Q.(a)
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🔒 Start your 14-day free trial to unlock the full solution →Part (a)Concept understanding — Biology Disease Control
Biology Disease Control — A First Look
Think of your body as a city. Every day, germs (bacteria, viruses, fungi, parasites) try to enter — through the air you breathe, the food you eat, a cut on your skin. Most of the time, your body's defence systems stop them before you even notice. That's immunity, your natural security force.
But sometimes the invaders break through. You get a fever, a cough, an infection. Now you need disease control — the set of actions that stop the illness from spreading and help you recover.
What exactly is disease control?
In biology, disease control means reducing the incidence (new cases), prevalence (total cases), or transmission of a disease. It's not about wiping out every germ — that's impossible. It's about keeping the disease at a level where it no longer threatens public health.
The NCERT textbook divides disease control into two broad approaches:
1. Preventive measures — stopping the disease before it starts
These are actions taken by individuals, communities, and governments to block the entry of pathogens.
- Vaccination — training your immune system to recognise a germ before it attacks. This is the single most powerful tool in disease control.
- Sanitation and hygiene — clean drinking water, proper sewage disposal, handwashing. Many diseases (cholera, typhoid, hepatitis A) spread through contaminated water or food.
- Vector control — killing or avoiding the organisms that carry disease. Mosquito nets, insect repellents, draining stagnant water — these control malaria, dengue, chikungunya.
- Quarantine and isolation — separating sick people from healthy ones during outbreaks. You saw this during COVID-19.
Prevention is always better than cure. Once a disease spreads in a population, controlling it becomes exponentially harder and more expensive. That's why governments invest heavily in vaccination drives and public sanitation.
2. Curative measures — treating the disease once it occurs
Even with the best prevention, some people will fall ill. Curative measures aim to:
- Reduce the severity of the illness (e.g., antibiotics for bacterial infections, antiviral drugs for flu)
- Shorten the duration of the illness
- Prevent complications and death
- Stop the patient from infecting others
The key point: treatment alone cannot control a disease in a population. If you only treat sick people without preventing new infections, the disease keeps circulating.
Why does disease control matter for society?
A single outbreak can paralyse a city. Schools close, hospitals overflow, businesses shut down. The economic cost is enormous. That's why disease control is not just a medical issue — it's a public health issue.
The NCERT textbook emphasises that disease control requires community participation. No matter how good the doctors or vaccines are, if people refuse to vaccinate their children or ignore hygiene, the disease will keep spreading. …
Part (b)Concept understanding — Cancer Cell Biology
Imagine a city where every cell is a citizen with a specific job. Skin cells form the outer wall, stomach cells digest food, nerve cells carry messages. Each citizen follows a strict rulebook: grow when needed, stop when the job is done, and eventually die to make room for younger replacements. This orderly cycle is what keeps the city healthy.
Now, what happens if one citizen suddenly stops listening to the rules? It starts growing uncontrollably, refuses to die, and begins crowding out its neighbours. Worse, it might break through the city walls and travel to a different district, setting up a new colony there. That rogue citizen is a cancer cell. Cancer cell biology is the study of how normal, well-behaved cells turn into these rebellious, destructive ones.
The core idea: a breakdown of cellular discipline
Every cell in your body contains a complete set of instructions — your DNA. Think of DNA as the city's master blueprint and rulebook. Inside that blueprint are specific genes that act like traffic lights: some tell the cell to grow (these are called proto-oncogenes), and others tell it to stop growing or to self-destruct when damaged (these are called tumour suppressor genes).
Cancer begins when these traffic lights break. A proto-oncogene might get stuck on green, so the cell grows non-stop. Or a tumour suppressor gene might get stuck on red, so the cell never gets the signal to stop or die. Usually, a single broken light isn't enough — the cell has backup systems. But over years, multiple lights break, and the cell loses all control.
Cancer is not one disease but a collection of diseases. All cancers share one fundamental property: uncontrolled cell division caused by accumulated damage to the DNA. The type of cancer depends on which original cell type went rogue (e.g., lung cells → lung cancer, skin cells → skin cancer).
How a normal cell becomes cancerous: a step-by-step intuition
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Initiation — A cell's DNA gets damaged by something (a chemical in cigarette smoke, UV radiation from the sun, a random copying error during cell division). This damage is a mutation. One mutation alone rarely causes cancer, but it's the first crack in the rulebook.
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Promotion — The damaged cell is now slightly more prone to grow. If it encounters more damaging agents (promoters), it accumulates more mutations. Each mutation pushes it further from normal behaviour.
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Progression — After several mutations, the cell now divides rapidly, ignores signals to stop, and refuses to die. It forms a mass of cells called a tumour. Not all tumours are cancerous — benign tumours stay in one place and don't invade neighbours. Malignant tumours are the dangerous ones: they invade nearby tissues and can break off to travel through blood or lymph vessels.
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Metastasis — This is the most dangerous step. A few cancer cells detach from the original tumour, travel through the bloodstream or lymphatic system, and settle in a distant organ (like the liver, lungs, or brain). There, they start a new tumour. This spread is what makes cancer so hard to treat.
Why does this matter for you?
You don't need to memorise gene names or pathways. What matters is understanding the logic behind prevention and treatment:
- Prevention works because most cancers take years to develop. Avoiding known DNA-damaging agents (tobacco, excessive sun, certain viruses like HPV) reduces the chance of those first mutations.
- Early detection works because a small, localised tumour can often be surgically removed before it metastasises. …
Concept: Life cycle of Plasmodium / malaria (a); tumours and cancer diagnostics (b).
Part (a)
(i) In the human body: When an infected female Anopheles bites, it injects sporozoites (the infective stage) with its saliva. These reach the liver, multiply, and then enter the red blood cells (RBCs), where they multiply asexually and rupture the RBCs, releasing a toxin (haemozoin) that causes the recurring high fever and chills. Some parasites in the RBCs form the sexual stages, the male and female gametocytes, which circulate in the blood ready to be picked up by a mosquito.
(ii) Two events inside the female Anopheles:
- Fertilization / fusion of gametes — the gametocytes taken up in the blood meal form gametes that fuse to form a zygote (which develops further in the gut wall). …
Part (a): In humans, Plasmodium sporozoites multiply in the liver, then in RBCs (releasing haemozoin → fever) and form gametocytes; inside the female Anopheles the two events are fertilization (gamete fusion → zygote) and sporogony (formation of sporozoites that reach the salivary glands).
Part (b): Malignant tumours invade tissues and metastasise, unlike localised benign tumours; cancer is detected by biopsy/histopathology, imaging (X-ray/CT/MRI) and antibody/molecular techniques.
Part (a) Life cycle of Plasmodium
(i) In the human body.
- A bite by an infected female Anopheles mosquito injects the infective sporozoites with the mosquito's saliva into the human blood.
- The sporozoites reach the liver cells and multiply there.
- They then enter the red blood cells (RBCs), where they multiply asexually, and the RBCs rupture, releasing more parasites and a toxic substance called haemozoin. Haemozoin is responsible for the characteristic recurring high fever and chills every 3–4 days.
- After several such cycles, some parasites within the RBCs develop into the sexual forms — male and female gametocytes, which circulate in the blood. These are the stages that continue the cycle when a mosquito bites the infected person.
(ii) Two events inside the female Anopheles.
When a female Anopheles bites an infected person, it sucks up blood containing gametocytes; inside the mosquito's gut:
- Fertilization (gametogony): the gametocytes mature into male and female gametes, which fuse to form a zygote (the zygote develops further in the wall of the mosquito's gut). …
- KCET 2024Set B-41 markMCQQ.The principle of vaccination is based on which property of immune system? (A) Memory (B) Specificity (C) Diversity (D) Plasticity
›Reveal solutionSolution
A vaccine protects only because the immune system stores memory cells from the first (primed) exposure — memory is the property being exploited.
Step 1 — What a vaccine actually delivers.
In immunisation, a preparation of antigenic proteins of a pathogen, or a weakened/inactivated pathogen (the vaccine), is introduced into the body. It is not itself protective — it cannot fight anything. Its job is to be seen.
Step 2 — What the body does with it.
The antigens generate a primary response: antibodies are produced, and crucially, memory B-cells and memory T-cells are generated that recognise that specific pathogen.
Step 3 — What happens on real infection.
When the vaccinated person is later actually infected, the existing memory cells recognise the pathogen at once and mount a secondary (anamnestic) response — faster, of much higher magnitude, and dominated by high-affinity antibodies. The pathogen is neutralised before disease develops.
Vaccine→primary response+memory cellslater infectionrapid massive secondary response
This two-step logic is the principle of vaccination, and its load-bearing element is memory.
Step 4 — Why the other properties, though real, are not the principle. …
- KCET 2022Set A-11 markMCQQ.Identify the most infectious and fatal type of malarial parasite: (A) Plasmodium falciparum (B) Plasmodium vivax (C) Plasmodium ovale (D) Plasmodium malariae
›Reveal solutionSolution
Among the four human malarial parasites, P. falciparum causes the malignant, often fatal form of malaria.
Step 1 — The four species that infect humans.
Species Type of malaria Severity P. vivax Benign tertian (48 h cycle) Rarely fatal; relapses P. ovale Benign tertian Mild, uncommon P. malariae Quartan (72 h cycle) Mild, chronic P. falciparum Malignant tertian Most severe — can be fatal Step 2 — Why falciparum is the fatal one. …
- KCET 2021Set C-31 markMCQQ.The development of quick immune response in a person infected with deadly microbes by administering preformed antibodies is (A) Active immunity (B) Cell-mediated immunity (C) Innate immunity (D) Passive immunisation
›Reveal solutionSolution
The question asks about the type of immunity when preformed antibodies are given directly to fight an infection. This is passive immunisation — the body does not produce its own antibodies, so the protection is immediate but temporary.
The key here is understanding how the immune response is generated. When a person is infected with a deadly microbe, time is critical. The body's own immune system (active immunity) takes days to weeks to mount a full response — it needs to recognise the pathogen, activate B-cells, and then produce antibodies. That delay can be fatal.
So instead, we give preformed antibodies — antibodies that were already made in another organism (like a horse or another human) and are injected directly into the patient. This bypasses the entire production process. The immune response is immediate because the antibodies are ready to neutralise the microbe right away.
This is the defining feature of passive immunisation: the host receives ready-made immune components, rather than producing them itself. The protection is fast but short-lived, because the injected antibodies are eventually broken down and no memory cells are formed.
Now let's look at each option:
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Active immunity — This is when the body's own immune system is activated and produces antibodies and memory cells. It can happen naturally (after an infection) or artificially (via vaccination). It takes time to develop but provides long-lasting protection. That's not what's happening here — the antibodies are given, not made by the patient.
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Cell-mediated immunity — This involves T-cells directly attacking infected cells, not antibodies. The question specifically mentions preformed antibodies, which are part of the humoral (antibody-mediated) response, not cell-mediated. So this is incorrect. …
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- KCET 2021Set C-31 markMCQQ.Identify the techniques useful in detecting the cancers of internal organs (A) CT (B) MRI (C) Radiography (D) All of the above
›Reveal solutionSolution
Internal-organ cancers are detected by imaging techniques — radiography, CT and MRI are all standard tools, so all three are correct.
Step 1 — What the question is really asking
A cancer of an internal organ (lung, liver, brain, kidney...) gives no visible lump on the surface. Detection therefore relies on imaging — techniques that build a picture of the inside of the body without opening it.
Step 2 — Examine each technique
- Radiography (X-ray): X-rays pass through the body and are absorbed differently by tissues of different density. A tumour mass shows up as an abnormal shadow. This is the oldest and cheapest screening tool (e.g. chest X-ray for lung cancer).
- CT (Computed Tomography): uses X-rays taken from many angles and reconstructs a three-dimensional image of the internal organs by computer — far better contrast and localisation than a plain X-ray. …
- KCET 2019Set A-11 markMCQQ.Identify the incorrect statement. (A) Pneumonia is a bacterial disease. (B) Ringworm is a fungal disease. (C) HIV is transmitted by mosquito bite. (D) Cancer is a non-infectious disease.
›Reveal solutionSolution
The key idea is to match each disease with its correct causative agent and transmission mode. The incorrect statement is (C), because HIV is not transmitted by mosquito bites — it requires direct exchange of infected body fluids.
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Pneumonia — bacterial disease (Statement A)
Pneumonia is most commonly caused by the bacterium Streptococcus pneumoniae (though viral and fungal pneumonias also exist). In the context of this question, the statement is taken as correct because the classic, textbook form of pneumonia is bacterial. So (A) is true.
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Ringworm — fungal disease (Statement B)
Ringworm is a superficial fungal infection of the skin, caused by dermatophytes like Trichophyton, Microsporum, and Epidermophyton. It is not a worm at all — the name comes from the ring‑shaped rash. Statement (B) is correct.
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HIV transmission — mosquito bite (Statement C)
HIV (Human Immunodeficiency Virus) is transmitted through direct contact with infected blood, semen, vaginal fluids, or breast milk. Mosquitoes do not transmit HIV. Even if a mosquito bites an infected person, the virus does not replicate inside the insect and is not injected into the next person. The mosquito’s proboscis is a one‑way valve — it only injects saliva (which does not contain HIV), not blood from a previous meal. This is a classic misconception. Statement (C) is false. …
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- KCET 2019Set A-11 markMCQQ.Cells in the quiescent stage (G0) (A) show indefinite proliferation. (B) remain metabolically active (C) always become cancerous (D) remain metabolically inactive
›Reveal solutionSolution
G0 means out of the division cycle, not out of action — such cells are metabolically active, just non-dividing.
Step 1 — What G0 actually is.
At the G1 checkpoint a cell chooses one of two paths:
- Continue into S phase and divide, or
- Exit the cycle into the quiescent stage G0.
Cells in G0 have stopped proliferating. That is a statement about the cell cycle, not about the cell's metabolism.
Step 2 — The key distinction (the whole point of the question).
A G0 cell:
- does not replicate its DNA and does not divide, but
- is metabolically active — it transcribes genes, synthesises proteins, respires, and performs its specialised tissue function.
Classic examples: mature neurons and cardiac muscle cells sit in G0 permanently yet are among the most metabolically demanding cells in the body. Liver cells sit in G0 but can be recalled into G1 and divide again after injury.
Step 3 — Eliminate the other options. …
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