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Cyclospora cayetanensis

2200 GI Effects Comprehensive Profile - Stool, Genova Diagnostics

Reference range:   Not Detected, Detected

Cyclospora cayetanensis is a coccidian (= intestinal) parasite that causes a diarrheal disease known as cyclosporiasis in humans and possibly in other primates.

It belongs to the phylum Apicomplexa and the genus Cyclospora. The species name, "cayetanensis," refers to the Cayetano Heredia University in Lima, Peru, where early epidemiological and taxonomic work on this parasite was conducted.

Symptoms of cyclosporiasis include watery diarrhea, loss of appetite, weight loss, abdominal cramps, nausea, and sometimes low-grade fever. The severity of the illness can vary based on factors such as age, the condition of the host, and the size of the infectious dose.

Infection with Cyclospora cayetanensis occurs when individuals consume food or water contaminated with the parasite. People living or traveling in countries where cyclosporiasis is endemic may be at an increased risk of infection. The oocysts are shed in the stool of infected individuals and need favorable laboratory conditions to sporulate and become infective. Cyclosporiasis can also be acquired from contaminated produce, leading to outbreaks in developed countries.

How is Cyclospora infection treated?

The recommended treatment is a combination of two antibiotics, trimethoprim-sulfamethoxazole, also known as Bactrim, Septra, or Cotrim. People who have diarrhea should also rest and drink plenty of fluids.

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Cyclospora spp.

GI-MAP Interpretive Guide by Diagnostic Solutions, Diagnostic Solutions Laboratory | GI-MAP & Food Sensitivity Tests

Optimal range:   0 - 50000 Units

This parasite causes an intestinal infection called cyclosporiasis.

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CYFRA 21-1 (Cytokeratin 19 Fragment)

Tumor / Cancer screening tests

Optimal range:   0 - 2.08 ug/L

The CYFRA 21-1 is well known as tumor maker of lung cancer and is not influenced by environmental factors.

CYRFA 21-1 (cytokeratin 19 fragment) has been demonstrated as clinically useful in the prognostication and monitoring of non-small cell lung cancer (NSCLC). Elevated pre-treatment levels may be associated with unfavorable prognosis, and decreasing levels during therapy predict an objective response to treatment. However, the level of CYFRA 21-1 cannot be used as absolute evidence for the presence or absence of disease and results must be viewed in context with other clinical evidence.

Cytokeratins are epithelial markers whose expression is not lost during malignant transformation. CYFRA 21-1 is a cytokeratin-19 fragment that is soluble in serum and can be used as circulating tumor marker. Although expressed in all body tissues, its major occurrence is in the lung, particularly in lung cancer tissues.

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CYP450, mimic Hepatitis C Peptide

Array 12 – Pathogen-Associated Immune Reactivity Screen, Cyrex Laboratories

Optimal range:   0.2 - 2.4 ELISA Index

Hepatitis C virus (HCV) is an enveloped, positive-sense single-stranded RNA virus of the Flaviviridae family.

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Cyst(e)ine

NutrEval Plasma - Urine and Blood, Genova Diagnostics

Optimal range:   5.9 - 19.9 Units

Cysteine is a nonessential sulfur-containing amino acid. It is obtained from the diet and is also endogenously made from the intermediate amino acid cystathionine.

Dietary cysteine sources include poultry, eggs, beef, and whole grains.

This amino acid should not be confused with the oxidized derivative of cysteine called cystine. Cystine is formed by combining two cysteine molecules within a redox reaction.

The urinary FMV amino acid test reports cysteine and cystine separately.

The plasma amino acid test combines both cysteine and cystine as one biomarker called "Cyst(e)ine".

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Cyst(e)ine

3102 ION (Blood/Urine) Amino Acids 40, Genova Diagnostics

Optimal range:   5.9 - 19.9 qmol/dL

Cysteine is a nonessential sulfur-containing amino acid. It is obtained from the diet and is also endogenously made from the intermediate amino acid cystathionine.

Dietary cysteine sources include poultry, eggs, beef, and whole grains.

This amino acid should not be confused with the oxidized derivative of cysteine called cystine. Cystine is formed by combining two cysteine molecules within a redox reaction.

The urinary FMV amino acid test reports cysteine and cystine separately.

The plasma amino acid test combines both cysteine and cystine as one biomarker called "Cyst(e)ine".

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Cyst(e)ine

Methylation Panel, Genova Diagnostics

Optimal range:   271 - 392 micromol/L

Cysteine is a nonessential sulfur-containing amino acid. It is obtained from the diet and is also endogenously made from cystathionine. Dietary cysteine sources include poultry, eggs, beef, and whole grains. [L]

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Cystathionine

Methylation Panel, Genova Diagnostics

Optimal range:   74 - 369 nanomol/L

Because cystathionine is an intermediate of the transsulfuration pathway, elevation of this biomarker may indicate a backup of the transsulfuration pathway. Conversion of cystathionine to glutathione requires necessary cofactors, such as vitamin B6, zinc, glycine, and magnesium. Therefore, transient elevations of this metabolite may indicate increased need for these cofactors.

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Cystathionine

Amino Acid Analysis, Quest Diagnostics

Optimal range:   0 - 1 umol/L

Cystathionine is an intermediate dipeptide within the process of transsulfuration. Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle. Currently, there is no known source or physiologic function for cystathionine other than serving as a transsulfuration intermediate. Some literature suggests that cystathionine may exert protection against endoplasmic reticulum stress-induced tissue damage and cell death, but studies are sparse.

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Cystathionine

Amino Acid Profile, Qn (Urine), LabCorp

Optimal range:   0.5 - 80.8 umol/g Cr

Cystathionine is an intermediate dipeptide within the process of transsulfuration.

Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle.

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Cystathionine

3102 ION (Blood/Urine) Amino Acids 40, Genova Diagnostics

Optimal range:   0 - 0.09 qmol/dL

Cystathionine is an intermediate dipeptide within the process of transsulfuration. Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle. Currently, there is no known source or physiologic function for cystathionine other than serving as a transsulfuration intermediate. Some literature suggests that cystathionine may exert protection against endoplasmic reticulum stress-induced tissue damage and cell death, but studies are sparse.

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Cystathionine

Urine

Amino Acids; Urine 24-hour (Doctor's Data), Doctor's Data

Optimal range:   9 - 65 qmol/24 hours

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Cystathionine

Blood

NutriStat Basic Profile, US BioTek

Optimal range:   0.1 - 0.6 umol/L

Cystathionine is an intermediate dipeptide within the process of transsulfuration. Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle. Currently, there is no known source or physiologic function for cystathionine other than serving as a transsulfuration intermediate. Some literature suggests that cystathionine may exert protection against endoplasmic reticulum stress-induced tissue damage and cell death, but studies are sparse.

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Cystathionine

Amino Acids test [Great Plains Laboratory / Doctor's Data], Doctor's Data

Optimal range:   7 - 40 qM/g creatinine

Cystathionine is an intermediate dipeptide within the process of transsulfuration. Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle. Currently, there is no known source or physiologic function for cystathionine other than serving as a transsulfuration intermediate. Some literature suggests that cystathionine may exert protection against endoplasmic reticulum stress-induced tissue damage and cell death, but studies are sparse.

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Cystathionine

Amino Acid Profile, Qn (Plasma), LabCorp

Optimal range:   0 - 0.7 umol/L

Cystathionine is an intermediary metabolite that is formed in the sequential enzymatic conversion of methionine to cysteine. Cystathionine is normally detected at very low levels in plasma. It is found between homocysteine and cysteine and is formed by the enzyme cystathionine beta-synthase (CBS).

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Cystathionine

NutrEval Plasma - Urine and Blood, Genova Diagnostics

Optimal range:   0 - 0.09 Units

Cystathionine is an intermediate dipeptide within the process of transsulfuration.

Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle.

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Cystathionine

Metabolimix+, Genova Diagnostics

Optimal range:   4 - 48 micromol/g creatinine

Cystathionine is an intermediate dipeptide within the process of transsulfuration. Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle. Currently, there is no known source or physiologic function for cystathionine other than serving as a transsulfuration intermediate. Some literature suggests that cystathionine may exert protection against endoplasmic reticulum stress-induced tissue damage and cell death, but studies are sparse.

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Cystathionine

Urinary Amino Acids (Synlab), SYNLAB

Optimal range:   0 - 1 mmol/mol creatinine

Cystathionine is an intermediate dipeptide within the process of transsulfuration. Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle. Currently, there is no known source or physiologic function for cystathionine other than serving as a transsulfuration intermediate. Some literature suggests that cystathionine may exert protection against endoplasmic reticulum stress-induced tissue damage and cell death, but studies are sparse.

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CYSTATHIONINE

Urine

Amino Acid Analysis, LC/MS, Quest Diagnostics

Optimal range:   0 - 10 mmol/mol creatinine

Cystathionine is an intermediate dipeptide within the process of transsulfuration. Transsulfuration is the main route for irreversible homocysteine disposal, glutathione production, and energy. The initial step involves the enzyme cystathionine β-synthase enzyme (CBS). This reaction requires nutrient cofactors such as vitamin B6 and iron. Cystathionine is then converted to cysteine, and eventually goes on to either make glutathione or feed the Kreb’s cycle. Currently, there is no known source or physiologic function for cystathionine other than serving as a transsulfuration intermediate. Some literature suggests that cystathionine may exert protection against endoplasmic reticulum stress-induced tissue damage and cell death, but studies are sparse.

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Cystathionine

OMX Organic Metabolomics / Diagnostic Solutions, Diagnostic Solutions Laboratory | GI-MAP & Food Sensitivity Tests

Optimal range:   2.5 - 57.5 nmol/mg Creatinine

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