Biochemistry
1 questionsWhat is the number of variable regions present on each light and heavy chain of an antibody?
NEET-PG 2013 - Biochemistry NEET-PG Practice Questions and MCQs
Question 541: What is the number of variable regions present on each light and heavy chain of an antibody?
- A. 1 (Correct Answer)
- B. 2
- C. 3
- D. 4
Explanation: ***1*** - Each **light chain** and **heavy chain** within an antibody molecule contains **one variable region (V domain)**. - These variable regions are crucial for **antigen binding specificity**, as they combine to form the antigen-binding site. - The variable domain is located at the **N-terminal end** of each chain. *2* - While a complete antibody molecule has **two antigen-binding sites** (bivalent), each formed by pairing of VH and VL domains, individual chains possess only **one variable region each**. - The number '2' refers to the total number of identical binding sites on the intact antibody, not the number of variable regions per chain. *3* - The number **3** does not correspond to the number of variable regions on individual chains. - This might be confused with the **three complementarity-determining regions (CDRs)** present within each variable domain (CDR1, CDR2, CDR3), which are hypervariable loops that directly contact the antigen. *4* - The number **4** is incorrect for variable regions. - This number corresponds to the total number of **polypeptide chains** in a complete IgG antibody (2 heavy + 2 light chains), or the number of **constant domains** in some heavy chain isotypes (IgM, IgE have 4 CH domains).
Community Medicine
1 questionsWhat is the schedule of intradermal rabies vaccine?
NEET-PG 2013 - Community Medicine NEET-PG Practice Questions and MCQs
Question 541: What is the schedule of intradermal rabies vaccine?
- A. 2-2-0-1-0-1
- B. 8-4-4-1-0-1
- C. 2-2-2-0-1-1
- D. 2-0-2-0-1-1 (Correct Answer)
Explanation: ***2-0-2-0-1-1*** - This schedule represents the **Thai Red Cross (TRC) regimen** for intradermal rabies vaccination that was standard at the time of this exam (2013). - The numbers indicate the number of vaccine doses administered at different sites: **2 doses on day 0** (bilateral deltoids), **0 doses on day 3**, **2 doses on day 7** (bilateral deltoids), **0 doses on day 14**, **1 dose on day 28**, and **1 dose on day 90**. - This was the **answer expected for NEET 2013** based on the guidelines prevalent at that time. - **Note:** Current WHO guidelines (post-2013) recommend the updated 2-2-2-0-1-1 schedule (4-site ID regimen) which includes doses on days 0, 3, 7, and 28. *2-2-0-1-0-1* - This schedule is **not a recognized** intradermal rabies vaccination protocol. - Does not match any standard WHO-approved regimen for intradermal administration. *2-2-2-0-1-1* - While this may appear incorrect for the 2013 exam context, this schedule actually represents the **current updated Thai Red Cross (4-site ID) regimen** recommended by WHO in recent guidelines. - This regimen provides doses on **days 0, 3, 7, 28, and 90**, which is now the preferred intradermal schedule. - However, for the NEET 2013 exam, the older 2-0-2-0-1-1 schedule was the expected answer. *8-4-4-1-0-1* - This schedule is **not a standard regimen** and involves an impractically high number of doses. - No recognized intradermal rabies protocol uses this many doses on initial days. - Would be **unnecessary and impractical** for effective post-exposure prophylaxis.
Internal Medicine
1 questionsWhich of the following symptoms is commonly associated with giardiasis?
NEET-PG 2013 - Internal Medicine NEET-PG Practice Questions and MCQs
Question 541: Which of the following symptoms is commonly associated with giardiasis?
- A. Steatorrhea and flatulence (Correct Answer)
- B. All of the options
- C. Nausea and vomiting
- D. Abdominal pain
Explanation: ***Steatorrhea and flatulence*** - **Giardiasis** is an intestinal infection caused by the parasite *Giardia lamblia*, leading to malabsorption and characteristic symptoms [1]. - The parasite attaches to the intestinal lining, interfering with fat absorption, which results in **steatorrhea** (fatty, foul-smelling stools) and increased gas production causing **flatulence** [1]. *Nausea and vomiting* - While **nausea** can occur in giardiasis, **vomiting** is less common as a primary or dominant symptom. - These symptoms are more characteristic of other gastrointestinal infections like **viral gastroenteritis**. *Abdominal pain* - **Abdominal pain** is a general symptom that can occur with many gastrointestinal issues, including giardiasis [1]. - However, it's not as specific or as clinically defining for giardiasis as **steatorrhea** and **flatulence**, which are direct consequences of the parasite's impact on fat absorption. *All of the options* - Although some patients with giardiasis may experience nausea and abdominal pain, **steatorrhea** and **flatulence** are the most direct and specific indicators of the malabsorption caused by *Giardia lamblia* [1]. - Choosing "all of the above" would imply that all listed symptoms are equally common and specific, which is not the case for giardiasis.
Microbiology
7 questionsCutaneous larva migrans is due to ?
Infective form of Hookworms?
What type of spore is produced by Ascomycota during sexual reproduction?
What does the hookworm primarily feed on?
The fungus with septate hyphae and dichotomous branching is?
In malaria, pre-erythrocytic schizogony occurs in -
What is the infective form of Trypanosoma brucei?
NEET-PG 2013 - Microbiology NEET-PG Practice Questions and MCQs
Question 541: Cutaneous larva migrans is due to ?
- A. W.bancrofti
- B. B. Malayi
- C. D. medinensis
- D. Ancylostoma braziliense (Correct Answer)
Explanation: ***Ancylostoma braziliense*** - **Cutaneous larva migrans** is primarily caused by the larvae of **dog and cat hookworms**, especially *Ancylostoma braziliense*. - Humans become **accidental hosts** when these larvae penetrate the skin but cannot complete their life cycle, leading to **serpiginous tracks**. *W. bancrofti* - This parasite, **Wuchereria bancrofti**, is a filarial nematode that causes **lymphatic filariasis** (elephantiasis). - Its effects are characterized by **lymphedema** and **hydrocele**, not migrating skin lesions. *B. Malayi* - **Brugia malayi** is another filarial nematode responsible for **lymphatic filariasis** in humans, similar to *W. bancrofti*. - It primarily causes **swelling of the limbs** and scrotum, not cutaneous larva migrans. *D. medinensis* - **Dracunculus medinensis** is the parasite that causes **dracunculiasis**, also known as **Guinea worm disease**. - This infection is characterized by a **painful blister** and subsequent emergence of the adult worm, which is distinct from creeping eruptions.
Question 542: Infective form of Hookworms?
- A. Egg
- B. Rhabditiform larva
- C. Filariform larva (Correct Answer)
- D. Adult worm
Explanation: ***Filariform larva*** - The **filariform larva (L3)** is the infective stage of hookworms, capable of penetrating intact skin. - Upon penetration, these larvae migrate through the bloodstream to the lungs, then up the bronchial tree to be swallowed, eventually maturing in the intestines. *Egg* - Hookworm **eggs** are passed in the feces of infected individuals and are not infective to humans directly. - They require favorable conditions (warm, moist soil) to embryonate and hatch into rhabditiform larvae. *Rhabditiform larva* - The **rhabditiform larva (L1)** is the first larval stage that hatches from the egg in the soil. - It is a non-infective, free-living stage that feeds on bacteria and molts twice to become the infective filariform larva. *Adult worm* - **Adult worms** reside in the small intestine of the host and are not the infective form. - They attach to the intestinal mucosa and feed on blood, causing the characteristic anemia associated with hookworm infection.
Question 543: What type of spore is produced by Ascomycota during sexual reproduction?
- A. Asexual spores
- B. Ascospores (Correct Answer)
- C. Conidia
- D. None of the options
Explanation: ***Ascospores*** - **Ascospores** are the sexual spores produced by fungi belonging to the phylum **Ascomycota** during their sexual reproductive cycle. - These spores are formed inside a sac-like structure called an **ascus** after **karyogamy (nuclear fusion)** and **meiosis**. - Each ascus typically contains **4-8 ascospores** arranged in a characteristic pattern. - Examples of Ascomycota include *Aspergillus*, *Penicillium*, *Candida*, and yeasts like *Saccharomyces*. *Asexual spores* - **Asexual spores** are produced during **asexual reproduction** without the fusion of gametes or meiosis. - Examples include **conidia** and **sporangiospores**, which allow for rapid proliferation and dispersal. *Conidia* - **Conidia** are a specific type of **asexual spore**, not sexual spores. - They are formed exogenously on specialized structures called **conidiophores**. - While Ascomycota can produce conidia asexually, the question asks specifically about sexual reproduction. *None of the options* - This option is incorrect because **ascospores** are indeed the sexual spores of Ascomycota.
Question 544: What does the hookworm primarily feed on?
- A. Plasma proteins
- B. Lymphatic fluid
- C. Interstitial fluid
- D. Blood from intestinal mucosa (Correct Answer)
Explanation: ***Blood from intestinal mucosa*** - Hookworms attach to the **intestinal wall** and ingest host blood, leading to blood loss and potential **anemia**. - They produce **anticoagulants** to facilitate continuous feeding from the mucosal capillaries. *Plasma proteins* - While plasma contains proteins, hookworms primarily feed directly on **whole blood**, not just isolated plasma proteins. - Feeding mainly on plasma proteins would not explain the significant **iron-deficiency anemia** associated with hookworm infection. *Lymphatic fluid* - Hookworms reside in the **small intestine** and do not typically feed on lymphatic fluid. - Other parasites, like **filarial worms**, are known to inhabit and obstruct the lymphatic system. *Interstitial fluid* - Interstitial fluid is found in the spaces between cells; hookworms feed from the **vascular supply** within the intestinal mucosa. - Feeding on interstitial fluid would not cause the characteristic **blood loss** seen in hookworm infections.
Question 545: The fungus with septate hyphae and dichotomous branching is?
- A. Aspergillus (Correct Answer)
- B. Penicillium
- C. Mucor
- D. Rhizopus
Explanation: ***Aspergillus*** - *Aspergillus* species are characterized by their **septate hyphae** and **acute-angle branching** (branching at approximately 45-degree angles), which are key distinguishing features in histopathology. - This branching pattern is sometimes referred to as "dichotomous branching" in medical literature, though true dichotomous branching is more characteristic of certain tissue forms. - This fungal morphology is often seen in infections such as **invasive aspergillosis** in immunocompromised patients. *Penicillium* - *Penicillium* also has **septate hyphae**, but its branching pattern is typically *not acute-angled or dichotomous*. - It is more commonly known for its **brush-like** conidiophores (penicillus) in culture rather than distinctive tissue branching patterns. *Mucor* - *Mucor* is a type of **zygomycete** (now classified under Mucorales) and is characterized by **aseptate or sparsely septate hyphae** with **irregular, right-angle branching**. - This is a key histological feature distinguishing it from *Aspergillus* in cases of **mucormycosis**. *Rhizopus* - Similar to *Mucor*, *Rhizopus* is also a zygomycete with **aseptate or sparsely septate hyphae** and **irregular, wide-angle branching**. - It is often identified in culture by the presence of **rhizoids** (root-like structures) and sporangiophores.
Question 546: In malaria, pre-erythrocytic schizogony occurs in -
- A. Lung
- B. Liver (Correct Answer)
- C. Spleen
- D. Kidney
Explanation: ***Liver*** - After being introduced by a mosquito bite, **Plasmodium sporozoites** rapidly travel to the liver - In the liver, they invade **hepatocytes** and undergo asexual reproduction, known as **pre-erythrocytic (or hepatic) schizogony**, forming merozoites - This is the exo-erythrocytic cycle that occurs before red blood cell invasion *Lung* - The lungs are not a primary site for **Plasmodium** development or asexual reproduction in the human host - While some parasite components or host immune responses might involve the lungs in severe malaria, it is not where pre-erythrocytic schizogony occurs *Spleen* - The **spleen** is primarily involved in clearing infected red blood cells and acts as a site for immune responses to malaria, but not for initial schizogony - It plays a significant role in the **erythrocytic stage** of malaria by filtering and destroying parasitized red blood cells *Kidney* - The **kidneys** are not involved in the life cycle of the **Plasmodium parasite** during pre-erythrocytic schizogony - While malaria can cause **renal complications** (such as acute kidney injury in severe cases), this is a pathological effect, not a site of parasite development
Question 547: What is the infective form of Trypanosoma brucei?
- A. Trypomastigote (Correct Answer)
- B. Amastigote form
- C. Egg stage
- D. No infective form
Explanation: ***Trypomastigote*** - The **trypomastigote** is the infective form of *Trypanosoma brucei* transmitted to humans by the **tsetse fly** bite. - In the human host, trypomastigotes multiply in the **blood and lymphatic system**, eventually invading the central nervous system. *Amastigote form* - The **amastigote** form is characteristic of *Trypanosoma cruzi* and *Leishmania* species, not *Trypanosoma brucei*. - **Amastigotes** are found intracellularly and lack a flagellum, responsible for replication within host cells for these other parasites. *Egg stage* - *Trypanosoma brucei* is a **protozoan parasite** and does not have an **egg stage** in its life cycle. - Egg stages are typical for helminths, such as **tapeworms** or **flukes**. *No infective form* - This statement is incorrect; **all parasitic organisms** must have an infective stage to be transmitted to their hosts. - The **trypomastigote** is specifically adapted for transmission and survival in the human host and vector.