NEET-PG 2013 Practice Questions

Q: What anatomical structure is formed after the obliteration of the umbilical vein?

Round ligament of the liver (ligamentum teres). ***Round ligament of the liver (ligamentum teres)*** - The **umbilical vein** carries oxygenated blood from the placenta to the fetus during development [1]. - After birth, the umbilical vein obliterates and forms the **round ligament of the liver**, also known as the **ligamentum teres hepatis**. *Ligamentum venosum* - This structure is the obliterated remnant of the **ductus venosus**, which shunted blood from the umbilical vein to the inferior vena cava, bypassing the fetal liver [1]. - It is located in a fissure on the posterior surface of the liver, separate from the round ligament. *Ligamentum arteriosum* - This ligament is the remnant of the **ductus arteriosus**, a fetal blood vessel connecting the pulmonary artery to the aorta. - Its obliteration allows blood to flow through the lungs after birth. *Medial umbilical ligament* - This ligament is formed from the obliterated **umbilical arteries**, which carry deoxygenated blood from the fetus back to the placenta. - There are two medial umbilical ligaments, one from each umbilical artery.

Q: Which of the following diseases is classified under category-B of bioterrorism?

Cholera. ***Cholera*** - **Cholera** is classified under **Category B** agents due to its moderate ease of dissemination, moderate morbidity rates, and low mortality rates. - While it can cause severe diarrheal disease, its treatment is relatively straightforward with **rehydration therapy**, and it poses a lower risk of mass casualties compared to Category A agents. *Anthrax* - **Anthrax** is a **Category A** bioterrorism agent, characterized by its high mortality rate, ease of dissemination, and potential for major public health impact. - It poses a significant threat due to its ability to form **spores** that are highly resistant and can cause severe lung infection. *Plague* - **Plague** is designated as a **Category A** agent because of its high potential for mass dissemination, high mortality if untreated, and potential to cause widespread panic. - It can be spread via **aerosols** and can lead to severe systemic illness. *Botulism* - **Botulism** is classified as a **Category A** agent due to the extreme potency of the **botulinum toxin**, even in minute quantities, which can cause severe flaccid paralysis and death. - It has a high potential for causing severe public health impact and requires complex medical interventions.

Q: An adolescent male developed vomiting and diarrhea 1 hour after having food from a restaurant. The most likely pathogen is?

Staphylococcus aureus. ***Staphylococcus aureus*** - The rapid onset of symptoms (within 1 hour) strongly suggests **pre-formed toxin ingestion**, which is characteristic of *Staphylococcus aureus* food poisoning. - While the typical incubation period is **1-6 hours** (average 2-4 hours), onset within 1 hour can occur with **high toxin loads** in contaminated food. - **Vomiting** is often the predominant symptom, occurring shortly after consuming contaminated food, which distinguishes it from other bacterial causes. *Clostridium perfringens* - Onset of symptoms caused by *Clostridium perfringens* is typically **8-16 hours** after ingestion, which is much longer than observed here. - It primarily causes **diarrhea and abdominal cramps** due to toxin production in the intestine, with minimal vomiting. *Vibrio parahaemolyticus* - Symptoms usually appear **4-96 hours** (average 12-24 hours) after consuming contaminated seafood, which is a longer incubation period than described. - It typically causes **watery diarrhea**, abdominal cramps, nausea, and occasional vomiting, but not within 1 hour. *Salmonella* - The incubation period for *Salmonella* infection is typically **6-72 hours** (average 12-36 hours), making it highly unlikely for symptoms to appear within 1 hour. - **Diarrhea, fever, and abdominal cramps** are common with *Salmonella*, but rapid-onset vomiting from pre-formed toxin is not its mechanism.

Q: Which of the following is a superantigen ?

TSST. ***TSST*** - **Toxic Shock Syndrome Toxin-1 (TSST-1)** is a classic example of a superantigen produced by *Staphylococcus aureus*. - Superantigens **bind directly to MHC class II molecules and T-cell receptors (TCRs)** outside of the antigen-binding groove, leading to non-specific activation of a large percentage of T cells and a massive release of cytokines. *Cholera toxin* - **Cholera toxin** is an exotoxin produced by *Vibrio cholerae* that causes massive fluid secretion in the intestine by **activating adenylate cyclase** in enterocytes. - It functions by **ADP-ribosylating the Gs alpha subunit**, leading to constitutive activation of cyclic AMP production, but it is not a superantigen. *Diphtheria toxin* - **Diphtheria toxin**, produced by *Corynebacterium diphtheriae*, inhibits protein synthesis in eukaryotic cells by **ADP-ribosylating elongation factor-2 (EF-2)**. - This action leads to cell death and the characteristic pseudomembrane formation in diphtheria, but it does not act as a superantigen. *Vero-cytoxin* - **Vero-cytoxin** (also known as Shiga toxin or Shiga-like toxin) is produced by *E. coli* O157:H7 and other Shiga toxin-producing *E. coli* (STEC). - It inhibits protein synthesis by **cleaving ribosomal RNA**, primarily causing damage to intestinal cells and renal endothelial cells, but it is not a superantigen.

Q: What is the primary use of the Hybridoma technique?

Monoclonal antibodies. ***Monoclonal antibodies*** - The **hybridoma technique** is primarily used to produce **monoclonal antibodies (MAbs)**, which are highly specific antibodies derived from a single B-cell clone. - These antibodies recognize a **single epitope** on an antigen, providing exceptional specificity and uniformity. - The technique involves **fusing a B-lymphocyte** (antibody-producing cell) with a **myeloma cell** (immortal cancer cell) to create a hybridoma that continuously produces identical antibodies. - This is the **gold standard** for producing large quantities of identical, highly specific antibodies for diagnostic and therapeutic use. *Specific antibodies* - While monoclonal antibodies are indeed specific, this term is **too vague** and could refer to any antibody with specificity, including polyclonal antibodies. - **Polyclonal antibodies** are also specific but are produced through conventional immunization, not the hybridoma technique. - The defining characteristic of the hybridoma technique is that it produces **monoclonal** (single clone) antibodies, not just "specific" ones. *Antigen* - An **antigen** is a molecule that elicits an immune response and is used to immunize animals during antibody production. - However, antigens are the **input** for antibody production, not the **product** of the hybridoma technique. *Cytokines* - **Cytokines** are signaling molecules involved in immune cell communication and regulation. - They are not produced by the hybridoma technique, which is specifically designed for **antibody production**.

Q: Rosette formation with sheep RBCs (SRBCs) indicates functioning of -

T-cells. ***T-cells*** - **T-cells** possess specific receptors, like **CD2** on their surface, that can bind to ligands on sheep red blood cells (SRBCs). - This binding leads to the formation of characteristic **rosettes**, where SRBCs cluster around the T-lymphocytes, indicating functional T-cells. *B-cells* - **B-cells** primarily function in **humoral immunity** by producing antibodies and do not typically form rosettes with sheep RBCs. - While B-cells have surface receptors, they are not CD2 and thus do not facilitate this specific type of rosette formation. *Neutrophils* - **Neutrophils** are **phagocytic cells** involved in innate immunity, primarily combating bacterial and fungal infections. - They lack the specific surface receptors (like CD2) required to form rosettes with sheep RBCs. *Monocytes* - **Monocytes** are precursors to macrophages and dendritic cells, involved in phagocytosis and antigen presentation. - They do not possess the necessary surface markers to form rosettes with sheep RBCs.

Q: Cytolytic activity of membrane attack complex is modulated by ?

Factor S (vitronectin). ***Correct Option: Factor S (vitronectin)*** - Vitronectin (S-protein) is a **plasma protein** that directly modulates the **cytolytic activity of the membrane attack complex (MAC)**. - It binds to the **C5b-7 complex** in the fluid phase, preventing its insertion into target cell membranes and thereby blocking the formation of the complete, functional MAC. - By inhibiting membrane insertion of C5b-7, vitronectin prevents the subsequent binding of **C8 and C9**, which are essential for the cytolytic pore formation. - This is a **direct modulation** of MAC's cytolytic activity at the MAC assembly stage. *Incorrect Option: Factor H* - Factor H is a regulatory protein that controls the **alternative pathway** of complement activation by promoting degradation of **C3b**. - By degrading C3b, Factor H prevents formation of **C5 convertase**, thereby reducing downstream MAC formation. - However, Factor H acts **early in the complement cascade** and does not directly modulate the cytolytic activity of already-formed MAC components. - Its effect is on **preventing MAC formation**, not on modulating MAC's cytolytic function itself. *Incorrect Option: Factor I* - Factor I is a **serine protease** that cleaves and inactivates C3b and C4b, requiring cofactors like Factor H or C4bp. - Like Factor H, it regulates complement activation **upstream** of MAC formation. - It does not directly interact with or modulate the cytolytic activity of the MAC. *Incorrect Option: Factor B* - Factor B is a component of the **alternative pathway C3 convertase** (C3bBb). - It **promotes complement activation** rather than modulating MAC's cytolytic activity. - Factor B functions early in the cascade and has no direct role in regulating MAC function.

Q: ABO isoantibodies are of which class?

IgM. ***IgM*** - Naturally occurring **ABO isoantibodies** are predominantly of the **IgM class**. - These **pentameric antibodies** are highly effective at causing **agglutination** of incompatible red blood cells, which is crucial in transfusion reactions [1]. *IgG* - While IgG antibodies can be formed against ABO antigens (e.g., in hemolytic disease of the newborn), the **naturally occurring isoantibodies** are primarily IgM. - IgG antibodies are **monomeric** and can cross the **placenta**, which is a key difference from the primary IgM ABO antibodies. *IgD* - **IgD** antibodies are primarily found on the surface of **B cells** and play a role in B cell activation. - They are **not a primary mediator** of ABO isoantibody response or red blood cell agglutination. *IgA* - **IgA** antibodies are predominantly found in **mucosal secretions** and play a role in mucosal immunity. - While some IgA may be present, it is **not the predominant class** for naturally occurring ABO isoantibodies involved in transfusion reactions. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. (Basic Pathology) introduces the student to key general principles of pathology, both as a medical science and as a clinical activity with a vital role in patient care. Part 2 (Disease Mechanisms) provides fundamental knowledge about the cellular and molecular processes involved in diseases, providing the rationale for their treatment. Part 3 (Systematic Pathology) deals in detail with specific diseases, with emphasis on the clinically important aspects., pp. 154-155.

Q: Which of the following is not an acute phase reactant?

Endothelin. ***Endothelin*** - Endothelin is a **vasoconstrictive peptide** primarily involved in regulating **blood vessel tone** and blood pressure. - While it plays a role in processes like inflammation and tissue repair, it is not synthesized or regulated in the same rapid, systemic manner as a classic acute phase reactant. *C-reactive protein* - **C-reactive protein (CRP)** is a rapidly responding acute phase reactant produced by the liver in response to **inflammation**, infection, and tissue injury. - Its levels can rise dramatically within hours of an inflammatory stimulus and are used as a marker for disease activity. *Haptoglobin* - **Haptoglobin** is an acute phase reactant that binds to free **hemoglobin** released from red blood cells during hemolysis, preventing oxidative damage. - Its levels typically increase during acute inflammation or infection, although it can also decrease with severe hemolysis. *Fibrinogen* - **Fibrinogen** is a critical acute phase protein involved in the **coagulation cascade** and wound healing. - Its concentration increases significantly during acute inflammation, contributing to the elevated **erythrocyte sedimentation rate (ESR)**.

Q: Visual field monitoring is important before starting which of the following drugs for epilepsy treatment?

Vigabatrin. ***Vigabatrin*** - **Vigabatrin** is known to cause **irreversible concentric visual field constriction** (peripheral vision loss) due to retinal toxicity. - Regular **ophthalmological monitoring**, including **visual field testing**, is crucial before and during treatment to detect and manage this adverse effect early. *Topiramate* - Topiramate can cause **acute angle-closure glaucoma** and **myopia**, which affect vision, but regular visual field monitoring is not a primary requirement for this specific side effect. - Its main concerns often relate to cognitive side effects and kidney stones, rather than progressive visual field loss requiring baseline and ongoing field testing. *Valproic acid* - Valproic acid is not typically associated with specific visual field defects requiring routine monitoring. - Its major side effects often involve **hepatotoxicity**, **pancreatitis**, and **teratogenicity**. *Carbamazepine* - Carbamazepine's notable side effects include **aplastic anemia**, **hyponatremia**, and **Stevens-Johnson syndrome**. - While it can cause some ocular side effects like **diplopia** or **nystagmus**, it does not typically lead to the progressive and irreversible visual field constriction seen with vigabatrin, which necessitates strict monitoring.

Question 1

What anatomical structure is formed after the obliteration of the umbilical vein?

Accepted Answer

Round ligament of the liver (ligamentum teres)

Answer

Ligamentum venosum

Answer

Ligamentum arteriosum

Answer

Medial umbilical ligament

Question 2

Which of the following diseases is classified under category-B of bioterrorism?

Accepted Answer

Cholera

Answer

Anthrax

Answer

Plague

Answer

Botulism

Question 3

An adolescent male developed vomiting and diarrhea 1 hour after having food from a restaurant. The most likely pathogen is?

Accepted Answer

Staphylococcus aureus

Answer

Clostridium perfringens

Answer

Vibrio parahaemolyticus

Answer

Salmonella

Question 4

Which of the following is a superantigen ?

Accepted Answer

TSST

Answer

Cholera toxin

Answer

Diphtheria toxin

Answer

Vero-cytoxin

Question 5

What is the primary use of the Hybridoma technique?

Accepted Answer

Monoclonal antibodies

Answer

Antigen

Answer

Specific antibodies

Answer

Cytokines

Question 6

Rosette formation with sheep RBCs (SRBCs) indicates functioning of -

Accepted Answer

T-cells

Answer

B-cells

Answer

Neutrophils

Answer

Monocytes

Question 7

Cytolytic activity of membrane attack complex is modulated by ?

Accepted Answer

Factor S (vitronectin)

Answer

Factor I

Answer

Factor B

Answer

Factor H

Question 8

ABO isoantibodies are of which class?

Accepted Answer

IgM

Answer

IgG

Answer

IgD

Answer

IgA

Question 9

Which of the following is not an acute phase reactant?

Accepted Answer

Endothelin

Answer

C-reactive protein

Answer

Haptoglobin

Answer

Fibrinogen

Question 10

Visual field monitoring is important before starting which of the following drugs for epilepsy treatment?

Accepted Answer

Vigabatrin

Answer

Topiramate

Answer

Valproic acid

Answer

Carbamazepine

NEET-PG 2013

Anatomy

Community Medicine

Microbiology

Pathology

Pharmacology