Brucellosis pathophysiology: Difference between revisions
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* Humans are generally [[infected]] in one of three ways: | * Humans are generally [[infected]] in one of three ways: | ||
** ''Eating undercooked meat or consuming unpasteurized/raw dairy products'' | ** ''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. | ***The most common way to be [[infected]] is by eating or drinking unpasteurized/raw [[Dairy product|dairy products]]. | ||
***When sheep, goats, cows, or camels are [[infected]], their [[milk]] becomes contaminated with the [[bacteria]]. | ***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 | ***If the [[milk]] from [[infected]] [[animals]] is not pasteurized, the infection will be transmitted to people who consume [[Dairy product|dairy products]]. | ||
** ''[[Breathing]] in the [[bacteria]] that cause brucellosis ([[inhalation]])'' | ** ''[[Breathing]] in the [[bacteria]] that cause brucellosis ([[inhalation]])'' | ||
***This risk is generally greater for people in [[laboratories]] that work with the [[bacteria]]. | ***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]]. | ***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]]. | ** [[Bacteria|''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 [[Animals|animal]] [[Excretion|excretions]] ([[newborn]] [[animals]], [[fetuses]], and [[Excretion|excretions]] that may result from [[birth]]). | ***This poses a problem for workers who have close contact with [[animals]] or [[Animals|animal]] [[Excretion|excretions]] ([[newborn]] [[animals]], [[fetuses]], and [[Excretion|excretions]] that may result from [[birth]]). | ||
***Such workers may include: | ***Such workers may include: | ||
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===Pathogenesis=== | ===Pathogenesis=== | ||
*[[Virulent]] [[Brucella|''Brucella'']] [[organisms]] can [[infect]] both nonphagocytic and [[phagocytic cells]]. | *[[Virulent]] [[Brucella|''Brucella'']] [[organisms]] can [[infect]] both nonphagocytic and [[phagocytic cells]]. | ||
*When [[Brucella|''Brucella'']] enters the body [[White blood cells|white blood cells (WBC)]], particularly [[neutrophils]] and [[macrophages]] [[phagocyte]] the [[pathogen]]. | *When [[Brucella|''Brucella'']] enters the body [[White blood cells|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|reticuloendothelial system (RES)]]. | **[[WBC]] transports the [[pathogen]] via the [[hematologic]] and [[lymphatic]] routes to different organs, specially to those from the[[Reticuloendothelial system|reticuloendothelial system (RES)]]. | ||
**[[Brucella]] multiplies themselves within the [[vacuoles]] of the [[phagocytes]] without being destructed. | **[[Brucella]] multiplies themselves within the [[vacuoles]] of the [[phagocytes]] without being destructed. | ||
*Different [[Brucella]] species are classified as smooth and rough [[lipopolysaccharide]] phenotypes. | *Different [[Brucella]] species are classified as smooth and rough [[lipopolysaccharide]] phenotypes. | ||
**Smooth [[lipopolysaccharides]] (S-LPS): | **Smooth [[lipopolysaccharides]] (S-LPS): | ||
***''B. abortus'', ''B. melitensis'', ''B. suis'' and ''B. neotoma'' | ***''[[Brucella abortus|B. abortus]]'', ''[[Brucella melitensis|B. melitensis]]'', ''B. suis'' and ''B. neotoma'' | ||
***S-LPS are more [[virulent]] than R-LPS | ***S-LPS are more [[virulent]] than R-LPS | ||
***S-LPS survive much more effectively than nonsmooth ones | ***S-LPS survive much more effectively than nonsmooth ones | ||
**Rough lipopolysaccharides (R-LPS): | **Rough [[lipopolysaccharides]] (R-LPS): | ||
***''B. ovis'' and ''B. canis'' | ***''B. ovis'' and ''[[Brucella canis|B. canis]]'' | ||
*In [[Polymorphonuclear cells|polymorphonuclear]] or [[Mononuclear phagocytic system|mononuclear phagocytic cells]], ''[[Brucella]] spp.'' uses a number of mechanisms for avoiding or suppressing bactericidal responses: | *In [[Polymorphonuclear cells|polymorphonuclear]] or [[Mononuclear phagocytic system|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. | **[[Lipopolysaccharide]] and outer membrane [[proteins]] probably play a substantial role in [[intracellular]] survival. | ||
***This may be due to the [[mannose]] and [[integrins]] receptors. | ***This may be due to the [[mannose]] and [[integrins]] [[receptors]]. | ||
**[[Brucella]] stays within the cells because it inhibits [[cellular]] mechanisms of [[programmed cell death]] ([[apoptosis]]). | **[[Brucella|''Brucella'']] stays within the [[Cells (biology)|cells]] because it inhibits [[cellular]] mechanisms of [[programmed cell death]] ([[apoptosis]]). | ||
**The survival of [[Brucella]] within the cells has been associated with: | **The survival of [[Brucella|''Brucella'']] within the cells has been associated with: | ||
***Synthesis of [[antioxidant]] [[enzymes]] | ***[[Synthesis]] of [[antioxidant]] [[enzymes]] | ||
***Production of [[Guanosine monophosphate|guanosine 5 monophosphate (GMP)]] | ***Production of [[Guanosine monophosphate|guanosine 5 monophosphate (GMP)]] | ||
**** [[GMP]] inhibits: [[phagolysosome]] fusion, degranulation and activation of the myelo-peroxidase-halide system, and production of [[Tumor necrosis factor-alpha|tumor necrosis factor]]. | **** [[GMP]] inhibits: [[phagolysosome]] fusion, degranulation and activation of the myelo-peroxidase-halide system, and production of [[Tumor necrosis factor-alpha|tumor necrosis factor]]. | ||
***Synthesis of [[proteins]] of molecular weight 17, 24, 28, 60, and 62 kDa. | ***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 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 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]]. | *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|''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="aa">Brucelosis. Wikipedia. https://es.wikipedia.org/wiki/Brucelosis. Accessed on February 2, 2016</ref> | *The mechanisms of [[pathogenesis]] of [[Brucella|''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=== | ||
[[Image:Brucella-histo.jpg|thumb|200px|Brucella spp. are poorly staining, small gram-negative coccobacilli (0.5-0.7 x 0.6-1.5 µm), and are seen mostly as single cells and appearing like “fine sand”.]] | [[Image:Brucella-histo.jpg|thumb|200px|Brucella spp. are poorly staining, small gram-negative coccobacilli (0.5-0.7 x 0.6-1.5 µm), and are seen mostly as single cells and appearing like “fine sand”.]] | ||
[[Image:Bruce-granulomanecrosis.jpg|thumb|200px|Histopathology of guinea pig liver in experimental Brucella suis infection. Granuloma with necrosis]] | [[Image:Bruce-granulomanecrosis.jpg|thumb|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="a">Brucellosis. Wikipedia. https://en.wikipedia.org/wiki/Brucellosis. Accessed on January 29, 2016</ref> | *[[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 19:23, 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
Overview
Brucella is usually transmitted via the digestive route to the human host. Following transmission, white blood cells phagocyte the pathogen and transports it via the hematologic or lymphatic route to different organs, specially to those of the reticuloendothelial system.[1][2]
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 dairy 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.[3]
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 the hematologic and lymphatic routes to different organs, specially to those from thereticuloendothelial 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.[1][2]
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
- ↑ 1.0 1.1 Corbel MJ (1997). "Brucellosis: an overview". Emerg Infect Dis. 3 (2): 213–21. doi:10.3201/eid0302.970219. PMC 2627605. PMID 9204307.
- ↑ 2.0 2.1 Brucelosis. Wikipedia. https://es.wikipedia.org/wiki/Brucelosis. Accessed on February 2, 2016
- ↑ Brucellosis. CDC. http://www.cdc.gov/brucellosis/transmission/index.html. Accessed on February 1, 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