Page 856 - Veterinary Immunology, 10th Edition
P. 856

Moraxella bovis also secretes a leukotoxin for bovine neutrophils.
  VetBooks.ir  Actinobacillus pleuropneumoniae secretes a toxin that kills porcine

               macrophages. Mycoplasma mycoides can kill bovine T cells. Other
               bacteria trigger lymphocyte death by apoptosis. These include B.

               anthracis, Streptococci, Shigella, L. monocytogenes, S. aureus, and
               Yersinia. Leukotoxins are a relatively crude method of
               assassination. Some bacteria use much more sophisticated methods
               such as injecting toxins into their targets. Gram-negative bacteria

               such as Salmonella, Pseudomonas, and E. coli have developed an
               elaborate needle complex, a type III secretion system, to convey
               effector molecules directly into the cytosol of effector cells. These
               injection systems are turned on when a bacterium is ingested by a

               cell and exposed to a low pH within the phagosome. Once the
               needle complex enters the cytosol and detects its neutral pH,
               injection of effector molecules occurs. These molecules activate
               guanosine triphosphatases and disrupt intracellular signaling

               pathways. At high concentrations, they produce transmembrane
               pores and kill the cells.
                  Although killing leukocytes is an effective way to avoid being
               eaten, other bacteria are content to simply prevent intracellular

               destruction. Some bacteria generate a resistant cell wall to protect
               themselves against lysosomal enzymes. For example, the cell wall
               waxes of Corynebacterium pseudotuberculosis make it resistant to
               lysosomal enzymes. S. aureus uses a cell wall peptidoglycan that is

               completely resistant to lysozyme. Some bacteria produce
               antioxidants that neutralize the products of the respiratory burst.
               For example, the carotenoid pigments responsible for the yellow
               color of S. aureus can quench singlet oxygen. Salmonella enterica

               Typhimurium can prevent assembly of the NADPH-oxidase
               complex and down-regulate host NOS2 activity. Pasteurella
               multocida and Histophilus somni are also able to inhibit the
               respiratory burst. Anthrax toxins LF and EF also inhibit NAPDH

               oxidase activity. Staphylococcus aureus produces catalase that
               inactivates hydrogen peroxide and the free radicals produced
               during the respiratory burst. It also produces lactate dehydrogenase
               that also helps it to resist NO-mediated oxidation. Some bacteria
               can defend themselves against hypochlorite through the actions of a

               molecular chaperone called Hsp33. This protein unfolds on





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