Microbe-Human Interactions (Ch 13 & 14) PDF

Summary

This document provides an overview of the interactions between microbes and humans, including colonization, infection, and disease. It covers various aspects such as factors causing disease, the human microbiome, and the benefits of normal microbiota. It also describes pathogens and virulence.

Full Transcript

‭Health and Disease‬ ‭Colonization, infection, and disease‬ ‭‬ ‭Colonization‬ ‭○‬ ‭Microbes living in or on human body‬ ‭‬ ‭Bacteria, fungi, protozoa, viruses‬ ‭○‬ ‭Resident microbiota (normal flora) → don’t cause disease‬...

‭Health and Disease‬ ‭Colonization, infection, and disease‬ ‭‬ ‭Colonization‬ ‭○‬ ‭Microbes living in or on human body‬ ‭‬ ‭Bacteria, fungi, protozoa, viruses‬ ‭○‬ ‭Resident microbiota (normal flora) → don’t cause disease‬ ‭‬ ‭Fend off other pathogens‬ ‭‬ ‭Ex: Vitamin K‬ ‭○‬ ‭Transient microbiota → come and go‬ ‭‬ ‭Infection‬ ‭○‬ ‭Pathogenic microbes penetrate host defenses, enter tissues, and multiply‬ ‭‬ ‭Disease‬ ‭○‬ ‭Deviation from normal health‬ ‭○‬ ‭Disruption of body‬ ‭Disease‬ ‭‬ ‭Factors‬‭that cause disease‬ ‭○‬ ‭Infections‬ ‭○‬ ‭Genetics and aging‬ ‭○‬ ‭Environmental agents / chemicals‬ ‭○‬ ‭Malfunctions of systems or organs‬ ‭‬ ‭Infectious disease‬ ‭○‬ ‭Disruption of tissues or organs caused by microbes or their products‬ ‭‬ ‭Pathogen‬ ‭○‬ ‭Microbe capable of causing disease‬ ‭‬ ‭Pathology‬ ‭○‬ ‭Study of disease‬ ‭‬ ‭Etiology‬ ‭○‬ ‭Cause of disease‬ ‭‬ ‭Pathogenesis‬ ‭○‬ ‭Development of disease‬ ‭Normal microbiota‬ ‭‬ ‭ ome microbes may cross placenta‬ S ‭‬ ‭Microbes are picked up when baby passes through birth canal‬ ‭‬ ‭Gut is colonized by ingestion of microorganisms‬ ‭‬ ‭Skin, eyes, respiratory system, mouth, intestines, urogenital system (urethra, vagina)‬ ‭○‬ ‭Microbes are in tissues previously thought to be sterile‬ ‭‬ ‭Lungs, bladder, breast milk, placenta‬ ‭Human microbiome project‬ ‭‬ S ‭ equencing biota of humans‬ ‭‬ ‭Human cells contain 21,000 protein encoding genes‬ ‭○‬ ‭Microbes that inhabit humans contain 8 million‬ ‭‬ ‭All healthy people harbor potentially dangerous pathogens, but in low numbers‬ ‭‬ ‭Can study changes in microbiome due to disease‬ ‭Benefits of normal microbiota‬ ‭ ‬ I‭ nfluence development of organs‬ ‭‬ ‭Aid digestion‬ ‭‬ ‭Make products for use by humans‬ ‭○‬ ‭Ex: Vitamin K → gut bacteria‬ ‭‬ ‭Prevent overgrowth of harmful microorganisms‬ ‭○‬ ‭Microbial antagonism‬ ‭‬ ‭Microbes in a steady, established relationship are unlikely to be displaced‬ ‭by incoming microbes‬ ‭‬ ‭Outcompete pathogens that try to come in and take over‬ ‭Pathogens‬ ‭‬ ‭True pathogens‬ ‭○‬ ‭Capable of causing disease in healthy persons w/ normal immune systems‬ ‭‬ ‭Opportunistic pathogens‬ ‭○‬ ‭Cause disease when‬ ‭‬ ‭Host’s defenses are compromised‬ ‭‬ ‭When they become established in a part of the body that is not natural to‬ ‭them‬ ‭Virulence‬ ‭‬ ‭Virulence‬ ‭○‬ ‭Degree of pathogenicity‬ ‭‬ ‭Indicated by microbe’s ability to establish itself in the host and cause‬ ‭damage‬ ‭○‬ ‭Comparing one microbe to another to determine intensity‬ ‭○‬ ‭May be enhanced by rapid passage through susceptible hosts‬ ‭○‬ ‭Can be weakened by growth in lab → attenuation‬ ‭‬ ‭Ex: vaccines‬ ‭‬ ‭Virulence factor‬ ‭○‬ ‭Any characteristic or structure of microbe that contributes to toxin production or‬ ‭induction of an injurious host response‬ ‭‬ ‭Microbes w/ smaller infectious does have greater virulence‬ ‭Infectious dose (ID) and lethal dose (LD)‬ ‭‬ I‭ D‬‭50‬ ‭→ number of microorganisms re‬‭quired to produce‬‭demonstrable in 50% of test host‬ ‭population‬ ‭‬ ‭LD‬‭50‬ ‭→ lethal dose for 50% of inoculated hosts within‬‭a given period‬ ‭○‬ ‭How many it takes to kill you‬ ‭○‬ ‭Potency of toxin‬ ‭‬ ‭Which organism is more virulent? (lower the number = causes diseases more easily)‬ ‭○‬ ‭Organism A LD‬‭50‬ ‭= 2‬ ‭○‬ ‭Organism B LD‬‭50‬ ‭= 20,000‬ ‭Causing disease‬ 1‭.‬ ‭ ntrance‬ E ‭2.‬ ‭Attachment / adhesion‬ ‭3.‬ ‭Establishment → evading host defenses‬ ‭4.‬ ‭Causing disease → pathogenesis‬ ‭5.‬ ‭Exiting‬ ‭Step 1: Entrance‬ ‭‬ ‭Usually through skin and mucous membranes‬ ‭○‬ ‭Parenteral route‬ ‭‬ ‭Microbes deposited directly beneath skin‬ ‭‬ ‭Ex: punctures, injections, bites, cuts, wounds, surgery‬ ‭○‬ ‭Ingestion‬ ‭‬ ‭Adapted to survive digestive enzymes and abrupt pH changes‬ ‭○‬ ‭Inhalation (airborne)‬ ‭‬ ‭Extent to which an agent is carried into respiratory tree is based on its size‬ ‭‬ ‭Small cells and particles are inhaled more deeply than larger ones‬ ‭○‬ ‭Sexually transmitted‬ ‭‬ ‭Urogenital tract‬ ‭Portals of entry‬ ‭‬ S ‭ kin, ears, eyes, nose, mouth, mammary glands, urethra, vagina, anus‬ ‭‬ ‭Few microbes can penetrate unbroken skin‬ ‭Entry ≠ disease‬ ‭‬ O ‭ ne microbe gained entrance to body → do not necessarily cause disease‬ ‭‬ ‭Host defenses, normal flora, and the ID may not allow organism to become established or‬ ‭cause disease‬ ‭○‬ ‭Ex: In order to cause infection in normal large intestine,‬‭Salmonella‬‭needs 1,000‬ ‭bacterial cells present ID‬‭50‬ ‭= 1,000; for‬‭Shigella‬‭,‬‭ID‬‭50‬ ‭= 10‬ ‭Step 2: Attaching to host (becoming established)‬ ‭‬ ‭Adhesion → microbes attach to host tissues‬ ‭○‬ ‭Specificity → binding b/t specific molecules on both host and pathogen‬ ‭‬ ‭Particular pathogen is limited to limited types of cells and organisms‬ ‭‬ ‭Can only reside to certain parts in body‬ ‭○‬ ‭Once attached → pathogen can invade body compartments‬ ‭‬ ‭Quorum sensing‬ ‭‬ C ○ ‭ hemical communication b/t nearby bacteria‬ ‭○‬ ‭Critical to establishment of infection‬ ‭Microbes attach to host cells‬ ‭‬ ‭Bacteria, fungi and protozoa most often use surface molecules‬ ‭○‬ ‭Adhesions or ligands‬ ‭‬ ‭Specific proteins, glycoproteins or lipoproteins‬ ‭‬ ‭Located on pili, fimbriae, flagella or glycocalyx (capsule)‬ ‭‬ ‭Viruses use spikes‬ ‭Step 3: Surviving host defenses (becoming established)‬ ‭‬ ‭Phagocytes‬ ‭○‬ ‭White blood cells that engulf and destroy pathogens using enzymes and‬ ‭antimicrobial chemicals‬ ‭‬ ‭Antiphagocytic factors‬ ‭○‬ ‭Virulence factors used by pathogens to avoid phagocytes‬ ‭○‬ ‭Capsules → resist phagocytosis‬ ‭‬ ‭Not being able to grab onto‬ ‭○‬ ‭Leukocidins → chemicals that kill WBCs‬ ‭○‬ ‭Some can survive inside phagocytes‬ ‭‬ ‭Use WBC as incubator‬ ‭Step 4: Causing disease‬ ‭‬ M ‭ icrobes secrete enzymes and toxins‬ ‭‬ ‭Host defenses damage healthy tissue‬ ‭‬ ‭Microbes induce epigenic changes in host cells‬ ‭○‬ ‭Turn genes on / off‬ ‭Direct damage via enzymes‬ ‭‬ ‭Exoenzymes‬ ‭○‬ ‭Secreted by pathogenic bacteria, fungi, protozoa, and worms‬ ‭○‬ ‭Break down and inflict damage on tissues‬ ‭○‬ ‭Dissolve host’s defense barriers and promote the spread of microbes into deeper‬ ‭tissues‬ ‭○‬ ‭Ex:‬ ‭‬ ‭Mucinase → breaks down mucus to maneuver around wherever‬ ‭‬ ‭Keratinase → breaks down keratin of skin and go deeper in body‬ ‭‬ ‭Refer to microbial metabolism lecture‬ ‭Toxins: Potent sources of cellular damage‬ ‭‬ ‭Toxin‬ ‭○‬ S ‭ pecific chemical product of microbes, plants, and some animals that is poisonous‬ ‭to other organisms‬ ‭‬ ‭Exotoxin → secreted by living bacteria‬ ‭○‬ ‭Many types‬ ‭‬ ‭Ex: hemolysins (protein) → break down red blood cells‬ ‭‬ ‭Endotoxin → not actively secreted‬ ‭‬ S ○ ‭ hed from outer membrane when organism dies‬ ‭○‬ ‭Only found in gram-negative bacteria‬ ‭‬ ‭Ex: lipopolysaccharide (LPS) → stays in membrane until dying‬ ‭Exotoxins‬ ‭‬ W ‭ ater soluble substances secreted into host tissues‬ ‭‬ ‭Soluble in body fluids‬ ‭○‬ ‭Quickly spread via bloodstream‬ ‭○‬ ‭Can be carried through circulatory system‬ ‭‬ ‭Destroy specific parts of host cells‬ ‭○‬ ‭Ex: membrane, proteins, interfere w/ protein synthesis‬ ‭‬ ‭Among most lethal substances‬ ‭‬ ‭Body produces antitoxins (antibodies) against toxins‬ ‭Origins and effects of circulating exotoxins and endotoxins‬ ‭Naming exotoxins‬ ‭‬ ‭Type of host cell attacked‬ ‭○‬ ‭Neurotoxins → act on nervous tissue‬ ‭○‬ ‭Hepatotoxins → liver cells‬ ‭○‬ ‭Enterotoxins → act on enteric tissue (gut)‬ ‭‬ ‭Type of disease caused‬ ‭○‬ ‭Diphtheria toxin, tetanus toxin‬ ‭‬ ‭Type of bacteria‬ ‭○‬ ‭Botulinum toxin →‬‭Clostridium botulinum‬ ‭○‬ ‭Vibrio enterotoxin →‬‭Vibrio cholerae‬ ‭Endotoxin production‬ ‭‬ ‭Part of bacterial cell wall‬ ‭○‬ ‭Ex: LPS → gram-negative cell walls‬ ‭‬ ‭Released into tissues when organisms die‬ ‭‬ ‭Weak toxins compared to exotoxins‬ ‭‬ ‭Cause phagocytic WBCs to produce cytokines‬ ‭‬ ‭Can activate blood clotting‬ ‭‬ ‭Can lead to necrosis (death) of tissues‬ ‭‬ ‭Pyrogenic (fever causing)‬ ‭‬ ‭Do not have specific method of action‬ ‭‬ ‭Produce same effect no matter what the organism‬ ‭Exotoxins vs endotoxins‬ ‭‬ E ‭ xotoxins → mostly gram-positive‬ ‭‬ ‭Endotoxins → only gram-negative‬ ‭Pathogenesis‬ ‭Step 5: Vacating the host - Portals of exit‬ ‭‬ ‭Portal of exit‬ ‭○‬ ‭Avenue for pathogens to exit host‬ ‭○‬ ‭Secretion‬ ‭○‬ ‭Excretion‬ ‭○‬ ‭Discharge‬ ‭○‬ ‭Sloughed tissue (shedding)‬ ‭Respiratory and salivary portals‬ ‭‬ ‭Escape media for pathogens that infect upper and lower respiratory tract‬ ‭○‬ ‭Mucus‬ ‭○‬ ‭Sputum‬ ‭○‬ ‭Nasal drainage‬ ‭○‬ ‭Other moist secretions‬ ‭Skin scales‬ ‭‬ O ‭ uter layer of skin and scalp is constantly being shed into environment‬ ‭‬ ‭Household dust is composed of skin cells‬ ‭‬ ‭Ex:‬ ‭○‬ ‭Dermatophytes (fungi) → athlete’s foot‬ ‭○‬ ‭Viruses → warts, herpes, smallpox‬ ‭○‬ ‭Bacteria → syphilis, impetigo‬ ‭Fecal exit‬ ‭‬ S ‭ ome intestinal pathogens cause irritation in the intestinal mucosa that increases motility‬ ‭of bowel‬ ‭‬ ‭Resulting diarrhea provides rapid exit for pathogen‬ ‭‬ ‭Helminth worms release eggs and cysts through feces‬ ‭‬ ‭Feces containing pathogens are public health problem when allowed to contaminate‬ ‭drinking water or when used to fertilize crops‬ ‭Urogenital tract‬ ‭‬ A ‭ gents involved in STDs leave host in vaginal discharge or semen‬ ‭‬ ‭Source of neonatal infections that infect infant as it passes through birth canal‬ ‭○‬ ‭Herpes simplex‬ ‭○‬ ‭Chlamydia‬‭(bacterial)‬ ‭○‬ ‭Candida albicans‬‭(yeast infection)‬ ‭‬ ‭Pathogens that affect kidney are discharged in urine‬ ‭Removal of blood or bleeding‬ ‭‬ B ‭ lood has portal of exit when removed or released through vascular puncture‬ ‭‬ ‭Blood-feeding insects are common transmitters of pathogens‬ ‭○‬ ‭Ticks‬ ‭○‬ ‭Fleas‬ ‭○‬ ‭Mosquitos‬ ‭Clicker Questions‬ ‭1.‬ ‭Which of the following areas is least likely to have resident microbiota?‬ ‭a.‬ ‭Digestive system‬ ‭b.‬ ‭Urinary system‬ ‭c.‬ ‭Reproductive system‬ ‭d.‬ ‭Respiratory system‬ ‭e.‬ ‭Nervous system‬ ‭2.‬ ‭Which of the following would not be an example of microbial antagonism?‬ ‭a.‬ ‭Taking up space‬ ‭b.‬ ‭Secreting antibiotics‬ ‭c.‬ ‭Conjugation‬ ‭d.‬ ‭Using up nutrients‬ ‭e.‬ ‭Secreting acids‬ ‭3.‬ ‭The majority of pathogenic microbes gain access to the human body through:‬ ‭a.‬ ‭Blood‬ ‭b.‬ ‭Skin‬ ‭c.‬ ‭Wounds‬ ‭d.‬ ‭Mucous membranes‬ ‭e.‬ ‭Placenta‬ ‭4.‬ ‭Which of the following enzymes is a clot buster?‬ ‭a.‬ ‭Coagulase‬ ‭b.‬ ‭Kinase‬ ‭c.‬ ‭IgA protease‬ ‭d.‬ ‭Hyaluronidase‬ ‭e.‬ ‭Collagenase‬ ‭5.‬ ‭Which of the following pathogen and portal of exit are mismatched?‬ ‭a.‬ ‭Influenza – respiratory route‬ ‭b.‬ ‭Athlete’s foot – skin scales‬ ‭c.‬ ‭Giardia – fecal route‬ ‭d.‬ ‭Chlamydia – blood‬ ‭e.‬ ‭COVID-19 – salivary‬ ‭Infections and Epidemiology‬ ‭Patterns of infection‬ ‭‬ ‭ ocalized‬ L ‭‬ ‭Systemic‬ ‭‬ ‭Focal‬ ‭‬ ‭Mixed‬ ‭‬ ‭Primary‬ ‭‬ ‭Secondary‬ ‭‬ ‭Acute‬ ‭‬ ‭Chronic‬ ‭Localized infection‬ ‭‬ ‭Microbe enters body and remains confined to specific tissue‬ ‭○‬ ‭Boils‬ ‭○‬ ‭Fungal skin infections‬ ‭○‬ ‭Warts‬ ‭Systemic infection‬ ‭‬ ‭When infection spreads to several sites and tissue fluids, usually in bloodstream‬ ‭○‬ ‭Viral → measles, rubella, chickenpox, AIDS‬ ‭○‬ ‭Bacterial → anthrax, typhoid fever, syphilis‬ ‭○‬ ‭Fungal → valley fever, cryptococcosis‬ ‭‬ ‭Infectious agents can also travel by means of nerves (rabies) or cerebrospinal fluid‬ ‭(meningitis)‬ ‭Focal infection‬ ‭‬ C ‭ an be local in one, but spread in another‬ ‭‬ ‭Exists when infectious agent breaks loose from local infection and is carried to other‬ ‭tissues‬ ‭‬ ‭Examples:‬ ‭○‬ ‭Tuberculosis‬ ‭○‬ ‭Streptococcal pharyngitis (strep throat → scarlet fever)‬ ‭○‬ ‭Toxemia (infection remains localized → toxins carried through blood to target‬ ‭tissue)‬ ‭Mixed infection‬ ‭‬ ‭Several agents establish themselves simultaneously at infection site‬ ‭‬ ‭Polymicrobial diseases‬ ‭○‬ ‭Wound infections, dental caries, human bite infections‬ ‭Primary and secondary infections‬ ‭‬ N ‭ ot at the same time‬ ‭‬ ‭Primary infection‬ ‭○‬ ‭Initial infection‬ ‭‬ ‭Secondary infection‬ ‭○‬ ‭Occurs when primary infection is complicated by another infection caused by‬ ‭different microbe‬ ‭Acute vs. chronic infections‬ ‭‬ ‭Acute infections‬ ‭○‬ ‭Come on rapidly‬ ‭○‬ ‭Often have short-lived effects‬ ‭○‬ ‭Ex: flu‬ ‭‬ ‭Chronic infections‬ ‭○‬ ‭Progress and persist over a long period of time‬ ‭○‬ ‭Ex: Valley fever (fungal)‬ ‭Signs and symptoms: Warning signals of disease‬ ‭‬ ‭Sign‬ ‭○‬ O ‭ bjective changes that can be observed and measured by someone other than‬ ‭patient‬ ‭○‬ ‭More precise than symptoms‬ ‭○‬ ‭Ex: tachycardia, heart murmur, fever‬ ‭‬ ‭Symptom‬ ‭○‬ ‭Subjective evidence of disease as sensed by patient‬ ‭○‬ ‭Only patient can describe‬ ‭○‬ ‭Ex: stomachache, headache‬ ‭‬ ‭Syndrome‬ ‭○‬ ‭Disease identified or defined by a certain complex of signs and symptoms‬ ‭Common signs and symptoms of infectious diseases‬ ‭‬ ‭Signs‬ ‭○‬ ‭ ever‬ F ‭○‬ ‭Septicemia (bacteria multiplying in blood)‬ ‭○‬ ‭Microbes in tissue fluids‬ ‭○‬ ‭Chest sounds‬ ‭ ‬ ‭Skin eruptions‬ ○ ‭○‬ ‭Leukocytosis (high WBC count) / leukopenia (low WBCs)‬ ‭○‬ ‭Swollen lymph nodes‬ ‭○‬ ‭Abscesses‬ ‭○‬ ‭Tachycardia (increased heart rate)‬ ‭○‬ ‭Antibodies in serum‬ ‭ ‬ ‭Symptoms‬ ‭○‬ ‭Chills‬ ‭○‬ ‭Pain, ache, soreness, irritation‬ ‭○‬ ‭Tiredness, brain fog‬ ‭‬ ‭Malaise‬ ‭‬ ‭Fatigue‬ ‭○‬ ‭Chest tightness‬ ‭○‬ ‭Itching‬ ‭○‬ ‭Headache‬ ‭○‬ ‭Nausea‬ ‭Infections that go unnoticed‬ ‭‬ ‭Asymptomatic, subclinical, or inapparent infections‬ ‭○‬ ‭Carriers‬ ‭‬ ‭Host is infected but does not manifest disease‬ ‭○‬ ‭Patient experiences no symptoms or disease and does not seek medical attention‬ ‭○‬ ‭Most infections are intended by some sort of sign‬ ‭Long-term infections & long-term effects‬ ‭‬ ‭Latency‬ ‭○‬ ‭Dormant state of infectious agent‬ ‭○‬ ‭During this state, microbe can periodically become active and produce recurrent‬ ‭disease‬ ‭○‬ ‭Agents of syphilis, typhoid fever, tuberculosis, and malaria also enter into latent‬ ‭stages‬ ‭‬ ‭Sequelae‬ ‭○‬ ‭Long-term or permanent damage to organs and tissues‬ ‭‬ ‭Meningitis → deafness‬ ‭‬ ‭Strep throat → rheumatic heart disease‬ ‭‬ ‭Lyme disease → arthritis‬ ‭‬ ‭Polio → paralysis‬ ‭Course of an infection‬ ‭‬ ‭Incubation period‬ ‭○‬ ‭Time from initial contact w/ infectious agent to appearance of first symptoms‬ ‭‬ ‭Prodromal period‬ ‭○‬ ‭When the earliest notable symptoms of infection appear‬ ‭‬ ‭Acute period‬ ‭○‬ ‭Infectious agent multiplies at high levels, exhibits its greatest virulence, and‬ ‭becomes well established in its target tissue‬ ‭‬ ‭Convalescent stage‬ ‭○‬ ‭Patient responds to infection and symptoms decline‬ ‭Stages in the course of infection and disease‬ ‭‬ ‭Some diseases have 5th phase‬ ‭○‬ ‭Continuation period‬ ‭‬ ‭Patient experiences sequelae‬ ‭Reservoirs: Where pathogens persist‬ ‭‬ ‭Reservoir‬ ‭○‬ ‭Primary habitat in natural world from which a pathogen originates‬ ‭○‬ ‭Human or animal carrier; soil, water, or plants‬ ‭○‬ ‭Ex: giardia → body of water‬ ‭‬ ‭Source‬ ‭○‬ ‭Distinct from reservoir‬ ‭○‬ ‭Individual or object from which an infection is acquired‬ ‭○‬ ‭Ex: giardia → Lake Pleasant‬ ‭Living reservoirs‬ ‭‬ ‭Animals (other than humans and arthropods)‬ ‭○‬ ‭Can be directly transmitted to humans‬ ‭○‬ ‭Can be transmitted to humans via vectors‬ ‭○‬ ‭Can be transmitted through vehicles (ex: water)‬ ‭‬ ‭Actively ill humans‬ ‭○‬ ‭Indirect transmission‬ ‭‬ ‭Person w/ a cold contaminates a pen, which is then picked up by a healthy‬ ‭person‬ ‭○‬ ‭Direct transmission‬ ‭‬ ‭Sick person sneezing on healthy person‬ ‭‬ ‭Human carriers‬ ‭○‬ ‭Person who is fully recovered from hepatitis but is still shedding hepatitis A virus‬ ‭in feces uses suboptimal hand-washing technique and then contaminates food‬ ‭which a healthy person ingests‬ ‭○‬ ‭Incubating carrier of HIV, who doesn’t know she is infected, transmits virus‬ ‭through sexual contact‬ ‭‬ ‭Arthropods‬ ‭○‬ ‭Fleas, mosquitoes, flies, ticks, etc.‬ ‭○‬ ‭Host (and reservoir) of pathogen can also be the most of transmission‬ ‭Carrier states‬ ‭‬ ‭Asymptomatic carriers‬ ‭○‬ ‭Infected but show no symptoms‬ ‭○‬ ‭Ex: gonorrhea, genital herpes w/ no lesions‬ ‭‬ ‭Incubating carriers‬ ‭○‬ ‭Infected but show no symptoms‬ ‭○‬ ‭Ex: infectious mononucleosis‬ ‭‬ ‭Convalescent carriers‬ ‭○‬ ‭Recuperating patients w/o symptoms‬ ‭○‬ ‭Continue to shed viable microbes and infect others (Hepatitis A)‬ ‭‬ ‭Chronic carriers‬ ‭○‬ ‭Individuals who shelter infectious agent for long period after recovery due to‬ ‭latency of agent‬ ‭○‬ ‭Ex: tuberculosis, typhoid fever‬ ‭‬ ‭Passive carriers‬ ‭○‬ M ‭ edical / dental personnel who handle patient materials that are contaminated w/‬ ‭patient secretions / blood‬ ‭○‬ ‭Ex: risk picking up pathogens mechanically and accidentally transferring them to‬ ‭other patients‬ ‭Vectors‬ ‭‬ ‭Epidemiology‬ ‭○‬ ‭Live animal that transmits infectious agent from one host to another‬ ‭‬ ‭Majority of vectors are arthropods‬ ‭‬ ‭Biological vector‬ ‭○‬ ‭Actively participates in pathogen’s life cycle, serving as site in which pathogen‬ ‭can multiply or complete its life cycle‬ ‭○‬ ‭Communicates infectious agent to human host by biting, aerosol formation, or‬ ‭touch‬ ‭○‬ ‭Ex: mosquito transmitting malaria, chicken, bats‬ ‭‬ ‭Mechanical vectors‬ ‭○‬ ‭Not necessary to life cycle of infectious agent‬ ‭○‬ ‭Merely transport pathogen w/o being infected‬ ‭○‬ ‭Ex: cockroaches, flies‬ ‭Zoonosis‬ ‭‬ I‭ nfection indigenous to animals but also transmissible to humans‬ ‭‬ ‭Human is dead-end host and does not contribute to natural persistence of microbe‬ ‭‬ ‭Spread of disease is promoted by close associations of humans w/ animals‬ ‭‬ ‭People in animal-oriented or outdoor professions are at greatest risk‬ ‭‬ ‭Ex: rabies, hantavirus, West Nile virus, anthrax, plague, ringworm, toxoplasmosis,‬ ‭tapeworm‬ ‭Nonliving reservoirs‬ ‭‬ M ‭ icrobes have adapted to nearly every habitat in biosphere‬ ‭‬ ‭Soil, water, air, built environment‬ ‭‬ ‭Types‬ ‭○‬ ‭Most are saprobic (decomposers) and cause little harm to humans‬ ‭○‬ ‭Some are opportunists‬ ‭○‬ ‭Few are regular pathogens‬ ‭‬ ‭Ex: TB bacterium can be directly transmitted to humans when they come in contact with‬ ‭contaminated soil, water, or air‬ ‭Acquisition and transmission of infectious agents‬ ‭‬ ‭Communicable disease‬ ‭○‬ ‭Occurs when infected host can transmit infectious agent to another host and‬ ‭establish infection in that host‬ ‭○‬ ‭Ex: giardia, malaria, lyme disease‬ ‭‬ ‭Contagious‬ ‭○‬ ‭Agent is highly communicable, especially through direct contact‬ ‭○‬ ‭Ex: COVID-19, flu, common cold‬ ‭‬ ‭Noncommunicable‬ ‭○‬ ‭Does not arise through transmission of infectious agent from host to host‬ ‭○‬ ‭Ex: Valley fever, tetanus‬ ‭Horizontal vs vertical transmission‬ ‭‬ ‭Horizontal transmission‬ ‭○‬ ‭Disease is spread through population from one infected individual to another‬ ‭○‬ ‭Direct (contact) transmission‬ ‭‬ ‭Kissing, sex‬ ‭○‬ ‭Indirect transmission‬ ‭‬ ‭Fomites, vehicles, parenteral (via injection into deeper tissues)‬ ‭○‬ ‭Vector transmission‬ ‭‬ ‭Vertical transmission‬ ‭○‬ ‭Transmission from parent to offspring via ovum, sperm, placenta, or milk‬ ‭○‬ ‭Congenital disease‬ ‭‬ ‭Born w/ it‬ ‭Indirect transmission‬ ‭‬ ‭Vehicle‬ ‭○‬ ‭Natural, non-living material‬ ‭○‬ ‭Air, water, soil, food‬ ‭‬ ‭Fomite‬ ‭○‬ ‭Inanimate object that harbors and transmits pathogens‬ ‭○‬ ‭Not continuous source of infection‬ ‭‬ ‭Oral-fecal route‬ ‭○‬ ‭Fecal carrier w/ inadequate personal hygiene contaminates food during handling,‬ ‭and an unsuspecting person ingests it‬ ‭Droplet nuclei and aerosols‬ ‭‬ ‭Droplet nuclei‬ ‭○‬ D ‭ ried microscopic residues created when microscopic pellets of mucus and saliva‬ ‭are ejected from mouth and nose‬ ‭ ‬ ‭Aerosols‬ ‭○‬ ‭Suspensions of fine dust or moisture particles in air that contain live pathogens‬ ‭Healthcare-associated infections (HAI)‬ ‭‬ ‭Nosocomial infections‬ ‭○‬ ‭Infectious diseases that are acquired or develop during hospital stay or stay in‬ ‭another health-care facility‬ ‭‬ ‭Rates of HAIs can range from 0.1 - 20% of all admitted patients‬ ‭‬ ‭Iatrogenic infections‬ ‭○‬ ‭Due to medical treatment‬ ‭○‬ ‭Antibiotics that are used to treat bacterial infection, may result in yeast infection‬ ‭Control of nosocomial infections‬ ‭‬ R ‭ educe number of pathogens‬ ‭‬ ‭Aseptic techniques‬ ‭○‬ ‭Medical asepsis‬ ‭‬ ‭Practices that lower microbial load in patients, caregivers, and hospital‬ ‭environment‬ ‭○‬ ‭Surgical asepsis‬ ‭‬ ‭Ensuring all surgical procedures are conducted under sterile conditions‬ ‭‬ ‭Handle contaminated materials carefully‬ ‭‬ ‭Frequent and thorough hand washing‬ ‭○‬ ‭Single most important means of prevention‬ ‭‬ ‭Isolation rooms and wards‬ ‭‬ ‭Disinfect or sterilize materials and equipment‬ ‭Using Koch’s Postulates to determine etiology‬ ‭‬ E ‭ ssential aim of study of infection and disease → determining etiologic agent (causative‬ ‭agent)‬ ‭‬ ‭Series of proofs that established classic criteria for etiologic studies‬ ‭1.‬ ‭Same pathogen must be present in every case of disease‬ ‭2.‬ ‭Pathogen must be isolated from diseased host and grown in pure culture‬ ‭3.‬ ‭Pathogen from pure culture must cause disease when it is inoculated into healthy,‬ ‭susceptible laboratory animal‬ ‭4.‬ ‭Pathogen must be isolated from inoculated animal and must be shown to be‬ ‭original organism‬ ‭Exceptions to Koch’s Postulates‬ ‭‬ ‭Unique culture requirements‬ ‭○‬ ‭Some microbes cannot be cultured on artificial media‬ ‭○‬ ‭Treponema pallidum, Mycobacterium leprae‬ ‭○‬ ‭Rickettsia‬‭and many viruses (multiply only within‬‭cells)‬ ‭‬ ‭One pathogen can cause different disease states‬ ‭○‬ ‭Mycobacterium tuberculosis‬‭→ lungs, skin, bones, etc.‬ ‭○‬ ‭Streptococcus pyogenes‬‭→ sore throat, scarlet fever,‬‭skin infections‬ ‭‬ ‭Similar symptoms caused by several different pathogen‬ ‭○‬ ‭Pneumonia → fluid in lungs‬ ‭○‬ ‭Nephritis → inflammation of kidneys‬ ‭‬ ‭Idiopathic disease‬ ‭○‬ ‭Cause unknown‬ ‭Epidemiology: Study of disease in populations‬ ‭‬ ‭Epidemiology‬ ‭○‬ ‭Effects of diseases on community‬ ‭○‬ ‭Involves study of frequency and distribution of disease and distribution of disease‬ ‭and other health-related factors in defined populations‬ ‭‬ ‭Reportable diseases‬ ‭○‬ ‭Notifiable diseases‬ ‭○‬ ‭By law, some diseases must be reported to authorities‬ ‭○‬ ‭Other diseases are reported on voluntary basis‬ ‭Centers for Diseases Control and Prevention (CDC)‬ ‭‬ R ‭ esponsible for keeping track of infectious diseases nationwide‬ ‭‬ ‭Part of the U.S. Public Health Service‬ ‭‬ ‭Morbidity and Mortality Report‬ ‭○‬ ‭Weekly notice of diseases published by CDC‬ ‭‬ ‭CDC shares stats on disease w/ World Health Organization (WHO) for worldwide‬ ‭tabulation and control‬ ‭Epidemiological Statistics‬ ‭‬ ‭Prevalence of disease‬ ‭○‬ ‭Total number of existing cases w/ respect to entire population‬ ‭‬ ‭Incidence of disease‬ ‭○‬ ‭Measures number of new cases over certain time period‬ ‭○‬ ‭Aka case or morbidity rate‬ ‭‬ ‭Mortality rate‬ ‭○‬ ‭Measures number of deaths in population due to certain disease‬ ‭Epidemics‬ ‭‬ ‭Point-source epidemic‬ ‭○‬ ‭Infectious agents came from single source‬ ‭‬ ‭Common-source epidemic‬ ‭○‬ ‭Common exposure to single source of infection that can occur over period of time‬ ‭‬ ‭Propagated epidemic‬ ‭○‬ ‭Infectious agent that is communicable from person to person and is sustained over‬ ‭time in population‬ ‭‬ ‭Pandemic‬ ‭○‬ ‭Spread of epidemic across continents‬ ‭‬ ‭Index case‬ ‭○‬ ‭First patient found in epidemiological investigation‬ ‭‬ ‭Endemic‬ ‭○‬ ‭Infectious disease that exhibits relatively steady frequency over long time period‬ ‭in particular geographic locale‬ ‭○‬ ‭Ex: Valley fever in South America‬ ‭‬ ‭Sporadic disease‬ ‭○‬ ‭Occasional cases are reported at irregular intervals in random locales‬ ‭Patterns of infectious disease occurrence‬ ‭Global issues in epidemiology‬ ‭‬ ‭Emerging Infectious Diseases (EIDs)‬ ‭○‬ ‭Newly identified microbes‬ ‭○‬ ‭COVID-19, HIV, SARS, novel strains of influenza‬ ‭‬ ‭Re-emerging diseases‬ ‭○‬ ‭Dengue fever, tuberculosis, yellow fever‬ ‭‬ ‭Contributing factors‬ ‭○‬ ‭Widespread antibiotic use‬ ‭○‬ ‭Climate change leads to distribution changes in microbe habitats‬ ‭○‬ ‭Modern transportation‬ ‭○‬ ‭Natural disaster, construction, expanding settlement‬ ‭○‬ ‭Animal control → loss of “balance”‬ ‭○‬ ‭Public health measure failures‬ ‭Clicker Questions‬ ‭1.‬ ‭Malaria would be which type of infection?‬ ‭a.‬ ‭Local‬ ‭b.‬ ‭Systemic‬ ‭c.‬ ‭Focal‬ ‭d.‬ ‭Mixed‬ ‭2.‬ ‭A headache is an example of a:‬ ‭a.‬ ‭Sign‬ ‭b.‬ ‭Symptom‬ ‭c.‬ ‭Syndrome‬ ‭3.‬ ‭Which of the following is an example of a disease with a continuation period?‬ ‭a.‬ ‭Influenza‬ ‭b.‬ ‭The common cold‬ ‭c.‬ ‭Yeast infection‬ ‭d.‬ ‭COVID-19‬ ‭e.‬ ‭Salmonella food poisoning‬ ‭4.‬ ‭True or False: Since the reservoir of the Ebola virus has never been determined, we can‬ ‭assume that it is a man-made virus created in a laboratory.‬ ‭a.‬ ‭True‬ ‭b.‬ ‭False‬ ‭5.‬ ‭Match the following diseases with their descriptions:‬ ‭_‬‭A‬‭_‬‭1. Spread via mosquitoes‬ ‭_‬‭E‭_‬ ‬‭2. Contagious cold sores‬ ‭_‬‭C‬‭_‬‭3. Serious, rare disease contracted through the‬‭bite of an infected animal‬ ‭_‬‭B‭_‬ ‬‭4. Highly contagious, seasonal disease‬ ‭_‬‭D‬‭_‬‭5. Highly contagious; 90% of population is vaccinated‬ ‭. West Nile Virus‬ A ‭B. Common cold‬ ‭C. Rabies‬ ‭. Measles‬ D ‭E. Herpes‬ ‭6.‬ ‭Which of the following trends would be indicative of West Nile Virus?‬ ‭a.‬ ‭A‬ ‭b.‬ ‭B‬ ‭c.‬ ‭C‬ ‭d.‬ ‭D‬ ‭e.‬ ‭E‬ ‭7.‬ ‭Which of the following trends would be indicative of herpes?‬ ‭a.‬ ‭A‬ ‭b.‬ ‭B‬ ‭c.‬ ‭C‬ ‭d.‬ ‭D‬ ‭e.‬ ‭E‬ ‭8.‬ ‭Which of the following trends would be indicative of rabies?‬ ‭a.‬ ‭A‬ ‭b.‬ ‭B‬ ‭c.‬ ‭C‬ ‭d.‬ ‭D‬ ‭e.‬ ‭E‬ ‭9.‬ ‭Which of the following trends would be indicative of the common cold?‬ ‭a.‬ ‭A‬ ‭b.‬ ‭B‬ ‭c.‬ ‭C‬ ‭d.‬ ‭D‬ e‭.‬ ‭E‬ ‭10.‬‭Which of the following trends would be indicative of a measles outbreak?‬ ‭a.‬ ‭A‬ ‭b.‬ ‭B‬ ‭c.‬ ‭C‬ ‭d.‬ ‭D‬ ‭e.‬ ‭E‬

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