Shigellosis

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Shigella bacteria, in red, shown on the surface of an He-La cell. From: http://www.cimst.ethz.ch/ [1]

Etiology/Bacteriology

Shigellosis is caused by a bacterial infection of the Shigella genus. The Shigella genus is a Gram-negative, rod-shaped facultative anaerobe that does not form spores. There are four Shigella species, only three of which are the major disease causing species. S. flexneri accounts for roughly 60 percent of shigellosis cases in developing world and is the most frequently isolated species of Shigella worldwide [1]. S. sonnei is the cause of 77% of cases in the developed world while only causing 15 percent of cases in the developing world, and it is also causes two-thirds of shigellosis cases in the United States [1]. S. dysenteriae is the most common cause of dysentery epidemics, usually in confined populations with poor hygiene and little to no sanitation such as refugee camps. S. dysenteriae is a major concern because it is the only species of Shigella that produces the Shiga toxin.

Pathogenesis

Virulence factors

Shigella spp posses a wide variety of virulence factors that allow it to adhere to the epithelium of the intestine, survive the acidic stomach, invade host cells, evade immune responses and introduce toxins into the body.

Acid tolerance

Acid tolerance contributes to Shigella’s low infectious dose, but research has shown that acid tolerance changes according to growth phase [2]. Stationary phase seems to be necessary in order for the pathogen to survive conditions of low pH.

Effector proteins

Several effector proteins encoded on Shigella’s virulence plasmid allow the pathogen to invade host cells and move through the eukaryotic cytoplasm. Many of these same proteins help the pathogen adhere to the host cell wall. Invasion plasmid antigen B (IpaB) initiates binding to the host cell while also initiating pathways that kill macrophages upon infection, IpaC activates proteins to form the actin-polymerizing complex that allows Shigella to move and spread within host cells [3].

The Mxi-Spa T3SS

Shigella utilizes a Type III Secretion System to deliver its effector protein to the cytoplasm of host cells. Transmission electron microscopy has revealed the ATPase- dependent T3SS to consist of a 45 to 60 nm needle that extends out from the bacterium nested in a complex composed of seven rings primarily made of MxiD [4]. The whole complex spans the inner membrane, periplasm, and outer membrane of the pathogen and continues to allow for binding to host cells. As the internal of the diameter of the needle is only 2 to 3 nm across, effector proteins pass through the complex in a denatured form.

In order to control and time secretion of effector proteins, Shigella senses environmental oxygen conditions and utilizes essential effector proteins. In low oxygen environments, the pathogen elongates the T3SS needle thus preventing effector proteins from being secreted. As the bacterium approaches host cells, which require oxygen, it glycosylates its LPS in order to shorten them and thus expose the T3SS needle [5]. Once Shigella has translocated IpaB and IpaC to the tip of the needle, IpaB binds to the host cell surface, enduces changes in the cell membrane of the host cell, and works with IpaC to insert the needle into the host cell.

Toxins

Shiga toxin molecular structure. A subunit is shown in green associated with pentamer of B subunits. From: RCSB Protein Data Bank [2]

Three toxins are princiapally associated with Shigella spp and account for or are hypothesized to account for the emergence of bloody diarrhea in infected humans. Shigella enterotoxin 1 and 2 (ShET1 and ShET2) were shown to induce fluid secretion in the intestine and thus thought to produe the watery part of diarrhea, but the exact mechanism that produces diarrhea is still unknown [6].

Shiga toxin, on the other hand, is only associated with S. dysenteriae and accounts for the life-threatening symptoms found in some Shigella infections. Shiga toxin is an AB toxin consisting of a ~32 kDa A subunit and a pentamer of ~7 kDa B subunits. Once released from the bacterium, the B subunits bind globotriaosylceramide on the surface of the host cell. The toxin is then internalized and moved toward the cell by the Golgi network through a process called retrograde transport [6]. During this process, the A subunit is cleaved to created a A1 fragment with N- glycosidase acivity which cleaves an adenine from the 28s rRNA component of the 60s ribosomal subunit once the toxin reaches the endoplasmic reticulum. The cleavage inhibits EF1 mediated tRNA bonding and halts elongation of peptides.

Mechanism

An overview of Shigella's pathogenesis. Translocation across the intestinal epithelial allows the pathogen to invade more host cells and induce a host immune response. From: Clin. Microbiol. Rev. January 2008 vol. 21 no. 1 134-156 [3]

The pathogenesis of "Shigella" revolves around the cell's ability to enter host cells and hijack cellular machinery in order to evade immune responses and renew its replicative space. By utilizing an injectisome, the pathogen can inject effector proteins into the host cell that allow it to manipulate the eukaryotic cell's cytoskeleton, primarily actin fibers. Actin polymerization drives the process that leads to uptake of the pathogen and gives the bacterium a way to achieve intracellular motility as well as a way to pass laterally to other host cells. In addition, Shigella can mediate the cell death of macrophages to further evade the host's immune system.

Adherence

Once Shigella spp passes through the stomach, the pathogen approaches the large intestine where it will eventually cross the intestinal epitheial through a microfold cell to induce its pathogenicity. M cells, located in the Peyer’s patch, facilitate the development of immune response by absorbing antigens and passing them on to lymphoid tissues, and Shigella utilizes this function to gain access to the basolateral side of the epithelial cells.

Shigella adheres to M cells by binding CD44 and α5β1 found in areas of cell membrane high in cholestoral content known as lipid rafts [7]. These rafts are known to contain bunches of specific proteins, and in this case, the rafts contain the aforementioned receptors recognized by IpaB and the IpaBCD effector proteins on the pathogen’s surface. Binding initiates the introduction of the T3SS needle into the cell membrane which initiates the rearrangement of the membrane to bring more lipid rafts to the bacterial entry site and thus bringing more receptors to the cell and creating a signaling platform [7].

Entering the cell

Successful adherence prompts the pathogen to secrete various effector proteins through its T3SS that will help force the cell to ingest the bacterium by rearranging the eukaryotic cytoskeleton. IpgD and IpaA work to break down existing actin polymers and disconnect the cytoskeleton from the cytoplasmic side of the membrane respectively. VirA destabilizes microtubules and simultaneously activates a GTPase called Rac1. VirA works alongside IpaC and IpgB2 to activate Rac1 and Cdc42, another GTPase, which recruit Arp2/3 to initiate actin nucleation [8]. The following actin polymerization creates protrusions that extend from the host cell and then engulf the pathogen thus enclosing Shigella in a phagosome and giving it access to the inside of the cell.

Having passed into the M cell, Shigella utilizes its effector proteins and T3SS to escape from the phagosome—a process which occurs within the span of 15 minutes [9] . Shigella begins to multiply inside of the host cell after breaking down the phagosome and secretes IscB, which competitively binds to IscA, to avoid autophagy in the cell. In addition, IpgD actives signal pathways that prevent the host cell from inducing apoptosis in order the pathogen to multiply without interruption.

Actin-mediated motility

Movement within the cytoplasm of the cell is achieved by hijacking actin-nucleating machinery. Surface-bound IscA binds and activates N-WASP which recruits Arp2/3. Polymerization of actin on one end of the pathogen pushes it through the cytoplasm in the opposite direction, and VirA destabilizes microtubules surrounding the pathogen in order to allow movement through the cytoskeleton [10]. This induced motility allows the pathogen to evade extracellular immune defenses and invade neighboring epithelial cells by pressing against the cell membrane to create a protrusion that is endocytosis by the neighboring cell where it will multiply and continue to infect the epithelium [11]. Shigella can use the same mechanism to break through the basolateral cell membrane and reach the intestinal mucosa. The spread of Shigella in the epithelium through this process results in pronounced death of epithelial cells and subsequently a strong immune response.

Encountering macrophages

Shigella encounters macrophages shortly after reaching the intestinal mucosa. Shigella breaks through the phagosome upon being phagocytized and begins to secrete IpaB in the cytoplasm of the macrophage. IpaB binds to caspase-1, a protease in the macrophage, to induce pyroptosis through a variety of pathways including DNA fragmentation, ATP loss and cell membrane rupture [3]. The death of the macrophage triggers a release of cytokines that play a role in the massive inflammatory response associated with Shigella infection. This ability to invade and destroy macrophages allows the pathogen to evade a key part of the host’s innate immune response and constitutes a key part of its pathogenesis.

Clinical features

Symptoms commonly set in one to two days after being exposed to the bacteria and include bloody diarrhea, fever, and stomach cramps. Shigellosis typically passes within five to seven days. The Shiga toxin produced by S. dysenteriae can cause Hemolytic-uremic syndrome (HUS). HUS symptoms include bloody urine, kidney failure, and low blood platelet count, which help to clot blood. These symptoms usually set in 5 to 10 days after diarrhea manifests itself.

Diagnosis

Observation of bloody diarrhea alone cannot be used to determine Shigella to be the causative agent. Stool samples from the patient are needed to culture bacteria and confirm the presence of a Shigella species. The presence of leukocytes in the stool also signifies Shigella as the probable causative agent. Approximately 70 percent of patients suffering from shigellosis have leukocytes or fecal blood detected in the stool sample.

Treatment

Mild cases of Shigellosis can be managed without antibiotics, and recovery can be fairly quick. Antibiotics can limit the spread of the disease in the intestine and reduce the time it takes for the disease to pass through the body. For immunocompromised patients or patients demonstrating severe complications, antibiotics can be necessary. Susceptibility tests should be run to see if the bacterium is resistant to drugs like ampicillin. If so, antibiotics like flouroquinolones and azithromycin may be needed. Typically, the use of antidiarrheal medicines is not recommended because it may make the disease worsen.

Vaccination

Vaccination is difficult for Shigellosis because it is based on a narrow, type-specific O-somatic antigen. However, there are multiple research groups that working on vaccines using very unique approaches. One group passively administered Immunoglobulin from cows milk with a High-titer of S. flexneri antibodies which resulted in protection from wild type infection of S. flexneri. Yet, the administration of low titer antibodies in cow's milk did not yield protection. Also, another group has made progress through live oral vaccinations, but a difficult problem they are facing is that there is a small margin between under and over attenuation. Children seem to develop under attenuation to the vaccine which causes excessive reactogenicity. Developing countries have the other problem of over attenuation to the live oral vaccinations which doesn't provide sufficient immmunogenicity. Whole cell vaccines are being tested as vaccinations at John's Hopkins using S.sonnei and at Antex using Shigella. Clinical testing of these two vaccines is near. Vaccines are being tested on pigs where the toxins of the Shigella species are placed on other bacteria, results have yielded protection

Prevention

No effective vaccine for shigellosis currently exists. Person-to-person trasmission can be prevented through frequent, thorough hand washing. Children should also practice good hand washing to prevent infection obtained from a daycare center or through improper toilet use. Special care should be taken when a child in diapers demonstrates shigellosis. Diapers should be disposed in closed-lid waste bins, and whoever handled the diaper should wash his or her hands as well as the child’s hands once the changing is over. The changing area should also be thoroughly cleaned with bactericidal agents. Child-to-child contact should be avoided if possible if a child has shigellosis.

People with shigellosis should not prepare food for others until they have proven that they are no longer infected. Typical food and water safety precautions should be sufficient to prevent the disease. Greater food safety should be taken when in the developing world. Food should only be consumed if you have treated, cooked, or peeled it for yourself, and water should be treated or boiled before consumption.

Host Immune Response

Massive inflammatory response is principal feature of shigellosis is induced by the pathogen through a variety of pathways. Epithelial cells possess pathogen recognition receptors that trigger signaling pathways once Shigella enters the cytoplasm, and macrophages induce similar responses upon being invaded by the pathogen. In the face of through immune response, Shigella employs strategies that allow the bacterium to downregulate certain pathways and avoid intricate defense mechanisms.

Inside epithelial cells

Peptidoglycan molecules released by Shigella are recognized by nucleotide-binding oligomerization domain-containing protein 1 (NOD1) once the bacterium enters the cytoplasm, and a signal transduction event follows that activates MAPK and NF-kB pathways to initiate the secretion of cytokines and antimicrobial peptides which trigger an inflammatory response. These signaling molecules travel to neighboring cells through connexin gap junctions thus activating inflammatory response pathways in these cells. Since Shigella can travel between cells without leaving the cytoplasm, this universal response helps prep the epithelial lining for further invasion.

Autophagic recognition

Autophagy protein 5(Atg5) recognizes and binds VirG, an effector protein that helps activate the actin polymerization needed for Shigella to achieve intracellular motility, to initiate autophagosome formation. Binding of Atg5 to VirG also induces a response that causes proteins called septins to accumulate at bacterial entry foci and form cages that trap the invading bacterium. Once incased in the septin cage, the pathogen cannot move throughout the cell and subsequently destroy by autophagic pathways.

Effector protein IcsB, however, competitively binds to VirG to prevent recognition by Atg5. Without an Atg5-mediated response, Shigella is able to move and multiply in the cytoplasm out of grasp of autophagy. Such avoidance strategies help illustrate the pathogen’s detailed pathogenesis.

Recruitment of leukocytes

Chemokines released by infected epithelial cells and macrophages attract leukocytes to the site of infection—one the first steps toward resolving the infection. Apart from phagocytizing and killing the pathogen, neutrophils specifically utilize a proteinase that preferentially degrades Shigella effector proteins and produce neutrophil extracellular traps that catch extracellular pathogens and further degrade effector proteins.

Extravasation of neutrophils, however, initially makes the infection worse by disrupting cell-to-cell junctions that would otherwise limit Shigella's access to the basolateral surface of epithelial tissue.

In macrophages

While the invasion and destruction of macrophages is a key part of Shigella pathogenesis, the leukocyte still induces responses that predispose the body to counteracting the infection. Macrophages mediate an immune response through the secretion of cytokines IL-1beta and IL-18. Eventual death of the macrophage also releases molecules that help the mucosal immune system respond to the infection. A notable response is the secretion of IgA, which helps neutralize the pathogen and prevent its adherence, and IgG, which specifically targets LPS on the Gram-negative pathogen. This is a key part that helps prevent infection with the same serotype of pathogen.