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1.
Vaccines (Basel) ; 11(2)2023 Jan 27.
Article in English | MEDLINE | ID: mdl-36851153

ABSTRACT

There is increasing interest to replace animal-based potency assays used routinely to test vaccines, since they are highly variable, are costly, and present ethical concerns. The development of relevant in vitro assays is part of the solution. Using pertactin (PRN) antigen as an example in DTaP-IPV (diphtheria, tetanus, acellular pertussis, and inactivated poliovirus) vaccines, a PRN antigenicity ELISA was developed using two monoclonal antibodies with a high affinity to unique PRN epitopes, relevance to human immune responses, and evidence of functionality. The ELISA measured consistent PRN antigenicity between the vaccine lots and was validated to demonstrate its accuracy, precision, linearity, and specificity. Notably, the PRN antigenicity ELISA was more sensitive than the mouse-based potency test and could more effectively differentiate between degraded and intact vaccine lots compared to the in vivo test. From these studies, the PRN antigenicity ELISA is proposed as an in vitro replacement for the in vivo potency test for PRN in DTaP-IPV-based formulations. Important considerations in this study included comprehensive antibody characterization, testing of multiple vaccine lots, method validation, and comparison to animal-based potency. Together, these factors form part of an overall strategy that ensures reliable and relevant in vitro assays are developed to replace animal tests.

2.
Biochemistry ; 58(6): 646-656, 2019 02 12.
Article in English | MEDLINE | ID: mdl-30560647

ABSTRACT

The diphtheria toxoid (DT) antigen is one of the major components in pediatric and booster combination vaccines and is known to raise a protective humoral immune response upon vaccination. However, a structurally resolved analysis of diphtheria toxin (DTx) epitopes with underlying molecular mechanisms of antibody neutralization has not yet been reported. Using hydrogen-deuterium exchange mass spectrometry (HDX-MS) and Biolayer Interferometry (BLI) assays, we have characterized two neutralizing anti-DTx monoclonal antibodies (mAbs), 2-25 and 2-18, by identifying the specific epitopes on the diphtheria toxin responsible for antibody binding. Our results show that both epitopes are conformational, and mechanistically distinct. Monoclonal antibody 2-25 binds selectively to the B-subunit (translocation and receptor domain) of DTx, blocking the heparin-binding EGF-like growth factor (HBEGF) binding site. In contrast, mAb 2-18 binds to the A-subunit (catalytic domain), partially covering the catalytic loop region that shuttles NAD during catalysis. The results are discussed in the context of antigen neutralization mechanisms and can ultimately help to reveal the underlying factors that contribute to Diptheria vaccine efficacy.


Subject(s)
Antibodies, Monoclonal/immunology , Antibodies, Neutralizing/immunology , Diphtheria Toxin/immunology , Epitopes/immunology , Antibodies, Monoclonal/metabolism , Antibodies, Neutralizing/metabolism , Corynebacterium diphtheriae/chemistry , Deuterium/chemistry , Deuterium Exchange Measurement , Diphtheria Toxin/chemistry , Diphtheria Toxin/metabolism , Epitope Mapping , Epitopes/metabolism , Kinetics , NAD/metabolism , Protein Binding/immunology , Protein Conformation , Protein Domains/immunology
3.
Infect Immun ; 80(6): 2212-20, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22473606

ABSTRACT

Streptococcus pneumoniae pneumolysin (PLY) is a virulence factor that causes toxic effects contributing to pneumococcal pneumonia. To date, deriving a PLY candidate vaccine with the appropriate detoxification and immune profile has been challenging. A pneumolysin protein that is appropriately detoxified and that retains its immunogenicity is a desirable vaccine candidate. In this study, we assessed the protective efficacy of our novel PlyD1 detoxified PLY variant and investigated its underlying mechanism of protection. Results have shown that PlyD1 immunization protected mice against lethal intranasal (i.n.) challenge with pneumococci and lung injury mediated by PLY challenge. Protection was associated with PlyD1-specific IgG titers and in vitro neutralization titers. Pretreatment of PLY with PlyD1-specific rat polyclonal antiserum prior to i.n. delivery of toxin reduced PLY-mediated lung lesions, interleukin-6 (IL-6) production, and neutrophil infiltration into lungs, indicating that protection from lung lesions induced by PLY is antibody mediated. Preincubation of PLY with a neutralizing monoclonal PLY antibody also specifically reduced the cytotoxic effects of PLY after i.n. inoculation in comparison to nonneutralizing monoclonal antibodies. These results indicate that the induction of neutralizing antibodies against PLY can contribute to protection against bacterial pneumonia by preventing the development of PLY-induced lung lesions and inflammation. Our detoxified PlyD1 antigen elicits such PLY neutralizing antibodies, thus serving as a candidate vaccine antigen for the prevention of pneumococcal pneumonia.


Subject(s)
Antibodies, Bacterial/blood , Antibodies, Neutralizing/blood , Bacterial Vaccines , Lung Injury/prevention & control , Pneumonia, Pneumococcal/prevention & control , Streptolysins/immunology , Animals , Antibodies, Bacterial/immunology , Antibodies, Neutralizing/immunology , Antigens, Bacterial/immunology , Antigens, Bacterial/metabolism , Bacterial Proteins/chemistry , Bacterial Proteins/immunology , Bacterial Vaccines/immunology , Bronchoalveolar Lavage Fluid , Female , Lung Injury/pathology , Mice , Mice, Inbred BALB C , Mice, Inbred CBA , Streptococcus pneumoniae/metabolism , Streptolysins/chemistry
4.
Infect Immun ; 77(3): 996-1007, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19103768

ABSTRACT

Intracellular Salmonella enterica serovar Typhimurium (serovar Typhimurium) occupies a Salmonella-containing vacuole (SCV) where bacterial effector proteins are secreted into the host cell using type III secretion systems (T3SS). Cytoskeletal motor proteins and T3SS-delivered effector proteins facilitate SCV positioning to juxtanuclear positions where bacterial replication occurs. Here, we show that this characteristic SCV positioning is not maintained by all SCVs during infection of HeLa cells. Notably, juxtanuclear SCV localization that occurs by 8 to 14 h postinfection is followed by significant centrifugal displacement of a subset of SCVs toward the host cell periphery by 24 h postinfection. This novel phenotype requires bacterial protein synthesis, a functional Salmonella pathogenicity island 2 (SPI-2)-encoded T3SS, intact microtubules, and kinesin-1 motor protein. Bacteria lacking PipB2, a kinesin-recruiting T3SS effector, did not exhibit centrifugal displacement and remained at juxtanuclear positions throughout 24 h of infection. While levels of the SPI-2 effectors PipB2 and SifA increased during 24 h postinfection, a corresponding decrease in levels of the SPI-1 T3SS effectors SipA and SopB, both known to mediate juxtanuclear SCV positioning, was observed. A fluorescence-based assay indicated that wild-type serovar Typhimurium transferred from infected to uninfected epithelial cells while strains deficient in SPI-2 T3SS secretion or PipB2 did not. Our results reveal a novel SCV phenotype implicated in the cell-to-cell spread of serovar Typhimurium during infection.


Subject(s)
Cell Communication/physiology , Epithelial Cells/microbiology , Salmonella Infections/microbiology , Salmonella enterica/pathogenicity , Vacuoles/microbiology , Bacterial Proteins/metabolism , Epithelial Cells/metabolism , Fluorescent Antibody Technique , HeLa Cells , Humans , Kinesins/metabolism , Membrane Proteins/metabolism , Salmonella Infections/metabolism , Salmonella enterica/metabolism , Transfection , Vacuoles/metabolism
5.
Infect Immun ; 76(6): 2722-35, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18411289

ABSTRACT

Salmonella enterica serovar Typhimurium grows within host cells in a permissive compartment termed the Salmonella-containing vacuole (SCV). These bacteria use two distinct type III secretion systems (T3SS) to deliver virulence proteins (effectors) into cells. Effectors secreted by the Salmonella pathogenicity island 1 (SPI-1)-encoded T3SS mediate invasion and early SCV maturation steps, while those secreted by the SPI-2 T3SS affect the SCV at later stages postinfection. Some SPI-2 effectors modulate microtubule motor activity on the SCV. Here, we show that the actin-based motor myosin II also affects SCV dynamics during infection. Following invasion, myosin II is required for SCV positioning near the nucleus of host cells. Later, myosin II counteracts the activities of the SPI-2 effectors PipB2 and SseJ to maintain SCV positioning and stability, respectively. Myosin II activity was required for maximal bacterial growth in macrophages. Rho kinase activity was required for SCV positioning. The effector SopB, a known activator of Rho GTPases, was found to be required for SCV positioning, and transfection of cells with SopB was sufficient to induce myosin II phosphorylation. These studies reveal a novel role for myosin II in controlling SCV dynamics during infection and suggest that SopB activates myosin II.


Subject(s)
Myosin Type II/metabolism , Salmonella typhimurium/physiology , Vacuoles/microbiology , Animals , Bacterial Proteins/metabolism , Cell Division/physiology , Cell Nucleus , Gene Expression Regulation , HeLa Cells , Heterocyclic Compounds, 4 or More Rings/pharmacology , Humans , Macrophages/microbiology , Mice , Myosin Type II/antagonists & inhibitors , Myosin Type II/genetics , Salmonella typhimurium/cytology , Salmonella typhimurium/pathogenicity , Vacuoles/drug effects , rho-Associated Kinases/metabolism
6.
Autophagy ; 2(3): 189-99, 2006.
Article in English | MEDLINE | ID: mdl-16874109

ABSTRACT

Misfolded proteins can be directed into cytoplasmic aggregates such as aggresomes and dendritic cell aggresome-like induced structures (DALIS). DALIS were originally identified in lipopolysaccharide-stimulated dendritic cells and act as storage compartments for polyubiquitinated Defective Ribosomal Products (DRiPs) prior to their clearance by the proteasome. Here we demonstrate that ubiquitinated protein aggregates that are similar to DALIS, and not related to aggresomes, can be observed in several cell types in response to stress, including oxidative stress, transfection, and starvation. Significantly, both immune and nonimmune cells could form these aggresome-like induced structures (ALIS). Protein synthesis was essential for ALIS formation in response to oxidative stress, indicating that DRiP formation was required. Furthermore, puromycin, which increases DRiP formation, was sufficient to induce ALIS formation. Inhibition of either proteasomes or of autophagy interfered with ALIS clearance in puromycin treated cells. Autophagy inhibition enhanced ALIS formation under a variety of stress conditions. During starvation, ALIS formation in autophagy-deficient cells was only partially inhibited by protein synthesis inhibitors, indicating that both long-lived proteins and DRiPs can be targeted to ALIS. Together, these findings demonstrate that ALIS act as generalized stress-induced protein storage compartments for substrates of the proteasome and autophagy.


Subject(s)
Autophagy/physiology , Cell Compartmentation/physiology , Inclusion Bodies/physiology , Proteasome Endopeptidase Complex/physiology , Protein Transport/physiology , Animals , COS Cells , Chlorocebus aethiops , HeLa Cells , Humans , Inclusion Bodies/metabolism , Macrophages/metabolism , Mice , Models, Biological , Proteins/metabolism , Rats , Stress, Physiological/metabolism , Tumor Cells, Cultured , Ubiquitin/metabolism
7.
Microbiology (Reading) ; 152(Pt 8): 2323-2343, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16849798

ABSTRACT

Salmonella enterica serovar Typhimurium is a facultative intracellular pathogen causing disease in several hosts. These bacteria use two distinct type III secretion systems that inject effector proteins into the host cell for invasion and to alter maturation of the Salmonella-containing vacuole. Members of the Salmonella translocated effector (STE) family contain a conserved N-terminal translocation signal of approximately 140 aa. In this study, the STE family member SifA was examined using deletion strategies. Small deletions (approx. 20 residues long) throughout SifA were sufficient to block its secretion and/or translocation into host cells. Transfection of HeLa cells with a GFP-SifA fusion was previously shown to be sufficient to induce formation of Sif-like tubules resembling structures present in Salmonella-infected cells. The present study showed that both N- and C-terminal domains of SifA are required for this phenotype. Furthermore, both domains could induce aggregation of Lamp1-positive compartments, provided they were coupled to the minimal C-terminal membrane-anchoring motif of SifA. Mutation or deletion of the conserved STE N-terminal WEK(I/M)xxFF translocation motif of SopD2 disrupted its association with Lamp1-positive compartments, implicating these residues in both effector translocation and subcellular localization. Interestingly, one GFP-SifA deletion mutant lacking residues 42-101, but retaining the WEK(I/M)xxFF motif, targeted the Golgi apparatus. In addition, short peptides containing the signature WEK(I/M)xxFF motif derived from the N-termini of Salmonella effectors SopD2, SseJ and SspH2 were sufficient to localize GFP to the Golgi. These studies suggest that Salmonella effectors contain multifunctional motifs or domains that regulate several effector traits, including protein secretion/translocation, localization and subversion of host cell systems. Conditions that perturb the tertiary structure of effectors can influence their localization in host cells by liberating cryptic intracellular targeting motifs.


Subject(s)
Bacterial Proteins/physiology , Glycoproteins/physiology , Amino Acid Motifs , Amino Acid Sequence , Animals , Bacterial Proteins/analysis , Bacterial Proteins/chemistry , Base Sequence , Cell Line , Glycoproteins/analysis , Glycoproteins/chemistry , Golgi Apparatus/metabolism , Humans , Mice , Molecular Sequence Data , Protein Structure, Tertiary , Protein Transport , Structure-Activity Relationship
8.
Res Microbiol ; 157(4): 333-44, 2006 May.
Article in English | MEDLINE | ID: mdl-16376524

ABSTRACT

MinE regulates the proper placement of the cytokinetic FtsZ ring at midcell by inducing the pole-to-pole movement of MinCD complexes. While the N-terminus of MinE has been implicated in MinD binding, a clear functional role of the C-terminus has not been elucidated. We previously determined that MinE from Neisseria gonorrhoeae (Ng) was functional in Escherichia coli (Ec). Thus, using E. coli as a model organism, gonococcal MinE (MinE(Ng)) function was examined by generating amino acid substitutions of highly conserved MinE(Ng) residues and by testing the ability of the mutant proteins to interact with gonococcal MinD (MinD(Ng)), to induce a minicell phenotype upon overexpression, to initiate MinD(Ng) oscillation, and to stimulate MinD(Ng) ATPase activity. N-terminal MinE(Ng) mutants were unable to bind to MinD(Ng); thus, they did not induce a minicell phenotype, promote MinD(Ng) oscillation or stimulate MinD(Ng) ATPase activity. While C-terminal MinE(Ng) mutants exhibited reduced abilities to bind to MinD(Ng), we show that differences in MinD(Ng) binding to the C-terminus of MinE(Ng) alter the ability of MinE(Ng) to properly stimulate MinD(Ng) activity. We present four major findings from our studies of MinE(Ng): both the N- and C-termini of MinE(Ng) interact with MinD(Ng); interaction between MinD(Ng) and MinE(Ng) is required for the recruitment of MinD(Ng) to the coiled array; oscillation of MinD(Ng) does not require ATPase stimulation; and, the extent of MinD(Ng) ATPase stimulation depends on the binding strength between MinD(Ng) and the C-terminus of MinE(Ng.).


Subject(s)
Adenosine Triphosphatases/physiology , Bacterial Proteins/physiology , Cell Division , Escherichia coli/metabolism , Neisseria gonorrhoeae/metabolism , Adenosine Triphosphatases/genetics , Amino Acid Sequence , Amino Acid Substitution , Bacterial Proteins/genetics , Enzyme Activation , Escherichia coli/cytology , Molecular Sequence Data , Protein Binding , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/physiology , Sequence Homology, Amino Acid
9.
J Immunol ; 174(5): 2471-5, 2005 Mar 01.
Article in English | MEDLINE | ID: mdl-15728449

ABSTRACT

In response to a maturation stimulus, dendritic cells undergo the formation of ubiquitinated protein aggregates known as dendritic cell aggresome-like induced structures (DALIS). DALIS are thought to act as Ag storage structures, allowing for the prioritized degradation of proteins during infection. In this study, we demonstrate that murine macrophages can also form ubiquitinated protein aggregates that are indistinguishable from DALIS. These were formed in a dose- and time-dependent manner, and in response to a variety of microbial products. Surprisingly, the proteasome did not accumulate on these ubiquitinated protein structures, further underlining the difference between DALIS and aggresomes. Our studies suggest that DALIS formation is important for the function of Ag-presenting immune cells during infection.


Subject(s)
Dendritic Cells/metabolism , Dendritic Cells/microbiology , Macrophages/metabolism , Macrophages/microbiology , Animals , Antigen-Presenting Cells/enzymology , Antigen-Presenting Cells/immunology , Antigen-Presenting Cells/metabolism , Antigen-Presenting Cells/microbiology , Cell Line , Cells, Cultured , Dendritic Cells/enzymology , Dendritic Cells/immunology , HeLa Cells , Humans , Listeria monocytogenes/immunology , Macrophages/enzymology , Macrophages/immunology , Mice , Microscopy, Confocal , Microscopy, Fluorescence , Proteasome Endopeptidase Complex/metabolism , Rats , Salmonella typhimurium/immunology , Transfection , Ubiquitin/genetics , Ubiquitin/metabolism
10.
Res Microbiol ; 156(1): 17-29, 2005.
Article in English | MEDLINE | ID: mdl-15636744

ABSTRACT

A region in the cell division site determinant MinD required for stimulation by MinE and which determines MinD topological specificity along coil-like structures has been identified. Structural modeling of dimeric MinD and sequence alignment of 24 MinD proteins revealed a conserved polar region in Gram-negative bacterial MinD proteins, corresponding to residues 92-94 of Neisseria gonorrhoeae MinD (MinD(Ng)). Using MinD(Ng) as a paradigm for MinD functionality in Gram-negative organisms, mutation of these conserved residues did not abrogate MinD(Ng) self-association, nor its interaction with MinE(Ng) and the cell division inhibitor MinC. Although the MinD(Ng) mutant dimerized in the presence of ATP, its ATPase activity was not stimulated by MinE(Ng), unlike wild-type MinD(Ng). GFP fusions to either MinD(Ng) or to Escherichia coli MinD bearing simultaneous or individual mutations to residues 92-94 localized within coiled arrays along the E. coli inner cell periphery, similar to wild-type GFP-MinD. However, unlike wild-type GFP-fusions, the mutant proteins were distributed uniformly throughout the array, despite the presence of MinE, which normally imparts topological specificity to MinD by inducing the latter to oscillate from pole-to-pole and away from midcell. Hence, despite localizing along the inner cell periphery as a polymeric structure, the mutant MinD proteins in this study have lost the ability to be efficiently stimulated by MinE(Ng), resulting in a loss of distinct pole-to-pole oscillation.


Subject(s)
Adenosine Triphosphatases/chemistry , Adenosine Triphosphatases/metabolism , Bacterial Proteins/chemistry , Bacterial Proteins/metabolism , Neisseria gonorrhoeae/metabolism , Protein Structure, Tertiary , Adenosine Triphosphatases/genetics , Adenosine Triphosphate/metabolism , Amino Acid Sequence , Bacterial Proteins/genetics , Conserved Sequence , Cytoplasm/chemistry , Dimerization , Escherichia coli Proteins/genetics , Escherichia coli Proteins/metabolism , Genes, Reporter , Green Fluorescent Proteins/analysis , Green Fluorescent Proteins/genetics , Models, Molecular , Molecular Sequence Data , Mutation , Neisseria gonorrhoeae/genetics , Neisseria gonorrhoeae/growth & development , Protein Binding , Protein Conformation , Recombinant Fusion Proteins/analysis , Sequence Homology, Amino Acid
11.
EcoSal Plus ; 1(2)2005 Nov.
Article in English | MEDLINE | ID: mdl-26443522

ABSTRACT

Salmonella spp. can infect host cells by gaining entry through phagocytosis or by inducing host cell membrane ruffling that facilitates bacterial uptake. With its wide host range, Salmonella enterica serovar Typhimurium has proven to be an important model organism for studying intracellular bacterial pathogenesis. Upon entry into host cells, serovar Typhimurium typically resides within a membrane-bound compartment termed the Salmonella-containing vacuole (SCV). From the SCV, serovar Typhimurium can inject several effector proteins that subvert many normal host cell systems, including endocytic trafficking, cytoskeletal rearrangements, lipid signaling and distribution, and innate and adaptive host defenses. The study of these intracellular events has been made possible through the use of various imaging techniques, ranging from classic methods of transmission electron microscopy to advanced livecell fluorescence confocal microscopy. In addition, DNA microarrays have now been used to provide a "snapshot" of global gene expression in serovar Typhimurium residing within the infected host cell. This review describes key aspects of Salmonella-induced subversion of host cell activities, providing examples of imaging that have been used to elucidate these events. Serovar Typhimurium engages specific host cell machinery from initial contact with the host cell to replication within the SCV. This continuous interaction with the host cell has likely contributed to the extensive arsenal that serovar Typhimurium now possesses, including two type III secretion systems, a range of ammunition in the form of TTSS effectors, and a complex genetic regulatory network that coordinates the expression of hundreds of virulence factors.

12.
J Bacteriol ; 186(21): 7175-85, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15489428

ABSTRACT

MinD is involved in regulating the proper placement of the cytokinetic machinery in some bacteria, including Neisseria gonorrhoeae and Escherichia coli. Stimulation of the ATPase activity of MinD by MinE has been proposed to induce dynamic, pole-to-pole oscillations of MinD in E. coli. Here, we investigated the effects of deleting or mutating conserved residues within the N terminus of N. gonorrhoeae MinD (MinD(Ng)) on protein dynamism, localization, and interactions with MinD(Ng) and with MinE(Ng). Deletions or mutations were generated in the first five residues of MinD(Ng), and mutant proteins were evaluated by several functional assays. Truncation or mutation of N-terminal residues disrupted MinD(Ng) interactions with itself and with MinE. Although the majority of green fluorescent protein (GFP)-MinD(Ng) mutants could still oscillate from pole to pole in E. coli, the GFP-MinD(Ng) oscillation cycles were significantly faster and were accompanied by increased cytoplasmic localization. Interestingly, in vitro ATPase assays indicated that MinD(Ng) proteins lacking the first three residues or with an I5E substitution possessed higher MinE(Ng)-independent ATPase activities than the wild-type protein. These results indicate that determinants found within the extreme N terminus of MinD(Ng) are implicated in regulating the enzymatic activity and dynamic localization of the protein.


Subject(s)
Adenosine Triphosphatases/chemistry , Adenosine Triphosphatases/metabolism , Bacterial Proteins/chemistry , Bacterial Proteins/metabolism , Gene Expression Regulation, Enzymologic , Neisseria gonorrhoeae/enzymology , Adenosine Triphosphatases/genetics , Amino Acid Sequence , Bacterial Proteins/genetics , Escherichia coli/enzymology , Escherichia coli/genetics , Models, Molecular , Molecular Sequence Data , Mutation , Neisseria gonorrhoeae/genetics , Recombinant Fusion Proteins , Saccharomyces cerevisiae/enzymology , Saccharomyces cerevisiae/genetics , Two-Hybrid System Techniques
13.
Mol Microbiol ; 46(2): 493-504, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12406224

ABSTRACT

Min proteins are involved in the correct placement of division septa in many bacterial species. In Escherichia coli (Ec) cells, these proteins oscillate from pole to pole, ostensibly to prevent unwanted polar septation. Here, we show that Min proteins from the coccus Neisseria gonorrhoeae (Ng) also oscillate in E. coli. Green fluorescent protein (GFP) fusions to gonococcal MinD and MinE localized dynamically in different E. coli backgrounds. GFP-MinDNg moved from pole to pole in rod-shaped E. coli cells with a 70 +/- 25 s localization cycle when MinENg was expressed in cis. The oscillation time of GFP-MinDNg was reduced when wild-type MinENg was replaced with MinENg carrying a R30D mutation, but lengthened by 15 s when activated by MinEEc. Several mutations in the N-terminal domain of MinDNg, including K16Q and 4- and 19-amino acid truncations, prevented oscillation; these MinDNg mutants showed decreased or lost interaction with themselves and MinENg. Like MinEEc-GFP, MinENg-GFP formed MinE rings and oscillated in E. coli cells when MinDEc was expressed in cis. Finally, in round E. coli cells, GFP-MinDNg appeared to move in a plane parallel to completed septa. This pattern of movement is predicted to be similar in gonococcal cells, which also divide in alternating perpendicular planes.


Subject(s)
Adenosine Triphosphatases/physiology , Bacterial Proteins , Escherichia coli Proteins/physiology , Escherichia coli/genetics , Escherichia coli/physiology , Neisseria gonorrhoeae/genetics , Adenosine Triphosphatases/genetics , Cell Cycle Proteins , Cell Division , Cell Polarity , Escherichia coli Proteins/genetics , Gene Expression Regulation, Bacterial , Green Fluorescent Proteins , Luminescent Proteins/metabolism , Mutation , Recombinant Fusion Proteins/metabolism
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