Chapter 6 with our Microbiology MCQs and explanations! Test your knowledge and understanding of key concepts with our complete set of multiple choice questions with detailed explanations for each answer. Increase your confidence and understanding of the fascinating world of microorganisms!

Microbiology MCQs 251 to 300
- a) Lipolytic
- b) Proteolytic
- c) Lysozyme
- d) Both Lipolytic and Proteolytic
Why other options are incorrect:
- • Lipolytic: While correct, it is incomplete as it only refers to the breakdown of lipids.
- • Proteolytic: While correct, it is incomplete as it only refers to the breakdown of proteins.
- • Lysozyme: This is an antimicrobial enzyme found in secretions like tears and saliva that attacks bacterial cell walls; it is not the primary enzyme responsible for the general decomposition of organic matter.
- a) Micrococcus sps.
- b) Nitrosomonas sps.
- c) Proteus sps.
- d) Both Micrococcus sps. and Proteus sps.
Why other options are incorrect:
- • Micrococcus sps.: While these do decompose urea, this option is incomplete because Proteus is also a major decomposer.
- • Nitrosomonas sps.: These are nitrifying bacteria that oxidize ammonia into nitrites; they are not the primary organisms responsible for the initial decomposition of urea.
- • Proteus sps.: While Proteus is famous for rapid urea hydrolysis, this option is incomplete as Micrococcus also possesses this capability.
- a) The algal part in Lichens
- b) The fungal part in Lichens
- c) Laustoria formation
- d) None of these
Why other options are incorrect:
- • The fungal part in Lichens: This is known as the Mycobiont, which provides the structural support and absorbs water/minerals.
- • Laustoria formation: This likely refers to Haustoria, which are specialized fungal structures used to penetrate host cells for nutrient absorption, rather than a component name for the lichen partnership.
- • None of these: Incorrect because option ‘a’ accurately defines the term phycobiont.
- a) Capsules
- b) Cell-wall
- c) Endospores
- d) Flagella
Why other options are incorrect:
- • Cell-wall: While most bacteria have cell walls, this is common to both free-living and parasitic forms; it is not a specific requirement unique to the “parasitic” mode of life.
- • Endospores: These are highly resistant structures formed for survival in harsh external environments (like soil), not necessarily for the parasitic state inside a host.
- • Flagella: These are used for motility. Many parasitic organisms are non-motile and do not require flagella to infect a host.
- a) Genome
- b) Gene map
- c) Gene pool
- d) None of these
Why other options are incorrect:
- • Genome: This refers to the complete set of genetic material present in a single organism or cell, rather than the entire group/population.
- • Gene map: This is a graphic representation or physical location of genes on a chromosome; it does not represent the total number of genes in a group.
- • None of these: Incorrect because option ‘c’ is the standard biological term for this concept.
- a) Virulent
- b) A virulent
- c) Useful
- d) Symbiotic
Why other options are incorrect:
- • A virulent: This refers to bacteria that do not cause disease. Non-capsulated strains are often avirulent because the host immune system can easily destroy them.
- • Useful: While some bacteria are useful (like probiotics), the presence of a capsule is a specific structural feature associated with survival and pathogenicity within a host.
- • Symbiotic: While some symbiotic bacteria might have capsules, the term is most significantly used in microbiology to distinguish between virulent and non-virulent strains of pathogens (e.g., Streptococcus pneumoniae).
- a) Conjugants
- b) Fertile cells
- c) Exconjugants
- d) None of these
Why other options are incorrect:
- • Fertile cells: While the “F-factor” (Fertility factor) determines the donor’s ability to conjugate, the general term for both the donor and recipient during the process is “conjugants.”
- • Exconjugants: This term refers to the cells after they have completed the process of conjugation and separated from each other.
- • None of these: Incorrect because option ‘a’ is the standard biological term for participating cells.
- a) Monocytes
- b) Basophils
- c) Macrophages
- d) All of these
Why other options are incorrect:
- • Monocytes: These are phagocytic cells found in the blood, but they are not the only ones.
- • Basophils: While they have very limited phagocytic capability compared to neutrophils or macrophages, they are part of the myeloid white blood cell group.
- • Macrophages: These are the most active phagocytes in the tissues, but they originate from monocytes, making both ‘a’ and ‘c’ correct.
- a) Phagosome
- b) Lysosome
- c) both Phagosome and Lysosome
- d) None of these
Why other options are incorrect:
- • Lysosome: This is a pre-existing organelle in the cytoplasm containing digestive enzymes. It later fuses with the phagosome to destroy the microbe.
- • both Phagosome and Lysosome: Incorrect because they are two distinct structures. The combination of the two after fusion is specifically called a phagolysosome.
- • None of these: Incorrect because option ‘a’ is the scientifically accurate term for the vacuole.
- a) H2 SO4
- b) Singlet O2
- c) Superoxide radicals
- d) All of these
Why other options are involved:
- • H2 SO4: While hydrochloric acid or organic acids are more common, this option represents the extreme acidification within the vacuole used to denature microbial proteins.
- • Singlet O2: A highly reactive form of oxygen that causes lipid peroxidation and membrane damage to the microbe.
- • Superoxide radicals: These are the first products of the oxidative burst (produced by NADPH oxidase) and are precursors to other toxic agents like hydrogen peroxide.
- a) Opsonization
- b) Agglutination
- c) CFT
- d) None of these
Why other options are incorrect:
- • Agglutination: This is the clumping together of particles (like bacteria or red blood cells) when they react with specific antibodies; it does not specifically refer to the “coating” for phagocytosis.
- • CFT (Complement Fixation Test): This is a laboratory medical test used to detect the presence of specific antibodies or antigens in a patient’s serum using the complement system.
- • None of these: Incorrect because option ‘a’ is the precise term for this immunological process.
- a) Killing of the bacteria (microorganism)
- b) Inactivation of bacteria
- c) More activating the bacteria
- d) Both Killing of the bacteria (microorganism) and Inactivation of bacteria
Why other options are incorrect:
- • Killing of the bacteria: If the bacteria are killed, it is referred to as a “Killed Vaccine” or “Inactivated Vaccine” in the strict sense. Attenuation specifically implies the organism is still alive but weakened.
- • More activating the bacteria: This is the opposite of attenuation; increasing virulence would make the organism more dangerous.
- • Both Killing and Inactivation: In microbiology, “Killed” and “Attenuated” are two different categories of preparation. Therefore, they cannot both define attenuation.
- a) Streptococcus pyogenes
- b) Str. pneumoniae
- c) Str. viridans
- d) Str. faecalis
Why other options are incorrect:
- • Str. pneumoniae: These are α-haemolytic (Alpha-hemolytic), meaning they cause partial hemolysis, which produces a greenish discoloration on blood agar.
- • Str. viridans: This group is also primarily α-haemolytic.
- • Str. faecalis: Now classified as Enterococcus faecalis, these are usually γ-haemolytic (Gamma-hemolytic), meaning they produce no hemolysis at all on blood agar.
- a) Cellwall component
- b) Plasma component
- c) Serum component
- d) Cytoplasm component
Why other options are incorrect:
- • Cellwall component: Opsonins are produced by the host immune system, not by the bacteria’s own cell wall.
- • Plasma component: While plasma does contain these factors, “Serum” is the more specific immunological term for the fluid containing circulating antibodies and complement proteins.
- • Cytoplasm component: Opsonins act in the extracellular fluid (blood and tissues) to mark pathogens; they are not structural components of the cell’s internal cytoplasm.
- a) Viraemia
- b) Bacteraemia
- c) Septicaemia
- d) Pyemia
Why other options are incorrect:
- • Bacteraemia: This refers specifically to the presence of bacteria in the bloodstream.
- • Septicaemia: Also known as blood poisoning, this is a more severe condition where bacteria are not just present, but are actively multiplying and producing toxins in the blood.
- • Pyemia: This is a form of septicaemia where pus-forming (pyogenic) bacteria spread through the bloodstream, leading to the formation of multiple abscesses in various organs.
- a) Viraemia
- b) Septicaemia
- c) Bacteraemia
- d) Bactericidal
Why other options are incorrect:
- • Viraemia: This refers to the presence of viruses in the blood, not bacteria.
- • Septicaemia: This is a more serious condition where bacteria are not only present but are actively multiplying and producing toxins in the blood, leading to a systemic inflammatory response.
- • Bactericidal: This is an adjective describing an agent (like an antibiotic or disinfectant) that kills bacteria. It is not a term for a medical condition of the blood.
- a) Focal infection
- b) Acute infection
- c) Pyogenic infection
- d) Chronic infection
Why other options are incorrect:
- • Focal infection: This refers to a localized infection (like a tooth abscess) that sends bacteria or toxins to other parts of the body.
- • Acute infection: This describes the timing and severity of an infection (rapid onset, short duration), which may or may not produce pus.
- • Chronic infection: This refers to a long-term infection that persists for weeks, months, or years.
- a) Protected water supply
- b) Environmental sanitation
- c) Immunisation with killed vaccines
- d) All of these
Why all options are correct:
- • Protected water supply: Cholera is primarily spread through contaminated water. Providing treated or boiled water is the most effective way to break the transmission cycle.
- • Environmental sanitation: Proper disposal of sewage prevents human waste from contaminating soil and water sources, which is critical in controlling outbreaks.
- • Immunisation with killed vaccines: Oral cholera vaccines (containing killed whole cells of V. cholerae) provide significant protection for individuals in endemic areas or during outbreaks.
- a) 1 – 3 months
- b) 3 – 6 months
- c) 6 – 9 months
- d) None of These
Why other options are incorrect:
- • 1 – 3 months: This duration is too short; even basic cholera vaccines typically cover at least one peak season of the disease (about 6 months).
- • 6 – 9 months: This exceeds the standard duration of protection recognized for the traditional killed vaccines in most medical textbooks.
- • None of These: Incorrect because the range of 3–6 months is the standard accepted answer in microbiology examinations.
- a) It shares some Inaba, Ogawa subtypes with eltor
- b) Resistant to polymyxin
- c) Eltor is non-motile
- d) Causes less subclinical infections as compared to eltor
Why other options are incorrect:
- • It shares some Inaba, Ogawa subtypes: This is a similarity between the two biotypes, not a difference. Both can belong to these serotypes.
- • Resistant to polymyxin: This is incorrect for the Classical biotype. The Classical biotype is sensitive to polymyxin B (50 units), whereas El Tor is resistant.
- • Eltor is non-motile: Both biotypes are highly motile, exhibiting characteristic “darting motility” due to a single polar flagellum.
- a) Poverty and insanitation
- b) Mosquitoes
- c) Toxin produced by pesticides
- d) None of these
Why other options are incorrect:
- • Mosquitoes: These are vectors for diseases like Malaria, Dengue, and Zika, but they do not transmit Cholera.
- • Toxin produced by pesticides: Pesticides are chemical agents that may cause chemical poisoning, but Cholera is a biological infection caused by a specific bacterium.
- • None of these: Incorrect because option ‘a’ is widely recognized as the primary socio-economic driver of cholera epidemics.
- a) Flies
- b) Horse
- c) Man
- d) None of these
Why other options are incorrect:
- • Flies: While flies can act as mechanical vectors (carrying the bacteria from feces to food on their feet/bodies), they are not reservoirs where the bacteria naturally live and multiply.
- • Horse: Horses are not involved in the transmission cycle or the biological maintenance of cholera.
- • None of these: Incorrect because ‘Man’ is the scientifically recognized reservoir for this specific pathogen.
- a) Fever
- b) Zoonotic
- c) Pyogenic
- d) None of these
Why other options are incorrect:
- • Fever: Fever is a clinical symptom of an infection, not a “type” of infection classification itself.
- • Zoonotic: Zoonotic infections are diseases transmitted from animals to humans. While some streptococci can be found in animals, the primary pathogenic forms in humans (like S. pyogenes or S. pneumoniae) are generally spread human-to-human.
- • None of these: Incorrect because ‘Pyogenic’ is the standard medical classification for these organisms.
- a) Corynebacterium
- b) M. tuberculosis
- c) M. bovis
- d) M. avium
Why other options are incorrect:
- • Corynebacterium: This is a different genus of bacteria entirely; the niacin test is specifically used for the differential identification within the genus Mycobacterium.
- • M. bovis: This species is niacin-negative, which is a major diagnostic feature used to distinguish it from M. tuberculosis.
- • M. avium: As a member of the atypical mycobacteria (MAC), it is generally niacin-negative.
- a) Gram’s staining
- b) Simple staining
- c) Both Gram’s staining and Simple staining
- d) Ziehl – Neelsen’s staining
Why other options are incorrect:
- • Gram’s staining: Mycobacteria do not take up Gram stain well because the crystal violet cannot penetrate the thick, waxy cell wall. They often appear as “ghosts” or unstained cells.
- • Simple staining: Standard dyes used in simple staining (like methylene blue) cannot penetrate the mycolic acid layer effectively without a specific mordant or heat.
- • Both Gram’s and Simple: Since neither individual method is effective for identifying Mycobacteria, this combination is also incorrect.
- a) Neisseria
- b) Staphylococci
- c) Mycobacteria
- d) All of the above
Why other options are incorrect:
- • Neisseria: These are Gram-negative diplococci and are not acid-fast.
- • Staphylococci: These are Gram-positive cocci and do not contain the mycolic acid layer required for acid-fastness.
- • All of the above: This is incorrect because only the genus Mycobacterium (and a few others like Nocardia to a lesser extent) exhibit acid-fast properties.
- a) Sh.shiga
- b) Sh.schmitzi
- c) Both Sh.shiga and Sh.schmitzi
- d) Sh.para dysenteriae
Why other options are incorrect:
- • Sh.shiga: Refers only to Serotype 1 of Shigella dysenteriae.
- • Sh.schmitzi: Refers only to Serotype 2 of Shigella dysenteriae.
- • Sh.para dysenteriae: Historically associated with Shigella flexneri, not Shigella dysenteriae.
- a) Protein M
- b) Protein T
- c) Protein R
- d) Polysaccharide C
Why other options are incorrect:
- • Protein M: While M protein is a major virulence factor and is used for Griffith typing (serotyping within Group A), it is not the basis for the broad classification into groups.
- • Protein T & R: These are surface proteins used for further epidemiological typing of strains but do not determine the primary Lancefield group.
- a) Str. pyogenes
- b) Virulence group
- c) Viridans group
- d) None of these
Why other options are incorrect:
- • Str. pyogenes: This organism is a β-haemolytic (beta-hemolytic) bacterium, meaning it causes complete lysis of red blood cells on blood agar.
- • Virulence group: This is a general term describing the degree of pathogenicity of a microorganism; it is not a specific taxonomic name for α-haemolytic streptococci.
- • None of these: This is incorrect because “Viridans group” is the standard clinical terminology for these organisms.
- a) CO2
- b) Nitrogen
- c) Oxygen
- d) Serum
Why other options are incorrect:
- • CO2 & Nitrogen: These gases do not inactivate Streptolysin O; in fact, Streptolysin O is active under anaerobic conditions (lack of oxygen).
- • Serum: Serum does not inactivate Streptolysin O. In contrast, Streptolysin S (the other hemolysin) is oxygen-stable but is often associated with serum proteins for stability.
- a) A typical mycobacteria
- b) Brucella
- c) Streptococcus
- d) Bordetella pertusis
Why other options are incorrect:
- • Atypical mycobacteria: Diagnosis is primarily through culture and molecular methods, not standard agglutination tests where prozone is a primary concern.
- • Streptococcus: While serology (like ASO) is used, the prozone effect is not a hallmark diagnostic pitfall for this genus as it is for Brucella.
- • Bordetella pertusis: Diagnosis is usually made via PCR or culture from nasopharyngeal swabs rather than the specific agglutination tests associated with prozone.
- a) B. abortus
- b) B. melitensis
- c) B. suis
- d) B. canis
Oxidative Patterns:
- • B. abortus, B. melitensis, & B. suis: These species characteristically oxidize Glutamic acid, Ornithine, and Ribose.
- • B. canis: This species shows a distinct pattern and does not oxidize glutamic acid or ribose.
- a) Cytopathic effects
- b) Hela cells
- c) Both Cytopathic effects and Hela cells
- d) None of these
Why other options are incorrect:
- • Cytopathic effects: Influenza viruses typically do not produce distinct or rapid Cytopathic Effects (CPE) in most primary cell cultures. Therefore, CPE is not a reliable method for identifying its growth.
- • HeLa cells: Influenza virus does not grow well in HeLa cells. It prefers MDCK (Madin-Darby Canine Kidney) cell lines or the amniotic/allantoic cavities of embryonated chicken eggs.
- • None of these: Since the standard identification methods (Hemagglutination/Hemadsorption) are not listed, this is the correct choice.
- a) Haemaggulutinin inhibition test
- b) Tissue culture method
- c) Embryonated eggs
- d) Plaque formation
Why other options are incorrect:
- • Tissue culture method & Embryonated eggs: These are methods used for the isolation and cultivation (growth) of the virus, but they do not specifically identify the virus strain on their own.
- • Plaque formation: This technique is primarily used to quantify (titrate) infectious virus particles by counting “plaques” or areas of cell death, rather than for primary identification.
- a) Oxygen unstable
- b) Thermostable
- c) Oxygen stable
- d) None of these
Why other options are incorrect:
- • Oxygen unstable: This refers to Streptolysin O (SLO), which is inactivated by oxygen (oxygen-labile).
- • Thermostable: Streptolysin S is heat-labile (destroyed by heat), not thermostable.
- • None of these: This is incorrect as “Oxygen stable” is a fundamental characteristic of Streptolysin S.
- a) Salmonella
- b) Staphylococcus
- c) Bordetella
- d) Pneumococcus
Why other options are incorrect:
- • Salmonella: Identified through biochemical tests (like the TSI test) and serotyping (Widal test).
- • Bordetella: Identified via specialized culture media (Bordet-Gengou) and molecular methods; it does not produce coagulase.
- • Pneumococcus: Streptococcus pneumoniae is identified by its sensitivity to Optochin and its solubility in bile.
- a) Facultative anaerobe
- b) Obligate anaerobe
- c) Facultative aerobe
- d) Obligate aerobe
Why other options are incorrect:
- • Facultative anaerobe: These organisms (like E. coli) can grow in both aerobic and anaerobic conditions. Clostridium cannot survive in oxygenated environments.
- • Facultative aerobe: This term is rarely used in standard microbiology but would imply an organism that prefers anaerobic conditions but can live in oxygen; Clostridium is strictly anaerobic.
- • Obligate aerobe: These organisms (like Mycobacterium tuberculosis) require oxygen to survive and cannot grow under anaerobic conditions.
- a) Bacillus anthracis
- b) Brucella
- c) Corynaebacterium
- d) None of these
Why other options are incorrect:
- • Brucella: These are identified using culture methods and serological tests (like the milk ring test or Rose Bengal plate test), not McFadyean’s stain.
- • Corynebacterium: C. diphtheriae is traditionally identified using Albert’s stain or Neisser’s stain to demonstrate metachromatic (volutin) granules.
- • None of these: This is incorrect because Bacillus anthracis is the classic organism associated with this reaction.
- a) Vector borne
- b) Zoonotic infection
- c) Wound borne
- d) Soil borne
Why other options are incorrect:
- • Vector borne: Anthrax does not require an arthropod vector (like a mosquito or tick) for transmission to humans.
- • Wound borne: While “Cutaneous Anthrax” enters through skin abrasions, the disease as a whole is classified by its animal origin (Zoonosis).
- • Soil borne: While Bacillus anthracis spores can persist in the soil for decades and infect grazing animals, the term “Zoonotic” more accurately describes the clinical and epidemiological nature of human infection.
- a) Bacillus anthracis
- b) Escherichia-coli
- c) Corynebacterium
- d) Brucella
Why other options are incorrect:
- • Escherichia coli: While some specific strains of E. coli (like K1) can possess a capsule, the genus as a whole is not typically defined by a capsule in the same way B. anthracis is.
- • Corynebacterium: Most species, including C. diphtheriae, are non-capsulated, non-motile, Gram-positive rods.
- • Brucella: These are small, Gram-negative coccobacilli that are characteristically non-capsulated and non-motile.
- a) 3 weeks
- b) 6 weeks
- c) 9 weeks
- d) 12 weeks
Key Points:
- • Window Period: The time between initial infection and the point when a test can reliably detect the virus or antibodies.
- • 3-6 Weeks: Some individuals may seroconvert early (often associated with acute retroviral syndrome symptoms), but a negative test at this stage is not conclusive.
- • 12 Weeks: This is the standard timeframe used in clinical guidelines to confirm a negative status after a potential exposure.
- a) HTLV – I
- b) Bunya virus
- c) HTLV – III
- d) All
Why other options are incorrect:
- • HTLV-I: This virus is associated with adult T-cell leukemia/lymphoma (ATL) and a neurological disorder called HAM/TSP, but it does not cause AIDS.
- • Bunya virus: This refers to a large family of viruses (Bunyaviridae) that cause diseases like Hantavirus pulmonary syndrome or Rift Valley fever, not AIDS.
- • All: Since only HTLV-III is an old name for HIV, “All” is incorrect.
- a) RNA virus
- b) DNA virus
- c) Retro virus
- d) Entero virus
Why other options are incorrect:
- • RNA virus: While HIV is technically an RNA virus, “Retro virus” is the more specific and accurate taxonomic classification provided in the options.
- • DNA virus: HIV does not store its genetic information as DNA; it only creates a DNA copy (provirus) during its replication cycle inside the host.
- • Entero virus: Enteroviruses are a genus of viruses (like Poliovirus) transmitted via the fecal-oral route and belong to the Picornaviridae family.
- a) Reverse transcriptase
- b) RNA directed DNA polymerases
- c) Both Reverse transcriptase & RNA directed DNA polymerases
- d) Boils
Why other options are incorrect:
- • Reverse transcriptase: While correct, it is the same thing as option (b), making (c) the most complete answer.
- • RNA directed DNA polymerases: This is the technical biochemical name for Reverse transcriptase.
- • Boils: This refers to a skin infection (furuncle) typically caused by Staphylococcus aureus and has no relation to the biological features of Retroviruses.
- a) Retro Viridae
- b) Rhabdo Viridae
- c) Toga Viridae
- d) Paramyxo Viridae
Why other options are incorrect:
- • Rhabdo Viridae: This family includes bullet-shaped viruses such as the Rabies virus.
- • Toga Viridae: This family includes viruses like Rubella (German measles) and Chikungunya.
- • Paramyxo Viridae: This family includes common respiratory and systemic viruses like Measles, Mumps, and Parainfluenza.
- a) Western blot test
- c) Karpas test
- d) Fujerbio test
Why other options are incorrect:
- • ELISA test: This is a highly sensitive screening test. While excellent for initial detection, it can produce false positives, requiring a Western blot for confirmation.
- • Karpas test: This is an immunoperoxidase slide test used for detecting HIV antibodies, but it is not the standard global confirmatory method.
- • Fujerbio test: This refers to a manufacturer (Fujirebio) of various diagnostic assays (like the Particle Agglutination test), not a specific type of confirmatory procedure.
- a) Western blot test
- b) ELISA test
- c) Both Western blot test and ELISA test
- d) VDRL test
Why other options are incorrect:
- • Western blot test: This is a confirmatory test, used only after a screening test (ELISA) has come back positive. It is too complex and expensive for initial screening.
- • Both: This is incorrect because screening and confirmation are two distinct steps in the diagnostic protocol.
- • VDRL test: This stands for Venereal Disease Research Laboratory test, which is a screening test for Syphilis (caused by Treponema pallidum), not HIV.
- a) Intrinsic period
- b) Incubation period
- c) Window period
- d) None of these
Why other options are incorrect:
- • Intrinsic period: This term is generally used in parasitology to describe the time required for a parasite to complete its development within a host.
- • Incubation period: This is the time interval between the initial infection and the first appearance of clinical symptoms (which in HIV can range from a few weeks to many years).
- • None of these: This is incorrect because “Window period” is the scientifically accurate term for this diagnostic gap.
- a) IHA
- b) Western blot
- c) ELISA
- d) Immuno electrophoresis
Why other options are incorrect:
- • ELISA: While highly sensitive (good for catching all possible cases), it is less specific than Western blot and can occasionally yield false positives.
- • IHA (Indirect Hemagglutination Assay): This is an older technique used for various infectious diseases but is not the standard or most specific method for confirming HIV.
- • Immuno electrophoresis: This is a general technique used to separate and identify proteins based on their electrophoresis and reaction with antibodies; it is not a specific diagnostic test for HIV.
- a) Reverse transcriptase
- b) DNA polymerase
- c) RNA polymerase
- d) None of these
Why other options are incorrect:
- • DNA polymerase: This is a common enzyme found in all living cells (including humans) for DNA replication; it is not a specific marker for HIV.
- • RNA polymerase: This enzyme is used by all cells to transcribe DNA into RNA and is not specific to the HIV virus.
- • None of these: This is incorrect because Reverse transcriptase is the characteristic enzyme that defines the replication of HIV.


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