Brucellosis pathophysiology: Difference between revisions
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*Infected mothers who are [[breast-feeding]] may transmit the [[infection]] to their [[infants]]. | *Infected mothers who are [[breast-feeding]] may transmit the [[infection]] to their [[infants]]. | ||
*[[Sexual]] [[transmission]] has been rarely reported. | *[[Sexual]] [[transmission]] has been rarely reported. | ||
*While uncommon, [[transmission]] may also occur via [[tissue]] [[transplantation]] or [[blood transfusions]].<ref name=" | *While uncommon, [[transmission]] may also occur via [[tissue]] [[transplantation]] or [[blood transfusions]].<ref name="b">Brucellosis. CDC. http://www.cdc.gov/brucellosis/transmission/index.html. Accessed on February 1, 2016</ref> | ||
===Pathogenesis=== | ===Pathogenesis=== | ||
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*The elimination of [[virulent]] [[Brucella]] depends on activated [[macrophages]] and hence requires development of Th1 type cell-mediated responses to [[protein]] [[antigens]]. | *The elimination of [[virulent]] [[Brucella]] depends on activated [[macrophages]] and hence requires development of Th1 type cell-mediated responses to [[protein]] [[antigens]]. | ||
*High [[iron]] [[concentrations]] promote the killing of [[Brucella]], probably by favoring production of [[hydroxylamine]] and [[hydroxyl radical]]. | *High [[iron]] [[concentrations]] promote the killing of [[Brucella]], probably by favoring production of [[hydroxylamine]] and [[hydroxyl radical]]. | ||
*The mechanisms of [[pathogenesis]] of [[Brucella]] infection in its natural host species and in humans are still not completely understood, and further studies are needed.<ref name="pmid9204307">{{cite journal| author=Corbel MJ| title=Brucellosis: an overview. | journal=Emerg Infect Dis | year= 1997 | volume= 3 | issue= 2 | pages= 213-21 | pmid=9204307 | doi=10.3201/eid0302.970219 | pmc=PMC2627605 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9204307 }} </ref><ref name=" | *The mechanisms of [[pathogenesis]] of [[Brucella]] infection in its natural host species and in humans are still not completely understood, and further studies are needed.<ref name="pmid9204307">{{cite journal| author=Corbel MJ| title=Brucellosis: an overview. | journal=Emerg Infect Dis | year= 1997 | volume= 3 | issue= 2 | pages= 213-21 | pmid=9204307 | doi=10.3201/eid0302.970219 | pmc=PMC2627605 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9204307 }} </ref><ref name="aa">Brucelosis. Wikipedia. https://es.wikipedia.org/wiki/Brucelosis. Accessed on February 2, 2016</ref> | ||
===Microscopic Pathology=== | ===Microscopic Pathology=== | ||
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[[Image:Bruce-granulomanecrosis.jpg|thumb|left|200px|Histopathology of guinea pig liver in experimental Brucella suis infection. Granuloma with necrosis]] | [[Image:Bruce-granulomanecrosis.jpg|thumb|left|200px|Histopathology of guinea pig liver in experimental Brucella suis infection. Granuloma with necrosis]] | ||
*[[Brucella|Brucella spp.]] are poorly staining, small [[gram-negative]] [[coccobacilli]] (0.5-0.7 x 0.6-1.5 µm). | *[[Brucella|Brucella spp.]] are poorly staining, small [[gram-negative]] [[coccobacilli]] (0.5-0.7 x 0.6-1.5 µm). | ||
*[[Brucella|Brucella spp.]] are seen mostly as single cells and appearing like “fine sand”.<ref name=" | *[[Brucella|Brucella spp.]] are seen mostly as single cells and appearing like “fine sand”.<ref name="a">Brucellosis. Wikipedia. https://en.wikipedia.org/wiki/Brucellosis. Accessed on January 29, 2016</ref> | ||
*On [[microscopic]] [[histopathological]] analysis of the [[liver]], common findings are: | *On [[microscopic]] [[histopathological]] analysis of the [[liver]], common findings are: | ||
**[[Granulomas]] with centrilobular [[necrosis]] or focal [[necrosis]] and [[parenchyma]] destruction.<ref>Hunt A, Bothwell P. Histological findings in human brucellosis. ''J Clin Pathol''. 1967; 20: 267-272</ref> | **[[Granulomas]] with centrilobular [[necrosis]] or focal [[necrosis]] and [[parenchyma]] destruction.<ref>Hunt A, Bothwell P. Histological findings in human brucellosis. ''J Clin Pathol''. 1967; 20: 267-272</ref> |
Revision as of 19:00, 5 February 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2] Danitza Lukac
Pathophysiology
Transmission
- Brucella spp. are primarily passed among animals, and they cause disease in many different vertebrates.
- Various Brucella species affect sheep, goats, cattle, deer, elk, pigs, dogs, american bishop and several other animals.
- Humans are generally infected in one of three ways:
- Eating undercooked meat or consuming unpasteurized/raw dairy products
- The most common way to be infected is by eating or drinking unpasteurized/raw dairy products.
- When sheep, goats, cows, or camels are infected, their milk becomes contaminated with the bacteria.
- If the milk from infected animals is not pasteurized, the infection will be transmitted to people who consume the milk and/or cheese products.
- Breathing in the bacteria that cause brucellosis (inhalation)
- This risk is generally greater for people in laboratories that work with the bacteria.
- Slaughterhouse and meat-packing employees have also been known to be exposed to the bacteria and ultimately become infected.
- Bacteria entering the body through skin wounds or mucous membranes through contact with infected animals.
- This poses a problem for workers who have close contact with animals or animal excretions (newborn animals, fetuses, and excretions that may result from birth).
- Such workers may include:
- Slaughterhouse workers
- Meat-packing plant employees
- Veterinarians
- Eating undercooked meat or consuming unpasteurized/raw dairy products
- Person-to-person spread of brucellosis is extremely rare.
- Infected mothers who are breast-feeding may transmit the infection to their infants.
- Sexual transmission has been rarely reported.
- While uncommon, transmission may also occur via tissue transplantation or blood transfusions.[1]
Pathogenesis
- Virulent Brucella organisms can infect both nonphagocytic and phagocytic cells.
- When Brucella enters the body white blood cells (WBC), particularly neutrophils and macrophages phagocyte the pathogen.
- WBC transports the pathogen via hematologic and lymphatic routes to different organs, specially to the reticuloendothelial system (RES).
- Brucella multiplies themselves within the vacuoles of the phagocytes without being destructed.
- Different Brucella species are classified as smooth and rough lipopolysaccharide phenotypes.
- Smooth lipopolysaccharides (S-LPS):
- B. abortus, B. melitensis, B. suis and B. neotoma
- S-LPS are more virulent than R-LPS
- S-LPS survive much more effectively than nonsmooth ones
- Rough lipopolysaccharides (R-LPS):
- B. ovis and B. canis
- Smooth lipopolysaccharides (S-LPS):
- In polymorphonuclear or mononuclear phagocytic cells, Brucella spp. uses a number of mechanisms for avoiding or suppressing bactericidal responses:
- Lipopolysaccharide and outer membrane proteins probably play a substantial role in intracellular survival.
- Brucella stays within the cells because it inhibits cellular mechanisms of programmed cell death (apoptosis).
- The survival of Brucella within the cells has been associated with:
- Synthesis of antioxidant enzymes
- Production of guanosine 5 monophosphate (GMP)
- GMP inhibits: phagolysosome fusion, degranulation and activation of the myelo-peroxidase-halide system, and production of tumor necrosis factor.
- Synthesis of proteins of molecular weight 17, 24, 28, 60, and 62 kDa.
- The 24 kDa protein is acid-induced, and its production correlates with bacterial survival under acidic conditions (<pH4).
- The 17 and 28 kDa proteins are apparently specifically induced by macrophages and correlated with intracellular survival.
- The elimination of virulent Brucella depends on activated macrophages and hence requires development of Th1 type cell-mediated responses to protein antigens.
- High iron concentrations promote the killing of Brucella, probably by favoring production of hydroxylamine and hydroxyl radical.
- The mechanisms of pathogenesis of Brucella infection in its natural host species and in humans are still not completely understood, and further studies are needed.[2][3]
Microscopic Pathology
- Brucella spp. are poorly staining, small gram-negative coccobacilli (0.5-0.7 x 0.6-1.5 µm).
- Brucella spp. are seen mostly as single cells and appearing like “fine sand”.[4]
- On microscopic histopathological analysis of the liver, common findings are:
- Granulomas with centrilobular necrosis or focal necrosis and parenchyma destruction.[5]
Reference
- ↑ Brucellosis. CDC. http://www.cdc.gov/brucellosis/transmission/index.html. Accessed on February 1, 2016
- ↑ Corbel MJ (1997). "Brucellosis: an overview". Emerg Infect Dis. 3 (2): 213–21. doi:10.3201/eid0302.970219. PMC 2627605. PMID 9204307.
- ↑ Brucelosis. Wikipedia. https://es.wikipedia.org/wiki/Brucelosis. Accessed on February 2, 2016
- ↑ Brucellosis. Wikipedia. https://en.wikipedia.org/wiki/Brucellosis. Accessed on January 29, 2016
- ↑ Hunt A, Bothwell P. Histological findings in human brucellosis. J Clin Pathol. 1967; 20: 267-272