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==Overview==
==Overview==
For symptomatic patients, diagnosis is confirmed only after isolation of ''Listeria monocytogenes'' from a normally sterile site, such as [[blood]], [[spinal fluid]] (in the setting of [[nervous system]] involvement), or [[amniotic fluid]]/[[placenta]] (in the setting of [[pregnancy]]). Stool samples are of limited use and are not recommended. ''Listeria monocytogenes'' may be isolated readily on routine media, but distinguishing ''Listeria'' from other Gram-positive organisms (such as diphtheroids) may be difficult. Selective enrichment media improve rates of isolation from contaminated specimens. The cultures typically require 1-2 days for growth. A negative culture does not rule out infection in the presence of strong clinical suspicion. Serological tests are unreliable and currently not recommended. Laboratory testing on asymptomatic patients (including high-risk asymptomatic patients) is not recommended.<ref name=CDC>{{cite web | title = Listeria | url = http://www.cdc.gov/listeria/diagnosis.html }}</ref>
For symptomatic patients, diagnosis is confirmed only after isolation of ''Listeria monocytogenes'' from a normally sterile site, such as [[blood]], [[spinal fluid]] (in the setting of [[nervous system]] involvement), or [[amniotic fluid]]/[[placenta]] (in the setting of [[pregnancy]]). Cultures from non-sterile sites, such as stool samples, are not recommended (1-15% carriage rate) but may still be useful in gastroenteritis with high suspicion of listeriosis. ''Listeria monocytogenes'' may be isolated readily on routine media. Since ''Listeria'' is an intracellular organism, only 1/3 of cultures yield positive Gram-stains. Selective enrichment media improve rates of isolation from contaminated specimens. The cultures typically require 1-2 days for growth. A negative culture does not rule out infection in the presence of strong clinical suspicion. Serological tests are unreliable and currently not recommended. Laboratory testing on asymptomatic patients (including high-risk asymptomatic patients) is not recommended.<ref name=CDC>{{cite web | title = Listeria | url = http://www.cdc.gov/listeria/diagnosis.html }}</ref>


==Laboratory Tests==
==Laboratory Tests==
===Cell Culture===
''The gold standard for the diagnosis of listeriosis is culture from sterile sites.''
* [[Listeria]] grows on media such as Mueller-Hinton agar.<ref>Chapter 13. Non-Spore-Forming Gram-Positive Bacilli: Corynebacterium, Propionibacterium, Listeria, Erysipelothrix, Actinomycetes, & Related Pathogens ,Jawetz, Melnick, & Adelberg's Medical Microbiology, 24th Edition ,The McGraw-Hill Companies</ref>
 
* Identification is enhanced if the primary cultures are done on agar containing sheep blood because the characteristic small zone of [[hemolysis]] can be observed around, and under the colonies.  
===Culture===
*Diagnosis of listeriosis is made by culturing ''Listeria'' from sterile sites (e.g.  blood, spinal fluid).
*Cultures from non-sterile sites, such as stool culture or vaginal culture, are not helpful for the diagnosis of listeriosis (approximately 5% to 15% fecal carriage, especially among patients who receive [[PPI]] therapy).<ref name="pmid6701102">{{cite journal| author=Lennon D, Lewis B, Mantell C, Becroft D, Dove B, Farmer K et al.| title=Epidemic perinatal listeriosis. | journal=Pediatr Infect Dis | year= 1984 | volume= 3 | issue= 1 | pages= 30-4 | pmid=6701102 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6701102  }} </ref>
*Gram-stain may yield positive results in approximately 1/3 of infected patients (''Listeria'' is an intracellular organism).
* ''Listeria'' grows on media such as Mueller-Hinton agar.
* Identification is enhanced if the primary cultures are performed on agar containing sheep blood given the characteristic small zone of [[hemolysis]] that can be observed around, and under the colonies.  
* Isolation can be enhanced if the tissue is kept at 4°C for some days before inoculation into bacteriologic media.
* Isolation can be enhanced if the tissue is kept at 4°C for some days before inoculation into bacteriologic media.
* The [[motility]] at room temperature and [[hemolysin]] production are primary findings that help differentiate [[listeria]] from coryneform bacteria.
* The [[motility]] at room temperature and [[hemolysin]] production are primary findings that help differentiate listeria from other organisms (e.g. coryneform bacteria).


===Stool Cultures===
===Stool Cultures===
Line 16: Line 21:
*In cases of outbreaks of [[listeriosis]] or individual patients with suspected ''listerial'' [[gastroenteritis]], special selected media can be used.  
*In cases of outbreaks of [[listeriosis]] or individual patients with suspected ''listerial'' [[gastroenteritis]], special selected media can be used.  


===Anton Test===
===Listeriolysin O Titers===
* Anton test can be used in the identification of ''[[Listeria monocytogenes]]'' and diagnosis of listeriosis.
*Elevated titers of listeriolysin O titers may distinguish patients with active ''Listeria'' infections from those who are carriers of the organism.
 
*The use of listeriolysin O for the diagnosis of listeriosis is still controversial.<ref name="pmid8972666">{{cite journal| author=Salamina G, Dalle Donne E, Niccolini A, Poda G, Cesaroni D, Bucci M et al.| title=A foodborne outbreak of gastroenteritis involving Listeria monocytogenes. | journal=Epidemiol Infect | year= 1996 | volume= 117 | issue= 3 | pages= 429-36 | pmid=8972666 | doi= | pmc=PMC2271639 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8972666  }} </ref><ref name="pmid8988887">{{cite journal| author=Dalton CB, Austin CC, Sobel J, Hayes PS, Bibb WF, Graves LM et al.| title=An outbreak of gastroenteritis and fever due to Listeria monocytogenes in milk. | journal=N Engl J Med | year= 1997 | volume= 336 | issue= 2 | pages= 100-5 | pmid=8988887 | doi=10.1056/NEJM199701093360204 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8988887  }} </ref>
==References==
==References==
{{reflist|2}}
{{reflist|2}}
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[[Category:Bacterial diseases]]
[[Category:Bacterial diseases]]
[[Category:Disease]]
[[Category:Disease]]
[[Category:Infectious disease]]
[[Category:Infectious disease]]

Revision as of 15:26, 26 January 2016

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2]

Overview

For symptomatic patients, diagnosis is confirmed only after isolation of Listeria monocytogenes from a normally sterile site, such as blood, spinal fluid (in the setting of nervous system involvement), or amniotic fluid/placenta (in the setting of pregnancy). Cultures from non-sterile sites, such as stool samples, are not recommended (1-15% carriage rate) but may still be useful in gastroenteritis with high suspicion of listeriosis. Listeria monocytogenes may be isolated readily on routine media. Since Listeria is an intracellular organism, only 1/3 of cultures yield positive Gram-stains. Selective enrichment media improve rates of isolation from contaminated specimens. The cultures typically require 1-2 days for growth. A negative culture does not rule out infection in the presence of strong clinical suspicion. Serological tests are unreliable and currently not recommended. Laboratory testing on asymptomatic patients (including high-risk asymptomatic patients) is not recommended.[1]

Laboratory Tests

The gold standard for the diagnosis of listeriosis is culture from sterile sites.

Culture

  • Diagnosis of listeriosis is made by culturing Listeria from sterile sites (e.g. blood, spinal fluid).
  • Cultures from non-sterile sites, such as stool culture or vaginal culture, are not helpful for the diagnosis of listeriosis (approximately 5% to 15% fecal carriage, especially among patients who receive PPI therapy).[2]
  • Gram-stain may yield positive results in approximately 1/3 of infected patients (Listeria is an intracellular organism).
  • Listeria grows on media such as Mueller-Hinton agar.
  • Identification is enhanced if the primary cultures are performed on agar containing sheep blood given the characteristic small zone of hemolysis that can be observed around, and under the colonies.
  • Isolation can be enhanced if the tissue is kept at 4°C for some days before inoculation into bacteriologic media.
  • The motility at room temperature and hemolysin production are primary findings that help differentiate listeria from other organisms (e.g. coryneform bacteria).

Stool Cultures

  • Stool cultures are not indicated in systemic listeriosis patients because routine culture media for enteric pathogens are not appropriate for the growth of Listeria.
  • In cases of outbreaks of listeriosis or individual patients with suspected listerial gastroenteritis, special selected media can be used.

Listeriolysin O Titers

  • Elevated titers of listeriolysin O titers may distinguish patients with active Listeria infections from those who are carriers of the organism.
  • The use of listeriolysin O for the diagnosis of listeriosis is still controversial.[3][4]

References

  1. "Listeria".
  2. Lennon D, Lewis B, Mantell C, Becroft D, Dove B, Farmer K; et al. (1984). "Epidemic perinatal listeriosis". Pediatr Infect Dis. 3 (1): 30–4. PMID 6701102.
  3. Salamina G, Dalle Donne E, Niccolini A, Poda G, Cesaroni D, Bucci M; et al. (1996). "A foodborne outbreak of gastroenteritis involving Listeria monocytogenes". Epidemiol Infect. 117 (3): 429–36. PMC 2271639. PMID 8972666.
  4. Dalton CB, Austin CC, Sobel J, Hayes PS, Bibb WF, Graves LM; et al. (1997). "An outbreak of gastroenteritis and fever due to Listeria monocytogenes in milk". N Engl J Med. 336 (2): 100–5. doi:10.1056/NEJM199701093360204. PMID 8988887.