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📖 Lesson 4 ⏱ ~25 min Year 9 · Unit 1 ⚡ +115 XP

Types of Pathogens

You'll be able to classify a disease by the type of pathogen that causes it.

In 2023, CSIRO researchers identified 5 distinct pathogen types responsible for Australia's most common infections, bacteria, viruses, fungi, protists, and parasitic worms, each demanding a completely different treatment strategy.

Today's hook: In 2023, CSIRO's Health and Biosecurity division catalogued the 5 major pathogen groups responsible for most human infectious disease in Australia. A bacterium that causes tuberculosis is structurally nothing like the SARS-CoV-2 virus that caused COVID-19, yet both can kill. What makes such different organisms dangerous, and why does it matter which type you have?
0/5QUESTS
Warm-up
Think First
+5 XP each

Q1 · List three different topics you have learned about disease so far, and explain how they might connect to each other.

Q2 · What do you think makes a good scientific investigation question? How is it different from a question you could just Google?

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Learning objectives
What you'll master
3 areas

● Know

  • Identify the five main types of pathogen, bacteria, viruses, fungi, protists, and parasitic worms
  • Recall an example disease caused by each type of pathogen
  • Recognise the ways pathogens cause harm, including toxins, cell destruction, and immune evasion

● Understand

  • Explain the structural differences between bacteria, viruses, fungi, protists, and worms
  • Describe how toxins and other mechanisms damage host tissues
  • Compare why bacterial and viral infections need different treatments

● Can do

  • Classify a disease by the type of pathogen that causes it
  • Match each pathogen type to a suitable treatment
  • Explain why antibiotics do not work against viruses
Cross-lesson links: This synthesis lesson pulls together ideas from Lesson 1 (what disease is) and Lesson 5 (how disease spreads). As you plan your depth study, you can use your understanding of transmission routes and body defences from Lessons 5-8 to help frame a strong investigation question.
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Vocabulary · tap to flip
Words You Need
6 terms
Core term Concept Skill Reference
Pathogen
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Pathogen
A microorganism, such as a bacterium, virus, fungus, or protozoan, that causes disease in its host.
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Bacterium
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Bacterium
A single-celled living organism with no nucleus that can multiply rapidly and cause diseases such as tetanus and food poisoning.
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Virus
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Virus
A non-living infectious particle that can only reproduce by invading a host cell and hijacking its machinery, causing diseases such as influenza.
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Fungus
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Fungus
An organism such as a yeast or mould that can grow on or in the body and cause infections such as tinea and thrush.
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Protozoan
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Protozoan
A single-celled organism, often spread by water or insects, that causes diseases such as malaria.
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Toxin
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Toxin
A poisonous substance produced by some pathogens that damages body cells and causes the symptoms of disease.
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5
Classifying pathogens
The Five Types of Pathogen
+5 XP

Imagine a hospital ward in 2023: one patient has a bacterial lung infection treated with antibiotics, the patient beside them has a viral cold that antibiotics cannot touch, and a third has a fungal skin infection requiring a completely different drug. This is the practical reality that pathogens create, organisms that cause disease, and they come in five main types, each with distinct structures and behaviours that demand different treatments.

Bacteria

Single-celled prokaryotes with no nucleus. They reproduce rapidly by binary fission. Some bacteria are beneficial (gut flora), but pathogenic bacteria cause diseases like tuberculosis, strep throat, and urinary tract infections. Bacteria can be treated with antibiotics.

Viruses

Non-cellular particles consisting of genetic material (DNA or RNA) inside a protein coat. They cannot reproduce independently, they hijack host cells to replicate. Viral diseases include influenza, COVID-19, measles, and HIV. Antibiotics do NOT work on viruses.

Fungi

Eukaryotic organisms including yeasts and moulds. Fungal infections include athlete foot, ringworm, and thrush. They are treated with antifungal medications.

Protozoa

Single-celled eukaryotes. Malaria (Plasmodium) and giardiasis are protozoan diseases. They are treated with antiparasitic drugs.

Parasites (helminths)

Multicellular worms including tapeworms and hookworms. They are treated with antiparasitic medications.

Five pathogen groups with structures and example diseasesPathogen TypesBacteria~1-5 μmCell walle.g. TBAntibioticsVirus~0.1 μmNo celle.g. FluAntiviralsFungusHyphaeEukaryotee.g. Athlete's footAntifungalsProtistNNucleus~10-100 μme.g. MalariaAntiparasiticsParasitic worms (helminths)Multicellular eukaryotic parasitee.g. tapeworm · antiparasitic medicinesSize comparison: protist > bacteria >> virus
Five pathogen groups: bacteria, viruses, fungi, protozoa and parasitic worms (helminths).
Text description
  • Bacteria: about 1–5 μm, with a cell wall; e.g. tuberculosis (TB); treated with antibiotics.
  • Virus: about 0.1 μm, not a cell; e.g. flu; treated with antivirals.
  • Fungus: made of hyphae, a eukaryote; e.g. athlete's foot; treated with antifungals.
  • Protist (protozoan): has a nucleus, about 10–100 μm; e.g. malaria; treated with antiparasitics.
  • Parasitic worms (helminths): multicellular eukaryotic parasites; e.g. tapeworm; treated with antiparasitic medicines.
  • Size comparison shown: protist > bacteria >> virus.
Example

Streptococcus pyogenes is a bacterium that causes strep throat. It is a spherical bacterium (coccus) that chains together and produces toxins that damage throat tissues. In contrast, SARS-CoV-2 (the virus that causes COVID-19) is a tiny particle about 100 times smaller than Streptococcus. It has RNA genetic material inside a lipid envelope studded with spike proteins. It cannot reproduce on its own, it must enter human cells and hijack their machinery. This fundamental difference explains why strep throat is treated with antibiotics (which target bacterial cell walls) while COVID-19 is treated with antivirals and supportive care, antibiotics would be completely ineffective against a virus.

Real-world anchor

Australian pathogen surveillance: The National Notifiable Diseases Surveillance System (NNDSS) tracks infectious diseases across Australia, categorising them by pathogen type. NSW Health and the Burnet Institute monitor emerging pathogens including drug-resistant bacteria and novel viruses. Australia unique wildlife harbours viruses with pandemic potential (like Hendra virus), and the Australian Centre for Disease Preparedness at CSIRO Geelong researches these pathogens to develop diagnostics and vaccines. Understanding pathogen classification is essential for Australia biosecurity and pandemic preparedness.

Mix & match+8 XP

Match each pathogen type to an example disease it causes.

Items
Bacteria
Virus
Fungi
Protozoa
Parasite (helminth)
Categories
Bacterial
e.g., tuberculosis, strep throat
Viral
e.g., influenza, COVID-19
Fungal
e.g., athlete foot, ringworm
Protozoan
e.g., malaria, giardia
Parasitic
e.g., tapeworm, hookworm
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Stop & Check, Planning Your Depth Study
Quick Check
+5 XP

Pathogens cause disease through several mechanisms:

1. Toxin production: Many bacteria produce toxins, poisonous substances that damage host tissues. Exotoxins are proteins secreted by living bacteria. Examples: tetanus toxin (causes muscle spasms), cholera toxin (causes severe diarrhoea), botulinum toxin (causes paralysis, also used in Botox). Endotoxins are lipopolysaccharides in the outer membrane of Gram-negative bacteria, released when bacteria die. They trigger fever and inflammation.

2. Cell destruction: Some pathogens directly destroy host cells. Viruses replicate inside cells until they burst (lyse), releasing new virus particles. The common cold virus destroys nasal epithelial cells, causing runny nose and congestion.

3. Immune system hijacking: Some pathogens evade or manipulate the immune system. HIV infects and destroys T-helper cells, crippling the immune response. Some bacteria form biofilms, protective slime layers that shield them from immune attack and antibiotics.

Example

Clostridioides difficile (C. diff) is a bacterium that causes severe diarrhoea, particularly in hospital patients who have received antibiotics. It produces two toxins (TcdA and TcdB) that damage the intestinal lining and trigger inflammation. Normally, harmless gut bacteria keep C. diff under control. But broad-spectrum antibiotics kill these protective bacteria, allowing C. diff to multiply and produce toxins. This is why C. diff infections are a major problem in healthcare settings. Australian hospitals monitor C. diff rates closely and use targeted antibiotic stewardship to prevent outbreaks. The NSW Clinical Excellence Commission publishes guidelines for C. diff prevention and management.

Real-world anchor

Australian toxin research: The Queensland Museum and University of Queensland researchers study Australian venomous animals (snakes, spiders, jellyfish, cone snails) whose toxins have yielded valuable medical compounds. Captopril (a blood pressure drug) was developed from jararaca snake venom. Prialt (a painkiller) comes from cone snail venom. While these are animal toxins rather than pathogen toxins, they illustrate how understanding toxin structure and function leads to medical breakthroughs. Australian researchers also study bacterial toxins to develop new antibiotics and antitoxin therapies.

A bacterium produces a substance that damages human tissues. What is this substance called?
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Explore
Explore
+5 XP

One of the most important distinctions in medicine is between bacterial and viral infections, because the treatments are completely different.

Bacterial infections can be treated with antibiotics drugs that kill bacteria or stop them from reproducing. Antibiotics target structures unique to bacteria, such as cell walls (penicillins), ribosomes (macrolides), or DNA replication (fluoroquinolones). Because human cells do not have these bacterial structures, antibiotics can kill bacteria without harming human cells.

Viral infections cannot be treated with antibiotics because viruses lack the structures antibiotics target. Viruses use host cell machinery to replicate, so killing the virus without killing the host cell is difficult. Antiviral medications target specific viral enzymes (like neuraminidase in influenza or reverse transcriptase in HIV) but are less effective than antibiotics and must be given early.

Why the distinction matters: Taking antibiotics for viral infections (like colds and flu) is useless, causes side effects, and drives the evolution of antibiotic-resistant bacteria, one of the greatest threats to global health.

Example

During the COVID-19 pandemic, some people demanded antibiotics from their doctors, believing they would help. They did not, COVID-19 is caused by a virus (SARS-CoV-2), and antibiotics have no effect on viruses. In fact, widespread antibiotic use during the pandemic may have accelerated antibiotic resistance. Australian data from the NPS MedicineWise program showed that antibiotic prescribing for respiratory infections actually decreased during the pandemic, partly because lockdowns reduced circulating infections and partly because public awareness improved. However, inappropriate antibiotic use remains a major problem globally, with the World Health Organisation estimating that 50% of antibiotics are prescribed unnecessarily.

Real-world anchor

Australian antibiotic stewardship: Australia has one of the highest rates of antibiotic prescribing in the OECD. The Australian Commission on Safety and Quality in Health Care runs the National Antimicrobial Resistance Strategy, promoting appropriate antibiotic use in hospitals and communities. The NPS MedicineWise program educates the public that antibiotics do not treat viral infections. Australian researchers at the Peter Doherty Institute study how antibiotic resistance spreads and develop rapid diagnostics to distinguish bacterial from viral infections, ensuring antibiotics are only used when truly needed. This work is critical for preserving the effectiveness of existing antibiotics.

Spot the slip-up+5 XP

Find the error in this student advice about treating illness.

A student tells their friend: "You have a cold? Take these leftover antibiotics from when I had a chest infection, they will kill the virus faster."
  1. Colds are caused by viruses, not bacteria.
  2. Antibiotics only work against bacteria, not viruses.
  3. Taking antibiotics for a viral infection contributes to antibiotic resistance.
  4. Sharing prescription antibiotics with friends is safe and effective.
Heads-up · common traps
Spot the Trap
3 myths
✗

Wrong: "A depth study is just a long essay about a disease." No, a depth study is an investigation. It requires you to ask a question, gather evidence, analyse data, and draw conclusions. It is active science, not just research.

✓

Right: A depth study is an active scientific investigation where you pose a question, gather and analyse evidence, and draw conclusions. It is hands-on inquiry, not just a literature review or essay.

✗

Wrong: "The different topics in this unit have no connection to each other." No, they are deeply connected. Pathogens cause disease, which the immune system fights, which vaccines train, which antibiotics treat, which resistance limits, which public health prevents. Every topic links to others.

✓

Right: The topics in this unit form an integrated network: pathogens cause disease, the immune system fights back, vaccines train immunity, antibiotics treat bacterial infections, resistance limits treatments, and public health strategies prevent spread. Each concept connects to the others.

✗

Wrong: "Once you memorise facts about disease, you understand it." No, true understanding means being able to explain connections, apply concepts to new situations, and evaluate evidence. Facts are tools; understanding is the ability to use them.

✓

Right: True understanding in science means you can explain connections between concepts, apply ideas to new situations, and evaluate evidence critically. Memorised facts are only useful when you know how to use them.

Australian Context

Australian Scientists Fighting Disease

Professor Fiona Stanley (AC): An Australian epidemiologist who founded the Telethon Kids Institute in Perth. Her research on birth defects, Indigenous health, and population health methods transformed Australian public health. She championed the use of population data to guide health policy.

Professor Ian Frazer: Co-developer of the HPV vaccine at the University of Queensland. His work has prevented countless cases of cervical cancer worldwide and put Australia on track to eliminate cervical cancer entirely.

Modern Australian research: Today, Australian scientists at WEHI, the Doherty Institute, CSIRO, and universities across the country continue to fight disease. During COVID-19, Australian researchers contributed to vaccine development, genomic surveillance, and long COVID research. Aboriginal and Torres Strait Islander researchers are increasingly leading health research that addresses community priorities with cultural authority.

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From the lesson
Copy Into Books

✍ Copy Into Your Books

▾

Unit Connections

  • Pathogen -> Transmission -> Defence -> Treatment
  • Infectious vs non-infectious disease
  • Local, national, and global perspectives

Key Formulas

  • Herd immunity threshold ≈ 1 - 1/R0
  • Incidence rate = (new cases/population) × multiplier
  • Case fatality rate = (deaths/cases) × 100%

Depth Study Steps

  • Choose topic -> Formulate question -> Research -> Hypothesis -> Method -> Data collection -> Analysis -> Conclusions -> Communication
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From the lesson
Diagram
9
From the lesson
Activity 1
Activity 1

Classify Pathogens Using Evidence

Compare structures, classify examples and justify your decisions using this lesson.

1 Make a comparison table for the five pathogen groups taught in this lesson: bacteria, viruses, fungi, protozoa and parasitic worms. For each group, give a structural feature and a named example of a disease or infection. Then explain one important difference between a virus and a bacterium.
Answer in your book.
2 Classify these three profiles using the five groups in Question 1, and justify each answer with the evidence given. A: a non-cellular particle with genetic material inside a protein coat that replicates only inside host cells. B: a single-celled organism with no nucleus. C: the malaria-causing organism Plasmodium, which is a single cell with a nucleus. Explain why the evidence distinguishes B from C.
Answer in your book.
3 Malaria is caused by Plasmodium and can be passed to a person through the bite of an infected mosquito. A student labels the mosquito as the malaria pathogen because it is the animal that bites. Explain the error, identify the pathogen group, and describe the mosquito's different role using only the information given.
Answer in your book.
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From the lesson
Activity 2
Activity 2

Explain Harm and Evaluate Treatment Evidence

Build causal explanations and evaluate a supplied model. This is a paper-based activity, not an experiment to perform.

1 Compare two ways pathogens can harm the body. Use one bacterial toxin example from this lesson and the example of HIV damaging T-helper cells. For each, write a cause-and-effect chain from the pathogen to the harm. Explain why a toxin and a pathogen are not the same thing.
Answer in your book.
2 At the level of treatment categories taught here, match each infection group (bacterial, viral and fungal) to a category that may be used for some infections in that group: antifungals, antibiotics or antivirals. Then explain why an antibiotic that blocks bacterial cell-wall construction cannot directly stop a virus by the same mechanism. Why does matching a category not mean every infection in that group needs the same medicine?
Answer in your book.
3 Evaluate these fictional results from two separate, controlled laboratory systems. In each system, the untreated control is set to 100%. With the same cell-wall-targeting antibiotic added, bacterial growth is 20% of its untreated control, while viral replication in suitable host cells is 100% of its untreated control. (a) State a conclusion supported by the results and explain it using Question 2. (b) Name one condition that should be kept the same between the treated and untreated groups within each system. (c) Explain why these results do not prove that this antibiotic works against every bacterium or that it is safe for every person. Do not plan or perform a pathogen experiment.
Answer in your book.
Reflect
Revisit your thinking
reflect

At the start of this lesson, you thought about how wildly different organisms, bacteria, viruses, fungi, and worms, all have the power to cause disease despite being as unrelated as a tree is to a smartphone.

Now that you've worked through the lesson, what do these different pathogens actually have in common that makes them capable of causing illness? Did anything surprise you?

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Quick check
Which type of pathogen is not made of cells and can only reproduce by taking over a host cell?
+10 XP
2
Quick check
Malaria is caused by Plasmodium, a single-celled organism spread by mosquitoes. Which type of pathogen is this?
+10 XP
3
Quick check
Some bacteria cause the symptoms of disease by producing a poisonous substance that damages body cells. What is this substance called?
+10 XP
4
Quick check
Why do antibiotics work against a bacterial infection but not against a viral infection like the flu?
+10 XP
5
Quick check
Tinea (athlete's foot) and thrush are infections caused by which type of pathogen?
+10 XP
0
From the lesson
Additional content
Short answer · explain in your own words
Show your reasoning
3 questions
Recall Core 2 marks

Q1. Name the five main types of pathogen and give one example disease caused by each. (2 marks)

Evaluate Core 3 marks

Q2. Explain two different ways that pathogens cause harm to the body, using an example for each. (3 marks)

Create Core 3 marks

Q3. A doctor tells a patient that antibiotics will not help their cold. Explain why this is correct, referring to the type of pathogen involved. (3 marks)

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From the lesson
Revisit

Revisit Your Thinking

Go back to your Think First answer. Has your understanding changed?

  • How has your understanding of disease and health developed across this entire unit?
  • What connections between concepts do you find most powerful or surprising?
Update your thinking in your book.
Model answers (click to reveal)

Answers

▾

MCQ 1

A A virus is not made of cells. It is a particle of genetic material in a protein coat that can only reproduce by invading a host cell and hijacking its machinery.

MCQ 2

C Plasmodium is a single-celled organism (a protozoan) spread by mosquitoes. Malaria is the classic protozoan disease.

MCQ 3

B A toxin is a poisonous substance produced by some pathogens (often bacteria) that damages body cells and causes the symptoms of disease.

MCQ 4

D Antibiotics target structures unique to bacteria, such as cell walls and bacterial ribosomes. Viruses are not cells and do not have these structures, so antibiotics have no effect on them.

MCQ 5

A Tinea (athlete's foot) and thrush are fungal infections, caused by fungi such as yeasts and moulds, and are treated with antifungal medications.

Short Answer 1

Model answer: The five main types of pathogen are: Bacteria, single-celled organisms with no nucleus (e.g. tuberculosis or strep throat); Viruses, non-living particles that hijack host cells to reproduce (e.g. influenza or COVID-19); Fungi, including yeasts and moulds (e.g. tinea / athlete's foot or thrush); Protozoa, single-celled organisms often spread by water or insects (e.g. malaria); and Parasitic worms (helminths), multicellular worms (e.g. tapeworm or hookworm). Award marks for correctly naming the types and matching a sensible example disease to each.

Short Answer 2

Model answer: Pathogens harm the body in several ways. Toxin production: many bacteria release toxins, poisonous substances that damage host tissues, for example tetanus toxin causes painful muscle spasms and cholera toxin causes severe diarrhoea. Cell destruction: some pathogens directly destroy host cells, for example a cold virus replicates inside nasal cells until they burst (lyse), releasing new virus particles and causing a runny nose. Immune evasion: some pathogens damage or hide from the immune system, for example HIV infects and destroys T-helper cells, weakening the body's defences. A full-mark answer clearly explains two of these mechanisms and links each to a specific example.

Short Answer 3

Model answer: The doctor is correct because a cold is caused by a virus, not a bacterium. Antibiotics work by targeting structures that are unique to bacteria, such as bacterial cell walls and ribosomes. Viruses are not living cells and do not have these structures, instead they invade the body's own cells and use the host's machinery to reproduce. Because there is no bacterial cell wall or ribosome for the antibiotic to attack, antibiotics have no effect on the virus that causes a cold. Taking antibiotics for a viral infection is therefore useless, can cause side effects, and helps drive the development of antibiotic-resistant bacteria.

Activity 1: Classify Pathogens Using Evidence

  1. Accept: bacteria are single cells without a nucleus, e.g. tuberculosis or strep throat; viruses are non-cellular particles containing genetic material in a protein coat, e.g. influenza or COVID-19; fungi have cells with nuclei and include yeasts and moulds, e.g. tinea or thrush; protozoa are single-celled organisms with nuclei, e.g. malaria caused by Plasmodium; parasitic worms are multicellular animals, e.g. tapeworm or hookworm infection. A bacterium is a cell and can reproduce by cell division under suitable conditions; a virus depends on a host cell's machinery to replicate. Credit accurate alternatives from the lesson. Do not require students to describe all fungi as multicellular or all bacteria as harmful.
  2. A is a virus: it is non-cellular, has genetic material in a protein coat and depends on a host cell for replication. B is a bacterium within the five groups used here: it is a single cell without a nucleus. C is a protozoan: Plasmodium is the malaria-causing single-celled eukaryote taught in the lesson. Both B and C are single-celled, so cell number alone does not distinguish them; the nucleus does. A nucleus alone would not identify every unknown organism as a protozoan, because fungi also have nuclei; C's named example supplies the additional evidence.
  3. Plasmodium is the disease-causing pathogen, classified here as a protozoan. The infected mosquito carries and transmits the parasite during a bite; it is the carrier or vector rather than the malaria pathogen. Naming 'vector' is optional because the role is supplied in the question. Do not infer that all mosquitoes carry malaria or that the mosquito itself is a protozoan.

Activity 2: Explain Harm and Evaluate Treatment Evidence

  1. For example: cholera-causing bacteria produce a toxin that disrupts normal intestinal function, causing severe diarrhoea; or tetanus-causing bacteria produce a toxin that disrupts nerve control of muscles, causing spasms. HIV is a virus that infects and damages T-helper cells, weakening the body's immune defences. Credit the level of mechanism taught: students need not explain molecular signalling or detailed immune coordination. A pathogen is the infectious disease-causing agent. A toxin is a harmful substance produced by an organism; in these examples it is produced by bacteria. A toxin is not itself a bacterium or virus. Credit another accurate toxin example from the lesson.
  2. Antibiotics can treat certain bacterial infections; antivirals are used for some viral infections; antifungals treat fungal infections. The specified antibiotic targets bacterial cell-wall construction. Viruses are not bacterial cells and have no bacterial cell wall, so they lack that target. Different pathogens and medicines have different properties, and not every infection requires or responds to a medicine in its category. These are scientific categories, not advice to choose or take a particular drug. Accept the lesson's examples without requiring names of medicines, doses or clinical decisions.
  3. In these fictional systems, the antibiotic reduced bacterial growth relative to its matched control but did not reduce viral replication. This is consistent with a drug targeting bacterial cell-wall construction, a target viruses lack. Suitable controlled conditions include the duration of observation, temperature, starting amount of the relevant organism, or host-cell type/number within the viral comparison; compare like with like within each system, not bacterial cells directly with virus particles. The result concerns only the tested bacterium, virus, conditions and antibiotic. It cannot establish effectiveness against every bacterium, nor human safety, because other bacteria and effects in people were not tested. The 20% value describes remaining growth relative to a control; it does not prove that 80% of bacteria were killed. This is supplied model data for reasoning, not a practical method.