Phage protein Gp11 blocks Staphylococcus aureus cell division by inhibiting peptidoglycan biosynthesis

ABSTRACT Phages and bacteria have a long history of co-evolution. However, these dynamics of phage-host interactions are still largely unknown; identification of phage inhibitors that remodel host metabolism will provide valuable information for target development for antimicrobials. Here, we perform a comprehensive screen for early-gene products of ΦNM1 that inhibit cell growth in Staphylococcus aureus. A small membrane protein, Gp11, with inhibitory effects on S. aureus cell division was identified. A bacterial two-hybrid library containing 345 essential S. aureus genes was constructed to screen for targets of Gp11, and Gp11 was found to interact with MurG and DivIC. Defects in cell growth and division caused by Gp11 were dependent on MurG and DivIC, which was further confirmed using CRISPRi hypersensitivity assay. Gp11 interacts with MurG, the protein essential for cell wall formation, by inhibiting the production of lipid II to regulate peptidoglycan (PG) biosynthesis on the cell membrane. Gp11 also interacts with cell division protein DivIC, an essential part of the division machinery necessary for septal cell wall assembly, to disrupt the recruitment of division protein FtsW. Mutations in Gp11 result in loss of its ability to cause growth defects, whereas infection with phage in which the gp11 gene has been deleted showed a significant increase in lipid II production in S. aureus. Together, our findings reveal that a phage early-gene product interacts with essential host proteins to disrupt PG biosynthesis and block S. aureus cell division, suggesting a potential pathway for the development of therapeutic approaches to treat pathogenic bacterial infections. IMPORTANCE Understanding the interplay between phages and their hosts is important for the development of novel therapies against pathogenic bacteria. Although phages have been used to control methicillin-resistant Staphylococcus aureus infections, our knowledge related to the processes in the early stages of phage infection is still limited. Owing to the fact that most of the phage early proteins have been classified as hypothetical proteins with uncertain functions, we screened phage early-gene products that inhibit cell growth in S. aureus, and one protein, Gp11, selectively targets essential host genes to block the synthesis of the peptidoglycan component lipid II, ultimately leading to cell growth arrest in S. aureus. Our study provides a novel insight into the strategy by which Gp11 blocks essential host cellular metabolism to influence phage-host interaction. Importantly, dissecting the interactions between phages and host cells will contribute to the development of new and effective therapies to treat bacterial infections.

proteins are toxic to or damage the host by immediately inhibiting host biosynthesis in the early stages of infection (3).Investigating the role of these putative phage proteins, particularly those that negatively affect host growth, will not only provide comprehensive insight into phage biology but will also help to better understand how bacteria are reprogrammed during phage infection.Several phage gene products that control host metabolism, e.g., host replication, transcription, and translation machinery, have been documented (4)(5)(6).
Phages have evolved strategies to hijack or manipulate their host's biosynthetic pathways and machinery during infection, and therefore have evolved various mecha nisms to control bacteria in long-term co-evolution and adaptation (7).The majority of known phage-host interactions occur early in the infection process (8), with phage early-gene products interacting with the host proteins to control and functionally shut them down.Studies have shown that phage proteins inhibit bacterial DNA biosynthesis by targeting host DNA polymerase and DNA gyrase (9,10), and affect cell division by inhibiting the essential cell division proteins FtsZ and FtsL or the cytoskeletal protein MreB (11)(12)(13)(14), or modifying or inhibiting bacterial RNA polymerase (15)(16)(17)(18).In addition, other key host processes, such as quorum sensing and glycolysis, are also targeted by phages (19,20).
Understanding the mechanisms by which phage proteins control the host will be valuable for the discovery of new antimicrobial drugs (5).In fact, the discovery of interactions between phage early proteins and essential bacterial proteins has been applied to high-throughput selection of antibacterial compounds (21).Moreover, the characterization of the active sites of the phage-host interaction will be useful for the development of effective approaches to identify small compounds or antibiotic peptides that mimic the antimicrobial activity of phage proteins (22,23).
Although it is critical to understand the interaction between phages and bacteria, our knowledge of the different mechanisms that phages develop to control bacteria is still limited.Due to the lack of sequence similarity to known proteins and the lack of experimental evidence, most of the phage early proteins have been classified as hypothetical proteins with uncertain functions (24).Methicillin-resistant Staphylococcus aureus is one of the most common antibiotic-resistant bacterial pathogens and is considered as a major threat to human health, thus understanding phage-S.aureus interactions will help to develop phage-based antimicrobial strategies to control this notorious pathogen (21,25).
In this study, we first comprehensively screened phage early proteins with growth control effects on S. aureus.One such early protein, Gp11, exacerbated division defects.We further demonstrated that Gp11 interacts with the peptidoglycan (PG) biosynthesis enzyme MurG and ultimately reduces the production of the final precursor molecule, lipid II.Gp11 also interacts with the cell division protein DivIC, which is essential for septal cell wall assembly by disrupting the recruitment of the division protein FtsW.Our results suggest that Gp11 interacts with essential host proteins to disrupt key PG biosynthesis and may provide a strategy to control S. aureus by targeting essential genes.

Gp11 causes growth defects and suppresses S. aureus cell division
Phage early proteins will "shut down" and "take over" the host, leading to host growth defects.To detect bacterial growth inhibition caused by hypothetical phage proteins, we performed a screening for 20 open reading frames (ORFs) of unknown function from S. aureus phage ΦNM1 (26).These genes were cloned into a plasmid driven by the isopropyl-β-D-1-thiogalactopyranoside (IPTG)-inducible promoter.The phage protein Gp104, which has been reported to inhibit the growth of S. aureus (21), was used as a positive control.After dot plating on a solid medium with IPTG induction, expression of gp11 or gp16 caused a reduction in the growth of S. aureus strain RN4220 (Fig. S1).Herein, we focused on characterizing the detailed roles of phage gene gp11 as its overexpression showed the strongest inhibition of the growth of S. aureus (Fig. S1).
To exclude that the inhibitory effect caused by Gp11 was due to the IPTG induction system, a NaAsO 2 induction system was introduced, and the same inhibitory effect was observed (Fig. 1A).Changes in cell morphology were observed after staining with the cell membrane fluorescent dye Nile Red (27).Compared to the control, overexpression of gp11 resulted in a decrease in cell viability (Fig. 1A).Phenotypic defects of larger cell size and abnormal non-spherical morphology of cells were observed compared to the control (Fig. 1B).Strikingly, overexpression of gp11 led to a fraction of cells with misplacement of nascent septa, and multiple parallel septa were frequently seen (Fig. 1B).Altered volume and abnormal cell division were also observed compared to the control.Cell volume increased significantly (Fig. 1C), and overexpression of gp11 also led to the formation of abnormal cells with multiple septa (Fig. 1D).Taken together, these results suggest that Gp11 alters cell morphology and causes growth defects.

Validation of MurG and DivIC as the targets of Gp11
Having obtained the evidence that Gp11 causes growth defects, we hypothesized that it might interact with the essential genes in S. aureus by suppressing their functions.To identify such potential interacting genes, we constructed a bacterial adenylate cyclasebased two-hybrid (BACTH) essential gene library of S. aureus.Essential genes (n = 345) were cloned into plasmids pKT25 or pUT18, and Gp11 interaction targets were exten sively screened (Fig. 2A).To test the feasibility of the screening approach with this library, we applied the known interaction pair Gp104 and DnaI as a positive control (28).As shown in Fig. 2B, Gp104 successfully interacts with DnaI, and Gp11 interacts with both MurG, which encodes a glycosyltransferase involved in PG biosynthesis, and DivIC, which is involved in cell division.A membrane protein called MraY, which is involved in PG synthesis but does not interact with Gp11, was chosen to test the specificity of this assay (Fig. 2B).To further investigate if these interactions with Gp11 play a key role in S. aureus, we used CRISPRi hypersensitivity assay (29).By preventing transcription with a deactivated Cas9, CRISPRi allows sequence-specific knockdown of genes (Fig. S2A).Knockdown of murG, divIC significantly inhibited the growth of S. aureus (Fig. S2B); however, murG knockdown had no effect on bacterial morphology, whereas divIC knockdown showed significantly larger cell volumes (Fig. S2C).The phage-host interaction pair Gp104 and DnaI was used as a positive control, and Gp11 with its non-target DnaI was used as a negative control.The strain overexpressing Gp104 based on dnaI knockdown exhibited enhanced growth sensitivity compared to the control cells expressing Gp104 (Fig. S2D).However, reduction of dnaI levels by CRISPRi after expression of Gp11 showed no difference in growth (Fig. S2E).We conclude that the CRISPRi-based system effectively identifies phage-host interactions.
Next, we identified the targets of Gp11 in S. aureus using this CRISPRi hypersensitiv ity assay.Partial knockdown of the essential gene murG increased the sensitivity of cells overexpressing Gp11 (Fig. 2C).Furthermore, overexpression of Gp11 in the divIC knockdown cells sensitized the cells expressing Gp11 (Fig. 2D), further supporting our result that MurG and DivIC are physiologically important targets of Gp11 in S. aureus.Bacterial growth was impaired after mraY knockdown (Fig. S2B), but no difference was observed in Gp11-expressing cells with or without mraY knockdown (Fig. 2E).
Having confirmed that MurG and DivIC are the targets of Gp11, we hypothesized that growth inhibition by Gp11 could be rescued by overexpression of either MurG or DivIC.Moreover, as shown in Fig. 2F, cell growth could be partially restored when MurG or DivIC was co-expressed with Gp11 in S. aureus.In contrast to DivIC, MurG plays an important role in rescuing cell growth.As a negative control, MraY failed to rescue the growth inhibition caused by Gp11 (Fig. 2F).After staining the cells with the cell membrane fluorescent dye Nile Red, we used fluorescence microscopy to examine the cell morphological changes by evaluating the area of the cells.Cells co-expressing Gp11 with either MurG or DivIC restored the phenotypic defects (Fig. 2G) by showing a significant reversal in cell volume and reducing cell division defects compared to cells expressing Gp11 alone (Fig. 2H and I).Taken together, these results suggest that Gp11 controls cell growth by interacting with MurG and DivIC in vivo.

Gp11 blocks cell division
Gp11 is a 53-amino-acid protein with a predicted double transmembrane helix (Fig. S3A).We examined Gp11 localization using Gp11-green fluorescent protein (GFP) fusion and found that Gp11 was indeed localized on the membrane (Fig. S3B).We performed a screen for Gp11-resistant mutants by generating transformants under conditions of high IPTG to identify key residues in Gp11.By sequencing of potential candidates, three ORF-resistant mutants were screened out as Gp11 S33L , Gp11 G36R , and Gp11 A38E (Fig. 3A; Fig. S3C).Expression of these point mutants revealed that all lost their ability to inhibit S. aureus growth (Fig. S3D and E), but remained localized on the membrane (Fig. S3B).
To further identify the key residues in Gp11 that interact with MurG and DivIC, we performed the BACTH assay.Mutation of G36 and A38 in Gp11 resulted in no interac tion with MurG, whereas mutation of S33 decreased binding affinity to MurG (Fig. 3B).Regarding the interaction of Gp11 with DivIC, the A38E mutant does not make contact with MurG but still interacts with DivIC (Fig. 3C).These data indicate that Gp11 interacts with MurG and DivIC in a different pattern.
The division defects caused by Gp11 suggest that it disrupts the process of cell division.Using a MurG-GFP fusion protein, we observed that localization of MurG was frequently disrupted in cells expressing Gp11 (Fig. 3D).To confirm the role of the key residues of MurG in Gp11 function, the localization of MurG was assessed in the background of Gp11 expression or its point mutants.As shown in Fig. 3D, once the key amino acids were mutated, the localization of MurG was no longer affected.In addition, FtsW, the transglycosylase that is required for the formation of the septal cell wall, is recruited by the trimeric complex of DivIC, DivIB, and FtsL (31).We found that overexpression of Gp11, but not its mutants, disrupted the localization of FtsW, causing the fluorescence to be aggregated (Fig. 3D).We also observed fluorescence aggrega tion of DivIB, but the localization of the early division protein EzrA (32) appear to be unaffected in enlarged Gp11-expressing cells, cells with empty vector, or Gp11 mutants (Fig. 3D).These results suggest that Gp11 binds to MurG, resulting in its mis-localization, and interacts with DivIC to disrupt the recruitment of FtsW, which ultimately result in cell division defects.

Gp11 spatially regulates PG biosynthesis in cell division and promotes phage infection
The interactions of Gp11 with MurG and DivIC led us to hypothesize that Gp11 may affect PG biosynthesis.To evaluate the effect of Gp11 on PG synthesis and the impact on S. aureus cell division, we labeled the cells with the fluorescent D-amino acid 7-hydroxycoumarin carbonyl amino-D-alanine (HADA), a molecule that is incorporated into newly synthesized PGs (33).Compared with the control cells, Gp11-overexpressing cells exhibited a more diffusible HADA signal, which was seen to occur at multiple sites within the cell, including peripheral and multiple partial septa (Fig. 4A), and the newly synthesized PG was depleted at the septum relative to the periphery in Gp11overexpressing cells compared with controls (Fig. 4B), which is consistent with murG knockdown cells (Fig. S4A and B).
MurG is a glycosyltransferase in PG synthesis that transfers N-acetyl glucosamine (GlcNAc) from UDP-GlcNAc to the C4 position of lipid I to form a lipid-linked disaccharide peptide called lipid II (35).We therefore hypothesized that Gp11 targets MurG to inhibit its activity in producing lipid II, and performed an assay to detect cellular lipid II in S. aureus as previously described (34,36).We isolated lipid II from Gp11-overexpressing cells, and the fraction was detected after labeling the stem peptides with biotin-D-lysine (BDL) for immunoblotting (Fig. 4C).As shown in Fig. 4D, a reduction in lipid II was observed in the presence of Gp11, but not its mutants, suggesting that Gp11 inhibits MurG activity, resulting in a reduction in lipid II.Taken together, our results indicate that Gp11 spatially regulates PG synthesis to control cell size.
Because Gp11 has been shown to affect lipid II production, we finally characterized its effect on PG biosynthesis during phage infection in the absence of gp11.We constructed an in-frame gene deletion of gp11 named ΦNM1 Δgp11 and characterized the effect of Gp11 on phage fitness (Fig. 5A).ΦNM1 Δgp11 showed a reduced ability to lyse the host and resulted in smaller phage plaques compared to ΦNM1 (Fig. 5B and C).When Gp11 is expressed in the bacteria, the phage plaque size and phage infection are restored to the levels of wild type (Fig. 5C and D).This implies that Gp11 is an important phage protein involved in the takeover or manipulation of host bacteria.
Consistent with our finding that Gp11 overexpression reduced lipid II production, cells infected with ΦNM1 Δgp11 showed a significant increase in lipid II compared to the ΦNM1-infected strain 2 h after infection (Fig. 4E).Because MurG is a key enzyme in the PG synthesis pathway and directly regulates lipid II production, we therefore conclude that Gp11 inhibits MurG activity and blocks S. aureus cell division by inhibiting PG biosynthesis.

DISCUSSION
With increasing concern about bacterial drug resistance, characterizing new targets has become a strong research focus in infection control.Phages engage in a long evolution ary arms race with their hosts over a period in which early phage proteins "take over" and "shut down" the host (37).Furthermore, bacterial proteins that are preferentially blocked by phage proteins have the potential to serve as novel antibacterial targets, as their disruption could disrupt key processes and slow bacterial growth.In the present study, we performed a comprehensive screening of phage early proteins that inhibit bacterial growth.We have identified a phage protein, Gp11, that inhibits cell division by interfering with PG synthesis.Our results suggest a model in which Gp11 interacts with MurG, leading to reduced production of lipid II, and interacts with DivIC to disrupt recruitment of the divisome complex.We found that expression of gp11 from phage ΦNM1 inhibits bacterial growth and alters cell morphology in S. aureus RN4220 with cell lysis (data not shown), which differs from observations of a lethal but not lytic effect of the phage protein E on Staphylococcus carnosus (38).This lysis effect is also observed in Escherichia coli with empty cell walls (39).The inhibitory effect of Gp11 could be used as a potentially beneficial strategy to combat S. aureus.Our results also suggest that Gp11 alters cell morphology by increasing host cell size.Phage adsorption and replication are closely related to the cell size of bacterial hosts, which affect the fitness and mutual evolution of phages and bacteria (40).The larger size caused by overexpression of Gp11 is consistent with the conclusion that Gp11 promotes phage infection (Fig. 5), supporting the idea that phages inhibit host cell division to propagate their progeny (14).These results suggest that Gp11 is a critical protein for phage ΦNM1 to control its host.
After screening for candidates that interact with phage proteins, we employed a CRISPRi hypersensitivity assay to validate the targets of phage proteins in S. aureus, which allows for the identification of direct phage targets.In this way, we found that Gp11 directly interacts with MurG and DivIC (Fig. 2B).These analyses provide a rapid method for identifying major targets of phages in the host using a dual screening model.As a glycosyltransferase, MurG is essential for bacterial survival by catalyzing the transfer of the GlcNAc motif of UDP-GlcNAc to the C4 hydroxyl MurNAc in lipid I to form lipid II (41) and is also an important target for the development of antimicrobial drugs.Elucidation of the mechanism by which Gp11 impairs cell growth requires a protein-pro tein interaction with MurG.This will provide new information for the development of novel drugs that directly target S. aureus in the future.
Gp11 inhibits cell growth by targeting PG biosynthesis in cell division.It has been reported that the correct localization of the division machinery in the midcell is correlated with PG density, which has been shown to be a marker of cell division (42).Gp11-mediated delocalization of MurG most likely disrupted its function spatiotempor ally.Previous work has also shown that the phage protein DicB inhibits cell division by interacting with and affecting the localization of cell division proteins MinC and FtsZ (43,44).Another phage protein Tip, which interacts with PilB, also antagonizes PilB function by delocalizing PilB from the poles (45).This strategy for phages to affect cell division by disrupting the localization of host division-associated proteins may be a general method for phages to alter host cell shape.
PG synthesis and cell division are inextricably linked, with the cell division septum being the main region of PG synthesis in S. aureus (46).Cell wall attack is one of the major strategies for phage to infect the host, but targeting PG synthesis is uncommon.A small protein like Gp11 targets the essential proteins MurG and DivIC to control its host.This implies the strong evolutionary pressure on phages to develop strategies to control host function by targeting two proteins simultaneously (19,20,47).DivIC is a key component of cell wall dynamics during division, which is essential for proper septum formation (48).The interaction between Gp11 and DivIC prevents the recruitment of FtsW, which interferes with PG biosynthesis at the septum, and overexpression of Gp11 showed a more diffuse HADA signal at the cell periphery (Fig. 4A).These data also support that loss of DivIC causes disruption of cell division as well as increases PG production at the cell periphery, which negatively impacts septum formation and ultimately results in thicker peripheral cell walls (49).During cell division, the late divisome proteins such as FtsW interact with other regulatory proteins to form the mature divisome and initiate septal PG synthesis (50).FtsW is a well-known lipid II-interacting protein (51).In a recent study, FtsW was reported to serve as a peptidoglycan polymerase that polymerizes lipid II at the septum into peptidoglycan (52).The reduction of lipid II in Gp11-expressing cells is consistent with the finding that FtsW was frequently mislocalized (Fig. 3D).We propose that mislocalization of FtsW may contribute to lipid II reduction during phage infection.Since the biosynthesis of the bacterial cell wall is closely coordinated with cell division (48,53), we hypothesized that this could be a viable strategy for phages to influence PG synthesis during cell division and to lyse their host, which has been observed in E. coli (39,54).
The target of Gp11 is relevant to its function as an inhibitor of PG synthesis.Gp11 inhibits the production of the final lipid-linked PG precursor, lipid II, by affecting the activity of MurG (Fig. 4).The altered morphological phenotype of the Gp11 mutant was accompanied by a reduction in lipid II, which is incorporated into the PG layer, helps to maintain cell shape, provides strength to withstand turgor, and is involved in the processes of cell growth and division (55).Notably, we found that infection with ФNM1 Δgp11 significantly increased the production of lipid II (Fig. 4E), which is consistent with previous studies that phage infection inhibits host PG biosynthesis.Previous work has shown that the phage protein Lys M inhibits PG synthesis by targeting MurJ (56).The small RNA phage Qβ encoding the A 2 protein blocked MurA, and the DNA phage ΦX174 encoding E protein inhibited MraY, both of which disrupt PG synthesis (54,57).Although phage proteins have been shown to inhibit PG synthesis, the effect of this inhibition on the phage-infected cell has not been investigated.Here, we elucidated the effect of Gp11 on PG synthesis by comparing the results of wild-type ФNM1 and ФNM1 Δgp11 infections.Our results further explain that Gp11 inhibits S. aureus growth probably by affecting lipid II formation and thus preventing bacteria from maintaining normal morphology.
The exploitation of phage-host interaction has inspired the discovery of antibacterial targets (7).For example, a strategy to search for novel molecular targets of phages used time-resolved fluorescence resonance energy transfer to screen small molecules to disrupt the interaction between Gp104 and DnaI (21) and ultimately identified 11 molecules that were directly active against S. aureus.Recently, Zhang et al. (58) used small molecules to mimic the inhibitory effect of the phage protein Gp46 to develop a super-antibacterial drug that not only shortens the drug development cycle but also broadly inhibits most drug-resistant bacteria.Therefore, studying the Gp11-MurG interaction could provide information for the development of small molecules that mimic the inhibitory effect of Gp11.In summary, the strategy to affect cell division by disrupting the localization of host division-associated proteins may be a general way for phages to reshape the host, and the interaction partners identified here will lay the foundation for future antimicrobial treatment.

Bacterial strains and growth conditions
The strains used in this study are listed in Table S1.Plasmids were cloned in Escherichia coli DH5α.The E. coli BL21(DE3) strain was used for protein overexpression and purification.E. coli strains were grown in Luria-Bertani (LB) broth or on LB agar supplemented with 100 µg mL −1 ampicillin or 50 µg mL −1 kanamycin.S. aureus strains were grown in tryptic soy broth (TSB; Difco) or on tryptic soy agar (TSA; Difco) supplemented with 10 µg mL −1 erythromycin or 10 µg mL −1 chloramphenicol when needed.To induce gene expression, 0.1 or 0.5 mM isopropyl-β-D-1-thiogalactopyranoside (IPTG) was added to the bacterial cultures.

Plasmid construction
The plasmids used in this study are listed in Table S2.All oligonucleotides used in this study are listed in Table S3.Genes were cloned into plasmids using a ClonExpress II One-step Cloning Kit (Vazyme, Nanjing, China).Genomic DNA extracted from S. aureus strain RN4220 using a TIANAmp Bacteria DNA Kit (Tiangen, Beijing, China) was used as the template in the PCR reactions.The plasmid pTLS is for phage early protein overex pression in S. aureus and contains IPTG-inducible constructs with the Cm R marker.All plasmids were constructed via multiple steps of restriction-ligation or Gibson assembly.

Screening of phage genes that inhibit bacterial growth
To identify genes that inhibit bacterial growth, we cloned early genes of unknown function from ΦNM1 according to the previous RNA-seq results (59) into plasmid pTLS under the IPTG-inducible promoter.The plasmids were transformed into S. aureus RN4220 for a spot test.Cultures containing individual plasmids of the phage genes were inoculated onto TSA plates with or without 1 mM IPTG at 37°C for 12 h.

Growth curves and spot dilution assay of S. aureus
For growth curve determination, overnight cultures of the strains were diluted 1:100 in TSB supplemented with 10 µM NaAsO 2 .Cells were grown at 37°C, and the optical density (OD) 600 values were measured hourly using a plate reader (BioTek, Winooski, VT, USA).Cells used for dilutions and subsequent colony-forming unit (CFU) counting were taken from cultures under experimental conditions.Plates with dilutions that resulted in well-separated colonies were used for counting, and total CFUs were calculated.For the spot dilution assay, 10-fold serial dilutions of cultures were prepared in 500 µL phosphate-buffered saline (PBS), and 2 µL of these dilutions was plated on TSA and incubated at 37°C for 12 h.

Construction and screening of the S. aureus essential gene BACTH library
A plasmid library containing 345 essential genes of S. aureus was constructed.The genes were amplified by PCR and ligated to the bacterial two-hybrid vector pUT18 and pKT25 provided in a BACTH System Kit (Euromedex, France).Plasmids were purified from the assembled clones to generate plasmid libraries.To screen the targets of phage proteins, 1 µL of the mixed essential gene plasmids was transformed into competent BTH101 cells harboring bait plasmids expressing phage proteins, and the transformants were plated on a MacConkey agar plate according to the manufacturer's instructions.The red colonies were selected for assaying β-galactosidase activity (60).

Bacterial two-hybrid assay
The BACTH system was used to detect protein-protein interactions (61).Briefly, the "bait" and "prey" proteins were fused to pKT25 and pUT18, respectively, and heat-shocktransformed into BTH101 competent cells lacking a functional cyaA gene.Transformants were grown on LB agar for 2 days at 30°C.Three clones were selected and grown for 16 h at 30°C with shaking in LB containing 50 µg mL −1 kanamycin, 100 µg mL −1 ampi cillin, and 0.5 mM IPTG.The Miller assay was used to spectrophotometrically quantify β-galactosidase activity and to identify the protein-protein interactions (60).Results are representative of at least three independent replicates.

CRISPRi hypersensitivity assay
CRISPRi-mediated inhibition of essential gene expression was performed as described (62).Using pISA-IPTG, the base-pairing region was designed to target the essential gene on the coding strand adjacent to the protospacer motif NGG.dCas9 protein expres sion was induced with IPTG.Results are representative of at least three independent replicates.To test the efficacy of the essential gene knockdown strain, relative growth in liquid TSB containing 1 mM IPTG was measured and compared to the growth of the no-sgRNA control at mid-log phase using a plate reader (BioTek).To verify the targets of Gp11 in S. aureus, a low inducible concentration was selected to knock down essential genes without affecting bacterial growth, and the plasmid pTR-gp11 was transformed into a strain containing the CRISPRi system.The growth of CRISPRi S. aureus knockdown mutants relative to no-sgRNA control was measured after overexpression of Gp11 using a flat-bottomed 96-well plate.

Labeling of S. aureus strains
The S. aureus strains were labeled with cell membrane fluorescent dye 9-diethyla mino-5H-benzo [α] phenoxazine-5-one (Nile Red) as previously described for fluorescence microscopy (27).To label S. aureus membranes, cells were stained with Nile Red (MedChemExpress, New Jersey, USA) at a final concentration of 5 µg mL −1 for 5 min at room temperature, washed twice with PBS, and then 2 µL cultures was plated onto slides for imaging.To label the nascent PG of S. aureus, cells were incubated with fluorescent d-amino acid HADA (MedChemExpress) at a final concentration of 250 µM for 30 min at 37°C with shaking, washed with PBS to remove the unbound dye, and then plated on a slide for imaging (63,64).The labeled cells were observed using phase contrast and the 4′,6-diamidino-2-phenylindole channel on an Olympus microscope.

Microscopy and image analysis
To detect Gp11 overexpression in S. aureus growth, cells were stained with the cell membrane fluorescent dye Nile Red for 5 min at room temperature and washed twice with PBS before microscopy.To study the localization of Gp11 and its mutants, Gp11 or its mutants fused with GFP were cloned into expression vector pCI and then elec trotransferred into S. aureus.Transformants were grown at 37°C in TSB medium, induced with 1 mM IPTG, and harvested by centrifugation at 5,000 × g for 3 min at OD 600 = 0.4.Supernatants were decanted, and pellets were resuspended in PBS for imaging.To further evaluate the effect of Gp11 on MurG localization, Gp11 was co-transformed with MurG-GFP in S. aureus.Cells were harvested at OD 600 between 0.4 and 0.6 with the addition of 10 µM NaAsO 2 and 100 µM IPTG and then centrifuged at 5,000 × g for 3 min, the supernatant was discarded and washed twice with PBS and resuspended.Bacterial solution (2 µL) was placed on a slide for sampling and microscopic observation.The localization of the corresponding proteins was monitored by fluorescence visualization using an Olympus fluorescence microscope at 488 nm excitation.All images were taken on an Olympus inverted microscope at 10× and 100× magnification using a 100× oil immersion phase contrast objective.Microscope control and image acquisition were performed in NIS Elements (Nikon, Melville, NY, USA).Cell area was analyzed using the MicrobeJ (65) and ImageJ (66).

Gp11 point mutant isolation
Point mutations of Gp11 were isolated as previously described (5,13).Briefly, S. aureus RN4220 cells were transformed with pTLS-gp11 and cultured overnight on TSB agar with 1 mM IPTG.The resistant colonies were harvested, and plasmids were extracted using a FastPure Plasmid Mini Kit (Vazyme).The plasmids were then retransformed into competent S. aureus RN4220 cells, and the resultant colonies were picked for spot dilution assay as described above to check growth inhibi tion.Plasmids contained in clones that no longer inhibited bacterial growth were subjected to sequencing analysis.

Mutant construction of gp11 in ΦNM1
The ΦNM1 gp11 knockout strain was constructed using a CRISPR system.The plasmid pCas9 expressing Cas9 containing guide RNA spanning nucleotides 74-93 of gp11 with the upstream and downstream fragments of gp11 was transformed into S. aureus RN4220.A plaque assay was performed as previously described to select for the Gp11 knockout strain (26).Briefly, 100 µL S. aureus and 10 µL phage were mixed with 5 mL soft TSA and 5 mM CaCl 2 and poured on TSA containing 1 mM IPTG and 10 µg mL −1 erythromycin.Plaques were selected for validation using the primers listed in Table S2.

Phage infection assay
Overnight cultures of S. aureus RN4220 were diluted 1:100 in fresh TSB containing a final concentration of 5 mM CaCl 2 to OD 600 = 0.2, and 200 µL of cells was added to each well of a 96-well plate.ΦNM1 WT or ΦNM1 Δgp11 phages were immediately added to each well at the indicated multiplicity of infection of 1 and 0.01, respectively.After phage infection, growth was measured every 15 min at 37°C using a shaking plate reader (Biotek).The growth curve experiment was replicated at least three times independently.

Lipid II purification
Lipid II extraction from S. aureus cells was performed as described (34).Briefly, overnight cultures of S. aureus WT or overexpressing Gp11 were diluted to OD 600 = 0.01 and grown in TSB at 37°C to OD 600 of 0.5-0.6.Cells were harvested after centrifugation at 4,000 × g for 10 min, and the pellets were resuspended in PBS and added to 8.75 mL CHCl 3 :MeOH (1:2).The mixture was vortexed at 25°C for 10 min and then centrifuged at 4,000 × g for 10 min to remove cell debris.The supernatant was transferred into a new centrifuge tube containing 5 mL CHCl 3 and 3.75 mL PBS (pH 7.4).The mixture was vortexed for 10 min and centrifuged at 4,000 × g for 10 min to achieve phase separation.The material between the top aqueous and bottom organic layer was collected, dried in a vacuum desiccator, and resuspended in 20 µL of dimethyl sulfoxide (DMSO).

Western blot analysis of biotinylated lipid II
Biotinylation and detection of lipid II were performed as described (67).Briefly, 2 µL of lipid extraction solubilized in DMSO was added to a solution containing 4 µM PBP4, 3 mM BDL in reaction buffer (12.5 mM HEPES, 2 mM MnCl 2 , 250 µM Tween-80, pH 7.5) to a total volume of 10 µL.After incubation for 1.5 h at room temperature, the reaction was quenched with 10 µL of 2× SDS loading buffer.The final mixture (3 µL) was loaded onto a 4%-20% gradient polyacrylamide gel and run at 100 V for 1 h.The final mixture was transferred to an immunoblot polyvinylidene fluoride membrane (Bio-Rad, Hercules, CA, USA).BDL-lipid II was detected by blotting with streptavidin-horseradish peroxidase (1:10,000 dilution) (Beyotime, Shanghai, China).

Statistical analysis
Statistical significance between two groups was analyzed by unpaired Student's t-test (two-tailed) using GraphPad Prism 8 (GraphPad Software, Boston, MA, USA).

FIG 1
FIG 1 Overexpression of Gp11 in S. aureus alters cell morphology.(A) Effect of Gp11 overexpression on S. aureus cell growth.(B) Effect of Gp11 overexpression on S. aureus cell shape as visualized by phase-con trast and fluorescence microscopy.Arrows indicate septal defects as multiple.Cells were stained with membrane dye Nile Red.Scale bar, 2.5 µm.(C) Cell volume was measured using MicrobeJ.Cells were harvested after 2 h incubation with 10 µm NaAsO 2 .(D) Quantitation of cells with septal defects as multiple septa (abnormal), and nascent or complete septum (normal) after treatment with 10 µm NaAsO 2 for 2 h.In this plot, n = 198 (Vec) and 91 (Gp11) cells; P values were determined by unpaired Student's t-test.**P < 0.01 and *P < 0.05.

FIG 2
FIG 2 Validation of the targets of Gp11 in S. aureus.(A) Flowchart for screening Gp11-interacting proteins from S. aureus essential-gene BACTH libraries.With libraries being collected in an essential-gene plasmid pool and equimolar mix, the plasmid library was then transformed into Escherichia coli BTH101 reporter cells, which contain the phage gene, and plated on MacConkey agar plates.(B) In a bacterial two-hybrid assay of Gp11 interaction with MurG and DivIC, the known interaction pair Gp104 and DnaI was used as a positive control, while Gp11 and MraY as a negative control.(C) CRISPRi-based assay revealed MurG as the target of Gp11.The growth of S. aureus by knockdown of murG after expression of Gp11 (Gp11 + sgRNA murG ) relative to no sgRNA control (Vec 1 + Vec 2 ).(D) The growth of S. aureus by knockdown of divIC after expression of Gp11 (Gp11 + sgRNA divIC ) relative to no sgRNA control (Vec 1 + Vec 2 ).Each data point represents three independent replicates.P values were determined by unpaired Student's t-test.**P < 0.01, *P < 0.05, and n.s.: no significant difference.(E) The growth of S. aureus by knockdown of mraY after expression of Gp11 (Gp11 + sgRNA mraY ) relative to no sgRNA control (Vec 1 + Vec 2 ).(F) Growth assay of cells expressing Gp11, MurG, DivIC, or MraY on solid medium.(G) Microscopic images of S. aureus expressing Gp11, MurG, and DivIC.Cells were stained with membrane dye Nile Red.Scale bars, 2.5 µm.(H) Cell volume was measured using MicrobeJ.Cells were collected after 2 h incubation with 10 µM NaAsO 2 and 100 µM IPTG.From left to right, n = 467, 418, 118, and 510 cells.P values were determined by unpaired Student's t-test.**P < 0.01.(I) Quantitation of cells with septal defects (abnormal), and nascent or complete septum (normal) after cells were treated with 10 µM NaAsO 2 and 100 µM IPTG for 2 h.

FIG 3
FIG 3 Gp11 acts to block cell division.(A) Summary of the identified mutants, all of which map to a hypothetical protein encoded by the gene gp11 in S. aureus ΦNM1.The structural model of Gp11 predicted by AlphaFold (30), and the fraction of each mutant of Gp11 is indicated.(B) Analysis of the interactions between MurG and the mutants of Gp11 through the bacterial adenylate cyclase-based two-hybrid (BACTH) system.(C) Analysis of the interactions between DivIC and the mutants of Gp11 through BACTH.(D) The localization of MurG, DivIB, FtsW, and EzrA were monitored in the presence of Gp11 or its mutants.The cells were collected after 2 h incubation with 10 µM NaAsO 2 and 100 µM IPTG.Scale bars, 2.5 µm.

FIG 4
FIG 4 Gp11 targets peptidoglycan biosynthesis by inhibiting the activity of MurG.(A) S. aureus cells expressing Gp11 or its mutants were stained with the fluorescent cell wall marker D-amino acid 7-hydroxycoumarin carbonyl amino-D-alanine (HADA) and analyzed by phase-contrast and fluorescence microscopy.Scale bars, 2.5 µm.(B) Images of individual cells expressing Gp11 or its mutants were used to calculate the fluorescence ratio of the septal versus cell peripheral fluorescence signal.n ≥ 30.P values were determined by unpaired Student's t-test.**P < 0.01 and n.s.: no significant difference.(C) The terminal D-Ala residue of the lipid II stem peptide was labeled with the biotin-D-lysine probe BDL using S. aureus PBP4 (34).(D) Western blot of lipid II after overexpression of Gp11 and its point mutants in S. aureus strain RN4220.(E) Western blot of lipid II after cells were infected with ΦNM1 and ΦNM1 Δgp11 .