Medical Interventions · Unit 1 · Outbreak investigation

Evidence Portfolio

Everything the investigation has collected, in one place. Every exhibit except the one thing that names the organism.

Course
Medical Interventions
Date
Thursday, September 17, 2026
Exhibits
MI-1 to MI-6
Missing on purpose
the organism's name
Use
Open beside your packet
Keep
In your notebook
Your charge today

This portfolio holds every piece of evidence in the case. The name of the organism is not in it, and that is deliberate. Five exhibits narrow the field. The sixth is the read you take to BLAST yourself.

You turn in
  • Nothing. This is a reference document. Your work goes in the packet and the notebook.

Time: Open it at the start of the block and keep it open.

SEC 1The patient record
Why this matters

A patient record is the first evidence in any infection, and reading one in order, rather than hunting for the alarming line, is a clinical skill that takes practice. Read all of it before you decide anything.

Read this

Exhibit MI-1, the index patient record. This is the first person identified in a cluster of skin and soft tissue infections reported after a weekend sports tournament.

EXHIBIT MI-1 · index patient, de-identified
FieldRecorded value
Age band('teenager',)
Presenting symptoms('painful red swollen area on the forearm, spreading redness, drainage, fever',)
Onset('3 days after a weekend tournament where equipment and towels were shared',)
Temperature('38.6 C',)
White cell count('elevated',)
Wound and blood culture('both positive at 24 hours',)
Rapid viral panel('negative for all targets tested',)
Stool ova and parasite exam('no ova or parasites seen',)
Fungal culture('no growth at 48 hours',)
Antibiotic susceptibility test('SENT, result not back yet',)
Read this

Read the last four rows again. Four of the five classes of agent have a line in this record that argues against them. Finding those four lines is mini lab 1.

SEC 2The outbreak curve
Why this matters

The curve is the population's version of a patient record. It shows what happened to everybody, which is the only way to see a shared exposure.

EXHIBIT MI-2: new skin infections by date of symptom onset0510151Sep 4255697148119610311112date of symptom onsetnew casesOne sharp peak about one incubation period after a shared event points to a single common exposure.Several successive peaks would point to spread from person to person. Read the shape, not the height.
Exhibit MI-2. It does not supply the exposure date or the meaning of the shape.
SEC 3Stain and culture
Why this matters

A Gram stain costs pennies and still changes the first antibiotic a hospital gives. That is why it is run before almost anything else.

EXHIBIT MI-3: Gram stain, patient isolate and the stain controlPATIENT ISOLATE1000x, oil immersionSTAIN CONTROL, known organisms1000x, oil immersionWHY THE CONTROL IS HEREKnown purple and known pink onone slide. If both do not appear,the stain failed and the patientfield means nothing.
Exhibit MI-3. It does not supply the Gram result in words.
EXHIBIT MI-4: culture at 24 hours, 37 degrees CelsiusPATIENT SAMPLEcount and describe in your tablePOSITIVE CONTROLgrowth, as it should beSTERILE CONTROLno growth, as it should be
Exhibit MI-4. It does not supply a colony count or a conclusion.
SEC 4The gel
Why this matters

A gel turns an invisible molecule into a distance you can measure with a ruler, and a distance anyone else can check is what makes a laboratory result evidence.

EXHIBIT MI-5: PCR product against four candidate referenceswellsLadderPatient isolateCandidate A referenceCandidate B referenceCandidate C referenceCandidate D referenceNo-template control3000 bp2000 bp1500 bp1000 bp700 bp500 bp300 bp200 bp100 bpdirection of travel, negative to positiveLane 1 is the ladder. Its fragment sizes are printed because a ladder is the instrument you measure against, not an answer.No size is printed for any sample lane. You read those off your own standard curve in SEC 04.
Exhibit MI-5. It does not supply the size of the patient band.
SEC 5The isolate read
Why this matters

This read is the only exhibit that can name the organism, and it will only do it through a tool you drive yourself. That is not a trick. It is how identification actually works now.

Read this

Exhibit MI-6, one 500 base read of the 16S rRNA gene from the patient isolate.

>S2_practice_isolate 16S rRNA gene, one read of 500 bases
GGCTCAGGATGAACGCTGGCGGCGTGCCTAATACATGCAAGTCGAGCGAACGGACGAGAAGCTTGCTTCTCTGATGTTAGCGGCGGACGGGTGAGTAACACGTGGATAACCTACCTATAAGACTGGGATAACTTCGGGAAACCGGAGCTAATACCGGATAATATTTTGAACCGCATGGTTCAAAAGTGAAAGACGGTCTTGCTGTCACTTATAGATGGATCCGCGCTGCATTAGCTAGTTGGTAAGGTAACGGCTTACCAAGGCAACGATGCATAGCCGACCTGAGAGGGTGATCGGCCACACTGGAACTGAGACACGGTCCAGACTCCTACGGGAGGCAGCAGTAGGGAATCTTCCGCAATGGGCGAAAGCCTGACGGAGCAACGCCGCGTGAGTGATGAAGGTCTTCGGATCGTAAAACTCTGTTATTAGGGAAGAACATATGTGTAAGTAACTGTGCACATCTTGACGGTACCTAATCAGAAAGCCACGGCTAACTA
Control group · already set up for you

The organism this read belongs to is not named in this portfolio, in the packet, in the notebook, or on the portal. Run it through BLAST in SEC 06 of your packet.

INDEXReference tables and sources

Table 1: characteristics of the five classes of infectious agent

ClassWhat it isSizeSeen on a Gram stain?Grows on standard agar?What it responds toTypical onsetExample illnesses
BacteriaOne cell, no nucleus (prokaryote)0.5 to 5 micrometresYes, Gram stain shows themYes, on standard agarAntibiotics, chosen by susceptibilityHours to a few daysStrep throat, listeriosis, tuberculosis
VirusesGenetic material in a protein coat, not a cell20 to 300 nanometresNo, far too small for a light microscopeNo, they need living host cellsAntivirals. Antibiotics do nothingOne to fourteen daysInfluenza, measles, COVID-19
FungiCells with a nucleus and a chitin cell wall2 to 10 micrometres (yeasts), longer threads (moulds)Poorly. A KOH prep or a fungal stain is usedYes, on fungal media such as Sabouraud agarAntifungalsDays to weeksThrush, athlete's foot, histoplasmosis
ProtozoaOne cell, with a nucleus (eukaryote)10 to 50 micrometresNot by Gram. Seen on a stained smear or wet mountSpecial media only, often not cultured at allAntiprotozoal drugsDays to weeksMalaria, giardiasis, amoebic dysentery
Parasitic wormsMany cells, a whole animal (helminth)Millimetres to metresNo. Eggs are found in stool under a microscopeNot culturedAntiparasitic (antihelminthic) drugsWeeks to monthsTapeworm, hookworm, roundworm

Table 2: treatment and prognosis for the realistic candidates

OrganismClassFirst-line treatmentPrognosis and what it depends onHow it usually reaches people
Listeria monocytogenesBacteriumAmpicillin, often with gentamicin for severe or invasive diseaseDangerous in pregnancy, in newborns, over 65, and with a weakened immune system. Invasive disease is serious and treated in hospital.Food-borne, including deli meats, soft cheeses and unwashed produce
Staphylococcus aureusBacteriumDepends entirely on the susceptibility test. Methicillin-sensitive strains take a beta-lactam such as cefazolin; MRSA does not, and is treated with drugs such as vancomycinRanges from a minor skin infection to life-threatening bloodstream infection. The susceptibility result changes the drug, so the lab result changes the prognosis.Skin and nose carriage, wounds, healthcare contact
Streptococcus pyogenesBacteriumPenicillin or amoxicillin. Still reliably sensitiveGood with treatment. Untreated infection can lead to rheumatic fever, which is why a sore throat gets cultured.Person to person by droplets
Pseudomonas aeruginosaBacteriumAn antipseudomonal drug such as piperacillin-tazobactam or ceftazidime. Many ordinary antibiotics do not workOften affects people already in hospital or with weakened defences. Resistance is common, so treatment follows the susceptibility test.Water, moist surfaces and equipment
Salmonella entericaBacteriumUsually fluids and supportive care. Antibiotics are reserved for severe or invasive illnessMost healthy people recover. Antibiotics are not automatic, because they are not always helpful.Food-borne, including poultry, eggs and produce
Escherichia coli, Shiga toxin-producingBacteriumFluids and supportive care. Antibiotics are generally avoided, because they may raise the risk of a serious kidney complicationA case where the reflex answer is the wrong answer. This is why naming the organism matters before choosing a drug.Food-borne, including undercooked beef and produce
Bacillus subtilisBacteriumRarely causes disease in healthy people. Usually treated as an environmental or laboratory contaminantA hit on this organism is more often a contamination question than a diagnosis. Check your controls before you check the drug chart.Soil, dust and laboratory surfaces

Claim ceiling. This table is a classroom reference for naming and reasoning. It is not a prescribing guide, it is not medical advice, and no one in this room diagnoses or treats anybody.

Links you need today

  • NCBI Nucleotide BLAST (blastn): blast.ncbi.nlm.nih.gov, choose Nucleotide BLAST.
  • NCBI Taxonomy Browser: look your organism up by name to see its classification.
  • CDC health topics A to Z: cdc.gov, search the organism for the disease it causes.
  • MedlinePlus: medlineplus.gov, for plain-language descriptions of an illness.

Where these tables come from

Table 1 is standard microbiology: cell structure, size ranges, staining behaviour, culture requirements and drug classes as described by the CDC and the National Library of Medicine. Table 2 follows CDC treatment guidance and standard clinical references for each named organism. Both are printed here as reference, not derived by students, which is why they sit in the index and not in a work section.

The isolate read in SEC 06 is a real 16S rRNA sequence. The identification it produces is produced by you, in BLAST, on the day. It is recorded nowhere in this packet.