
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions β written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Salmonellosis laboratory tests
Introduction
Overview
Overview
Symptoms of salmonellosis are indistinguishable from those caused by other gastrointestinal pathogens, therefore Salmonella must be identified with further studies. Stool culture in appropriate culture media, such as blood and MacConkey agars, is the most common study to identify the bacteria. When there is not enough bacteria on the sample, enrichment broths may be used to grown more salmonella. Serologic tests with polyvalent and specific antisera may be used to identify the serotype of Salmonella. Blood results from patients with salmonellosis may show unspecific findings, such as: leukocytosis and elevated LFTs on the CBC; hypokalemia and hyper or hyponatremia; elevated inflammatory markers; and bacterial growth on blood cultures. Urinalysis may show hypercalciuria, hypocitraturia and increased ammonium excretion. The bacteria may also be identified in stool by microscopic examination, and lactoferrin tests, however, due to the high dependence on the experience of the operator, in microscopic examination, and high cost and rate of false-positives, of the lactoferrin test, these are not commonly used.
Laboratory Findings
Laboratory Findings
The table below displays nonspecific laboratory abnormalities associated with Salmonellosis, including:[1][2][3][4][5]
| Test | Findings |
|---|---|
| Complete Blood Count |
|
| Electrolytes |
|
| Inflammatory Markers | |
| Blood cultures |
|
| Urinalysis |
|
Stool Cultures
Stool Cultures
Stool cultures in adequate culture media, allow the correct identification of the pathogen responsible for infectious diarrhea. The organism should be isolated from fresh stool. The sample should be planted in different selective and nonselective culture agar media, such as:[6]
- Blood
- MacConkey
- Bismuth sulfite
- Eosin-methylene blue
- Salmonella-Shigella
In cases where there is reduced number of pathogens, enrichment broths, such as tetrathionate or selenite, may be used prior to culture of bacteria.[6]
Fecal leukocytes may also be identified in the specimen.[7]
The identification of the organism allows specific treatment of the disease, as well as appropriate follow-up recommendations.[8][9]
This test is not routinely performed due to its elevated cost, when compared with the accuracy of the results. Results from fecal cultures are often delayed and show an elevated rate of false-negatives.[10]
Stool culture may remain positive during 4 to 5 weeks, and in rare cases (chronic) for more than 1 year.[11]
Serologic Tests
Serologic Tests
After identification of Salmonella in stool cultures, the identification of the serologic type of the pathogen is given by serologic testing. Polyvalent and specific antisera should be used.[6]
For this classification the following bacterial structures are considered:[12]
- Capsular antigen
- Polysaccharide O antigens
- Flagellar antigens
Microscopic Examination
Microscopic Examination
The examination of stool samples, after staining with methylene blue, helps in the diagnosis of acute diarrhea. This test allows the identification of leukocytes in feces, suggesting an inflammatory etiology for the diarrhea. When the results indicate a serious form of the disease, further studies, such as stool cultures are indicated.[10] Limitations of this test include:
- Smear must be obtained from a fresh specimen, preferably collected in a cup (sensitivity 95%) [13]
- The result is dependent on the experience of the operator
Lactoferrin Testing
Some studies advocate the importance to test for fecal lactoferrin. This test is considered more sensitive than simple microscopic examination of PMN. The Lactoferrin Latex Agglutination (LFLA) is an in vitro test able to detect a highly sensitive leukocyte marker, indicative of the presence of PMN.[10]
Its cost and high rate of false-positives in breast-fed children, limit its application.[8][14][10][15]
Gallery
Gallery
-
Salmonella bacteria in tetrathionate enrichment broth stained using direct FA staining technique. From Public Health Image Library (PHIL). [16]
-
Salmonella bacteria in tetrathionate enrichment broth stained using direct FA staining technique. From Public Health Image Library (PHIL). [16]
-
Triple sugar iron agar (TSI) tested for Salmonella (H2S+) and (H2S-); Citrobacter sp. and S. arizonae. From Public Health Image Library (PHIL). [16]
-
Salmonella sp. bacteria. From Public Health Image Library (PHIL). [16]
-
SEM depicts a number of red-colored Salmonella sp. bacteria invading a mustard-colored ruffled immune cell. From Public Health Image Library (PHIL). [16]
-
Salmonella typhimurium bacteria isolated from a pure culture (8000x mag). From Public Health Image Library (PHIL). [16]
-
Salmonella typhimurium bacteria isolated from a pure culture (20000X mag). From Public Health Image Library (PHIL). [16]
-
Salmonella typhimurium bacteria isolated from a pure culture (25000X mag). From Public Health Image Library (PHIL). [16]
References
References
- β “Diarrhoea and Vomiting Caused by Gastroenteritis”.
- β Agarwal R, Afzalpurkar R, Fordtran JS (1994). “Pathophysiology of potassium absorption and secretion by the human intestine”. Gastroenterology. 107 (2): 548β71. PMIDΒ 8039632.
- β Wang F, Butler T, Rabbani GH, Jones PK (1986). “The acidosis of cholera. Contributions of hyperproteinemia, lactic acidemia, and hyperphosphatemia to an increased serum anion gap”. N Engl J Med. 315 (25): 1591β5. doi:10.1056/NEJM198612183152506. PMIDΒ 3785323.
- β Welbourne T, Weber M, Bank N (1972). “The effect of glutamine administration on urinary ammonium excretion in normal subjects and patients with renal disease”. J Clin Invest. 51 (7): 1852β60. doi:10.1172/JCI106987. PMCΒ 292333. PMIDΒ 4555786.
- β Batlle DC, von Riotte A, Schlueter W (1987). “Urinary sodium in the evaluation of hyperchloremic metabolic acidosis”. N Engl J Med. 316 (3): 140β4. doi:10.1056/NEJM198701153160305. PMIDΒ 3796685.
- β 6.0 6.1 6.2 “Salmonella”.
- β Granville LA, Cernoch P, Land GA, Davis JR (2004). “Performance assessment of the fecal leukocyte test for inpatients”. J Clin Microbiol. 42 (3): 1254β6. PMCΒ 356889. PMIDΒ 15004086.
- β 8.0 8.1 Guerrant RL, Van Gilder T, Steiner TS, Thielman NM, Slutsker L, Tauxe RV; et al. (2001). “Practice guidelines for the management of infectious diarrhea”. Clin Infect Dis. 32 (3): 331β51. doi:10.1086/318514. PMIDΒ 11170940.
- β Longo, Dan (2012). Harrison’s principles of internal medicine. New York: McGraw-Hill. ISBNΒ 007174889X.
- β 10.0 10.1 10.2 10.3 Choi SW, Park CH, Silva TM, Zaenker EI, Guerrant RL (1996). “To culture or not to culture: fecal lactoferrin screening for inflammatory bacterial diarrhea”. J Clin Microbiol. 34 (4): 928β32. PMCΒ 228919. PMIDΒ 8815110.
- β Thielman NM, Guerrant RL (2004). “Clinical practice. Acute infectious diarrhea”. N Engl J Med. 350 (1): 38β47. doi:10.1056/NEJMcp031534. PMIDΒ 14702426.
- β Murray, Patrick (2013). Medical microbiology. Philadelphia: Elsevier/Saunders. ISBNΒ 0323086926.
- β Korzeniowski OM, Barada FA, Rouse JD, Guerrant RL (1979). “Value of examination for fecal leukocytes in the early diagnosis of shigellosis”. Am J Trop Med Hyg. 28 (6): 1031β5. PMIDΒ 507279.
- β Hines J, Nachamkin I (1996). “Effective use of the clinical microbiology laboratory for diagnosing diarrheal diseases”. Clin Infect Dis. 23 (6): 1292β301. PMIDΒ 8953074.
- β Miller JR, Barrett LJ, Kotloff K, Guerrant RL (1994). “A rapid test for infectious and inflammatory enteritis”. Arch Intern Med. 154 (23): 2660β4. PMIDΒ 7993149.
- β 16.0 16.1 16.2 16.3 16.4 16.5 16.6 16.7 “Public Health Image Library (PHIL)”.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: JoΓ£o AndrΓ© Alves Silva, M.D. [2] Jolanta Marszalek, M.D. [3]

![Salmonella bacteria in tetrathionate enrichment broth stained using direct FA staining technique. From Public Health Image Library (PHIL). [16]](https://www.wikidoc.org/images/0/02/Enterobacteria64.jpeg)
![Salmonella bacteria in tetrathionate enrichment broth stained using direct FA staining technique. From Public Health Image Library (PHIL). [16]](https://www.wikidoc.org/images/d/d0/Enterobacteria63.jpeg)
![Triple sugar iron agar (TSI) tested for Salmonella (H2S+) and (H2S-); Citrobacter sp. and S. arizonae. From Public Health Image Library (PHIL). [16]](https://www.wikidoc.org/images/d/dc/Enterobacteria55.jpeg)
![Salmonella sp. bacteria. From Public Health Image Library (PHIL). [16]](https://www.wikidoc.org/images/2/28/Enterobacteria38.jpeg)
![SEM depicts a number of red-colored Salmonella sp. bacteria invading a mustard-colored ruffled immune cell. From Public Health Image Library (PHIL). [16]](https://www.wikidoc.org/images/0/07/Enterobacteria01.jpeg)
![Salmonella typhimurium bacteria isolated from a pure culture (8000x mag). From Public Health Image Library (PHIL). [16]](https://www.wikidoc.org/images/2/26/Enterobacteria37.jpeg)
![Salmonella typhimurium bacteria isolated from a pure culture (20000X mag). From Public Health Image Library (PHIL). [16]](https://www.wikidoc.org/images/2/25/Enterobacteria36.jpeg)
![Salmonella typhimurium bacteria isolated from a pure culture (25000X mag). From Public Health Image Library (PHIL). [16]](https://www.wikidoc.org/images/c/ce/Enterobacteria35.jpeg)