Bacterial morphological plasticity

Bacterial Shape and Size Under Selective Forces

Normally, bacteria have different shapes and sizes which include coccus, rod and helical/spiral (among others less common) and that allow for their classification. For instance, rod shapes may allow bacteria to attach more readily in environments with shear stress (e.g., in flowing water). Cocci may have access to small pores, creating more attachment sites per cell and hiding themselves from external shear forces. Spiral bacteria combine some of the characteristics cocci (small footprints) and of filaments (more surface area on which shear forces can act) and the ability to form an unbroken set of cells to build biofilms. Several bacteria alter their morphology in response to the types and concentrations of external compounds. Bacterial morphology changes help to optimize interactions with cells and the surfaces to which they attach. This mechanism has been described in bacteria such as Escherichia coli and Helicobacter pylori.

Physiological mechanisms

Oxidative stress, nutrient limitation, DNA damage and antibiotics exposure are some of stress conditions to which bacteria respond, altering their DNA replication and cell division. Filamentous bacteria have been considered to be over-stressed, sick and dying members of the population. However, the filamentous members of some communities have vital roles in the population´s continued existence, since the filamentous phenotype can confer protection against lethal environments. Filamentous E. coli can be up to 70 µm in length and has been identified playing an important role in pathogenesis in human cystitis. There are different mechanisms identified in some bacteria that are attributable to the development to filamentous forms.

Base Excision Repair (BER) mechanism, as a strategy to repair DNA damage observed in E. coli. This involves two types of enzymes:

Bifunctional glycosylases: the endonuclease III (encoded by nth gene)

Apurinic/Apirimidinic (AP)-endonucleases: endonuclease IV (encoded by nfo gene) and exonuclease III (encoded by xth gene).

Under this mechanism, daughter cells are protected from receiving damaged copies of the bacterial chromosome, and at the same time promoting bacterial survival. A mutant for these genes lack BER activity and a strong formation of filamentous structures is observed.

SulA/FtsZ mediated filamentation: This is a mechanism to halt cell division and repair DNA. In the presence of single-stranded DNA regions, due to the action of different external cues (that induce mutations), the major bacterial recombinase (RecA) binds to this DNA regions and is activated by the presence of free nucleotide triphosphates. This activated RecA stimulates the autoproteolysis of the SOS transcriptional repressor LexA. The LexA regulon includes a cell division inhibitor, SulA, that prevent the transmission of mutant DNA to the daughter cells. SulA is a dimer that binds FtsZ (a tubulin-like GTPase) in a 1:1 ratio and acts specifically on its polymerization which results in the formation of non-septated bacteria filaments. A similar mechanism may occur in Mycobacterium tuberculosis,which also elongates after being phagocytized.

Ssd encoded by rv3660c promotes filamentation in M. tuberculosis in response to the stressful intracellular environment. Recently, septum site determining protein (Ssd) was discovered in this bacteria as a septum inhibitor, leading to elongated cells (not only in this specie but also in and in Mycobacterium smegmatis). The bacterial filament ultrastructure is consistent with inhibition of FtsZ polymerization (previously described). Ssd is believed to be part of a global regulatory mechanism in this bacteria that promotes a shift into an altered metabolic state.

In Helycobacter pylori, a spriral-shaped Gram-negative bacterium, the filamentation mechanism are regulated by two mechanisms: the peptidases that cause peptidoglycan relaxation and the coiled-coil-rich proteins (Ccrp) that are responsible for the helical cell shape in vitro as well as in vivo. A rod shape could have probably an advantage for motility than the regular helical shape. In this model, there is another protein Mre, which is not exactly involved in the maintenance of cell shape but in the cell cycle. It has been demotrated that mutant cells were highly elongated due to a delay in cell division and contained non-segregated chromosomes.

Immune response

Some of the strategies for bacteria to bypass host defenses include the generation of filamentous structures. As it has been observed in other organisms (such as fungi), filamentous forms are resistant to phagocytosis. As an example of this, during urinary tract infection, filamentatious structures of uropathogenic E. coli (UPEC) start to develop in response to host innate immune response (more exactly in response to Toll-like receptor 4-TLR4). TLR-4 is stimulated by the lipopolysaccharide (LPS) and recruits neutrophils (PMN) which are important leukocytes to eliminate these bacteria. Adopting filamentous structures, bacteria resist these phagocytic cells and their neutralizing activity (which include antimicrobial peptides, degradative enzyme and reactive oxygen species). It is believed that filamentation is induced as a response of DNA damage (by the mechanisms previously exposed), participating SulA mechanism and additional factors. Furthermore, the length of the filamentous bacteria could have a stronger attachment to the epithelial cells, with an increased number of adhesins participating in the interaction, making even harder the work for (PMN). The interaction between phagocyte cells and adopting filamentous-shape bacteria provide an advantage to their survival. In this relate, filamentation could be not only a virulence, but also a resistance factor in these bacteria.

Predator protist

Bacteria exhibit a high degree of “morphological plasticity” that protects them from predation. Bacterial capture by protozoa is affected by size and irregularities in shape of bacteria. Oversized, filamentous, or prosthecate bacteria may be too large to be ingested. On the other hand, other factors such as extremely tiny cells, high-speed motility, tenacious attachment to surfaces, formation of biofilms and multicellular conglomerates may also reduce predation. Several phenotypic features of bacteria are adapted to escape protistan-grazing pressure.

Protistan grazing or bacterivory is a protozoan feeding on bacteria. It affects prokaryotic size and the distribution of microbial groups. There are several feeding mechanisms used to seek and capture prey, because the bacteria have to avoid being consumed from these factors. There are six feeding mechanisms listed by Kevin D. Young.

Filter feeding: transport water through a filter or sieve

Sedimentation: allows prey to settle into a capture device

Interception: capture by predator-induced current or motility and phagocytosis

Raptorial: predator craws and ingests prey through pharynx or by pseudopods

Pallium: prey engulfed e.g. by extrusion of feeding membrane

Myzocytosis: punctures prey and suck out cytoplasm and content

Bacterial responses are elicited depending on the predator and prey combinations because feeding mechanisms differ among the protists. Moreover, the grazing protists also produce the by-products, which directly lead to the morphological plasticity of prey bacteria. For example, the morphological phenotypes of Flectobacillus spp. were evaluated in the presence and absence of the flagellate grazer Orchromonas spp. in a laboratory that has environmental control within a chemostat. Without grazer and with adequate nutrient supply, the Flectobacillus spp. grew mainly in medium-sized rod (4-7 μm), remaining a typical 6.2 μm in length. With the predator, the Flectobacillus spp. size was altered to an average 18.6 μm and it is resistant to grazing. Interestingly, if the bacteria are exposed to the soluble by-products produced by grazing Orchromonas spp. and pass through a dialysis membrane, the bacterial length can increase to an average 11.4 μm. Filamentation occurs as a direct response to these effectors that are produced by the predator and there is a size preference for grazing that varies for each species of protist. The filamentous bacteria that are larger than 7 μm in length are generally inedible by marine protists. This morphological class is called grazing resistant. Thus, filamentation leads to the prevention of phagocytosis and killing by predator.

Bimodal effect

Bimodal effect is a situation that bacterial cell in an intermediate size range are consumed more rapidly than the very large or the very small. The bacteria, which are smaller than 0.5 μm in diameter, are grazed by protists four to six times less than larger cells. Moreover, the filamentous cells or cells with diameters greater than 3 μm are often too large to ingest by protists or are grazed at substantially lower rates than smaller bacteria. The specific effects vary with the size ratio between predator and prey. Pernthaler et al. classified susceptible bacteria into four groups by rough size.

Bacterial size < 0.4 μm were not grazed well

Bacterial size between 0.4 μm and 1.6 μm were “grazing vulnerable”

Bacterial size between 1.6 μm and 2.4 μm were “grazing suppressed”

Bacterial size > 2.4 μm were “grazing resistant”

Filamentous preys are resistant to protist predation in a number of marine environments. In fact, there is no bacterium entirely safe. Some predators graze the larger filaments to some degree. Morphological plasticity of some bacterial strains is able to show at different growth conditions. For instance, at enhanced growth rates, some strains can form large thread-like morphotypes. While filament formation in subpopulations can occur during starvation or at suboptimal growth conditions. These morphological shifts could be triggered by external chemical cues that might be released by the predator itself.

Besides bacterial size, there are several factors affecting the predation of protists. Bacterial shape, the spiral morphology may play a defensive role towards predation feedings. For example, Arthrospira may reduce its susceptibility to predation by altering its spiral pitch. This alteration inhibits some natural geometric feature of the protist’s ingestion apparatus. Multicellular complexes of bacterial cells also change the ability of protist’s ingestion. Cells in biofilms or microcolonies are often more resistant to predation. For instance, the swarm cells of Serratia liquefaciens resist predation by its predator, Tetrahymenu. Due to the normal-sized cells that first contact a surface are most susceptible, bacteria need elongating swarm cells to protect them from predation until the biofilm matures. For aquatic bacteria, they can produce a wide range of extracellular polymeric substances (EPS), which comprise protein, nucleic acids, lipids, polysaccharides and other biological macromolecules. EPS secretion protects bacteria from HNF grazing. The EPS-producing planktonic bacteria typically develop subpopulations of single cells and microcolonies that are embedded in an EPS matrix. The larger microcolonies are also protected from flagellate predation because of their size. The shift to the colonial type may be a passive consequence of selective feeding on single cells. However, the microcolony formation can be specifically induced in the presence of predators by cell-cell communication (quorum sensing).

As for bacterial motility, the bacteria with high-speed motility sometimes avoid grazing better than their nonmotile or slower strains especially the smallest, fastest bacteria. Moreover, a cell’s movement strategy may be altered by predation. The bacteria move by run-and-reverse strategy, which help them to beat a hasty retreat before being trapped instead of moving by the run-and-tumble strategy. However, there is a study showed that the probability of random contacts between predators and prey increases with bacterial swimming, and motile bacteria can be consumed at higher rates by HNFs. In addition, bacterial surface properties affect predation as well as other factors. For example, there is an evidence shows that protists prefer gram-negative bacteria than gram-positive bacteria. Protists consume gram-positive cells at much lower rates than consuming gram-negative cells. The heterotrophic nanoflagellates actively avoid grazing on gram-positive actinobacteria as well. Grazing on gram-positive cells takes longer digestion time than on gram-negative cells. As a result of this, the predator cannot handle more prey until the previous ingested material is consumed or expelled. Moreover, bacterial cell surface charge and hydrophobicity have also been suggested that might reduce grazing ability. Another strategy that bacteria can use for avoiding the predation is to poison their predator. For example, certain bacteria such as Chromobacterium violaceum and Pseudomonas aeruginosa can secrete toxin agents related to quorum sensing to kill their predators.

Antibiotic

Antimicrobial agent has obvious implications for microbial infection therapeutics. The ability of bacteria to decrease their susceptibility to antimicrobial drugs importantly affects both bacterial ecology and the treatment of infectious diseases. From patients who are treated with antibiotics, filamentous organisms are commonly found in their clinical specimens. The filamentation contributes to a pathogen’s resistance to this antimicrobial agent. The induction of bacterial filamentation by antibiotics can alter bacterial virulence, which would have important implications for the pathogenesis and treatment of the disease as well.

For Burkholderia pseudomallei, some clinical antibiotic agents that are used to treat its infection, mellioidosis, can induce morphological changes such as filamentation and physiological changes in this bacteria. These antibiotics are the β-lactam antibiotics, fluoroquinolones, and antibiotics that inhibit the synthesis of thymidine. The ability of some β-lactam antibiotics to induce filamentation in gram negative bacteria is to inhibit penicillin-binding proteins (PBPs). This inhibition stops the assembly of peptidoglycan network in bacterial cell wall. PBP-1 inhibition leads to rapid cell death. While PBP-2 and PBP-3 inhibition lead to morphological change, turn normal cells to spheroplasts and filamentous cells (elongated rods), respectively. PBP-3 forms the septum in dividing bacteria by involving transpeptidase so inhibition of this PBP-3 protein leads to the incomplete formation of septa in dividing bacteria resulting in the formation of long strands of bacteria (filaments). Kang Chen et al. mentioned that the filament was induced by sublethal concentrations of ceftazidime, ofloxacin, or trimethoprim. At or below the minimal inhibitory concentration (MIC), filamentation occurred mainly at these concentration and bacteria remained as viable within the vacuoles of immortalized human macrophages, not rapidly killed. However, the B.pseudomallei filaments revert to normal forms when the antibiotics are removed. Moreover, bacillary daughter cells maintained cell-division capacity and viability despite re-exposure to antibiotics such as ceftazidime. Thus, this developmental alteration may provide additionally survival advantages to bacteria. Furthermore, for Pseudomonas aeruginosa, filamentation induced by antibiotics appears to trigger bacteria to change from a normal growth phase to a stationary growth phase. Filamentous bacteria are also associated with an increase in endotoxin (lipopolysaccharide, LPS) release and the immune system of patients needs to cope with this characteristic. Chloramphenicol antibiotic can induce the formation of filamentous cells, which contain multiple copies of unsegregated chromosomes. These chromosomes lead to the unsuccessful division of elongated cells, and the formation of bacterial filament. Moreover, the filamentation also depends on the expression levels of an efflux pump (MexAB-OprM) and the minimum inhibitory concentration of chloramphenicol.

The molecular correlate of the filament formation was described. The exposure to β-lactam antibiotics induced the SOS response in Escherichia coli. During repair of DNA damage, the SOS response aids bacterial propagation by inhibiting cell division. Moreover, both β-lactam antibiotics and genetic mutation induce SOS in E.coli through the DpiBA two-component signal transduction system leading to the inactivation of the ftsl gene product, penicillin binding protein 3 (PBP-3). The ftsl gene is a group of filamentous temperature-sensitive genes implicated in cell division. In addition, it is a membrane transpeptidase required for peptidoglycan synthesis at the septum generated by cell division. The event to inactivate ftsl gene product requires the SOS-promoting recA and lexA genes as well as dpiA and transiently inhibits bacterial cell division. Consequently, the bactericidal effects of β-lactam antibiotics are limited. The DpiA is the effector for the DpiB two-component system. Interaction of DpiA with replication origins competes with the binding of the replication proteins DnaA and DnaB. When overexpressed, DpiA can interrupt DNA replication and induce the SOS response resulting in inhibition of cell division.

Nutritional stress

Nutritional stress can change bacterial morphology. A common shape alteration is filamentation which can be triggered by a limited availability of one or more substrates, nutrients or electron acceptors. Since the filament can increase a cell’s uptake–surface area without significantly changing its volume appreciably. Moreover, the filamentation benefits bacterial cells attaching to a surface because it increases specific surface area in direct contact with the solid medium. In addition, the filamentation may allows bacterial cells to access nutrients by enhancing the possibility that part of the filament will contact a nutrient-rich zone and pass compounds to the rest of the cell’s biomass. For example, Actinomyces israelii grows as filamentous rods or branched in the absence of phosphate, cysteine, or glutathione. However, it returns to a regular rod-like morphology when adding back these nutrients.