chp 11 – Microbiology – Flashcards
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Unlock answersDNA is a double stranded helical structure. ?It is composed of nucleotides. ?Each nucleotide is a |
phosphate, a sugar (deoxyribose), and a nucleotide base. |
The components of DNA bind together in a very specific way. ?This permits a ____ and ______ orientation of the nucleotide |
correct and precise |
Nucleotides join to each other to form a chain. ?The ___________ of a sugar joins to the __________ of another nucleotide. ?This makes the linkage inherently polarized ?And gives structural orientation to the growing chain. |
3' hydroxyl group 5' hydroxyl group |
adenine and guanine are large double-ring structures |
DNA has two types of base ?Purines |
thymine and cytosine have smaller single ring structures. |
DNA has two types of base Pyrimidines – |
DNA STRUCTURE: the strands are ____ one strand is orientented upsidedown relative to the other |
antiparallel |
DNA is a chemically stable molecule. Any mismatched pairing is |
chemically unstqable |
is ususally found in single strand form contains ribose |
RNA |
helps maintain the proper shape of ribosomes. |
rRNA (ribosomal RNA |
contains information derived from DNA (the messenge from the DNA that says this is what you make) |
mRNA (messenger RNA) |
–carries amino acids to ribosomes |
?Transfer RNA |
how DNA is copied incrediably accurate and fast critical cellular process |
DNA replication |
occurs when the helix twists around itself must be relaxed is a characteristic of helical structures (because of this everything has to loosen up (unwound) b4 you can replicate). |
supercoiling |
Strands must be uncoiled, unwound, and separated before replication. ?This is accomplished by two enzymes: |
topoisomerase and helicase |
–unwinds the supercoils unwinds the supercoils by breaking the DNa so the supercoil relaxes, and then resealing the break |
?Topoisomerase |
–once the supercoiling has been relaxed this enzyme separates and unwinds the strands |
?Helicase |
would produce two copies that each contained one of the original strands and one new strand. cause you are conserving half |
semiconservative replication |
There are two requirements for replication: |
An ample supply of each of the nucleotides adenine, thymine, cytosine, and guanine A primer: template junction |
( a sequence that tells replication to begins/ you have to have a starting point for replication) |
A primer: template junction |
eacxh single strand of DNA is a |
template |
a portion of DNA is paired w/ a short piece od RNA called a ________ |
primer |
DNA replication is |
unidirectional (preceeds in one direction) |
gives the DNA polymerase (adds a lot of nucleotides to a strand of DNA) a place to add the next base Binding is between the 3’end of one base and the 5’ end of the next base |
the primer:template junction |
DNA REPLICATION:Direction Elongation of the bases is from the 3’ end This is required for |
chemical stability |
?The binding of a new base uses energy released from |
pyrophosphate |
DNA replication is performed this enzyme forms new strands of DNA using the primer: template junction as a guide. |
DNA polymerase |
aids in accurate replication takes place @ the primer:template junction active site |
proofreading |
with proofreading improperly paired bases are removed by an _____ (cuts out a nucleotide) |
exonuclease |
the double helix is unwound and seperated here DNA rep occurs here |
replication fork |
The separated strands at the replication fork are anti-parallel and are identified as: |
leading strand and the lagging strand |
The leading strand is in the correct orientation for bases added to the 3’ end of the primer: template junction. ?Replication moves towards the |
replication fork |
is anti-parallel. ?It moves away from the replication fork. ?Bases are only added to the 3’ end of the primer: template junction is replicated in pieces called Okazaki fragments |
the lagging strand |
each _____ has its own short RNA primer. It is created by an RNA polymerase called primase. |
okazaki fragment |
When the fragment is finished, the enzyme _______ removes the primer. The gap is filled in by DNA polymerase. Fragments are linked together by DNA ligase- |
RNAase H |
(its job is to join together fragments of DNA/ DNA glue/ glue DNA pieces together because of DNA and okaski fragments need to be attached) |
DNA ligase |
INITIATION AND TERMINATION OF REPLICATION: Initiation begins at a specific site on the chromosome: the _________ |
orgin of replication |
INITIATION AND TERMINATION OF REPLICATION: Termination occurs when the entire chromosome has been |
copied |
INITIATION AND TERMINATION OF REPLICATION: ?Replicated chromosomes are separated by ________ |
topoisomerase. |
always read in one direction The message is translated in a fixed reading frame There is no overlap or gap in the code |
codons |
a segment of DNa that codes for a functional product |
gene |
is the production of the functional product two features: it involves specific interactions between DNA and RNA it is highly regulated |
gene expression |
?It does not require a primer: template junction. ?RNA does not remain base-paired to DNA. ?It is not as accurate as DNA synthesis (because the RNA polymerase doesn’t have any proofreading). |
transcription |
three steps to stranscription |
initiation elongation and termination |
RNA polymerase unwinds strands of DNA and synthesizes the RNA: It also re-anneals the strands( it puts the strands back together). |
elongation |
a sequence of DNA signals the end of transcription: RNA polymerase detaches from DNA |
termination |
a DNA sequence called the promoter initially binds the RNA polymerase: This produces a bubble in the DNA. |
initiation |
The sequence of nucleotides in messenger RNA is transformed into a sequence of amino acids. It is directly affected by any errors in either DNA or RNA |
translation |
It is a highly conserved (all cells do it) function seen in all cells. It requires high levels of energy. requires all three types of RNA –messenger, transfer, and ribosomal |
Translation |
indicates the start of an amino acid sequence. begins with a start codon. Translation moves from the 5’end to the 3’ end. ends with a stop codon |
An open reading frame (ORF) |
mRNA in translation: mRNA contains a segment that recruits the ribosomal subunits. Ribosome and mRNA bind here through _______ |
complementary base pairing |
tRNA in translation: Each tRNA attaches to a specific amino acid at the __________ |
acceptor arm |
It brings amino acids to the ribosome. It binds to the ribosome at the anti-codon region using complementary base pairing |
acceptor arm |
The ribosome is a honeycombed structure with tunnels. ?The components of protein synthesis enter these tunnels and move through them. ___ ________ ___________ |
?mRNA ?tRNA ?Growing polypeptide chain |
3 stages of translation |
initiation elongation and termination |
requires: Recruitment of the ribosome to the mRNA placement of a methionine tRNA complex at the P site Precise positioning of the ribosome over the start codon of mRNA. |
initiation in translation |
, three things must occur in order for amino acids to be added to methionine. A tRNA carrying the next amino acid is loaded into the A site. A peptide bond forms between the amino acids. Each tRNA moves (out one moves in)–the one at the A site to the P site, the one at the P site to the E site. |
elongation: after initiation |
in elongation the ________ moves along the mRNA |
ribosome |
Translation continues until a stop codon enters the A site. ?Stop codons are recognized by specialized proteins. ?These specialized proteins cause the translation complex to fall apart. |
termination |
during termination the peptide achain is released from the ribosome and begins to form ___________ and __________ structures |
seconday and tertiary |
is energetically expensive and highly regulatied: constituative genes repressible genes inducible genes |
regulation of gene expression: protein synthesis |
Some genes are on and can be turned off – (can turn off when need to). |
repressible genes |
Some genes are always turned on – (always on). |
constitutive genes |
Some genes are off and can be turned on –(can be turned on when needed) |
inducible genes |
Gene expression is controlled by regulatory proteins: _______. _____, |
activators, repressor |
Gene expression is controlled by regulatory proteins: _______. _____, |
activators, repressor |
nvolved in positive regulation DNa binding protein |
activators |
invovlved in negative regulation are DNA binding protein |
repressors |
Regulatory proteins recognize two sites on DNA near the genes they control. |
the promoter and the operator |
where the RNA polymerase binds. is adjacent to the operator |
the promotor |
where regulatory proteins bind. adjacent to the promoter |
the operator |
turns on genes that are off (repressed). ?The best example is the lac operon: |
induction |
an _____ is a set of genes that is regulated. ?There are many in the chromosome |
operon |
The lac system has two regulatory proteins Both proteins bind at the operator site on DNA |
the lac repressor and the lac activator- CAP (caraboilte activator protein) |
is always produced. ?It binds at the operator site and overlaps part of the promoter site |
the lac repressor |
The lac repressor binds @ the operator site and overlaps part of the promoter site: this blocks the RNA polymerase from _______ this prevents transcription of the _______ |
attaching lac gene |
also binds at the operator site ?It recruits RNA polymerase to the site. ?It then interacts with the polymerase so it binds properly |
cap |
For the genes of the lac operon to be turned on, the repressor must first be _____ occurs through an allosteric control mechanism |
inhibited |
it then interacts w/ the polymerase so it binds properly |
expression of lac Operon: allosteric control mechanism |
The expression of lac genes is leaky ?A few transcripts are made and there is always a low level of ______ ?This allows small amounts of __________ into the cell. |
?-galactosidase lactose |
the expression of the lac gene is leaky: Lactose is converted to ______. ?_______ binds the lac repressor. |
allolactose |
The expression of lac genes is leaky ?A few transcripts are made and there is always a low level of ?-galactosidase. ?This allows small amounts of lactose into the cell. ?Lactose is converted to allolactose. ?Allolactose binds the lac repressor. ?This changes the shape of the lac repressor and it _________________________________ |
can no longer bind to the operator site |
acts in a similar fashion to allolactose. ?Its activity is based on levels of cyclic AMP (cAMP). |
CAP |
When cAMP levels rise, cAMP binds to ____ |
CAP |
cAMP binding to CAP: causes a change to the _______ shape of cap the cap-cAMP complex binds to the promoter site of the ________ this helps the RNA polymerase to bind to the _______ the lac genes are expressed |
3 dimensional lac operon promoter site |
When cAMP levels fall, ___________ ?RNA polymerase does not bind to the promoter site. ?The lac genes are not expressed |
no complex is formed. |
There are also cellular mechanisms that turn off genes. ?This is very important for the conservation of energy. has similar mechanisms to feedback inhibition |
repression |
ex of repression ______ synthesis: repressor is always produced but cannot bind DNA in its normal form. ?Excess binds the repressor and changes its shape so it can bind DNA and prevent gene expression. ?is a co-repressor of its own synthesis |
tryptophan |
are changes in the DNA sequence. ?Change in DNA sequence can cause changes in proteins. so they must be kept to a minimum |
mutations |
simplest mutation one base switched for another |
point mutation |
drastic mutation caused by the insertion or deletion of bases
–¿This is caused by large insertion or deletion of bases •(things that are going to change the reading frame) change how you will read the message and change what it’ll become in the end |
frameshift mutations |
rates are low certain sections oof the chromosome have higher rate (hot spots) |
spontaneous mutations |
can reverse the primary mutation instead of making a faulty protein you dont make a protein @ all |
suppressor mutations |
by: ?Hydrolysis ?Deamination ?Chemical mutagens ?Alkylation ?Oxidation ?Base analogs ?Radiation |
DNa can be dammaged |
cause double-strand breaks in DNA. |
gamma radiation and ionizing radiation |
causes DNA damage through the formation of thymine dimers.
(big gap skipping 2 nucleotides/ reading frame mutations) |
ultraviolet radiation |
damage to DNA that prevents replication |
radiation |
look like DNA bases but aren’t. ?They can be mistakenly used in replication. ?This inhibits further replication. |
base analogs |
what are the 3 principle mechanisms of DNA repair |
nucelotide excision, base excision and photoreactivation |
?Repair enzymes look for damaged bases. ?The damaged base is removed from the double helix. ?A DNA polymerase fills in the gap. ?A DNA ligase repairs the break in the strand |
base excision |
•In all organisms, NER involves the following steps: •Damage recognition •Binding of a multi-protein complex at the damaged site •Double incision of the damaged strand several nucleotides away from the damaged site, on both the 5' and 3' sides •Removal of the damage-containing oligonucleotide from between the two nicks •Filling in of the resulting gap by a DNA polymerase •Ligation |
nucleotide excision repair |
•repairs thymine dimers. –¿It is accomplished by an enzyme called photolyase. –¿Photolyase binds to the dimer in the dark. –¿Photolyase is activated by light and breaks the thymine-thymine bond. |
Photoreactivation |
bacteria shuffling genes occurs by: transposition, transformation, conjugation, and transduction |
genetic recombination |
genetic recombination that takes place w/in the same cell |
transposition |
genetic recombination that takes place between cells: ______ __________ _____ |
transformation, conjugation and transduction |
transposition is caused by _______. ?move from one place on the chromosome to another. ?They can move into or out of the chromosome. ?They use cleavage and rejoining mechanisms |
transposons |
Transposition causes random ___________. ?The results can be beneficial or detrimental. ?Beneficial changes will be selected for and maintained. ?They may be the reason for several human diseases. |
rearrangments |
involves the shift of genetic material between cells. ?It involves naked DNA. |
transformation |
is taken up by a bacterial cell and recombines with genes of that cell |
naked DNA |
in transformation the ________ must be competent Must be able to take up large molecules such as pieces of DNA. ?Some bacteria are naturally competent, whereas others can become competent after chemical treatment. ?Only a small amount of DNA is actually taken up |
recipient cell |
involves the transfer of genetic material between cells. ?It is a common event in both Gram-positive and Gram-negative bacteria. ?It uses a bacterial virus (phage) for transfer |
transduction |
There are two forms of transduction: |
generalized- random specialized- specific |
?The original infected cell chromosome is cleaved into pieces. ?Some of this bacterial DNA is incorporated into a newly made phage. ?When these phages infect the next cell, original DNA recombines with host chromosome |
There are three phases to generalized transduction. |
?Phage DNA incorporates into the host chromosome. ?Phage DNA excises itself from the host chromosome. Part of the host DNA is taken along. ?Original host DNA is incorporated into the next host chromosome. |
During specialized transduction: |
?Specialized transduction is used in |
biotechnology. |
involves the transfer of material between cells. ?requires direct contact between the donor and recipient cells. ?DNA moves from the donor to recipient cell |
conjugation |
conjugation requires direct contact between the donor and reciepient cells ______ stick together ______ use pili as a conduit for DNA transfer |
gram positive cells gram negative cells |
?The sex pilus of the donor cell recognizes specific receptors on the cell wall of recipient cell. ?An enzyme in the donor cell causes the plasmid DNA to unwind. ?One of the two single strands of plasmid DNA stays in the donor cell. |
There are several steps in conjugation: |
The other moves across the plasmid into the recipient cell. Both single strands are replicated. After replication, the donor and the recipient contain identical plasmids |
There are several steps in conjugation: |
can have several outcomes for the recipient cell: ?The plasmid can remain as a plasmid. ?The plasmid can become incorporated into the recipient cell chromosome. ?When this happens, the recipient cell is then referred to as Hfr. |
conjugation |
Conjugation: ___________ from Hfrcan be moved into a new recipient. ?This replaces sections of the host chromosome |
DNA |
mechanisms are involved in making pathogens more dangerous. |
?Many genetic |
is closely associated with pathogenicity and virulence. ?It transfers virulence genes into bacteria that were previously harmless. |
genetic transfer |
Genes for antibiotic resistance and toxins are found on |
plasmids |
?Genes for resistance to disinfectants and environmental pressure are found on |
dissimilation plasmids |
are defined as obligate intracellular parasites -they cannot live outside a cellular host. have only one goal –a productive infection are specific for a certain cell type |
viruses |
Viruses can infect: |
?Bacteria (called bacteriophages) ?Plant cells ?Animal cells (human cells included in this group). |
An intact viral particle |
virion |
is surrounded by a protein coat called a capsid. |
viral nucleic acid |
each is made up of capsomeres |
capsid |
there are 2 types of viuses |
DNA and RNA viruses |
structure must overcome two basic problems:
It must be strong enough to protect the viral nucleic acid. ?It must be able to release the viral nucleic acid for infection |
Virion |
have specific nomenclature |
viruses |
•It is built from identical protein units called capsomeres. –¿Capsomeres bond together and give the _______ structural symmetry. –¿Viruses possess either helical or icosahedral symmetry |
capsid |
viruses possesss either ____ or _____ symmetry |
helical or icosahedral |
There are two shapes of helical viruses: |
?Rod –straight and relatively rigid ?Filamentous –flexible, curved, or coiled. |
Their shape is derived from 20 triangular faces that make up the capsid 2 types: simple and complex |
ICOSAHEDRAL VIRUSES |
Many viruses that infect humans and other animals have this form when viral glycoproteins and oligosaccharides associate with the plasma membrane of the host cell. all have a phospholipid bilayer |
viral envelopes |
Envelopes vary in: |
?Size ?Morphology ?Complexity ?Composition |
envelope glycoproteins are firmly embedded in the envelope bilayer this is facilitated by domains of host membrane proteins called |
spanners |
envelope glycoproteins can form spikes or other structures on the outside of the virion which can be used to attach to the |
host cell |
important in infection packaged either: directly in the capsid enclosed in special proteins or enclosed in proteins from the host cell |
genomic packaging |
the host cells fills with virions and bursts. ?The result is cell death. |
in a lytic infection |
are also known as latent infections. ?The viral genome becomes incorporated into the host cell’s DNA. ?It can remain this way for an extended period. ?The host cell lives |
lysogenic infections |
For animal viruses, there are six steps in lyticinfection: |
?Attachment ?Penetration ?Uncoating ?Biosynthesis ?Maturation ?Release |
occurs when a virion binds to specific receptors on a host cell |
virion attachment |
in virion attachment some viruses require a _______ to attach. without it theres no infection |
coreceptor |
interactions occur through random collisions. ?The number of viruses is extremely important. |
viral-host cell |
WHEN VIRUS MEETS HOST CELL: produce the maximum number of virions |
lytic infections |
must be permissive for the infection to succeed. ?It must contain all of the components required to make new virions. |
the host cell |
at the apical cell surface usually cause acute infection. at the basolateral cell surface can become systemic |
viral infection |
Many viruses attach only to specific areas of the host cell membrane _______. ?________ are rich in cholesterol, fatty acids, and other lipids. ?They are more reliable for stable attachment. ?They are also the site of release for many viruses. |
lipid rafts |
Many different host cell molecules can be used as _____: ?Some viruses use more than one type. ?Some are shared by many viruses. ?can determine host range of virus |
viral receptors |
is high affinity. ?There are conformational interactions. |
virus-receptor binding |
Binding takes place between viral capsid and receptor. |
non-enveloped viruses |
Binding takes place between viral envelope proteins and receptor |
enveloped viruses |
Once attached, the virus must gain entry to the host cell. ?It must also ______ or _______ the capsid. |
uncoat or remove |
?Uncoating can occur in three places: |
the plasma membrane in the cytoplasm @ the nuclear membrane |
Use receptor mediated endocytosisto gain entry into the host cell |
PENETRATION & UNCOATING:Non-enveloped Viruses |
?Virus is enclosed in a vesicle –the early endosome ?Early endosomesfuse with or become late endosomes. ?Late endosomesfuse with the lysosomewhere uncoatingbegins. |
receptor mediated endocytosis: non enveloped viruses |
some viruses pore in the host membrane |
PENETRATION & UNCOATING:Non-enveloped Viruses |
fuses with the host cell membrane ?Fusion is mediated by specialized fusion proteins of the host cell. ?It results in the formation of a fusion pore –a large opening allowing viral entry. ?For some viruses, fusion requires the presence of co-receptor molecules |
PENETRATION & UNCOATING:Enveloped Viruses |
Viral infection requires ____________ ?Viral genomes, capsids, and other viral proteins are synthesized in specific locations in the host cell. Newly synthesized viral components are moved to other locations for assembly of viral particles |
compartmentalization |
Viral infection requires compartmentalization. Newly synthesized viral components are moved to other locations for assembly of __________ |
viral compartments |
Viral components are moved in vesicles, using host cell ________. ?Specialized host cell proteins are sometimes used. |
microtubules |
DNA viruses use routine host cell _____ to cross the nuclear membrane. ?The pathways form pores in the nuclear membrane |
import pathways |
RNA viruses use ____________ to convert RNA to DNA. ?Newly converted viral DNA is put into a pre-integration complex. ?This moves into the host cell nucleus during mitosis when the nuclear membrane is broken down |
reverse scriptase |
are either DNA or RNA. ?Both can be single or double-stranded. |
viral genomes |
use the same mechanisms as the host cell for biosynthesis. ?One strand of viral DNA is transcribed into mRNA. ?It uses either the host cell or viral RNA polymerase |
Double-stranded DNA Viruses |
is used as a template to make a complementary copy of DNA. |
viral strand |
Viral strand is used as a template to make a complementary copy of DNA. ?This uses the host cell’s ______. ?The ________ is transcribed into mRNA. ?It is also used to make new copies of the __________ |
DNA polymerase complementary copy viral genome |
requires: ?The synthesis of at least one viral protein ?The expression of several viral genes. |
BIOSYNTHESIS:Replication of DNA Virus Genomes |
has the same configuration as host DNA. |
The viral genome |
is performed by the host cell machinery |
replication of Dna virus genomes |
viruses require much less DNA replication. |
latent DNA |
synthesis is inhibited by the virus. ?All polymerases and proteins concentrate on viral DNA synthesis. |
host DNA |
form in the host cell –replication compartments ? They contain both DNA templates and host cell replication machinery. ?They are essentially viral factories. |
Specialized sites |
allows exponential viral replication |
Compartmentalization |
do not kill host cells. ?The viral genome is inserted into a host chromosome. ?Maximum replication is not required. ?A small number of viral genes are expressed. ?A limited number of viral genomes are replicated |
BIOSYNTHESIS:Replication of Latent DNA Viruses |
Newly made viral DNA molecule is used as the template for is performed by the host cell’s RNA polymerase. |
transcription |
expression begins after DNA synthesis. ?Genes are expressed in a specific order. |
transcription: viral gene |
Transcription with single-stranded DNA viruses is more complicated. ?The single DNA strands must first be converted to |
double strands |
?Viral genes are transcribed at very high rates. ?This maximizes the number of |
new viruses being produced |
Rapid ______ of viral DNA is regulated by host cell proteins. ?______ is coordinated with viral DNA synthesis. ?All host cell _______ and protein synthesis is shut down by the virus. |
transcrition |
Mechanisms of biosynthesis are more complicated than in DNA viruses. ?Host cells do not possess RNA-dependent polymerases. |
RNA Viruses |
They are required to make viral mRNA and replicate genomes. ?Viruses must carry one |
RNA-dependent polymerases. |
are RNA viruses that contain the enzyme reverse transcriptase. cause latent infections. |
retroviruses |
converts RNA into DNA. ?Converted viral DNA can be inserted into the host cell _________ |
reverse transcriptase
chromosome |
Involves the movement of newly made viral components to specific sites in the host cell. |
maturation |
?There are two steps in maturation: |
?Intracellular trafficking ?Assembly |
Some viral components are synthesized in the cytoplasm, and some in the nucleus. ?They are transported through the cell by host cell microtubules to assembly sites. |
Intracellular Trafficking |
depend on: ?The type of genome (DNA or RNA) ?The mechanism of genome replication ?The presence or absence of an envelope |
?Assembly sites |
in intracellular trafficking many _______ viruses assemble near the host cell membrane ?Others assemble near membrane bound organelles. |
enveloped |
in intracellular tafficking these viruses assemble in the host cell nucleus |
Non-enveloped |
in intracellular traffiking travel from the assembly site to the cell membrane in vesicles. |
viral proteins |
in intracellular trafficking _____ transport depends in whether the virus has an envelope |
viral genome transport |
in intracellular traficking ___________ genomes move to sites near the membrane |
enveloped viruses |
in intracellular trafficking ________-genomes move to the host cell nucleus. |
?Non-enveloped viruses |
All virions must complete a common set of assembly reactions. ?Formation of structural subunits for the capsid ?Assembly of the capsid ?Association of viral genome within the capsid ?Assembly of viral envelope glycoproteins. |
Enveloped viruses: |
All virions must complete a common set of assembly reactions: ?Formation of structural subunits for the capsid ?Assembly of the capsid ?Association of the viral genome within the capsid.
|
non enveloped viruses |
Capsomeres are assembled 1st. ?Assembly is diff in DNA viruses & RNA viruses. ?The # of capsomeres produced is always more than the # required. ?This maximizes the chances of capsomeres finding each other. |
ASSEMBLY: Capsids |
can be assisted by host chaperone proteins. |
capsid assembly |
ASSEMBLY: Viral Genomes This is the most important part of assembly. ?There are two mechanisms: |
Concerted assembly and sequential assembly |
–the viral genome is inserted into already assembled capsid |
?Sequential assembly |
–the virion is assembled while the viral genome is being synthesized |
?Concerted assembly |
New virions can be released from the host cell in two ways: |
?Lysis ?Budding |
Non-enveloped viruses use _ forr release. ?This causes death of the host cell. |
lysis |
?Enveloped viruses use _____ for release. ?This allows the host cell to live for a while.
(picking up that piece of envelope on the way out of the cell). |
budding |
release: ?In some viral infections, ________ are non-infectious. ?Viral enzymes convert them into an infectious form after release. |
completed virions |
can spread from cell to cell. ?They can use tight junctions between cells. ?They can also spread through the formation of syncytia. |
viruses |
allow movement through the body without exposure to the immune system
large globs of viruses/ can move through the blood stream to make it to one part of the body to the other |
formation of synctica |
spread: Some viruses produce _____: ?These are empty capsids or non-infectious virions ?They confuse and distract the host defenses. |
decoy virons |
spread: Some viruses incorporate host proteins as a type of |
camouflage |
can be: Acute (rapid and self limiting) ?Persistent (long term) ?Latent (extreme versions of persistent infections) ?Slow or transforming (complicated types of persistent infections) |
Viral infections |
produce virions and kill host cells rapidly (cytopathology |
Cytopathic viruses |
viruses produce virions but do not cause cytopathology |
?Noncytopathic |
me viruses dont produce virions or cause cytopathology but |
still cause infection |
periods vary for different viruses. ?Some are as short as days. ?Some are as long as years. |
incubation periods |
during the incubation period the virus is ______ the host is beginning to ______ |
replicating respond |
varicella zoster is |
chicken pox |
rapid production of virions & elimination of infection; virions can be missed and spread to other tissues this then causes reinfection ex: varicella-zoster |
acute infections |
severe public health problem associated w/ epidemics short incubation period which causes a delay in indentifiable symptoms until the virus has already spread |
acute infections |
Acute infection epidemics are often seen in |
crowded populations. ?Schools ?Military bases ?Nursing homes |
hosts that survive acute infections are immune to __________ for life: some diseases escape this immunity |
reinfection |
(changes in virion structure) reinfection occurs because of this it is due to the specificity of the immune reponse the new structure isnt recog by the immune system memory |
antigenic variation |
there are 2 forms of antigenic variation |
antigenic drift and antigenic shift |
Involves major changes in virion structure ?Is due to the acquisition of new genes ?This is through co-infection or recombination |
?Antigenic shift |
Involves small changes in virion structure ?Results from mutations ?Occurs after the infection has begun |
antigenic drift |
Caused when host defenses are either modulated or completely bypassed. ?Virions are produced for months or even years. |
PERSISTENT INFECTIONS |
There are two variations of persistent infections |
chronic and latent infection |
the infection lasts for life |
latent infection |
the infection is eventually cleared |
chronic infection |
host defense mech against viral infec They must be given the signal to begin killing infected cells. Some viruses can kill them first. |
cytotoxic T cells |
some viruses escape killing by infecting tissues that have reduced immunosurveillance |
skin central nervous system |
?No large-scale production of virions ?Reduced or absent immune response ?Persistence of an intact viral genome so infections can reoccur |
latent infections |
can be reactivated years after entry into host. |
latent viruses |
are lethal. ?They are usually associated with brain infections. ?Signs may not be seen until years after the primary infection. ?Once signs and symptoms appear, death usually follows very quickly |
slow infections |
?Sufficient number of viruses present ?Access to susceptible and permissive host cells ?An ineffective host immune response |
There are three basic requirements for successful infection |
are disseminated within the host and transmitted from one host to another. |
viral infections |
refers to spread of virus within an infected body. ?There are common sites for viruses to enter into the body. |
viral disssemination |
what are the three main entry points for viral dissemination |
respiratory system, digestive system and the urogenital tract |
The most common portal of entry into the human body. ?It is always exposed to large numbers of potential pathogens. ?Viruses easily disseminate from here into other areas of the body |
respitory tract |
is the second most common portal of entry. ?Many viruses use this portal of entry. ?They must be resistant and resilient to harsh environments in order to survive. |
the digetive tract |
in the digestive tract some viruses use transcytosis through _______ to enter the body some viruses stay in the _____ and eventually destroy them |
M cells |
their destruction causes inflammation of the digestive tract and diarrhea |
M cells |
The primary point for sexually transmitted viruses to enter the body. ?Some remain in this tract and cause local infections e.g. genital warts. ?Some gain access to underlying tissues and disseminate throughout the body. |
urogenital tract |
viruses also use this like when they enter through the eyes ex: opthalmic herpes infection |
portals of entry |
Some viruses enter through the skin. ?Usually by _______ transmission from biting insects ?If they remain in the epidermis, a localized, ______ infection occurs. ?If they get into the dermis, a ____ infection can occur |
vector acute systemic |
They can disseminate throughout the entire body. ?Some target neurons. ?Some use neurons to get to their preferred target area. |
viral dissemination in the nerous system |
Viruses released from the apical surface host cells cause |
localized limited infection |
?Viruses released from the basement membrane of host cells can |
spread systemically |
?The bloodstream is the best route for systemic viral infection. ?Referred to as |
hematogenous dissemination |
refers to virus replicating in the blood |
viremia |
refers to the spread of the virus from one host to another |
viral transmission |
there are 2 patterns of viral transmission human to human and animal to human? |
transmission w/ in a single species transmission between species |
Viruses can be transmitted in several ways: ?Via _____ or inanimate objects ?Via poor techniques employed by health care workers: ___________ ?________ –the digestive tract |
fomites iatrogenic transmission Fecal-oral route |
Viruses can be transmitted in several ways: ?Respiratory tract Viruria Urogenital tract ? Contact with ? |
the sneeze is the best form of transmission transmission via urine sexual transmission skin |
infections are seasonal. ?Respiratory tract infections are higher in winter. ?Digestive tract infections are higher in summer. |
most acute viral |
in pregnant women can expose the fetus to infection |
viremia |
some virus transmission from mother to infant can occur through |
breast feeding |
the capacity of an infectious organsim to cause disease |
virulence |
viruses can cause significant damage |
virulent |
(attenuated) viruses cause little or no disease. |
nonvirulent |
–how much virus is required to paralyze 50% of a subject population. |
PD50 (way to measure viral virulence ID50 & LD50 as well) |
can be directly affected by: ?Route of entry ?Age and health of host ?The gender of the host |
virulence |
?Susceptible –can be infected and can also transmit the infection ?Immune –cannot be infected |
There are two types of host: |
caqn gender play a role in infection? |
?Males are more susceptible to viral infection than females. |
the most effective way to deal with viral infections. ?It allows for life-long immunity from a particular infection. ?It increases herd immunity |
vaccination |
what are the 3 groups of vaccines |
live attenuated cavvine inactivated or killed vaccine and subunit vaccine |
made of intact virions rendered non-infectious |
live attenuated vaccine |
composed of killed or dead virons |
inactivated or killed vaccine |
cposed of immunogenic parts of virions |
subunit vaccine |
antigen is administered and causes the onset of the immune response |
avtive immunization |
a preformed antiviral product, such as antibody, is administered |
passive immunization |
can inactivate genes responsible for suppressing tumor formation. |
retroviruses |
Some viruses can cause _____ in animals. ?An estimated 20% of human ______ involve viruses |
cancer |
Viruses associated with human cancers include: |
?Epstein-Barr virus ?Hepatitis B and C viruses ?HPV |
for many products that modify or block host defense. ?A battle wages between the host immune system and these modifications |
viral genomes code |
are usually opportunistic infections and have increased with the number of immunocompromised individuals |
fungal infections |
Parasites can be divided into two groups: |
? Protozoans – microscopic, single-celled eukaryotes. ? Helminths – macroscopic, multicellular worms. |
Disease causing parasites depend on their ______ for survival |
infected host |
are intestinal parasites that infect 10% of the world population |
entamoeba |
parasites infect 16 million people in Latin America each year |
trypanosoma |
vary in size. ?They contain membrane-bound nuclei and cytoplasm. |
paracytic protozoans |
the cytoplasm of parasitic protozoans are divided into |
inner form- endoplasm and outer form-ectoplasm |
parasitic protozoans can be classified on the basis of their methods of |
movement and reproduction |
Are facultative anaerobes ?Are heterotrophs ?Have a highly developed reproductive system |
most infectious protozoans |
some infectious protozoans form ____ as a way of protecting themselves. they can also be a mech of transmission from host to host |
cysts |
are worms. ?There are two types: ?Free living ?Parasitic ?They are bilaterally symmetrical and of various lengths |
helminths |
parasitic helminths body is covered by a tough cellular ______ some have suckers, hooks, or plates which are used for _______ |
cuticle attachment |
?Differentiated organs ?Primitive nervous systems ?Primitive excretory systems ?Highly developed reproductive systems ?They do not have a circulatory system. |
All helminths have: |
comes in 2 forms: gastrointestinal form and blood and tissue form |
nematodes (round worms) |
use only one host to complete their life cycle |
gastrointestinal form of nematodes |
uses multiple hosts to complete their life cycle |
blood and tissue form of nematode |
what are the three types of helminth that can infect humans |
cestodes (tapeworms), trematodes (flukes), nematodes (round worms) |
?Have a flat, ribbon-shaped body ?The head contains suckers and frequently has hooks for attachment. ?They generate proglottids– reproductive segments with male and female gonads. ?Have no digestive tract - nutrients are absorbed across their cuticle. ?Some use one host and others two for their life cycle. |
cestodes (tapeworms) |
Have leaf-shaped bodies ?They have two suckers. ?Oral sucker –takes in nutrients and regurgitates waste ?Distal sucker –used for attachment |
trematodes (flukes) |
Pathogenesis of protozoan diseases is variable. ?The severity of infection is related to the number of worms. ?A large worm load lead to increased disability of the host |
for helminths |
can cause: ?Tissue damage ?Allergic or anaphylactic reactions |
The host defense reaction |
are intracellular parasites. ?They alternate between sexual and asexual reproduction |
sporozonans |
most important sporozoans diseases that together affect 1/3 of the world's population |
malaria and toxoplasmosis |
febrile illness found worldwide transmission by bite of anopheles mosquito mortality mainly seen in children and immunocompromised adults |
malaria (plasmodium species) |
Male fertilizes female gametocytes ?Resulting zygote forms an oocyst filled with sporozoites ?Oocyst ruptures releasing sporozoites into body ?Sporozoites penetrate salivary glands |
(plamodium) Sexual life cycle begins when a mosquito ingests infected blood |
Sporozoites are introduced with mosquito saliva. ?Sporozoites move to the liver and produce merozoites. ?Hepatocytes rupture releasing the merozoites. ?Merozoites infect red blood cells (ring stage). |
Asexual life cycle begins when a mosquito bites new host. |
Within 72 hours, infected red blood cells begin to rupture. ?Merozoites are released. ?Some infect other RBCs. ?Some transform into the gametocyte form. ?Gametocytes are then taken up by the next mosquito |
life cycle of the plasmodium |
Fever ?Anemia ?Circulatory changes thrombocytopenia |
Symptoms of malaria include: |
is caused by the destruction of red blood cells. ?It is accompanied by depression of marrow function and an enlarged spleen |
anemia in malaria |
two factors involved in the treatment of malaria |
species of plasmodium and the immunocompetency of the infected individual |
are amebas. ?The most primitive form of protozoans that: ?Multiply by simple binary fission ?Move by using pseudopodia. ?Produce a chitin wall for protection |
rhizopods |
rhizopods produce a chitin wall for protection that is referred to as a |
cyst |
is an obligate intracellular parasite. ?It is passed from host to host as cysts. ?Uses the fecal-oral route of infection ?Ingestion of a single cyst can cause infection |
AMEBIASIS (ENTAMOEBA HISTOLYTICA) |
is the third highest parasitic cause of deaths worldwide. ?Only malaria and schistosomiasis are higher. ?is on the rise in the US |
amabiasis (entamoeba histolytica) |
LIFE CYCLE OF ENTAMOEBA HISTOLYTICA: ?It is found in either the ________ form. |
trophozoiter cyst |
Initial infection is via the fecal-oral route. ?Systemic ________ occurs only after the colon colonized |
PATHOGENESIS OF AMEBIASIS amebiasis |
pathogenesis of amebiasis the parasite produces several virulence factors and enzymes which can cause membrane ____ and _______ |
lesions and cellular death |
w/ amebiasis the infection is usually mild and asymptomatic. lesions can open the intestine for _______ and __________ |
bacterial and viral infection |
in amebiasis cysts can pass through the stomach and into the small intestine here they disintegrate and release four |
trophozoites |
are widespread in nature. ?They use flagella for movement through the host. ?They multiply by binary fission |
flagellates |
what are the four flagellates that cause disease in humans |
?Trichomonas ?Giardia Leishmania ?Trypanosoma |
these 2 flagettes are noninvasive, have low morbity rates and theres no intermediate host required |
Trichomonas ?Giardia |
these 2 flagellates are invasive, have high morbidity rates, are frequently lethal and required an intermediate host (associated w/ the sandfly) |
leishmania and tryanosoma |
is a sexually transmitted infection. It produces vaginitis in females with symptoms: Pain ?Dysuria ?Discharge |
TRICHOMONIASIS (TRICHOMONAS VAGINALIS) |
It may cause prostatitis or urethritis in males. ?It can last from weeks to months. ?An estimated 180 million people worldwide are infected each year. ?The peak age of infection is 16 to 35 years old. |
TRICHOMONIASIS(TRICHOMONAS VAGINALIS) |
does not form cysts. ?It can survive outside the host for 1 to 2 hours. ?In water, semen, or urine, it can survive for up to 24 hours. |
trichomonas |
Direct contact transmission to genital endothelial cells causes the infection. ?Cells are destroyed and inflammation occurs. ?It is accompanied by petechial hemorrhaging. is noninvasive |
pathogenesis of trichomoniasis |
TRICHOMONIASIS: ?Infection causes persistent ______. ?Symptoms can last for months. ?Severe cases can cause ________ and ________. |
vaginitis hemorrhaging and tissue errosion |
It is caused by the protozoan _______ ; Motile ?Fusiform ?Moves in a spiral fashion ; The vector is the tsetse fly (Glossina species). |
TRYPANOSOMIASIS ; Trypanosoma. |
there are 2 forms of trypanosomiasis the african form which causes ____ and the american form which causes _____ |
sleeping sickness ; chaga's disease |
is caused by trypanosomissis and is confined to central Africa. ?There are ten to twenty thousand cases each year. ?The reservoir is humans |
sleeping sickness |
PATHOGENESIS OF TRYPANOSOMIASIS: Parasitemia causes localization of parasites in __________ the heart and CNS are particularily vulnerable |
SMALL BLOOD VESSELS |
PATHOGENESIS OF TRYPANOSOMIASIS
|
Symptoms include: Hemorrhaging ?Demyelinating panencephalitis ?Headache ?Fever ?Lymph adenopathy ?Skin rash ?Impaired mental status |
TRYPANOSOMIASIS ?Symptoms can progress to: |
?Eventual diminished alertness. ?Indistinct speech, tremors, and coma. ?Coma can lead to death. |
what are the subgroups for nematodes |
intestinal nematodes and tissue nematodes |
have the following characteristics: ?Fusiformbody shape ?Tough outer cuticle ?Male and female forms ?Thousands of offspring are produced ?Eggs must incubate outside the host to become infective ?There is a larval form |
Intestinal nematodes |
what type of nematodes are these? Pinworms ?Whipworms Large roundworms
(eggs must incubate outside the host) |
intestinal nematodes |
can produce: ?Malnutrition ?Discomfort Anemia Occasionally death |
intestinal nematode infection |
severity of intestinal nemotodes in directly correlated to worm load. small worm load ? large worm load ? |
pinworm (enterobius vermicularis) |
pathogenesis of enterobiasis:
pinworms attach to the mucosa of the _______ females migrate down the ___________ to lay eggs |
cecum
perianal |
once pinworms lay eggs: eggs stick to tissue, bedding towels and fingers eggs can be inhaled or swallowed eggs hatch in the upper intestine larvaw migrate down to the ______ |
cecum |
?Tissue nematodes can induce disease in: |
tissue blood and lymph systems |
Four major types of ________ use humans as definitive hosts. ?They can live for years in subcutaneous tissues and lymph vessels. |
tissue nematodes |
?Tissue nematodes discharge live offspring called ________. ?Circulate through the blood or tissue ?Can be ingested by blood sucking insects |
microfilariae. |
Caused by the parasite Trichinella spiralis: Lives in the duodenum and jejunum of flesh eating mammals. ?Particularly found in swine and bears |
TRICHINOSIS |
enters through the host vascular system and is distributed widely. ?Only parasites that penetrate the skeletal muscle survive. ?It can become encapsulated in muscle. ?It can remain viable for 5-10 years. |
trichinella |
The disease is widespread amongst swine. ?Human infection results from eating undercooked meat. ?Over one million people in the US carry either living or dead worms. ?Most infections are asymptomatic |
TRICHINOSIS |
lesions |
in trichinosis ________ are nfound in striated muscle ?Heart muscle ?CNS |
PATHOGENESIS OF TRICHINOSIS
The area of infection is infiltrated by white blood cells, particularly ___________. Worms mature in 24-48 hours of eating ______ |
eosinophiles tainted meat |
symptomes of trichinosis include |
nausea, andominal pain and diarrhea |
PATHOGENESIS OF TRICHINOSIS: ?Larval invasion starts _______ later. Lasts one to ______ Low worm load – __________ ?Large worm load – ________ |
one week six weeks asymptomatic significant disease and poss death |
are commonly called tapeworms. ?The largest of the intestinal parasites ?Lack a vascular and respiratory system ?Lack a gut or body cavity ?Nutrients are absorbed across the cuticle |
cestodes |
pathogenesis of cestode infec: in the _____:
the worms stays in the lumen of the gut only minor symptoms are seen |
primary host |
pathogenesis of cestode infection: in the ____________: larval stages of the worm cause serious tissue invasion most patients are asymptomatic |
intermediate host |
PATHOGENESIS OF CESTODE INFECTION ?Symptoms include |
?Gastric disfunction ?Nausea ?Diarrhea ?Weight loss |
are known as flukes. ?Have a bilateral symmetry ?Have two deep suckers: ?One in the oral cavity ?One on the ventral side of the worm |
trematodes |
can live for decades in human tissue and blood vessels. ?They produce progressive damage to vital organs. |
trematodes |
Eggs are excreted from the human host. They must reach water in order to hatch. Hatching releases larvae called miracidia. Miracadia penetrate snails, the intermediate host |
TREMATODES life cycle |
LIFE CYCLE OF TREMATODES: Miracadia develop into _______. _______ are released from the snail. |
cercariae |
DISEASE CAUSING TREMATODES
Three major groups of flukes invade humans: |
?Lung flukes –?Liver flukes –?Blood flukes – |
?Infections are frequently caused by consuming infected shell fish ?Infections cause eosinophilia and inflammation. ?After infection a capsule forms around the fluke |
paragonimiasis: lung flukes |
is the study of fungi |
mycology |
are important for the environment are commensal organisms. ?They are normally harmless to humans. can be opportunistic pathogens |
fungi |
are eukaryotes. ?There are two forms: ?Molds –multicellular ?Yeasts –unicellular |
fungi |
Fungi use __________ metabolism
They obtain carbon from decaying organic matter. |
heterotrophic |
Most fungi are _______ aerobes but some are ___________ anaerobes. ?No fungi are _____ |
obligate facultative obligate anaerobes. |
?Fungi reproduce either sexually or asexually. ?Involves spores -ascospores, zygospores, or basidiospores |
sexual reproduction |
?Fungi reproduce either sexually or asexually. ?Through conidia ?Involves mitotic division and budding |
asexual reproduction |
•Some fungi can grow in mold or yeast form •The_____ form requires environmental conditions similar to in vivo • proper temperature • increased nutrients •The ________ form requires: • ambient temperatures minimal nutirents |
yeast
mold
|
form of fungi that requires environmental conditions similar to in vivo. ?Proper temperature ?Increased nutrients |
yeast |
form of fungi requires: ?Ambient temperatures ?Minimal nutrients |
mold |
fungi are classified by: ?Ribosomal RNA typing ?The tissue types they parasitize ?The diseases they produce |
medically important |
are classified into 4 groups:
Superficial mycoses ?Mucocutaneous mycoses ?Subcutaneous mycoses ?Deep mycoses |
?Fungal diseases |
Fungal infections that do not involve a tissue response: ?Piedra, Tinea nigra, Tinea capitis, favus, and pityriasis |
SUPERFICIAL MYCOSES |
–colonization of the hair shaft causing black or white nodules |
?Piedra |
brown or black superficial skin lesions |
Tinea nigra |
folliculitis on the scalp and eyebrows |
?Tinea capitis |
–destruction of the hair follicle. |
favus |
–dermatitis characterized by redness of the skin and itching: ?Caused by hypersensitivity reactions to fungi normally found on skin Mostly seen in immunocompromised patients |
pityriasis |
Associated with: ?Skin ?Eyes ?Sinuses ?Oropharynx and external ears ?Vagina |
CUTANEOUS AND MUCOCUTANEOUS MYCOSES |
(type of cutaneous and mucocutaneous mycoses) skin lesions characterized by red margins, scales and itching: ?Restricted to the stratum corneum. ?Classified based on location of infection |
ringworm |
ringworm on feet or between toes |
tineapedis |
ringworms between the fingers, in wrinkles on the palms |
tineacorporis |
ringworms lesions on the hairy skin around the genetalia |
tineacruses |
ringworms in scalp and eyebrows |
tineacapitis |
chronic infection of the nail bed ?Commonly seen in toes |
?Onychomycosis |
type of cutaneous and mucocutaneous mycoses that has extended scaly areas on the hands and feet |
Hyperkeratosis |
colonization of the mucous membranes ?Caused by the yeast Candida albicans ?Often associated with a loss of immunocompetence |
mucocutaneous candidiasis |
?There are two clinical types of mucocutaneous candidiasis: |
thrush and vulvovaginitis |
fungal growth in the oral cavity ?An indicator of immunodeficiency. |
thrush |
fungal growth in the vaginal canal ?Can be associated with a hormonal imbalance
Or can be caused by a superinfection caused by the use of an antibiotics which wipes out normal microflora in the body |
vulvovaginitis |
Can cause the development of cysts and granulomas. ?Provoke an innate immune response -eosinophilia |
localized primary infections of subcutaneous tissue |
Usually seen in immunosuppressed patients with: ?AIDS ?Cancer ?Diabetes |
deep mycoses |
?Can be acquired by: ?Inhalation of fungi or fungal spores ?Use of contaminated medical equipment |
deep mycoses |
?Deep mycoses can cause a systemic infection - __________ ?Can spread to the skin |
disseminated mycoses |
very uncommon in immunocompetent individuals are more common in immunodeficient patients |
fungal infections |
fungi can become invasive. ?They switch from yeast form to mold form. ?The hyphae invade tissues and disseminate |
some dimorphic |
?Fungi do not produce exotoxins in vivo. ?Primary ________ is due to host inflammatory response. |
tissue injury in fungal infections |
?Host defense against fungal infection is primarily through: |
?Phagocytosis ?Adaptive immune response |
cause antibiotic resistance |
mutations |
classification of viruses
1.Type of genetic material 2.Shape of the capsid 3.Number of the capsomere 4.Size of the capsid 5.Presece/absence of an envelope 6.Type of host it infects 7.Type of disease it produce 8.Target cell 9.Immmunological and antigenic properties |
1.Type of genetic material 2.Shape of the capsid 3.Number of the capsomere 4.Size of the capsid 5.Presece/absence of an envelope 6.Type of host it infects 7.Type of disease it produce 8.Target cell 9.Immmunological and antigenic properties |
protein molecule forming capsid |
capsomere |
protein shell surrounding nucleic acid protein coat |
capsid |
nucleic acid plus capsid |
nucleocapsid |
phospholipid bilayer w/ embedded glycoproteins surrounding the capsid in enveloped virus
viral membrane |
envelope |
complete infectious viral structure: nucleic acid plus capsid for non-enveloped virus; nucleic acid plus capsid plus envelope for enveloped virus
viral partical |
virion |
ribbon like protein that forms spiral around nucleic acid (ex: tobacco) |
–Helical capsid- |
many sided |
polyhedral |
triangular faces |
icosahedral |
combination of helical and icosahedral |
complex capsid |
•The infection cycle was first worked out in bacteriophages (bacterial viruses). •Bacteriaphages generally go thru 5 steps in replication process ending in lysis of the cell |
adsorbtion- bac attaches to cell , penetration- involves injection of virus into cell DNA synthesis- once in used to make more DNA maturation- pieces of viruses put together release- involves lysis or bursting of the cell |
Viral infections are _______ within the host and _____ from one host to another |
disseminated
transmitted |
antibiotic resistance, synthesis of pilus, utilization of unusual nutrients, increased virulence, toxin production, antibiotic synthesis |
thngs that can be transferred on plasmids |
- live on the surface of the host Ticks, lice |
Ectoparasites |
live w/in the body of the host Some protozoa and worms |
endoparasites |
must spend part of its lifecycle in or on the host Most parasites, plasmodium- protozoa |
obligate parasites- |
free living soil fungi, but can obtain nutrients from the host Fungi that cause skin infections |
Falcultative parasites- |
tapeworms, remain in or on host once they have invaded |
Permanent parasites- |
biting insects feed on host then leave (mosquito) |
Temporary parasites: |
invade organisms other than normal host. Tick invading human rather than dog or wild animals |
accidental parasites |
parasites that have parasites (mosquitos that have malaria) Vectors-agents that transmit |
Hyperparasitism- |
harbors host while it reproduce sexually Malaria- mosquito |
Definative host: |
- harbor parasite during a developmental stage human |
Intermediate host |
range of different host in which parasite can mature Anopheles mosquitoes (malaria) |
host specificity |
•caused by several species of Aspergillus –¿Associated with immunodeficiency –¿Can be invasive and disseminate to the blood and lungs •¿Causes acute pneumonia –¿Mortality is very high. ¿Death can occur in a matter of weeks |
aspergillosis |