Print Options

Card layout: ?

← Back to notecard set|Easy Notecards home page

Instructions for Side by Side Printing
  1. Print the notecards
  2. Fold each page in half along the solid vertical line
  3. Cut out the notecards by cutting along each horizontal dotted line
  4. Optional: Glue, tape or staple the ends of each notecard together
  1. Verify Front of pages is selected for Viewing and print the front of the notecards
  2. Select Back of pages for Viewing and print the back of the notecards
    NOTE: Since the back of the pages are printed in reverse order (last page is printed first), keep the pages in the same order as they were after Step 1. Also, be sure to feed the pages in the same direction as you did in Step 1.
  3. Cut out the notecards by cutting along each horizontal and vertical dotted line
To print: Ctrl+PPrint as a list

280 notecards = 70 pages (4 cards per page)

Viewing:

Microbiology Unit 3

front 1

Controlling Microbial Growth

back 1

temperature (dentures proteins)
moisture
filtration
safety cabinets
osmotic pressure
radiation
chemicals

front 2

Resident (normal) microflora

back 2

microbes that are supposed to be present in the environment or on a surface.

front 3

Antiseptic

back 3

a disinfectant safe enough for use on the skin

front 4

Transient Microbes

back 4

microbes that are transferred from objects or surfaces to the skin

front 5

Disinfectant

back 5

used to clean inanimate objects

front 6

Purpose of disinfectants and antiseptics

back 6

to reduce the population of microbes normally through chemicals

front 7

Biosafety levels

back 7

the four safety levels in labs dealing with pathogens

front 8

Biosafety Level 1 (BSL-1)

back 8

mostly environmental microbes or normal flora
Not much of a risk to handle
non-pathogenic

front 9

Biosafety Level 2 (BSL-2)

back 9

can cause infection but work with such small populations it never really poses a threat
must still use good aseptic technique to minimize the amount of contamination of objects

front 10

Biosafety Level 3 (BSL-3)

back 10

work with massive quantities of pathogenic microbes (can be a larger quantity of BSL-2)
must work in a more clean and secure environment
may need some vaccinations prior to the lab
need to use good aseptic technique

front 11

Biosafety Level 4 (BSL-4)

back 11

No vaccines or treatment for microbial infections
must use barrier protection
survival rate is very small if contaminated

front 12

Salmonella typhi

back 12

causes typhoid fever and salmonellosis
can be associated with contaminated water or milk cultures

front 13

Symptoms of typhoid fever

back 13

high fever and enters a coma

front 14

Symptoms of Salmonellosis

back 14

aka food poisoning
nausea, vomiting, diarrhea, and fever

front 15

Caused the decline in Salmonella typhi deaths in the US

back 15

water chlorination
milk pasteurization
detection of diseased persons
preventative vaccination
antibiotic therapy
Sewage treatment plants improvements

front 16

Joseph Lister

back 16

hand washing prior to surgery (decline in infection rates)
heat sterilization of surgical instruments
application of phenol (carbolic acid) to wounds
antiseptic and disinfectants during surgery
improved survival rate

front 17

Autoclave

back 17

device that gets to at least 121 degrees Celsius to clean instruments within the device

front 18

Best conditions for heat sterilization

back 18

steamed heat under pressure

front 19

5% phenol is used today as...

back 19

the comparative standard for new disinfectants

front 20

Aseptic

back 20

"against infection"
used to minimize bacterial growth of any sort

front 21

Degerming

back 21

removing germs by scrubbing with aseptic soap to reduce transient and residential flora

front 22

Sanitize/Sanitation

back 22

cleaning up using a cleaner to reduce the population of microbes.
ex. soap and solvents

front 23

Pasteurization

back 23

71.2 degrees Celsius for 15 seconds

front 24

Sterilization

back 24

killing of or elimination all (hazardous) microbes in or on a device

front 25

Bacterio-

back 25

referring to bacteria

front 26

Fungi-

back 26

referring to fungi

front 27

Viri-

back 27

referring to viruses

front 28

-cidal

back 28

killing (chemicals are normally used)

front 29

-static

back 29

slowing down growth enough to allow immune system to fight off or remove

front 30

Factors that affect the efficacy of antimicrobial methods

back 30

relative susceptibility of microorganisms

front 31

3 classifications of germicides.

back 31

high, intermediate, & low

front 32

Germicides are classified based on?

back 32

their effectiveness

front 33

Germicide

back 33

a chemical used to kill germs

front 34

Prions

back 34

most resistant microbes
almost impossible to destroy but not easily found or transmitted

front 35

Most gram-negative bacteria

back 35

found in the middle of the spectrum between most resistant and least resistant

front 36

Bacteria and viruses

back 36

some of the easiest microbes to destroy

front 37

High Temp with an antimicrobial chemical

back 37

only a few minutes needed to kill majority of microbes

front 38

Low temp with an antimicrobial chemical

back 38

longer than the high temp, but may be necessary for certain substances that cant withstand the extreme temps

front 39

Effects of high temps

back 39

denaturation of proteins, nucleic acids, lipids, and carbs
interference with cytoplasmic membrane and cell wall

front 40

Thermal Death Point (TDP)

back 40

lowest temperature that kills all cells in broth in 10 minutes
(highly standardized)

front 41

Thermal Death Time (TDT)

back 41

time to sterilize volume of liquid at a set temperature
(tries to find ideal time and temp)

front 42

Decimal Reduction Time

back 42

reduce the number of microbes present to a small value
D-value time to require at a given temperature to kill 90% of the organisms being studied (reducing to a small number)

front 43

Moist Heat

back 43

denatures
destroys cytoplasmic membranes

front 44

More effective: dry heat or moist heat?

back 44

moist heat

front 45

Why is moist heat more effective than dry heat?

back 45

because the water in the moist heat is good at absorbing choleric heat energy that can then be transferred

front 46

Methods of microbial control using moist heat

back 46

boiling
autoclaving
pasteuization
ultra-high temp. sterilization

front 47

Boiling

back 47

100 degrees Celsius

front 48

Autoclaving

back 48

121 degrees Celsius, 15 lb/in. squared.
this is the standard it is not the only autoclaving procedure

front 49

Flash Pasteurization

back 49

72 (71.2) degrees Celsius for 15 seconds

front 50

Methods of microbial control using dry heat

back 50

oven
incinerator

front 51

Using an oven

back 51

170 degrees Celsius for 2 hours

front 52

Historical (batch) Pasteurization

back 52

56 degrees Celsius for 30 minutes

front 53

Effects of refrigeration and freezing

back 53

causes a decrease in microbial metabolism, growth, and reproduction (similar to hibernation)
may lead to desiccation and lyophilization

front 54

Desiccation

back 54

drying and removing water

front 55

Lyophilization

back 55

freeze drying
they freeze the microbes and remove the water through a vacuum

front 56

Use of filtration equipment

back 56

take a solution and use a membrane filter to siphon out microbes including viruses
helps to determine if microbes are present
the only thing allowed through is sterile liquid

front 57

Use of Biological Safety Hood/Cabinet

back 57

keeps the field and environment clean and helps prevent the transmission of bacteria to the person using the hood

front 58

Safety Glass in Safety Hood

back 58

limit entrance and exit of bacteria

front 59

Air flow in the safety hood

back 59

is constant and should not be obstructed

front 60

Class I Safety Hood can hold

back 60

BSL 1, 2, & 3

front 61

Class II Safety Hood can hold

back 61

BSL 1, 2, & 3

front 62

Class III Safety Hood can hold

back 62

BSL 4

front 63

Microbial Growth can be controlled by

back 63

osmotic pressure
radiation

front 64

Osmotic Pressure

back 64

how much water and chemical is inside and outside of the cell

front 65

Tonicity

back 65

changing the osmotic pressure in or out of the cell

front 66

Hypertonic

back 66

lots of chemical within
(salt, sugars, etc)

front 67

High osmotic pressure on the outside of a cell and low osmotic pressure on the inside of the cell =

back 67

water leaving the cell
desiccation

front 68

Low osmotic pressure pressure outside the cell and high osmotic pressure on the inside of the cell =

back 68

water enters the cell
lysis

front 69

Ionizing ray examples

back 69

x-rays
gamma rays

front 70

Ionizing rays are

back 70

the most powerful source of sterilizing

front 71

Nonionizing ray examples

back 71

UV rays

front 72

Process of nonionizing rays

back 72

it is still powerful, but item must be exposed for a longer period of time to be sterilized

front 73

A longer wavelength =

back 73

less powerful

front 74

A shorter wavelength =

back 74

more powerful

front 75

Purpose of UV rays

back 75

surface sterilization

front 76

Purpose of x-rays and gamma rays

back 76

penetrating surfaces

front 77

Chemicals used to control microbial growth:

back 77

phenol & phenolics
halogens
alcohol
heavy metals

front 78

Use of Phenol

back 78

AKA carbolic acid
was first antiseptic used in surgery
now used as the golden standard for antiseptics to be compared to

front 79

Examples of Halogens

back 79

Idophores (iodine and betodine)
Bleach (chlorine)
Bromine gas

front 80

Use of Iodophores

back 80

can be an antiseptic

front 81

Why is bleach not an antiseptic?

back 81

because it begins to break down every 24 hours, and must be reapplied

front 82

Use of bromine gas

back 82

an antiseptic but very corrosive

front 83

Examples of heavy metals

back 83

silver, mercury, and copper

front 84

Use of heavy metals

back 84

natural antiseptic

front 85

Phenol Coefficient (PC)

back 85

quantified killing power of a standard quality control organism
the higher the number the more effective it is

front 86

Examples of surface active agents

back 86

soaps (alkaline),
detergents (dissolve cell membranes)
quats (can rub the microbes away)

front 87

What is Triclosan?

back 87

soap

front 88

Hexaclorophene can not be used on...

back 88

babies

front 89

Example of aldehydes and acids

back 89

formaldehyde

front 90

What do aldehydes and acids do?

back 90

change the pH

front 91

Example of gaseous sterilants

back 91

chlorine

front 92

How is chlorine used to sterilize water?

back 92

in its gaseous state

front 93

Examples of oxidizing agents

back 93

peroxides and ozone

front 94

What do enzymes do to microbes?

back 94

they can attack and break down parts of the organism

front 95

Quaternary Ammonium Compounds (quats)

back 95

popular use as a disinfectant in health professions & is fairly strong but some opportunistic microbes can use this as a food source and continue to grow.

front 96

Opportunistic Microbe

back 96

a microbe that takes the opportunity to cause an infection (at the wrong place at the wrong time) & has adapted to use the human skin tissue as a food source

front 97

Example of an opportunistic microbe

back 97

Pseudomonas (microbe found in soil and water)
can be transferred by contact.

front 98

Pseudomonas can be found...

back 98

in some wounds (especially extensively burned patients)
in soil and water
in buckets of disinfectants

front 99

Virulence factor

back 99

chemicals produced by frank pathogens that cause pathological changes

front 100

Saphylococcus aureus

back 100

the #1 cause of a wound infection
will produce a pale white pus
is a frank pathogen

front 101

Frank pathogen

back 101

an obligate
if there is enough present at the right time it will cause infection

front 102

Pseudomonas species

back 102

produces a blue-green pus

front 103

Chemical effectiveness can be tested by...

back 103

(tube) dilution test & filter paper-disk diffusion

front 104

(Tube) dilution test

back 104

also used for antibiotic testing
looking for Minimum Inhibitory Concentration (MIC)
dilutions of select disinfectants are inoculated with a controlled amount of microbes, incubated, and looked at for the minimum amount of disinfectant needed to have no visible growth

front 105

Filter paper-disk diffusion

back 105

a highly standardized procedure (pH of agar, correct depth, etc..) disks are placed in the disinfectant concentrate & placed on the agar plate. for results you look at the area of the growth of the zone of inhibition (measured in mm) tests for effectiveness and susceptibility of a bacteria to a disinfectant

front 106

Criteria for Disinfectant Selection

back 106

fast acting
only effective against microorganisms (safe enough to use on skin and work surfaces)
deep penetrating without damage to surface
stable, easy to prepare
inexpensive & easy to use
smell pleasant

front 107

Kelsey-sykes capacity test

back 107

european methodology
uses a dilution procedure in timed intervals that is spread on to separate agar plates and incubated to see possible growth of microbes after incubation

bacterium + chemical => sub culture => determine viability by turbidity

front 108

In-use test

back 108

environmental check before and after use of disinfectants and cleaning
reality check
sample everything (where microbes hide) & then clean & then swab same areas again. Compare results
ideally everything should be gone

front 109

Antimicrobials are deterred through

back 109

chemotherapy

front 110

Paul Ehrlich

back 110

the chemist the proposed the "Magic Bullet"
1910 Salvarsan
Coined the term chemotherapy

front 111

Magic Bullet

back 111

the idea that somewhere on Earth there is a chemical magic bullet that can reverse any infection

front 112

1910 Salvarsan

back 112

a chemical used to treat infections caused by Treponema palladium
although helpful, it is made with arsenic so it is toxic
FIRST SYNTHETIC ANTIMICROBIAL

front 113

Treponema pallidum

back 113

causes syphilis

front 114

Alexander Fleming

back 114

found lysozyme and penicillin (1928) useful against bacteria

front 115

Lysozyme

back 115

an enzyme that breaks down peptidoglycan (the building blocks of bacterial cell walls)

front 116

Penicillin (1928)

back 116

mold growing on bacteria
wasn't very stable in its natural state

front 117

Ernest Chain

back 117

the biochemist that figured out how to create penicillin in a stable state to be used for treatment

front 118

Howard Florey

back 118

the physician who was the first to use penicillin as a form of treatment

front 119

Gerhard Domagk

back 119

1932- synthesized Prontosil and sulfa drugs that could be sprinkled on battlefield wounds to prevent infections

front 120

Selman A. Waksman

back 120

1940-1948
a soil microbiologist who used extracts from the soil and fungi to produce actinomycin, streptomycin, & neomycin.

front 121

Streptomycin

back 121

first antimicrobial to treat tuberculosis

front 122

Neomycin

back 122

used in skin ointment

front 123

Beta Lactam Ring

back 123

the working part of penicillin that interferes with peptidoglycan formation in bacteria

front 124

Antibiotic

back 124

antibacterial made by fungi to kill or inhibit bacteria

front 125

Penicillium notatum

back 125

first historic species to produce penicillin

front 126

Penicillium chrysogenum

back 126

used in modern manufacturing of penicillin
(produced penicillin in a greater quantity than P. notatum)

front 127

Semisynthetics

back 127

chemically altered antibiotics that are more effective than naturally occurring ones

front 128

Synthetics

back 128

antimicrobials that are completely synthesized in a lab

front 129

Examples of Synthetics

back 129

Salvarsan & sulpha drugs

front 130

Needed for an Ideal antimicrobial agent

back 130

readily available
inexpensive
chemically stable
easily administered
nontoxic & nonallergenic
selectively toxic against a wide range of pathogens

front 131

Antimicrobials, antibacterials, antifungals, & antiprotozoans all must have :

back 131

selective toxicity
a spectrum of activity
mode of action
minimal side effects
minimal drug resistance from microorganisms

front 132

Selective toxicity

back 132

targeting the bug not the patient
drug kills the microorganism not the host

front 133

Therapeutic dosage level must be

back 133

very distant from toxic dosage level

front 134

Broad spectrum

back 134

both gram positive and gram negative bacteria are targeted

front 135

Narrow spectrum

back 135

a select few species ( or all species in one genus) are targeted

front 136

Modes of action

back 136

inhibition of cell wall synthesis (BEST ONE!)
disruption of membrane function
inhibition of protein synthesis
inhibition of nucleic acid synthesis

front 137

Penicillin V

back 137

penicillin derivative that is acid resistant

front 138

Methicillin

back 138

penicillin derivative that is penicillinase resistant

front 139

Dicloxacillin

back 139

penicillin derivative that is acid & penicillinase resistant

front 140

Examples of Inhibition of metabolic pathways

back 140

quinolones interfere with malaria parasites (deadliest parasite)
heavy metals inactivate enzymes (ex. silver, mercury, lead) problem: very toxic
antiparasitics disrupt tubulin polymerization & glucose uptake in parasitic protozoa & worms (destroys motility structure and starves parasite)

front 141

Antimetabolites

back 141

competitive inhibitors (sulfa drugs & trimethoprim)
look like enzymes such as Para-aminobenzic acid
bacteriostatic

front 142

Bacteriostatic

back 142

slow organism growth so the microorganism can be flushed out by the body or scrubbed away.

front 143

Antiviral

back 143

slow down the viruses so the immune system can take over.
medicines target viruses metabolisms, but the best way is to prevent viral entry into a cell.

front 144

Problem with treating viruses

back 144

viruses grow inside our cells so it is hard to target them with an antiviral

front 145

Alieve

back 145

could interfere with influenza

front 146

Antifungal

back 146

not a huge arsenal because of the similarities to our cell structures.
difficult to get past additional barrier that fungi have (fungal cell wall)
medicines target cell wall synthesis, plasma membrane synthesis, and nucleic acid formation

front 147

Routes of Administration

back 147

topical
oral
intramuscular
intravenous

front 148

Benefits and down falls to oral administration

back 148

takes a few days to reach therapeutic level, but can be easily administered at home

front 149

benefits and down falls to intramuscular administration

back 149

hits microbes with a high therapeutic level quickly, but must be given in a health care facility

front 150

benefits and down falls to intravenous administration

back 150

very high therapeutic level that is maintained consistently, but it must be given and monitored in a health care facility

front 151

Side effects of antimicrobial drugs

back 151

Drugs may be toxic to kidneys, liver, or nerves
It may or may not be safe during pregnancy
possible allergic reactions including anaphylactic shock

front 152

Anaphylactic shock

back 152

severe allergic reaction that is life threatening because the air ways begin to close

front 153

If disruption of normal microbiota (normal flora) occurs during the use of antimicrobial agents...

back 153

secondary infections and superinfections can occur

front 154

Disruption of normal microbiota (normal flora) means

back 154

an antimicrobial agent is so powerful that is has killed the microbe and has also significantly decreased the normal flora allowing space for new microbes to invade without protection

front 155

Amphotericin B

back 155

attaches to ergosterol in fungal membranes

puts a pore in the cytoplasmic membrane so the cells loses all of its content

front 156

Downfall to Amphotericin B

back 156

humans could be susceptible because cholesterol is so similar to ergosterol the bacteria may attack the human cells

bacteria lack sterols so they are not susceptible to this drug

front 157

Aminoglycosides - Gentamicin

back 157

block the inhibition of translation & cause the misreading of mRNA

front 158

Tetracyclines

back 158

block the attachment of tRNA to the ribosome

front 159

Macrolides

back 159

prevent continuation of protein synthesis

front 160

Chloramphenicol

back 160

prevents peptide bonds from being formed

front 161

Candida albicans

back 161

causes candidiasis, thrush, & vaginitis

front 162

Clostridium difficile

back 162

causes pseudomembranous colitis (inflammation of the colin at the surface of the membrane. causes constant diarrhea)

front 163

Lateral gene transfer

back 163

acquisition of R-plasmids by transformation, transduction, or conjugation

front 164

Antimicrobials have much less effect due to...

back 164

new mutations of the chromosomal genes

front 165

B-lactam drugs - penicillin & cephalosporin

back 165

interfere with the formation of peptide side chains between adjacent strands of peptidoglycan by inhibiting penicilling-binding proteins (peptide chains are broken)
alters the cell wall stability

front 166

Bacitracin

back 166

interferes with the transport of peptidoglycan precursors across the cytoplasmic membrane (the building blocks)
alters plasma membrane and cell wall

front 167

Inhibit cell wall synthesis

back 167

penicillins, cephalosporins, vancomycin, bacitracin, isoniazid, & ethambutol

front 168

Inhibit protein synthesis

back 168

aminoglycosides, tetracyclines, chloramphenicol, & macrolides

front 169

Cross Resistance & multiple resistance

back 169

pathogens can acquire resistance to more than one drug by transferring the resistance to different genre of organisms

front 170

R-plasmids being exchanged

back 170

the genes in the extra chromosomal fragments are transferred

front 171

Constant use of drugs has..

back 171

eliminated sensitive cells causing superbugs, cross resistance, and resistance to antimicrobial drugs

front 172

Cross resistance

back 172

resistant to more than one drug or resistant to all the drugs in the same family

front 173

Resistant S. aureus

back 173

first well-known resistant bacteria

front 174

Preventing resistance

back 174

maintain a high concentration of drug in patient for sufficient time
(kills all sensitive cells and inhibits others so the immune system can destroy)
Use antimicrobial agents in combination (two is better than one)

front 175

Synergism

back 175

combining drugs to assemble a greater affect than just hitting with one drug

front 176

Antagonism

back 176

drugs that work against one another (want to avoid)

front 177

Retarding the Resistance

back 177

use antimicrobials when necessary
develop new variations of existing drugs
search for new drugs
use bacteriocins

front 178

Bacteriocins

back 178

bacteria made substance used to kill other bacteria

front 179

Antibiotic Susceptibility/Sensitivity Testing (AST) includes

back 179

Minimum inhibitory concentration (MIC)
Minimum bactericidal concentration (MBC)
ETest

front 180

Kirby-Bauer Test

back 180

filter paper disc is placed on a bacterial lawn.
interpretative chart must be used to look at the zone of inhibition
Problem: technically difficult & only interprets outcome of what serum drug level is needed (doesn't tell for any other specific body fluids)

front 181

Minimum inhibitory concentration (MIC)

back 181

tubes lined up from most concentrated to least concentrated & exact number of bacterial cells is added to each tube
looking for the minimum concentration to have no turbidity seen in the tube (good for all body fluids)

front 182

Minimum bactericidal concentration (MBC)

back 182

one step farther than MIC
looking for bacteria in the clear tube
Subculture with no growth confirms the MIC
No growth must occur on the agar plate

front 183

ETest

back 183

a piece of membrane filter with varying concentrations of the drug are present
MIC value would be where the growth stops on the agar plate
helps to determine drug & dosage needed

front 184

Serum cidal level

back 184

reserved for patients who are not responding to an antibacterial
they take samples of the patients serum and infuse the agar plate with the pathogen to see what is going on

front 185

Vitek

back 185

company that manufactures things for micro lab that need to be very small; so small a light can be shown through them to record info

front 186

Domain Eukarya

back 186

common unicellular & multicellular
macroscopic & range in functionality including pathogenic
divided into classes by motility

front 187

Motility by pseudopodia

back 187

Ameboid cells such as Entamoeba histolytica and Naegleria fowleri
move by "false feet" that stretch out their plasma membrane and stick it on to a surface and pull itself that way

front 188

Entamoeba histolytica

back 188

can affect the digestion tract (mainly intestines) & cause diarrhea, colitis, & dysentary in amoebic form
thru oral-fecal transmission
can easily migrate to the liver or peritoneal cavity (triggers inflammation response)

front 189

Amoeba form is...

back 189

a trophozoite

front 190

Trophozoite

back 190

soft shell made of just the cytoplasmic membrane & you can see pseudopodia
susceptible to drugs in this form

front 191

Cyst

back 191

encapsulated form that has a very sturdy structure, is very spherical, and is the most difficult to treat

front 192

Naegleria fowleri

back 192

thermophile that is the primary cause of amoebic meningitis
found in warm, untreated stagnant water
migrates to the CNS via the oral cavity
100% mortality rate

front 193

Trichomonas vaginalis

back 193

primary cause of protozoan vaginitis
can also cause prolonged postpartum fever, endometritis, premature rupture of membranes, & cytological changes in the cervical cell morphology

front 194

Signs of Trichomonas vaginalis

back 194

no cyst forms
no mitochondria
most curable STD
lemon shaped with 2 pairs of flagella

front 195

How to ID Trichomonas vaginalitis

back 195

using a "hanging drop" wet mount - a drop of liquid with the organism is placed on a cover slip & suspended to be viewed (can also use a wet mount and get the same results)

front 196

Anaerobic flagellates

back 196

cells that move by flagella

front 197

Giardia lamblia

back 197

moves by flagella
tear drop shape with 2 nuclei
no mitochondria
AKA backpacker's diarrhea, or bever fever

front 198

Giardia duodenalis

back 198

trophozoite and cyst forms
trophs are tear drop in shape
they look like they are starring back

front 199

Cure for parasites

back 199

gin & tonic
cocktail introduced by the army of the British East Indian Company in India

front 200

Why does gin & tonic work?

back 200

the tonic water contains the chemical quinine, which helps prevent malaria

front 201

Eukaryotes that have no motility structures

back 201

Plasmodium vivax
P. falciparum
P. malaria
P. ovale
P. knowlesi

front 202

Plasmodium vivax

back 202

most common cause of malaria

front 203

Plasmodium falciparum

back 203

most lethal carrier of malaria
urine is black or brown
AKA "black water fever" or "malignant tertian malaria"

front 204

P. malaria
P. ovale
P. knowlesi

back 204

rare malaria in occurrence

front 205

Plasmodium knowlesi

back 205

newest malaria in humans (used to only be found in animals)

front 206

endemic diseases

back 206

more common in a specific geographic location & has ideal conditions for a particular disease

front 207

Malignant tertian malaria

back 207

symptoms occur every 2-3 days along with fever and chills

front 208

Plasmodium

back 208

causes malaria
egyptians described symptoms in 3000 BC
is an intracellular parasite
a biological vector (insect facilitates transfer of disease)

front 209

Biological vector of malaria

back 209

anopheles mosquito (female)
they are the most likely to carry malaria

front 210

Malaria

back 210

has a ring feature (not much cytoplasm)
will eat the innards of the red blood cell
its life cycle goes from the red blood cells to the liver.

front 211

Toxoplasma gondii

back 211

definitive host: intestines of cats
Intermediate hosts: mammals and birds (accidentally transmitted & does not stay in intestines, it migrates)
extraintestinal (humans- brain, heart, skeletal muscle)
oral-fecal or organ transplant & transplacental transmission
forms cysts that can be ingested and cause infection

front 212

Toxoplasma gondii causes

back 212

leading cause of spontaneous abortion due to protozoan parasite (pregnant women should avoid cleaning cat litter boxes)
could be infected for the rest of your life

front 213

Infective stage of Toxoplasma gondii

back 213

fecal oocyst in fecal & muscle of animals we eat, food, & water

front 214

Diagnostic stage of Toxoplasma gondii

back 214

transplanted tissue, in our muscles and organs, & abortion

front 215

Things that cause fetal neurological damage

back 215

"T"- Toxoplasma (protozoan)
"O"- others
"R"- Rubella
"C"- Cytomegalovirus
"H"- Herpesvirus

front 216

Viruses that cause fetal neurological damage

back 216

rubella
cytomegalovirus
herpesvirus

front 217

Complex of teratogens

back 217

chemicals that target developing fetal tissue & damage it

front 218

How to avoid Toxoplasma gondii

back 218

handwashing & throughly cooking meat

front 219

Trypanosoma cruzi

back 219

protozoan pathogen
causes chagas disease (aka american trypanosomiasis)
endemic throughout much of mexico, central america, and south america

front 220

endemic disease

back 220

a disease that is located in a specific geographical region

front 221

Trypanosoma cruzi

back 221

caused by triatomine bug (aka kissing bug)
causes an acute and a chronic disease
20-30% of infected people will develop debilitating or life-threatening conditions in the heart, liver, and spleen
display Romana's sign

front 222

Romana's sign

back 222

inflammatory response and swelling from the kissing bug

front 223

Aschelminth

back 223

rounded bodied worms that are long, thin, and tube shaped

front 224

platyhelminthes

back 224

flat, segmented bodied worms
ex. tape worm

front 225

Avoid Nematoda by

back 225

WASHING YOUR HANDS!

front 226

Ascaris lumbricoides

back 226

roundworm
largest, most common parasite found in humans (1,000,000,000 people infected)
causes ascaris pneumonia
can burrow through tissue (dragging along bacteria from intestines)
dioecious
MIGERATES

front 227

Infective stage of Ascaris lumbricoides

back 227

eggs, larvae, fertilized eggs

front 228

Diagnostic stage of Ascaris lumbricoides

back 228

finding the worm, deposit fertilized & unfertilized eggs, & larva]

front 229

Ascaris lumbricoides females are...

back 229

larger than the males
a result of the female carrying all of the eggs

front 230

dioecious

back 230

two separate sexes

front 231

Ascaris pneumonia

back 231

larvae migration causing hemorrhage and edema in lungs

front 232

Intestinal blockage

back 232

caused by ascaris lumbricoides blocking the intestinal tract (large mass of communities of worms)
notorious for migration

front 233

Sensitive to anesthetics

back 233

ascaris lumbricoides
patients in surgical recovery rooms have had worms migrate from the small intestine through the stomach and out of a patients nose, mouth, or even tracheotomy tubes

front 234

Enterobius vermicularis

back 234

pinworm
infects about 400,000,000 people world wide
"D" shaped infective eggs

front 235

Infective & Diagnostic stage for Enterobius vermicularis

back 235

eggs of perianal folds, larvae inside & eggs

front 236

Lifecycle of Enterobius vermicularis

back 236

entire life cycle is in the human host
female lays eggs at night around the perianal region causing an inflammatory response and the urge to itch

front 237

To collect a sample of Enterobius vermicularis

back 237

use Graham sticky tape method (aka "scotch tape" method)
repeat 3-5 times
the fertilized eggs are sticky and easily transferred

front 238

Avoiding Necator americanus

back 238

dont go barefoot in the woods!

front 239

Necator americanus

back 239

aka north american hook worm or creeping nematodes
has infective larvae
burrows through host skin, passes from blood stream, to lung to digestive tract where they live in the intestine of the host
adapted to go back and forth from lungs to digestive tract
latch onto intestines

front 240

Avoiding Trichinella spiralis

back 240

cook meat hot!

front 241

Trichinella spiralis

back 241

causes trichinosis
infective encysted larvae in the meat from a pig
need a biopsy to confirm trichinosis

front 242

life cycle of trichinella spiralis

back 242

reproduce in the small intestine
eggs hatch (stomach uncovers cyst form)
larvae migrate especially to skeletal muscle

front 243

eosinophils

back 243

white blood cells that respond to allergies & parasites
normal level- 0%-5%
25%-70% increase in level due to a parasite

front 244

Examples of platyhelminthes

back 244

tapeworms
cestoda
parasitic

front 245

Parts of a playhelminth

back 245

scolex
proglottids
hermaphroditic

front 246

Tapeworms

back 246

longest worm - up to 30 feet

front 247

scolex

back 247

head of tapeworm
has a circle of hooks & suction cups to latch on

front 248

proglottids

back 248

segments in the worm (relatively loose connection that will tear easily)

front 249

hermaphroditic

back 249

both sex organs are present in each segment

front 250

Taenia saginata

back 250

beef tapeworm

front 251

Taenia solium

back 251

pork tapeworm

front 252

Ways to contract Taenia

back 252

eating undercooked meat or touching undercooked meat and not properly washing your hands

front 253

Taenia solium is...

back 253

worse than taenia saginata

front 254

Best specimen to see Taenia

back 254

to see segments in the stool

front 255

infective stage of Taenia

back 255

larvae in cow and pig muscle
oncosphere in cysticerci

front 256

diagnostic stage of Taenia

back 256

fertilized eggs and segments

front 257

Cysticerci

back 257

infective larvae in the muscle of an animal

front 258

life cycle of taenia

back 258

infective cysticercus in raw or undercooked pork or beef muscle
adults tend to stay in the intestines, but other areas of the body including the leg can also be infected with cysticerci

front 259

cysticercosis

back 259

infection with cysticerci

front 260

neurocysticercosis

back 260

larval tape worm in the brain causing headaches, migraines, passing out, and seizures
treated with drugs or removal of the worms through surgery

front 261

neglected parasitic infections

back 261

receive relatively little attention through devotion to their surveillance, prevention, and/or treatment

front 262

Neglected parasites include

back 262

Chagas disease - trypanosoma cruzi
Cysticercosis - taenia solium
Toxocariasis - toxocara canis (less commonly toxocara cati)
Toxoplasmosis - toxoplasma gondii
Trichomoniasis - trachomonas vaginalis

front 263

Chagas disease

back 263

caused by trypanosoma cruzi

front 264

Cysticercosis

back 264

caused by taenia solium
leading cause of epilepsy among hispanics in the US

front 265

Toxocariasis

back 265

caused by toxocara canis (less commonly toxocara cati)

front 266

Toxoplasmosis

back 266

caused by toxoplasma gondii

front 267

Trichomoniasis

back 267

caused by trachomonas vaginalis

front 268

CDC works to...

back 268

protect people from health threats from things such as neglected parasites

front 269

People can be protected by...

back 269

increasing awareness among physicians and the public
synthesizing the existing data to help better understand these infections
improve diagnostic testing
advising treatment, including distributing otherwise unavailable drugs for certain infections (Chagas disease)

front 270

Dog round worm

back 270

Toxocariasis cani
phylum: nematoda
zoonotic disease
located worldwide
definitive host: dogs
Intermediate host: none
accidental host: humans and other mammals
children are more susceptible than adults

front 271

Zoonoses

back 271

a disease passed from animals to humans (especially from mammals)

front 272

Toxocarasis cati

back 272

the feline form of toxocarasis

front 273

Infection of Toxocarasis cani is transferred by/ found in ...

back 273

intestines (ingested eggs)
Transplacenta
transmammary

front 274

T. cannis infects...

back 274

puppies born with infection
puppies less than 5 weeks
humans (in the heart, liver, lung, brain, muscle, or eye)

front 275

Infective stage of T. cannis

back 275

eggs and larva

front 276

Diagnostic stage of T. cannis

back 276

eggs, larva, & tracks on skin

front 277

two types of larvae migration

back 277

ocular larvae migration (OLM)
visceral larvae migration (VLM)

front 278

Ocular larvae migration (OLM)

back 278

caused by larva migration to the retina

front 279

Visceral larvae migration (VLM)

back 279

caused by the movement of worm larvae throughout various organs of the body

front 280

Controlling creeping nematodes

back 280

treat dogs, especially puppies, regularly for worms
good hygiene practices when handling animals
don't let children play in areas dogs are allowed to defecate
teach children not to eat dirt or soil