesis, glucogenesis, and amino acid catabolism [24,25]. To date, six biotin-requiring enzymes are identified [26], namely i) acetyl-CoA carboxylase (ACC) [25,27]; ii) propionyl-CoA carboxylase (PCC) [28]; iii) pyruvate carboxylase (PC) [29,30]; iv) 3-methylcrotonyl-CoA (MCC) [31]; v) geranyl-CoA carboxylase (GCC) [32]; and vi) urea carboxylase (UC) [33]. Among them, ACC is regarded as a promising drug target against numbers of diseases (such as obesity plus type 2 diabetes) [26,34]. Mutations in either PCC or MCC can cause metabolic disorders in human neurodevelopment [35][36][37]. It is also noted that biotin, which serves as an essential micro-nutritional element, is generally produced by most of bacteria, fungi, and plants, whereas not in mammals and birds [38]. Increasingly-accumulated evidence supported that biotin is a nutritional virulence factor for certain bacterial pathogens [16][17][18]39] and that its metabolism behaves as an attractive target against severe bacterial infections [40][41][42][43]. Intriguingly, biotin is found to mediate host-microbiome interaction, and regulates intestinal stem mitosis [44]. This is in part (if not all) consistent with the clinical observation that the maintenance of gut microbiota biotin metabolism benefits the metabolic status of patients with severe obesity [45]. Therefore, it seems very true that biotin is an old vitamin but possesses new roles in the crosstalk of nutritional sensing with human health and/or metabolic diseases.
In this study, we aimed to examine the contribution of biotin synthesis to P. aeruginosa virulence. Genomic context and functional assignment suggested the existence of an "BioC-BioH" early pathway for biotin synthesis in P. aeruginosa (Fig 1A and 1B). Unlike the paradigm BioH that is encoded by the free-standing bioH in E. coli, the counterpart of P. aeruginosa is clustered with bioC in an operon (Fig 1A) [56]. Cao and coworkers reported the in vitro enzymatic activity of P. aeruginosa BioH and pointed out its expression is independent of genomic context [56]. However, the question whether genetic removal of the gatekeeper render P. aeruginosa biotin auxotrophic awaits answering. More importantly, the role of biotin synthesis in P. aeruginosa infectivity is poorly understood. Here we report that this is the case, and close the knowledge gap in the context of biotin metabolism along with bacterial virulence. This constitutes an additional example for biotin as a limited/nutritional virulence factor.

Diversified distribution of 'bioC-bioH' pair
The machinery of 'BioC-BioH' is a canonical route engaged in the formation of pimeloyl-ACP methyl ester (M-C7-ACP), a cognate precursor for biotin synthesis (Fig 1A and 1B). A modified type II fatty acid synthesis (FASII) pathway is hijacked by BioC and BioH [47]. In this case, BioC O-methyltransferase introduces a SAM-derived methyl moiety to the ω-carboxyl group of malonyl-CoA, giving an atypical primer malonyl-CoA methyl ester dedicated to two rounds of FASII cycles [46]. As a result, the methyl group of M-C7-ACP is no longer required, and eliminated by BioH demethylase to produce C7-ACP, a primer for late step of biotin synthesis catalyzed successively by BioF/A/D/B (Fig 1B) [24,47]. Genome analysis unveils that A role of PA0502 in biotin synthesis pathway A. Genetic context of Pseudomonas aeruginosa bioH (PA0502) and its counterparts in certain microorganisms B. A model for 'BioC-BioH' path of biotin synthesis in P. aeruginosa. C. Expression of PA0502 allows growth of the biotin auxotroph of E. coli ΔbioH on the non-permissive condition of M9 minimal medium. D. The removal of PA0502 renders P. aeruginosa biotin auxotrophic. A representative result from three independent experiments (in panels C & D) is given. E. Growth curves of the E. coli ΔbioH strains with or without plasmid-borne bioH (PA0502). F. Growth analyses of P. aeruginosa ΔbioH mutant and its complemented strain. As for plotting growth curves, the data is expressed in means ± standard deviation (SD) of three independent experiments (in panels E & F). Designations: SAM, S-adenosylmethionine; SAH, S-Adenosylhomocysteine; ACP, acyl carrier protein; FASII, Fatty acid synthesis type II; FabH, β-ketoacyl-ACP synthase III; FabF, β-ketoacyl-ACP synthase II; FabG, 3-keto-acyl-ACP reductase; FabZ, β-hydroxy-acyl-ACP dehydratase; FabI, enoyl-ACP reductase; BioC, Omethyltransferase of malonyl-ACP; BioH, demethylase of pimeloyl-ACP methyl ester; BioF, 8-

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Pseudomonas BioH is a fitness determinant the genetic organization of 'bioC-bioH' loci varies dramatically in diverse bioH-carrying bacterial species (Fig 1A). Totally, four types of genomic contexts are assigned to 'bioC-bioH' pair. The paradigm pattern refers to the bioA/BFCD operon of E. coli and Vibrio species, along with the free-standing bioH and birA (Fig 1A).
It is noted that BirA acts as a bifunctional biotin operon repressor having an additional activity of biotin-[acetyl-CoA-carboxylase subunit B, AccB] ligase [57,58]. In the Legionnaires diseases-causing bacterium, Legionella pneumophila, it gives a bioA/BFHD cluster, almost identical to the prototypic version of bioA/BFCD. The only exception lies in that bioC of E. coli is replaced with BioH of L. pneumophila, and vice versa (Fig 1A). It represents a second mode for 'bioC-bioH' distribution. In contrast to the paradigmatic version, the bio cluster of P. aeruginosa seems to be more domesticated because that bioH (PA0502) is also integrated, forming a unique bioBFHCD operon (Fig 1A). The genetic organization of bioBFHCD cluster can assure synergistic expression of BioC and BioH, the two enzymes responsible for primary step of biotin synthesis, benefitting efficient production of biotin [56]. In this case, unlike the bioA of E. coli that is encoded in an operon, the counterpart of Pseudomonas remains scattered on the chromosome and is exempt from the regulation of BirA bifunctional repressor (Fig 1A). This can be the third style of 'BioC-BioH' organization. Intriguingly, a similar scenario is seen in the soil bacterium Cellvibrio japonicus, and the carbohydrates-degrading marine bacterium Saccharophagus degradans (Fig 1A). However, bioH and bioC that are supposed to be two adjacent genes, appear to be fused into a single gene bioHC (Figs 1A and S1). Namely, they include CJA_0428 for C. japonicus, and Sde_3137 for S. degradans (Fig 1A). Here, the presence of fusion BioHC is provisionally termed as the fourth form of 'BioC-BioH' combination. Overall, the unexpected diversity is displayed among the genomic arrangement of bacterial 'BioC-BioH' paths.

Essentiality of bioH (PA0502) for P. aeruginosa viability
Unlike BioC that determines methyl malonyl-CoA to enter FASII as a disguised primer, BioH functions as a gatekeeper enzyme of biotin synthesis in that it informs the resultant product M-C7-ACP to exit the ongoing FASII cycle via demethylation (Fig 1B). To test the role of bioH (PA0502) in vivo, we performed two sets of genetic systems (E. coli and P. aeruginosa). As expected, arabinose-induced expression of bioH enables the biotin auxotroph of E. coli ΔbioH mutant to grow in a chemically-defined M9 medium lacking biotin (Fig 1C). This is generally consistent with an observation by Cao and coworkers [56]. The deletion of bioH renders P. aeruginosa biotin auxotrophic, and plasmid pAK1900-borne PA0502 expression restores the impaired growth phenotype the ΔbioH mutant, at a comparable level of the parental strain PAO1 (Fig 1D). Similar scenarios were seen with the measurement of growth curves. Namely, i) the introduction of bioH into E. coli ΔbioH mutant confers the re-gain of robust growth in biotin-lacking liquid media (Fig 1E); and ii) genetic removal of bioH impairs bacterial viability of P. aeruginosa ΔbioH on non-permissive growth condition (Fig 1F). In fact, growth defection of ΔbioH mutants is restored by the presence of exogenous biotin (Fig 2A). Unlike E. coli that requires biotin at minimal level of 0.5-1.0 nM, the opportunistic pathogen P. aeruginosa, physiologically demands the addition of exogenous biotin at 10 to 20-fold higher level (Fig 2A). Combined with the earlier observations of Cao et al. [56], our genetic evidence underscores the physiological role of bioH in P. aeruginosa biotin synthesis.

Physiological demand of biotin by Pseudomonas
An ELISA kit-based measurement revealed that cytosolic biotin in P. aeruginosa of mid-log phase is at over 3-fold higher level compared with that of E. coli (Fig 2B). It is thus reasonable

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Pseudomonas BioH is a fitness determinant to ask the question whether or not the much higher demand of biotin by P. aeruginosa is implicated into the existence of more biotin-requiring enzymes (Fig 2A and 2B). To test this hypothesis, we conducted genome-wide search for biotinylated proteins. As a result, five hits The requirement of biotin and protein biotinylation for P. aeruginosa. A. P. aeruginosa physiologically demands biotin at the level of 10 nM, 10-fold higher than that of E. coli. 0.5-1.0 nM biotin can restore growth of the biotin auxotrophic strain, E. coli ΔbioH mutant. In contrast, over 10 nM biotin is required to favor the appearance of P. aeruginosa ΔbioH mutant on the non-permissive growth condition lacking biotin. B. Biotin determination suggested that P. aeruginosa has much higher level of cytosolic biotin than E. coli does. Bacterial cultures in mid-log phase were sampled for the preparation of crude extracts used in cytosolic biotin determination. Data was expressed in an average ± standard deviations (SD). Each dot represented an independent measurement of biotin level. C. Sequence logo of biotinylation sites ubiquitously conserved in biotin-requiring enzymes of P. aeruginosa. Genome-wide mining of P. aeruginosa reveals five putative biotinylated enzymes, namely PA1400, PA2012, PA2891, PA4847, and PA5435 (S1 Table). D. Streptavidin blot analyses for crude extracts of E. coli and P. aeruginosa. Unlike E. coli displaying a well-known AccB subunit with biotinylation, the cytosol extract of P. aeruginosa is featuring with the presence of multiple biotinylated proteins. E. SDS-PAGE (12%) profile for three biotinylated enzymes (PA1400, PA2012, and PA2891). Three of five predictive biotinylated enzymes were overexpressed, purified, and judged with SDS-PAGE (12%). F. Western blot analysis of the three recombinant proteins (PA1400, PA2012, and PA2891) using anti-6x His primary antibody. G. Use of streptavidin blot to determine the biotin modification of the three recombinant proteins (PA1400, PA2012, and PA2891). Designations: CΔbioH, a genetically-complemented strain of the E. coli ΔbioH mutant with P. aeruginosa PA0502; CΔPA0502, the genetically-complemented strain of the P. aeruginosa ΔPA0502 mutant carrying a plasmid pAK1900-borne PA0502. https://doi.org/10.1371/journal.ppat.1011110.g002

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Pseudomonas BioH is a fitness determinant of P. aeruginosa were returned, all of which feature with a conserved motif (EAMKME) containing the constant lysine (K) residue biotinylated (Fig 2C). Namely, these enzymes include PA1400 (pyruvate carboxylase), PA2012 (α-subunit of methyl crotonyl-CoA carboxylase), PA2891 (α-subunit of geranyl-CoA carboxylase), PA4847 (AccB, biotin carboxyl carrier protein), and PA5435 (the probable transcarboxylase subunit) (S1 Table). To verify the bioinformatic output, we carried out streptavidin-based blot using bacterial crude extract. As expected, only one band of protein biotinylation was detected from the positive control strain, E. coli that is well-known in the biotinylated subunit of AccB (Fig 2D). It was noted that multiple bands of biotinylated proteins appear in our streptavidin blot for the crude extract derived from P. aeruginosa PAO1 (Fig 2D). Among them, three protein candidates (PA1400, PA2012, and PA2891) were selected for further consolidation of biotin modification. All the three recombinant enzymes were overexpressed and purified to homogeneity (Fig 2E). Their identities were respectively validated using western blot with anti-6x His primary antibody (Fig 2F). Meanwhile, streptavidin blot confirmed that they consistently contain biotinylated form ( Fig  2G). The data benefits our understanding of physiological explanation for the relatively-high demand of biotin by P. aeruginosa (Fig 2). In fact, similar scenarios had already been seen with the plant pathogen, Agrobacterium tumefaciens [59] and the human pathogen surrogate, Mycobacterium smegmatis [60,61]. Therefore, the accumulated evidence enabled us to raise the possibility that an arsenal of certain pathogens requires high-level of biotin for its central metabolism in an adaptation to the harsh host environments.

Enzymatic activity of P. aeruginosa BioH
An N-terminal hexa-histidine (6x His)-tagged version of P. aeruginosa BioH (PA0502) protein was overexpressed and purified to homogeneity (S2A Fig). Using a Superdex 75 column, gel filtration analysis elucidated that the wild-type BioH protein is eluted at the position of~12.5 ml (S2B and S3A Figs), which migrates relatively-slower than the fatty acid-binding protein FakB2 of a known monomer (~11.5 ml,~33 kDa). This suggested that BioH of P. aeruginosa appears as a monomer (~25 kDa), which is largely consistent with the monomeric solution states of the paradigm E. coli BioH [50] and its isoenzyme BioJ [17,54]. As described with BioJ [17], we also tested activity of P. aeruginosa BioH with its physiological substrate M-C7-ACP. The reaction mixture was separated with conformationally-sensitive gel of 0.5 M urea/17.5% PAGE (pH9.5), in which the product C7-ACP is supposed to migrate slower than its reactant M-C7-ACP due to the loss of methyl moiety [47]. Clearly, the in vitro activity of P. aeruginosa BioH behaves in a dose-dependent manner (S2C Fig). Of note, full activity of enzymatic demethylation can be reached when the P. aeruginosa BioH is added as low as 50 nM (S2D Fig). Subsequently, MALDI-TOF mass spectrometry was used to differentiate P. aeruginosa BioH reaction mixture. As predicted, the reactant M-C7-ACP exhibited a unique spectrum of 9002.281 m/z, close to its theoretical value of 9003.3 (S2E Fig), and the product of C7-ACP whose theoretical value is 8989.3 m/z was assigned with a distinct mass profile of 8988.772 m/z (S2F Fig). Collectively, along with the enzymatic analyses of Cao et al. [56], this study biochemically defined Pseudomonas BioH is a functional demethylase of M-C7-ACP.

Catalytic triad of P. aeruginosa BioH
BioH is a member of the α/β-hydrolase family with characteristics of a catalytic triad. Multiple sequence alignment of P. aeruginosa BioH with its homologues revealed the presence of three conserved resides forming a putative catalytic triad, namely S66, D189, and H216 (Figs 3A, S1 and S3A). The predicted structure of P. aeruginosa BioH with AlphaFold enabled us to illustrate a catalytic triad of which the configuration is almost identical to the counterpart of the

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Pseudomonas BioH is a fitness determinant is generated with PyMol, and the structural model of PA0502 was predicted with Alpha-fold [79]. The catalytic triad of E. coli BioH consists of S82, D207, and H235. Equivalently, they denote S66, D189, and H216 in PA0502. B. The in vitro enzymatic assays reveal that none of three single mutants defective in catalytic triad is active. Namely, the three single mutants of PA0502 include S66A, D189A, H216A. The conformationally-sensitive gel of 0.5 M urea/17.5% PAGE (pH9.5) was applied to distinguish the product C7-ACP from its reactant M-C7-ACP. The minus symbol denotes no addition of PA0502. The positive control refers to the addition of wild-type PA0502 (50 nM). The triangle on right hand denotes varied level of PA0502 mutant (ranging from 0.5, 5, 50, to 500 nM). C. Growth curve analysis of P. aeruginosa PAO1 suggested that catalytic triad is essential for PA0502 activity. The graph was plotted with data collected from three independent measurements, and presented in an average ± standard deviations (SD). D. The alanine substitution of catalytic triad inactivates the ability of PA0502 to restore bacterial growth of the biotin auxotrophic strain ΔPA0502 on the non-permissive, biotin-deficient condition of M9 minimal medium. https://doi.org/10.1371/journal.ppat.1011110.g003

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Pseudomonas BioH is a fitness determinant paradigm E. coli BioH (S82, D207, and H235, in Fig 3A). To test the function of this catalytic triad, we generated three single BioH mutants (S66A, D189A, and H216A, in S3A Fig), along with its wild-type whose identity was validated with mass spectrometry (S3B Fig). Except for the BioH mutant (H216A) that behaves as its wild-type to form a monomer, the remaining two mutated versions (S66A and D189A) are constantly eluted at the position of polymer in the analysis of size exclusion chromatography (S3A Fig). As expected, all the three mutants are enzymatically inactive with its cognate substrate M-C7-ACP, regardless of their solution structures (Fig 3B). Next, we examined the roles of these mutants in vivo by visualizing the viability of engineered E. coli carrying plasmid-borne PA0502 and its derivatives. Unlike its parental version PA0502, none of its three mutants with certain defection in catalytic triad can allow bacterial occurrence of the biotin auxotroph P. aeruginosa ΔbioH on the non-permissive condition of both defined M9 liquid media (Fig 3C) and M9 minimal agar plates (Fig 3D). Thus, this represents a functional proof of the catalytic triad of P. aeruginosa BioH.

P. aeruginosa BioH enables biotin synthesis in vitro
To visualize its metabolic role of P. aeruginosa BioH, we established the DTB/biotin bioassay coupled with the in vitro reconstituted system for DTB/biotin synthesis (Fig 4A and 4C) as described by different research groups [17,47,62]. In this BioH-including system, the cell-free crude extract was prepared from the biotin auxotroph of E. coli ΔbioH, providing an array of enzymes of FASII and late steps of biotin synthesis (Fig 4B). The detection of DTB/biotin production relies on an indicator strain FYJ283, the ΔbioBFDA deletion mutant of A. tumefaciens we previously developed (S2 Table) [49,59]. In principle, i) the indicator strain FYJ283 cannot grow on biotin-limiting M9 minimal agar plates, unless exogenous DTB/biotin is supplied; ii) bacterial growth of the reporter strain on such non-permissive condition demonstrates the generation of DTB/biotin in the reconstituted system in vitro; and iii) the biotin-dependent viability of an indicator strain reduces 2,3,5-triphenyl tetrazolium chloride (TTC), releasing an . Use of 2,3,5-triphenyl tetrazolium chloride (TTC, 0.001%) proceeds to probe bacterial viability of the ΔbioBFDA mutant. In principle, the occurrence of biotin is verified by the release of insoluble red pigment reduced from TTC that is precipitated to surround viable cells [17]. To prevent biotin cross-contamination, quadrant sectored plates were used, each sector of which is placed with a paper disc to spot biotin and/or DTB/biotin reaction mixture. https://doi.org/10.1371/journal.ppat.1011110.g004

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Pseudomonas BioH is a fitness determinant insoluble red pigment circle precipitated around alive cells. As expected, the indicator strain FYJ283 cannot be viable in the absence of exogenous biotin, but slightly grows in the presence of 1 pmol biotin (Fig 4A). It was noted that the supplementation of biotin (up to 5 pmol) can give robust bacterial growth (Fig 4A). As for the crude extract and PBS buffer used in the in vitro system, no contamination of trace DTB/biotin was sensitized with the indicator strain FYJ283, because of lacking an insoluble red pigment circle (Fig 4C). In contrast, the reaction mixture (10 μl)-arising DTB/biotin is enough to allow bacterial growth of the biotin auxotrophic strain, i.e., A. tumefaciens ΔbioBFDA mutant (Fig 4C). It is concluded that P. aeruginosa BioH enables the in vitro reconstitution of biotin synthesis.

BioH is necessary for bacterial survival within macrophages
In general agreement with the fact that the pathway of biotin synthesis and utilization participates in the intracellular pathogen Francisella infectivity [16][17][18], the BioA inhibitor MAC13772 was found to attenuate virulence of human pathogen P. aeruginosa by interfering the late step of biotin biosynthesis [15]. Thus, it is reasonable to speculate the involvement of bioH (PA0502) in the replication of P. aeruginosa within macrophages. To test this hypothesis, we carried out the analyses for macrophage infections. Murine bone marrow-derived macrophages (mBMDM) were prepared as Zhu et al. [63] described with little change. The prior exploration informed us that the appropriate value for multiplicity of infection (MOI) is estimated to be 5:1 (P. aeruginosa PAO1: mBMDM cell). In addition to the wild-type (WT) PAO1, the two derivatives of P. aeruginosa used to challenge mBMDM cells included i) the ΔbioH mutant, and ii) its complemented strain CΔbioH. Here, 6 hours of co-cultivation ensured bacterial invasion into macrophages. After 1 h post-infection, we noted that the intraphagosome persistence of ΔbioH is indistinguishable when compared with its parent type and the CΔbioH strain (Fig 5A). This indicated no role of the bioH in immunological invasion of P. aeruginosa PAO1. However, the intracellularly-phagocytosed cells of the ΔbioH mutant are almost completely cleaned at 24 h post-infection. This was evidenced by the fact the ratio of

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Pseudomonas BioH is a fitness determinant CFU (24 h:1 h) is around 0.5 for the ΔbioH mutant, which is roughly 20-fold lower than that of the wild-type (Fig 5B). Furthermore, genetic complementation of the ΔbioH mutant restored its reproduction within mBMDM macrophage to the level of wild-type (Fig 5B). Thus, it is likely that bioH is critical for the replication of P. aeruginosa within macrophages.

The repertoire of dynamic biotin levels within mouse tissues
The recent finding of Carfrae et al. [15] informed us that biotin level in mouse plasma is estimated to be 40-fold higher than human plasma. As Carfrae and colleagues [15] conducted, we also employed an ELISA-based Biotin Quantitative Determination Kit to investigate the abundance of biotin pools in a panel of samples. First, we analyzed plasma biotin from four healthy individuals, and found its concentration varying from 1.38 to 2.38 ng/ml (equivalently 5.65 to 9.74 nM, Fig 6A). Second, the average biotin level in mouse plasma of CD-1 (5-6 week) lineage was measured to be 10.61 ng/ml (i.e., 43.43 nM), which is 6-fold higher compared to the counterpart (average value: 1.7 ng/ml; 6.96 nM) in human plasma (Fig 6B). This generally supported the proposal by Carfrae et al. [15] regarding the variation in plasma biotin levels. Whereas we believed that the discrepancy in fold change is mainly due to the difference on human plasma sources used in the two studies. Third, we quantified biotin levels of eight mouse tissues, namely heart, liver, spleen, lungs, kidneys, large intestine, small intestine, and stomach (Fig 6C). Except that both liver and large intestine display relatively-higher biotin level (~20 ng/g tissue, Fig 6C), all the remaining 6 tissues possess biotin at close levels of~10 ng/g tissue, which is similar to that of mouse plasma (Fig 6B and 6C). Finally, we probed biotin abundance in three kinds of mouse organ contents, which separately refer to large intestine, small intestine, and stomach. Intriguingly, biotin levels in these organ contents (300 to 400 ng/ ml) were observed to be approximate 20-fold higher than those of the corresponding organs (Fig 6C and 6D). When compared to mouse plasma, they contain biotin at nearly 30 to 40-fold higher levels (Fig 6B and 6D). This can be explained partially by the fact that they are places where a large amount of biotin produced by the gut microbiota are secreted to feed certain biotin-consuming residents [44,64].
The use of an experimental model mimicking human biotin levels is a prerequisite for evaluating a role of bioH in P. aeruginosa infection. As recommended by Carfrae and coworkers [15], CD-1 mice were intraperitoneally administered with streptavidin (~2 mg/kg). Dynamic level of mouse biotin in vivo was monitored during the 12 h period post-administration with streptavidin. As expected, the mouse plasma biotin concentration remains at low level of less than 2 ng/ml, comparable to human plasma (Fig 7A). In particular, the lowest level of plasma biotin that is 0.79 ng/ml (3.23 nM), occurs at 1 h post-administration with streptavidin ( Fig  7A). Similar scenarios were observed with the contents arising from the bellowed organs, namely large intestine (Fig 7B), small intestine (Fig 7C), and stomach (Fig 7D). Also, the biotin concentrations dramatically dropped at 1 h after an intraperitoneal administration with streptavidin, regardless of its elevation over time (Fig 7A-7D). The landscape of biotin dynamic alteration was reproduced in the eight mouse tissues we examined (S4 These data combined with observations of Carfrae et al. [15] revealed that the challenge of CD-1 mice with P. aeruginosa at 1 h after the pre-administration with streptavidin (2 mg/kg) is supposed to mostly mimic human infection of with P. aeruginosa. In summary, we presented a repertoire of dynamic biotin levels in various organs/tissues of CD-1 mice. Along with findings of other research groups, this observation might benefit understanding multi-faceted roles of biotin in bacterial infection [15], and pathophysiology of mammalian animals [44,64].

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Pseudomonas BioH is a fitness determinant

Removal of bioH attenuates the pathogenicity of P. aeruginosa in a murine model of systemic infection
The experimental model for systemic infections we established here denotes an intraperitoneal challenge of CD-1 mice with 1x 10 7 CFU of P. aeruginosa, in which i) a pre-administration with 2 mg/kg of streptavidin proceeds one hour earlier, and ii) bacterial loads are determined by plating the dilution of homogenized tissues from the mouse euthanized 12 h post-infection (Fig 8A). In addition to the WT P. aeruginosa PAO1 strain as a positive control of strong invasiveness, the mutant strain of ΔbioH was evaluated, as well as its genetically-complemented strain, CΔbioH (S2 Table). Here, five different tissues/organs were sampled for the analyses of Relatively-low level of biotin is measured in human plasma samples. Blood plasmas of four human individuals (H1 to H4) were subjected for the routine biotin measurement. Biotin level of human plasma varies from 1.38 to 2.38 ng/ml (i.e., 5.65 nM to 9.74 nM), which is generally consistent with the observation with human biotin by Carfrae and coworkers [15]. B. Contrasting plasma biotin level in CD-1 mice and humans. The average biotin level (10.61 ng/ml; 43.43 nM) in mouse plasma is around 6-fold higher than the counterpart (1.70 ng/ml; 6.96 nM) in the human individual. C. The determined level of biotin assigned to an array of tissues of CD-1 mice Totally, eight tissues examined here include heart, liver, spleen, lungs, kidneys, large intestine, small intestine, and stomach. D. Measurement for biotin level in organ contents from CD-1 mice. Biotin level was measured using CD-1 mice (5-6 weeks). The organ contents were separately collected from large intestine, small intestine, and stomach. All the data are expressed in means ± SD, and assayed by two-tailed analysis of variance. Clearly, biotin level (300-400 ng/ml) in organ contents is over 20-fold higher than the equivalents (10-20 ng/ml) in associated tissues. https://doi.org/10.1371/journal.ppat.1011110.g006

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Pseudomonas BioH is a fitness determinant bacterial loads, namely heart (Fig 8B), liver (Fig 8C), spleen (Fig 8D), lungs (Fig 8E), and kidneys (Fig 8F). The bacterial loads of the ΔbioH mutant in all examined tissues declined greatly in comparison with its parental strain, and such a growth defect within host can be largely restored by genetic complementation of a plasmid-borne bioH (Fig 8B-8F). We also examined bacterial loads in the routine model of CD-1 mice without the pre-administration with streptavidin ( S5A Fig). As predicted, removal of bioH failed to exert any obvious effect on bacterial burden in the infected mouse tissues, including heart (S5B Fig), liver (S5C Fig), spleen (S5D  Fig), lungs (S5E Fig), and kidneys (S5F Fig). It demonstrated that we have success in the  [15] recommended, which is supposed to reduce the biotin levels in mouse plasma and other organ contents. All the data are given in means ± SD, and assayed by two-tailed analysis of variance. https://doi.org/10.1371/journal.ppat.1011110.g007

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Pseudomonas BioH is a fitness determinant

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Pseudomonas BioH is a fitness determinant establishment of systemic infection model of CD-1 mice mimicking the human environment, initially proposed by Carfrae and colleagues [15]. Importantly, the data indicated that the BioH gatekeeper links bacterial biotin synthesis to P. aeruginosa persistence within CD-1 mouse that mimics human plasma biotin levels.

Deletion of bioH reduces the virulence of P. aeruginosa in mouse lung infections
To further determine the role of bioH in P. aeruginosa virulence, we adopted a mouse lung infection model. In light that the abundance of biotin is 6-fold (40-fold in the measurement of Carfrae et al. [15]) higher in mouse plasma compared to human plasma (Fig 6B), we also leveraged streptavidin to mimic human biotin environment in CD-1 mice prior to lung infections (Fig 9A). Apart from the negative control group inoculated with PBS buffer, the remaining three groups of mice (10/group) were separately challenged with WT/PAO1, ΔbioH, and CΔbioH. Unlike the negative group of which all the 10 mice are not sacrificed within the whole monitoring period of 48 hours (Fig 9A and 9B), none of mice from the group injected with wild-type PAO1 (and/or the complemented strain CΔbioH) survived at 18 h post-infection ( Fig  9B). The survival ratio of the group challenged with ΔbioH was 80% (8/10) at 18 h post-infection, and two mice remained alive by the end of infection (Fig 9A and 9B). This suggested that the bioH plays a modest role in P. aeruginosa pathogenicity with CD-1 mouse model. The differences in the CFUs (substantial) versus survival curves (not substantial) could be a reflection of this point, where P. aeruginosa initially can be largely cleared in the host "nutrient adjustment period", but might eventually scavenge/compete host biotin to maintain an infection.
Next, we settled out to evaluate pathological roles through measuring i) bacterial load in lungs and ii) pulmonary edema at 12h post-infection. First, we found that the level of ΔbioH collected from lungs is over 2-log lower than the wild-type PAO1 (Fig 9C). As expected, the replication defect of ΔbioH in lungs was significantly reversed upon the introduction of a plasmid-borne PA0502 (Fig 9C). The symptom of pulmonary edema was routinely approached with the ratio of wet weight of lung to its dry weight. As for the lungs infected with wild-type PAO1, the ratio was calculated to be about 8, much higher than the equivalent value (~5) of negative control group inoculated with PBS buffer (Fig 9D). Whereas the ΔbioH-infecting group gave the count of~5, quite close to that of the PBS group. In the group challenged with the CΔbioH strain, the ratio was restored to the level of the PAO1 strain (Fig 9D). Clearly, the inactivation of bioH potently compromised pulmonary edema, a hallmark of severe lung injuries.
Using histopathological analyses of lungs, we observed that in contrast to the negative control (i.e., PBS group) that displays an intact alveolar structure (Fig 9E), the wild-type PAO1-injecting mice exhibited intensive lung symptoms featuring with thicken alveolar septa and inflammatory cell accumulation in certain regions (Fig 9F). Not surprisingly, the lung section arising from the group infected with ΔbioH mutant presented almost intact alveolar structure except for particular multifocal hemorrhage and homogeneously pink infiltration (Fig 9G). Of note, the re-introduction of plasmid-borne PA0502 expression also caused similar pathological lesions as the parental strain PAO1 does (Fig 9H). The combined data allowed us to conclude that BioH (PA0502) is important, if not essential, for lung infections of mice with P. aeruginosa PAO1.

Pseudomonas biotin synthesis is a druggable pathway
We next assessed the vulnerability of P. aeruginosa by intervening biotin metabolism. In addition to the representative virulent strain, P. aeruginosa PAO1, we also included two clinical

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Pseudomonas BioH is a fitness determinant

Fig 9. Intranasal infections of CD-1 mice elucidated that BioH (PA0502) plays a role in P. aeruginosa virulence. A.
A strategy designed for mice challenge with P. aeruginosa via an intranasal administration. As described in Fig 8A, the cartoon models were generated by ourselves. B. Survival curves of CD-1 mice infected with various strains of P. aeruginosa. C. Bacterial load of the lung tissues from mice post-infection with three types of P. aeruginosa strains. D. Relative ratio (wet weight: dry weight) of the lung tissues from mice post-infection with three types of P. aeruginosa strains. Data are shown as means ± SD, and were analyzed in two-tailed way of variance via Mann Whitney test. Representative histopathology of the lung tissue from mice inoculated with the blank control PBS (E) and the positive control, wild-type strain PAO1 of P. aeruginosa (F). G. Pathological section of the lung tissue from mice infected with the ΔbioH mutant of P. aeruginosa PAO1. H. Histopathological analyses of the lung tissues collected from mice challenged with the complemented strain (CΔbioH) of the P. aeruginosa ΔbioH mutant. The lung tissues were collected from infected and placebo mice, which were killed and necropsied on 2 dpi. Lung samples were stored in formalin for 7 days and subsequently embedded in paraffin. Finally, hematoxylin and eosin were applied in staining of sectioned samples. PBS denotes the blank control group, and WT is the positive control group. Scale bars are labeled on each

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Pseudomonas BioH is a fitness determinant CRPA isolates (Pa-1 and Pa-2, in Fig 10A) in the assays. The insusceptibility to meropenem was attributed to the existence of bla KPC-2 (Fig 10B). Unlike the two strains PAO1 and Pa-2, Pa-1 seemed to be a natural mutant defective in pyocyanin production. Since MAC13772 is known to efficiently inhibit the activity of BioA, an important enzyme responsible for late step of biotin synthesis (Fig 10C) [65], we evaluated bacterial viabilities on the cultivation conditions containing varied levels of MAC13772 inhibitor. In general consistency with the description of Carfrae et al. [15], we observed that all the three examined strains of P. aeruginosa are inhibited greatly, regardless of carbapenem resistance (Fig 10D). The half-maximal inhibitory concentrations (IC50) of MAC13772 are 310.7 μM for PAO1, 565.1 μM for Pa-1, and 528.5 μM for Pa-2, respectively (Fig 10D). Similarly, the reduction in bacterial growth was also seen with LB medium treated with streptavidin to minimize the availability of free biotin ( Fig  10E). As anticipated, the biotin-eliminated LB medium enables the production of two Pseudomonas virulence factors [i.e., biofilm [66,67] and pyocyanin [68,69]]. On such condition, we thereafter investigated the MAC13772-stressed formation of biofilms and pyocyanin. Although the presence of MAC13772 inhibitor had no obvious role in modulating formation of Pseudomonas biofilms (Fig 10F), it significantly attenuated production of the other virulence factor pyocyanin (Fig 10G). Thus, we concluded that Pseudomonas biotin synthesis can be a druggable metabolic pathway.

Conclusions
Prior to this study, bacterial biotin metabolism has already been connected with successful infections of two notorious intracellular pathogens, namely i) the TB-causing bacterium, M. tuberculosis [40,70]; and ii) the life-threatening agent, F. tularensis [16][17][18]. The data we reported here represents a first proof that BioH, an important member of the toolbox of biotin synthesis enzymes, is critical for the pathogenesis of P. aeruginosa, an extracellular pathogen (Figs 5, 8 and  9). The prototypical C7-ACP methyl ester demethylase BioH functions as a gatekeeping enzyme in the canonical biotin synthesis pathway, because that it determines the switching from the modified FASII cycle to the late step of biotin biosynthesis (Fig 1B). Notably, the BioH of KPC-2-producing clinical P. aeruginosa with carbapenem resistance is identical to the counterpart of the model P. aeruginosa PAO1. Although that its expression and activity is independently of genetic context [56], removal of bioH renders P. aeruginosa PAO1 biotin auxotrophic (Figs 1 and 2). In spite that genomic environment of 'BioC-BioH' path markedly varies in diverse microbes, BioH is paired with BioC at the constant ratio of 1:1. The advantage of this genetic arrangement is to prevent wasteful production of two enzymes dedicated to the primary stage of biotin synthesis. Whereas a rare example of exception was recently discovered in Mycobacterium smegmatis, i.e., three BioH isoforms (BioH1 to BioH3) combined with a single BioC, are programed into an early stage of mycobacterial biotin synthesis [62]. Presumably, the redundance of BioH-like activities is originated from the domestication of certain α/β-hydrolase to gain this promiscuous role of hydrolyzing M-C7-ACP ester. The evolutionary advantage of redundant BioH isoenzymes for mycobacterial pathogens is to guarantee efficient biotin production within harsh host niche. This is because that the BioH action proceeds smoothly even one or two isoenzymes are impaired or hijacked by host immunity to do another job. panel. In the two groups of mice infected with WT (F) and CΔbioH (H), lung lesions displayed i) thicken alveolar septa (red arrows); ii) multifocal hemorrhage in certain alveolar cavities (blue arrows) and bronchiolar cavities (green arrows); iii) homogeneously pink infiltration in partial alveolar cavities (black arrows); and iv) inflammatory cell accumulation in certain alveolar spaces and cavities [including lymphocytes, macrophages and neutrophils (yellow arrows)]. Designation: WT, P. aeruginosa PAO1; ΔbioH, the ΔPA0502 mutant of P. aeruginosa PAO1; CΔbioH, the complemented strain of the P. aeruginosa ΔPA0502 mutant with a plasmid pAK1900-borne PA0502. https://doi.org/10.1371/journal.ppat.1011110.g009

Pseudomonas BioH is a fitness determinant
To the best of our knowledge, Carfrae et al. shed light on the previously-unknown human plasma environment, of which biotin is unexpectedly 40-fold lower than that of mouse model involved in our routine infection study [15]. In contrast, we found that plasma biotin concentration of CD-1 mice is around 6-fold higher than that of human plasma (Fig 6A and 6B). The discrepancy is probably due to the altered origin of human plasmas. Nonetheless, these data Unlike Pa-2 producing the secreted virulence factor pyocyanin, the clinical isolate Pa-1 is a natural mutant defective in pyocyanin synthesis. C. Scheme for MAC13772 known as an inhibitor of BioA, an important enzyme responsible for late stage of Pseudomonas biotin synthesis. In addition to crystal structure of BioA (PDB: 6ED7), chemical structure of BioA inhibitor, MAC13772 was given [15]. D. Measurement for IC50 of MAC13772 in the viabilities of two CRPA isolates and PAO1 virulent strain. E. 18h-growth biomass of three P. aeruginosa in the biotin-lacking LB stressed with IC50 of MAC13772. F. No effect on the virulence factor biofilm production exerted by MAC13772 in the biotin-lacking LB growth condition. G. Evidence that MAC13772 can interfere profoundly synthesis of the virulence factor pyocyanin in P. aeruginosa isolates. https://doi.org/10.1371/journal.ppat.1011110.g010

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Pseudomonas BioH is a fitness determinant benefited the establishment for infection model of mouse mimicking human niches. In particular, we presented a repertoire of distinct biotin levels in various mouse tissues and organ contents, which is helpful to understand interplay between P. aeruginosa and host in views of competing for metabolic nutrients/cofactors. Similar to those of plant pathogen A. tumefaciens [59] and human pathogen M. tuberculosis [61], P. aeruginosa encodes up to 5 biotin-requiring enzymes (S1 Table and Fig 2B-2G). This explains in part, if not all, why the physiological requirement of biotin in P. aeruginosa is 10 to 20-fold higher than that of E. coli having a single biotinylated protein, AccB (Fig 2A-2C). Like the paradigm E. coli BioH [47] and its unrelated isoenzyme BioJ [17], P. aeruginosa BioH can enable the in vitro reconstitution of biotin synthesis (Fig 4), verifying its biochemical role. These observations highlight the importance of biotin cofactor in central metabolism and pathophysiology of the opportunistic agent, P. aeruginosa. As for Francisella, the category A tier 1 select agent, the gatekeeper enzyme BioH is wellknown to play a role in survival and immunity escape from macrophages [17,18]. Different from Francisella that is a facultative extracellular bacterium, P. aeruginosa is an obligate extracellular pathogen that causes opportunistic human infections. The finding that P. aeruginosa BioH participates into bacterial infections allowed us to believe that de novo biotin synthesis might benefit intramacrophage persistence rather than phagosome-inside replication ( Fig  5A). Given the promiscuity of BioH demethylase, it can't rule out the possibility that certain non-specific substrate selectivity other than biotin synthesis might be involved in P. aeruginosa pathogenesis. Whereas alternative mechanisms remain to be defined in the near future.
The catalytic triad (S82, D207 & H235 for E. coli BioH) is ubiquitously present amongst diverse BioH orthologs (Figs S1 and 3A) and non-homologous isoforms, exemplified with Francisella BioJ [17] and Helicobacter BioV [55]. Apart from the contribution to its enzymatic activity, the two residues (S66 and D189) of P. aeruginosa BioH catalytic triad are unexpectedly found to be critical for the maintenance of its solution structure (S3A Fig). Thus, it is of much interest to test if a similar scenario is seen with the paradigm E. coli BioH and its non-closely relative BioJ. Apart from biotin synthesis route, the machinery of biotin utilization is also implicated into bacterial pathogenicity [16,71]. It was noted that the biotin protein ligase, Bpl appears to be an alternative front-line anti-TB drug target [40]. The extracellular pathogen P. aeruginosa possesses a bifunctional Bpl/BirA that is also a repressor for biotin synthesis. It is reasonable to ask the question if P. aeruginosa Bpl/BirA is a restricted/nutritional virulence factor. In this work, we also approved that the known BioA inhibitor MAC13772 are active with both PAO1 and clinical CRPA isolates (Fig 10). More importantly, this inhibitor profoundly interferes formation of a well-known virulence factor pyocyanin, regardless of KPC-2 carbapenem resistance (Fig 10B and 10G). Notably, our epidemiological screen returned a natural mutant (designated as Pa-1) of P. aeruginosa that is defective in pyocyanin synthesis (Fig 10A and 10G). However, the underlying mechanism awaits further exploration in the near future.
Collectively, genetic and infection studies of P. aeruginosa BioH posed a link between intramacrophagic biotin and rapid phagosomal persistence/escape. The success of bacterial biotin metabolism in clinical anti-TB translation trials [43], prompted us to believe BioH-including enzyme toolbox as a promising drug target that can re-sensitize CRPA in the development of lead compounds and front-line antibiotics.

Ethics statement
The maintenance and manipulation of the opportunistic pathogen Pseudomonas aeruginosa was carried out in the biosafety level 2 (BSL-2) laboratories from Zhejiang University School of

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Pseudomonas BioH is a fitness determinant Medicine, and Shanghai Institute of Materia Medica, Chinese Academy of Sciences. The analyses of mice infections were conducted under the relevant guidelines and regulations from the Administration of Affairs Concerning Experimental Animals approved by the State Council of People's Republic of China (11-14-1988). The protocols of animal study were reviewed and approved by the Institutional Animal Care and Use Committee (IACUC) of the Shanghai Public Health Clinical Center (permit 2013P201). The laboratory animal usage license numbers included SYXK-HU-2010-0098 (certified by Shanghai Committee of Science and Technology, and ZJU20220126 (licensed by Laboratory Animal Welfare and Ethics Committee of Zhejiang University). Under appropriate regulation, four samples of healthy human plasma were kindly provided by Clinical Laboratory of the 2 nd Affiliated Hospital (School Hospital Branch), Zhejiang University School of Medicine.

Antibacterial analyses of BioA inhibitor, MAC13772
The known BioA inhibitor MAC13772 was also used to approve the feasibility of Pseudomonas biotin biosynthesis as a promising druggable target [65]. In addition to the wild-type strain PAO1, two clinical P. aeruginosa isolates with carbapenem resistance were explored for the susceptibility to MAC13772. To figure out the resistance determinant, PCR assays were performed with a pair of bla KPC-2 -specific primers. As Carfrae and coworkers described [15], all the three strains (PAO1, Pa-1, and Pa-2) were grown in biotin-free M9 minimal medium supplemented with MAC13772 in series of dilution. As a result, the plotting of growth curves gave the half-maximal inhibitory concentration (IC50) of MAC13772. Following the treatment with Streptavidin [15], the biotinlacking LB medium was given. The resultant LB medium mixed with MAC13772 inhibitor at the IC50 level, acted as 'selective medium' for production of two virulence factors (i.e., biofilms and pyocyanin) in different Pseudomonas strains. The biofilms produced from static cultures, were stained with the dye crystal violet (0.1%), rinsed with water, and then quantified with a plate reader at one of the following 3 wave-lengths (550 nm, 570 nm or 590 nm) [66,67]. The pyocyanin secreted into medium, were routinely extracted with chloroform solution, and measured in a plate reader at 520 nm [68,69]. Finally, the value of biofilm/pyocyanin production is determined by calculating the ratio of OD590 (or OD520) to bacterial cell density (OD600).

Genetic inactivation and complementation of PA0502 in P. aeruginosa
The sucrose counterselection against levansucrase (SacB)-aided approach was employed to inactive the bioH (PA0502) in the strain PAO1 of P. aeruginosa. The two adjacent regions

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Pseudomonas BioH is a fitness determinant (~1kb) of PA0502 were PCR amplified with 2 sets of specific primers (PA0502-up-F/R plus PA0502-down-F/R), and then fused together through overlapping PCR with the pair of primers (PA0502-up-F/PA0502-down-R, S3 Table). The resultant overlapped DNA fragment of around 2kb was directly cloned into the gene replacement vector pEX18Ap via two cuts of EcoRI and HindIII [72,73], yielding pEX18Ap::PA0502-UD (S2 Table). Subsequently, the gentamicin resistance cassette (~1.8 kb) cut from pPS858 with BamHI, was inserted into pEX18Ap::PA0502-UD, giving the knock-out plasmid of pEX18Ap::PA0502-UGD (S2 Table). The resultant plasmid of pEX18Ap::PA0502-UGD was electroporated into PAO1 competent cells with the selection for gentamicin resistance. Colonies of interest were screened for gentamicin sensitivity and loss of sucrose (5%) sensitivity, which typically indicates a double crossover event and thus marks the occurrence of gene replacement. The PA0502 deletion mutant of PAO1, designated FYJ5201, was verified with multiplex PCR and direct sequencing of the PCR amplicon. Additionally, the bioH (PA0502)-coding sequence was introduced into pAK1900 vector via HindIII/XbaI cuts, generating a complementary plasmid pAK1900::bioH (S2 Table). Finally, the resultant plasmid was electroporated into FYJ5201 (PAO1, ΔbioH), producing a genetically-complemented strain FYJ5202 that expresses a plasmid-borne PA0502, pAK1900::bioH (S2 Table).

Protein expression, purification and gel filtration
The strain FYJ5210 bearing pET28a::bioH was grown to mid-log phase (OD600:~0.8), and then subjected to 10h of induction with 0.5 mM IPTG at 16˚C. The harvested bacterial cells were suspended with lysis buffer [20 mM Tris-HCl (pH8.0), 300 mM NaCl, 5% glycerol, 20 mM imidazole and 1 mM PMSF], and passed through 3 rounds of French Pressure Cell [62]. Following the removal of bacterial debris by the centrifugation at 16800 rpm for 1 h at 4˚C, the resultant lysates were incubated with Ni-NTA agarose beads pre-equilibrated with lysis buffer for 1 h [17,54]. After removing the contaminants, the SUMO-tagged BioH protein was eluted with the elution buffer [20 mM Tris-HCl (pH8.0), 300 mM NaCl, 5% glycerol and 300 mM imidazole]. To liberate the SUMO tag, the fusion protein of BioH was digested with ULPI enzyme in the reaction buffer [20 mM Tris-HCl (pH 8.0), 150 mM NaCl] overnight. The purity of the required BioH protein was determined with 15% SDS-PAGE, and its solution state was determined using gel filtration with a Superdex 75 column.

Western blot analysis
To probe the presence of multiple biotinylated proteins, the cell lysates of P. aeruginosa PAO1 were subjected to the analysis of Western blot using Streptavidin AP-conjugate (Roche) as the primary antibody (1: 1000). The resultant chemiluminescent signals were detected with CDP-Star substrate [75]. Because that the recombinant biotin-requiring enzymes is tagged with N-terminal hexa-histidine, Western blot was carried out using mouse anti-6x his primary antibody, along with the goat anti-mouse IgG secondary antibody, prior to the assay of Streptavidin blot [59,61].

Macrophage infections
As Zhu et al. described [63], Mouse Bone Marrow-Derived Macrophages (mBMDM) were prepared. Briefly, the cells flushed out from femurs and tibiae of 8-week-old female C57BL/6 mice, were cultured in DMEM media containing 10% heat inactivated fetal bovine serum (FBS), 1% NEAA (Sigma), 1% Na-Pyruvate and 30% supernatant from L929 cells (as source of M-CSF). The cells were Following 5-day incubation at 37˚C with 5% CO 2 , the mBMDM cells were harvested. After removal of non-adherent cells by washing with 1x PBS buffer, the adherent cells were plated at 1.5×10 6 cells/ well, and cultivated overnight prior to the use in infection assays. In general, the mBMDMs were challenged with different bacterial strains (PAO1, ΔbioH, and CΔbioH) at a multiplicity of infection (MOI: bacterial counts vs cell counts) of 5. Extracellular bacteria were removed by washing with 1x PBS buffer, following 6h of incubation at 37˚C oven containing 5% CO 2 . Then the interested cells were separately harvested at 1h and 24 h post-infection, and lysed with 0.25% SDS. The lysates in appropriate dilution with 1x PBS were plated to measure colony forming unit (CFU). The bacterial survival percentage refers to the ratio of CFU at 24 h in relative to CFU at 1 h.

Measurement of biotin levels
To measure biotin levels of different origins, the commercial Enzyme-Linked Immunosorbent Assay (ELISA) kit (E-IR-R501, Elabscience) was applied as recommended by the manufacture. The sensitivity and range of this kit was 0.19 ng/ml, and 0.31-20 ng/ml, respectively. It was noted that the wells of Micro ELISA plate were pre-coated with biotin antigen. In general, 50 μl test sample was supplemented into each well of ELISA plate, and then incubated with 50 μl Avidin-HRP working solution for 30 min at 37˚C. After 3 rounds of wash, the substrate reagent (90 μl each well) was added, and then incubated for 15 min at 37˚C in dark. Finally, the optical density values of samples at the 450 nm wavelength (OD450), were recorded immediately after the addition of 50 μl stop solution. The biotin levels in different samples were calculated by comparing the OD450 values of the samples to a standard four parameter logistic curve.
The samples tested here included i) bacterial lysates of E. coli MG1655 and P. aeruginosa PAO1; ii) human and mouse plasma; iii) eight kinds of mouse tissues/organs (heart, liver, spleen, lungs, kidneys, large intestine, small intestine, and stomach); and iv) three types of organ contents (large intestine contents, small intestine contents, and stomach contents). First, the acquired bacterial pellets from E. coli MG1655 (and/or P. aeruginosa PAO1) in log-phase were washed three time with 1x PBS buffer, and subjected to the lysis by sonication. After the removal of cell debris by centrifugation, bacterial lysates were produced. Second, the plasma samples of four healthy individuals were kindly provided by Clinical Laboratory of the 2 nd Affiliated Hospital (School Hospital Branch), Zhejiang University School of Medicine. The blood collected in anticoagulation tube by mouse tail cutting, proceeded with the 15min of centrifugation (1000×g) at 4˚C, and the resultant supernatant was mouse plasma. Third, following the blood collection, mouse was euthanized and then dissected to harvest eight different tissues/organs, exemplified with lungs. To minimize side effects of the hemolyzed blood, mouse tissues were weighed, cut into small pieces, and rinsed in PBS. The acquired tissues were resuspended in appropriate volume of 1x PBS, and fully ground by glass bead. The resultant homogenates were centrifuged for 10 min at 5000×g at 4˚C, to generate the supernatant for subsequent biotin quantification. In addition, the contents of three organs (namely large intestine, small intestine, and stomach) were weighed, resuspended in 1ml PBS, and then centrifuged, giving the supernatant used in biotin detection.
When necessary, CD-1 mice (5-6 weeks) were intraperitoneally pre-administered with 2 mg/kg streptavidin to mimic the human environment. Then mouse plasma, tissues, and organ contents were collected at different time courses (1, 2, 4, and 12 h) to determine biotin levels.

Mouse systemic infections
The model of systemic infection was established by using CD-1 mice (5-6 weeks) intraperitoneally challenged with P. aeruginosa strains. The bacterial plating on LB agar in series of dilution informed us that OD600 equals to 1x10 9 CFU for P. aeruginosa. To remove excess biotin, log-phase culture of P. aeruginosa was washed three times, and resuspended in 1x PBS of appropriate volume to give 1x10 7 CFU/ml of inoculums. In general, 15 mice were divided into 3 groups (5 mice each). Apart from the WT, PAO1 strain, ΔbioH and its complemented strain CΔbioH were included. As for a standard model, CD-1 mice were intraperitoneally challenged with different strains of P. aeruginosa (1x10 7 CFU), and euthanized at 12 h post-infections. If required, CD-1 mice were intraperitoneally administered with 2 mg/kg streptavidin at 1 h before P. aeruginosa infections. The obtained mouse tissues (heart, liver, spleen, lungs, and kidneys) were weighed, homogenized in 1ml PBS, diluted, and plated on LB agar to calculate the bacterial loads. Eventually, the calculation of Log10(CFU/g), an indicator of bacterial loads, was employed to determine altered infectivity of ΔbioH mutant relative to its parental strain PAO1.

Mouse lung infections
The role of bioH in P. aeruginosa pathogenesis was addressed using the lung infection model of CD-1 mice (5-6 weeks) as recently established by Carfrae et al. with minor alteration [15]. In total, four groups of mice (six mice per group) were divided. Apart from the negative

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Pseudomonas BioH is a fitness determinant control, PBS group, the remaining three groups were separately challenged with the wild-type PAO1, ΔbioH mutant, and its complemented strain CΔbioH. Given that excess biotin in mouse plasma occurs at the level, 6-fold higher than that of human plasma, streptavidin (at 2 mg/kg) was administered intraperitoneally prior to mice infection. After the introduction of 5% chloral hydrate as anesthetic by intraperitoneal injection, mice were intratracheally infected at 1x10 7 CFU of PAO1 and/or its derivatives (ΔbioH, and CΔbioH). The survival was recorded during the whole period of 48 h infections, and mice were euthanized at the end of experiment. To better visualize the mouse lung lesions, HE dyeing (i.e., hematoxylin-eosin staining) was conducted. At 12 h post-infections, mouse lung tissues were collected for the preparation of homogenates, and bacterial loads in the lung was calculated by plating. In addition, the ratio of lungs (wet /dry), indicative of pulmonary edema was calculated, because it represents the severity of lung injuries caused by P. aeruginosa.
Supporting information S1 with its related homologs. ClustalOmega (http://www.clustal.org/omega/) was used to conduct sequence alignment. Identical residues are denoted with white letters in red background, similar residues are indicated with dark letters in yellow background, different residues are showed with dark letters, and dots refer to gaps. The catalytic triad of PA0502 consists of S66, D189, and H216 (showed with red arrows). Unlike the paradigm BioH, the E. coli b3412 product, the two homologs (CJA_0428 and Sde_3137) seem to possess an additional domain of BioC. Apart from E. coli b3412 and P. aeruginosa PA0502, the remaining five bioH-like cousins separately arise from i) the soil bacterium Cellvibrio japonicus Ueda107 for CJA_0428, ii) the marine bacterium Saccharophagus degradans strain 2-40 for Sde_3137, iii) the plant pathogen Xanthomonas campestris for Xcc_0385, iv) the intracellular pathogen Legionella pneumophila str. Corby for LPC_0888, and v) the opportunistic pathogen Vibrio cholerae N16961 for vc2718.

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Pseudomonas BioH is a fitness determinant chromatography analysis of the recombinant BioH (PA0502) protein. The Streptococcus suis FakB2 with known size (~33 kDa) [76], is used as a size control here. Using a Superdex 75 column, gel filtration assay unveils the monomeric form of PA0502 (~25 kDa). C. The recombinant BioH (PA0502) exhibits the activity of M-C7-ACP demethylation in a dose-dependent manner. D. The BioH (PA0502) enzyme (50 nM) displays full activity with M-C7-ACP within 1 min. The conformationally-sensitive gel of 0.5 M urea/17.5% PAGE (pH9.5) was utilized to separate the product C7-ACP from its reactant M-C7-ACP. The symbol of minus "-" denotes no addition of PA0502. The triangle on right hand (panel C) denotes varied level of PA0502 protein (ranging from 0, 1,5,10,15,20,25,30  Here, the mouse tissues were sampled at five different time points (0, 1, 2, 4, and 12 h) post-intraperitoneal administration with 2 mg/kg streptavidin as recently Carfrae et al. [15] described. All the data are given in means ± SD, and assayed by two-tailed analysis of variance. These findings consistently point to biotin abundance in the above eight kinds of mouse tissues we examined is greatly reduced at 1 h post-intraperitoneal administration with streptavidin. (TIF)

S5 Fig. No effects exerted by BioH on bacterial loads in the routine model of CD-1 mice without the pre-administration with streptavidin. A.
A scheme of CD-1 mice intraperitoneally challenged with P. aeruginosa derivatives. Using certain templates freely provided by ScienceSlides Online, we generated the cartoon models. The CD-1 (5-6 weeks) mice are inoculated with 10 7 CFU of P. aeruginosa, and euthanized at 12 h post-infection to collect various samples. It was note that, prior to bacterial challenge, CD-1 mice here are not subjected to the intraperitoneal administration with streptavidin. B. Minor variation in bacterial loads of the three strains (WT, ΔbioH, and CΔbioH) collected from the infected mouse heart. Using the infection model of CD-1 mice without pre-intraperitoneal administration with streptavidin, the impact of BioH on bacterial loads is indistinguishable between WT and its derivatives (ΔbioH and CΔbioH). Functional impairment of BioH does not influence bacterial persistence in various mouse tissues, namely liver (C), spleen (D), lungs (E), and kidneys (F). The fact that BioH lacks detectable role in bacterial survival within the infected CD-1 mouse reinforced the importance of mimicking the human environment in seeking for the relevance of host biotin to the infectivity of opportunistic pathogen P. aeruginosa [15]. The data here are presented in averages ± SD, and verified with two-tailed analysis of variance. Designations: WT, the wildtype strain of P. aeruginosa PAO1; ΔbioH, the mutant of P. aeruginosa devoid of bioH; CΔbioH, the genetically-complementary strain of ΔbioH mutant. (TIF)