The Gastrointestinal Microbial Assay Plus (GI-MAP)- Comprehensive panel of microbial targets, immune and digestive markers The Gastrointestinal Microbial Assay Plus (GI-MAP) was designed to assess a patient’s microbiome from a single stool sample, with particular attention to microbes that may be disturbing normal microbial balance and may contribute to perturbations in the gastrointestinal (GI) flora or illness. The panel is a comprehensive collection of microbial targets as well as immune and digestive markers, and relies exclusively on quantitative polymerase chain reaction (qPCR) technology to detect parasites, bacteria, fungi, and more by targeting the specific DNA of the organisms tested.
Zonulin has been identified as a key biomarker for intestinal permeability, which has been associated with celiac disease, non-celiac gluten sensitivity (NCGS), and other GI and systemic conditions.
Indications - Autoimmune molecular mimicry (if caused by pathogens)
- Diarrhea
- Digestion
- Foodborne illness
- Gastritis
- Gastroenteritis (if it has viral causes)
- Gut dysbiosis
- Immunity
- Inflammation
- Leaky gut
- Celiac disease / gluten sensitivity
- Suspected bacterial, parasitic or viral pathogenesis (incl. detection of antibiotic resistant bacteria)
Overview The Gastrointestinal Microbial Assay Plus (GI-MAP) was designed to assess a patient’s microbiome from a single stool sample, with particular attention to microbes that may be disturbing normal microbial balance and may contribute to perturbations in the gastrointestinal (GI) flora or illness. The panel is a comprehensive collection of microbial targets as well as immune and digestive markers. It screens for pathogenic bacteria, commensal bacteria, opportunistic pathogens, fungi, viruses, and parasites. It primarily uses multiplex, automated, DNA analysis to give integrative and functional medicine practitioners a better view into the gastrointestinal microbiome. Zonulin has been identified as a key biomarker for intestinal permeability, which has been associated with celiac disease, non-celiac gluten sensitivity (NCGS), and other GI and systemic conditions. Methodology Quantitative polymerase chain reaction (qPCR) Analytes
BACTERIAL PATHOGENS - Campylobacter
- C. difficile Toxin A
- C. difficile Toxin B
- Enterohemorrhagic E. coli
- E. coli O157
- Enteroinvasive E. coli/Shigella
- Enterotoxigenic E. coli LT/ST
- Shiga-like Toxin E. coli stx1
- Shiga-like Toxin E. coli stx2
- Salmonella
- Vibro cholerae
- Yersinia enterocolitica
- H. pylori
- Virulence Factor, babA
- Virulence Factor, cabA
- Virulence Factor, cabPAI
- Virulence Factor, dupA
- Virulence Factor, iceA
- Virulence Factor, opiA
- Virulence Factor, vacA
PARASITIC PATHOGENS - Cryptosporidium
- Entamoeba histolytica
- Giardia
VIRAL PATHOGENS - Adrenovirus 40/41
- Norovirus GI
- Norovirus GII
NORMAL/COMMENSAL BACTERIA - Akkermansia Mucinophilia
- Bacteroides fragilis
- Bifidobacterium spp.
- Clostridia (class)
- Enterobacter spp.
- Enterococcus spp.
- Escherichia spp.
- Faecalbacterium prausnitzii
- Lactobacillus spp.
BACTERIAL PHYLA - Bacteroidetes
- Firmicutes
- Firmicutes/Bacteroidetes Ratio
ADDITIONAL DYSBIOTIC/OVERGROWTH BACTERIA - Bacillus spp.
- Enterococcus faecalis
- Enterococcus faecium
- Methanobacteriaceae (family)
- Morganella spp.
- Pseudomonas spp.
- Pseudomonas aeruginosa
- Staphylococcus spp.
- Staphylococcus aureus
- Streptococcus spp.
POTENTIAL AUTOIMMUNE TRIGGERS - Citrobacter spp.
- Citrobacter freundii
- Fusobacterium spp.
- Klebsiella spp.
- Klebsiella pneumoniae
- Mycobacterium avium subsp. paratuberculosis
- Prevotella spp.
- Proteus spp.
- Proteus mirabilis
FUNGI/YEAST - Candida albicans
- Candida spp.
- Geotricum spp.
- Microsporidia spp.
- Rhodoturula spp.
OPPORTUNISTIC VIRUSES - CMV- Cytomegalovirus
- EBV- Epstein Bar Virus
Parasites & worms:PROTOZOA - Blastocystis hominis
- Chilomastix mesnelli
- Cyclospora spp.
- Dientamoeba fragilis
- Endolimax nana
- Entamoeba coli
- Pentatrichomonas hominis
WORMS - Ancyclostroma duodenale
- Ascaris lumbricoides
- Necator americanis
- Trichuris trichiura
- Taenia spp.
Intestinal health markers:DIGESTION IMMUNE RESPONSE INFLAMMATION GI MARKERS - ß-Glucuronidase
- Occult Blood - FIT
ZONULIN Antibiotic resistance genes (Optional add-on): Phenotypes | HELOBACTER - Amoxicillen
- Clarithromycin
- Fluroquinolines
- Tetracycline
Specimen Stool sample Container - 1x orange-capped stool vial
Patient preparation - Please refrain from taking aspirin for two days prior to collecting your sample.
- Never discontinue prescription medication without first consulting your physician.
Age requirements Can be used on all ages. However, often the microbiome of infants will appear very “dysbiotic”, as the microbiome and the infant’s immune system is very immature. Medications We recommend continuing all prescription medications prior to testing. Please carefully document any relevant recent or current medication use. Medications that may alter the composition of the microbiome include: - Antibiotics -(after finishing Antibiotics, wait 4-6 weeksbefore collecting sample)
- Immune Suppressants/ Oral steroids- will likely cause a lower Secretory IgA, Anti-gliadin, and calprotectin result (after finishing these meds, wait 4-6 weeks before collecting sample)
Supplements:
It is not necessary to discontinue most supplements before testing. It is the provider’s discretion to recommend discontinuing supplements. Many providers will want to understand the impact of supplements on the gut ecosystem and will want their patients to continue supplements during testing. If a provider wants more of a “baseline” assessment using the GI-MAP, they may recommend discontinuing supplements prior to testing. There are a few categories of supplements that deserve consideration:
Non-prescription anti-microbial agents:
While we don’t require that people discontinue antibiotics or antimicrobial substances before collection their stool sample, doing the test while taking these substances can influence the test results. If possible, we recommend discontinuing anti-microbial agents 4-6 weeks before testing.
Enzymes:
Oral enzyme use will not change the elastase-1 finding. If the enzyme contains lipase or ox bile, it may decrease the value for steatocrit.
Ox Bile/Lipase:
Ox bile/lipase intake will affect the steatocrit level but will not affect Elastase-1. If you would like to see your patient’s baseline without supplementation, discontinue at least 3 days before testing. If you would like to see how well-managed your patient is on their supplement, do not discontinue.
Probiotics:
Probiotic supplements can influence the normal and opportunistic bacteria flora. If you would like to assess your patient’s baseline microbial balance without supplementation, discontinue for ~2 weeks prior to testing. If you would like to see the influence of the current probiotic supplement, do not discontinue prior to testing.
Biofilm disruptors:
There is no published evidence to suggest that a biofilm disruptor will improve detection of organisms. However, some clinicians choose to use a biofilm disruptor with their patients up to 14 days before testing. This is an option but not a requirement for testing.
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See also Brochure under ‘Downloadable files’ for even more research.
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