Community Management of Smoking and Lung Cancer - Question and answers

Running head: QUESTION AND ANSWERS
Question and answers
Name of the Student
Name of the University
Author Note

COMMUNITY MANAGEMENT OF SMOKING AND LUNG CANCER1
Answer 1
A) According to the girl’s allergic reaction symptoms, and laboratory results, it is likely
that she is suffering from Type 1 hypersentivity reaction where the disease is allergic
asthma, form of anaphylaxis where airways are reversibly blocked preventing lung
tissues from receiving oxygen and increasing respiratory rate (Aulbach & Amuzie,
2017).
B) The most common environmental allergen that causes asthma is pollution or dust
containing dust mites.
Further diagnostic test to confirm specific allergen present in the serum are
molecular-based allergic test where panels containing allergens along with serum
containing allergen is tested to measure the presence of serum antibody, IgE specific
for the allergen. Radio allegro sorbent assay (RAST) is performed to detect the
presence of specific IgE for the allergen in the serum. Test for mast cell tryptase
released from mast cell granules as a sole mediator of inflammation during
anaphylaxis can be done within 1-2 hours of allergic response.
C) Medications for asthma in children include inhalers containing either short-acting
beta-2 agonists such as alvuterol or levalbuterol providing quick relief of
bronchioconstriction or long-acting corticosteroids such as aerosol form of Salmeterol
and Fluticasone that useful for persistant asthma. A nebulizer or face mask can aslo be
used (Chu & Bajaj, 2019).
D) Allergic specific immunotherapy or allergen-SIT is used as desensitizing therapy for
allergic diseases such as asthma. The mechanimsm include triggering peripheral T-
cell tolerance and development of regulatory T-cells along with release of interlukin

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10 and tumor growth factor-β, that helps in suppressing pro-inflammatory cells
including eosinophils, basophils and mast cells (Akdis & Akdis, 2015).
Answer 2:
Microscopic diagnosis of malaria is done by examination of patient blood smear that
is stained with Giemsa stain to distinguish the parasite from other cells in the blood under the
microscopei It gives a standard laboratory result for presence of malarial parasite and is easy
to perform however the results may vary if the quality of the reagents change. Rapid
Diagnostic Test s (RDTs) is an useful alternative to microscopic test. The patient’s blood
sample is collected for detection of specific antigens in the blood released by one of the
malarial parasite. RDTs rapidly determine malarial infection in patients however it shows
limitation when lower number of parasites are present in the bloodstream and therefore
requires microscopy to finally confirm the number of parasites present along with the RBCs
that are infected. Molecular diagnosis of malaria is more sensitive than microscopy but it is
unable to diagnose acute ill patients in a clinical setting. In molecular testing the genomic
DNA of the malarial parasite is extracted from the blood of the patient and real time PCR or
nested PCR is run with the DNA sample to confirm the presence of specific type of malarial
parasite (Who.int, 2020).
Answer 3:
A) i. Clostridium tetanus and Clostridium botulinum toxins are neurotoxins containing
three domains having three different functions including binding to neurospecific
receptor, translocation through membrane and proteolysis of specific molecules.
Clostridium neurotoxins have the capability to bind to the neuronal cells. C. tetani
releases tetanospasmin that interferers with motor neurons at the neuro-muscular
junction. The inhibitory neurotransmitters such as glycine released from the motor

COMMUNITY MANAGEMENT OF SMOKING AND LUNG CANCER3
neurons blocks the receptor at the neuromuscular junction leading to inhibition of the
excitory transmitter and suppression of muscle activity. However tetanus toxin when
internalized through a wound and reaches the neuromuscular junction, it binds to the
presynaptic tereminals and then transferred to the spinal cord where it binds to the
receptor binding site for inhibitory neurotransmittors on the muscle cell and destroys
the vesicular synaptic membrane protein causing “lockjaw” of muscles. On the other
hand botulinum toxin blocks the sites on the nerve endings which releases
acetylcholine into the synaptic cleft. Upon binding to the release site, the toxin
cleaves synaptobrevin and other membrane protein present on the nerve endings. This
leads to paralysis or weakness of the muscles because acetylcholine can no longer act
as a neurotransmitter. Diptheria toxin is a AB type of bacterial toxin released by
Corynebacterium diphtheria. The toxin has two subunits the A part is the catalytic
subunit and the B is the binding subunit. The toxin binds to the receptor on the host
cell membrane by its binding domain and enters into the host cell through
endocytosis. The catalytic part A cleaves from the toxin but remains attached to the
vesicle through disulphide bond and after acidification of the vesicle, the A subunit is
released and then the A subunit catalyses the transfer of ADP ribose from NAD+ to
elongation factor EF-2 protein leading to prevention of elongation during translation
of proteins and thereby leading to death of the cell. Shiga toxin (Stx) released by
Eschericia coli strain consists of pentamer of subunit B and single A subunit. Shiga
toxin binds to the receptor of the intestinal lumen of eukaryotes named Gb3 and is
internalised through endocytosis. Stx is transferred to the golgi complex and then to
endoplasmic reticulum where it inactivates ribosomes thereby causing inhibition of
translation and finally apoptosis of the cell (Henkel, Baldwin & Barbieri, 2010).

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ii. Amatoxin and phallotoxins are produced by two different groups of poisonous
mushrooms that is Amanita phalloides. Amatoxin shows its toxicity by binding
tightly to form complexes with DNA dependent RNA polymerase II enzyme found in
eukaryotes and specially attack liver cells after ingestion thereby inhibiting the
transcription process and further translation. This leads to the cell death by necrosis
because amatoxin shows syngergistic action with the tumor necrosis factor that is
TNF-α. On the other hand phallotoxins bind the protein receptors on the surface of
membrane of eukaryotic hepatocytes and induce the leakage of ions such as calcium
and potassium. The toxin is transferred to the cytoplasm by endocytosis and released
to destroy organelles (Wong, 2013). Virotoxins are derived from phallotoxins and are
formed of different compunds thus having structural and biological similarity.
Virotoxins are not absorbed properly after oral intake but it binds to the outer surface
of hepatocytes and casusing hepatic necrosis (Garcia et al., 2015).
iii. Ricin is a toxin produced by castor bean seeds that shows toxicity to mammalian
cells by catalysing the cleavage of N-glycosidic bond joining the adenine residue to
the 28S ribosomal RNA that is joined to a galactose binding lectin through a
disulphide bond. Thus the 28S RNA does not contain a purine residue and the
enzymatic activity of the ribosome is lost therefore no protein synthesis occurs. The
toxin binds to mammalian cells surface and transloactes itself through endocytosis
and delivers the catalytic subunit into the cytoplasm that renders protein synthesis and
causes cell death. Aflatoxin is a mycotoxin produced by Aspergillus flacus and
Aspergillus parasiticus that is genotoxic to the liver cells by inducing genetic changes
or mutation in the DNA of human through disruption of DNA bases or oxidative
damage and produces replication error (Eaton & Groopman, 2013). Taxol on the other
hand is an antitumor drug that reduces malignancies in human. It interacts with the

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microtubules and inhibits their depolymerisation. It has a igh affinity binding sites on
the microtubules and and polymerizes tubulin forming stable polymerization. It
inhibits the cell division by blocking the cells at the G2/M stage of the cell cycle thus
preventing mitosis.
B) Ciguatoxin is produced by a algae known as Gambierdiscus toxicus that shows
growth on the reefs in water near island which in turn is eaten by the fishes making
flesh of the fish poisonous. These fishe are eaten by human and the toxin is
transferred along the food chain. The disease caused by this toxin affects the
gastrointestinal as well as the neurological system causing diarrhoea, vomiting and
stomach pain which incur after few hours of ingestion of the toxic fish. It can also
lead to paralysis and death of the affected person (Robertson et al., 2014). Paralytic
shellfish poisoning occurred when different classes of molluscs consumed
dinoflagellates that are toxic in nature and the primary storage of the toxin occurred in
shell fishes. The ingestion of this toxin containing fishes by human causes
neurological defects within an hour of consumption and symptoms such as numbness
and dry mouth and throat, drowsiness and fever. In severe cases it can cause
respiratory problems and paralysis. Puffer fish poisoning occurred by ingestion of the
puffer fish belonging to the class of Tetraodontidae that produces tetrodoxin. The
toxin is present in the body of the fish due to the presence of marine vibrios that
produces the toxin inside the fish occurring as a normal microflora. The puffer fish
poisoning shows similar symptoms such as paralytic fish poisoning where in severe
cases death occur by asphyxiation (Cole et al., 2015).