How Pathogens Cause Disease

For most infectious diseases, the ability to accurately identify the causative pathogen is a critical step in finding or prescribing effective treatments. Today’s physicians, patients, and researchers owe a sizable debt to the physician Robert Koch (1843–1910), who devised a systematic approach for confirming causative relationships between diseases and specific pathogens.

Koch’s Postulates

In 1884, Koch published four postulates (below) that summarized his method for determining whether a particular microorganism was the cause of a particular disease. Each of Koch’s postulates represents a criterion that must be met before a disease can be positively linked with a pathogen. In order to determine whether the criteria are met, tests are performed on laboratory animals and cultures from healthy and diseased animals are compared (see the figure below).

Extended description

Reading left to right: a healthy mouse’s blood viewed under a microscope shows only red blood cells, and a petri dish cultured from that blood shows no growth — the suspected agent is absent from a healthy organism. A diseased mouse’s blood viewed under the microscope shows the suspected agent (drawn in green) scattered among the red blood cells, and a petri dish cultured from that blood shows bacterial growth — the agent is present in, and can be isolated from, the diseased organism. The cultured agent is then injected into a healthy mouse, which becomes sick. Finally, a petri dish cultured from this newly diseased mouse shows the same growth pattern as the second dish, confirming the same agent has been re-isolated.

In many ways, Koch’s postulates are still central to our current understanding of the causes of disease. However, advances in microbiology have revealed some important limitations in Koch’s criteria. Koch made several assumptions that we now know are untrue in many cases. The first relates to postulate 1, which assumes that pathogens are only found in diseased, not healthy, individuals. This is not true for many pathogens. For example, H. pylori, described earlier in this chapter as a pathogen causing chronic gastritis, is also part of the normal microbiota of the stomach in many healthy humans who never develop gastritis. It is estimated that upwards of 50% of the human population acquires H. pylori early in life, with most maintaining it as part of the normal microbiota for the rest of their life without ever developing disease. Similarly, when Alice Katherine Evans discovered that Brucella bacteria found in cows was responsible for a common human disease, she noted that the infected cattle could pass on the infection whether or not they displayed symptoms. This is an important distinction: Even without knowledge of microbiology, many people would not consume milk from a visibly sick cow, but the concept of a healthy cow being infectious is critical to understanding the risks posed by pathogens.

Koch’s second faulty assumption was that all healthy test subjects are equally susceptible to disease. We now know that individuals are not equally susceptible to disease. Individuals are unique in terms of their microbiota and the state of their immune system at any given time. The makeup of the resident microbiota can influence an individual’s susceptibility to an infection. Members of the normal microbiota play an important role in immunity by inhibiting the growth of transient pathogens. In some cases, the microbiota may prevent a pathogen from establishing an infection; in others, it may not prevent an infection altogether but may influence the severity or type of signs and symptoms. As a result, two individuals with the same disease may not always present with the same signs and symptoms. In addition, some individuals have stronger immune systems than others. Individuals with immune systems weakened by age or an unrelated illness are much more susceptible to certain infections than individuals with strong immune systems.

Koch also assumed that all pathogens are microorganisms that can be grown in pure culture (postulate 2) and that animals could serve as reliable models for human disease. However, we now know that not all pathogens can be grown in pure culture, and many human diseases cannot be reliably replicated in animal hosts. Viruses and certain bacteria, including Rickettsia and Chlamydia, are obligate intracellular pathogens that can grow only when inside a host cell. If a microbe cannot be cultured, a researcher cannot move past postulate 2. Likewise, without a suitable nonhuman host, a researcher cannot evaluate postulate 3 without deliberately infecting humans, which presents obvious ethical concerns. AIDS is an example of such a disease because the human immunodeficiency virus (HIV) only causes disease in humans.

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Molecular Koch’s Postulates

In 1988, Stanley Falkow (1934–) proposed a revised form of Koch’s postulates known as molecular Koch’s postulates. These are listed in the left column of the table below. The premise for molecular Koch’s postulates is not in the ability to isolate a particular pathogen but rather to identify a gene that may cause the organism to be pathogenic.

Falkow’s modifications to Koch’s original postulates explain not only infections caused by intracellular pathogens but also the existence of pathogenic strains of organisms that are usually nonpathogenic. For example, the predominant form of the bacterium Escherichia coli is a member of the normal microbiota of the human intestine and is generally considered harmless. However, there are pathogenic strains of E. coli such as enterotoxigenic E. coli (ETEC) and enterohemorrhagic E. coli (O157:H7) (EHEC). We now know ETEC and EHEC exist because of the acquisition of new genes by the once-harmless E. coli, which, in the form of these pathogenic strains, is now capable of producing toxins and causing illness. The pathogenic forms resulted from minor genetic changes. The right-side column of the table below illustrates how molecular Koch’s postulates can be applied to identify EHEC as a pathogenic bacterium.

As with Koch’s original postulates, the molecular Koch’s postulates have limitations. For example, genetic manipulation of some pathogens is not possible using current methods of molecular genetics. In a similar vein, some diseases do not have suitable animal models, which limits the utility of both the original and molecular postulates.

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Pathogenicity and Virulence

The ability of a microbial agent to cause disease is called pathogenicity, and the degree to which an organism is pathogenic is called virulence. Virulence is a continuum. On one end of the spectrum are organisms that are avirulent (not harmful) and on the other are organisms that are highly virulent. Highly virulent pathogens will almost always lead to a disease state when introduced to the body, and some may even cause multi-organ and body system failure in healthy individuals. Less virulent pathogens may cause an initial infection, but may not always cause severe illness. Pathogens with low virulence would more likely result in mild signs and symptoms of disease, such as low-grade fever, headache, or muscle aches. Some individuals might even be asymptomatic.

An example of a highly virulent microorganism is Bacillus anthracis, the pathogen responsible for anthrax. B. anthracis can produce different forms of disease, depending on the route of transmission (e.g., cutaneous injection, inhalation, ingestion). The most serious form of anthrax is inhalation anthrax. After B. anthracis spores are inhaled, they germinate. An active infection develops and the bacteria release potent toxins that cause edema (fluid buildup in tissues), hypoxia (a condition preventing oxygen from reaching tissues), and necrosis (cell death and inflammation). Signs and symptoms of inhalation anthrax include high fever, difficulty breathing, vomiting and coughing up blood, and severe chest pains suggestive of a heart attack. With inhalation anthrax, the toxins and bacteria enter the bloodstream, which can lead to multi-organ failure and death of the patient. If a gene (or genes) involved in pathogenesis is inactivated, the bacteria become less virulent or nonpathogenic.

Virulence of a pathogen can be quantified using controlled experiments with laboratory animals. Two important indicators of virulence are the median infectious dose (ID₅₀) and the median lethal dose (LD₅₀), both of which are typically determined experimentally using animal models. The ID₅₀ is the number of pathogen cells or virions required to cause active infection in 50% of inoculated animals. The LD₅₀ is the number of pathogenic cells, virions, or amount of toxin required to kill 50% of infected animals. To calculate these values, each group of animals is inoculated with one of a range of known numbers of pathogen cells or virions. In graphs like the one below, the percentage of animals that have been infected (for ID₅₀) or killed (for LD₅₀) is plotted against the concentration of pathogen inoculated. The graph below represents data graphed from a hypothetical experiment measuring the LD₅₀ of a pathogen. Interpretation of the data from this graph indicates that the LD₅₀ of the pathogen for the test animals is $10^4$ pathogen cells or virions (depending upon the pathogen studied).

Extended description

The curve starts at the origin (0, 0) and rises slowly at first, then steeply through the middle of its range, then levels off as it approaches 100%. A pair of dashed lines marks the curve’s midpoint: a vertical line up from 10⁴ on the x-axis meets a horizontal line across from 50% on the y-axis, showing that the LD₅₀ for this hypothetical pathogen is 10⁴ agents. The curve continues rising past that point and does not visibly flatten at 100% until roughly 10⁸ agents.

The table below lists selected foodborne pathogens and their ID₅₀ values in humans (as determined from epidemiologic data and studies on human volunteers). Keep in mind that these are median values. The actual infective dose for an individual can vary widely, depending on factors such as route of entry; the age, health, and immune status of the host; and environmental and pathogen-specific factors such as susceptibility to the acidic pH of the stomach. It is also important to note that a pathogen’s infective dose does not necessarily correlate with disease severity. For example, just a single cell of Salmonella enterica serotype Typhimurium can result in an active infection. The resultant disease, Salmonella gastroenteritis or salmonellosis, can cause nausea, vomiting, and diarrhea, but has a mortality rate of less than 1% in healthy adults. In contrast, S. enterica serotype Typhi has a much higher ID₅₀, typically requiring as many as 1,000 cells to produce infection. However, this serotype causes typhoid fever, a much more systemic and severe disease that has a mortality rate as high as 10% in untreated individuals.

ID₅₀ for Selected Foodborne Diseases (Food and Drug Administration. “Bad Bug Book, Foodborne Pathogenic Microorganisms and Natural Toxins.” 2nd ed. Silver Spring, MD: US Food and Drug Administration; 2012.)

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Primary Pathogens versus Opportunistic Pathogens

Pathogens can be classified as either primary pathogens or opportunistic pathogens. A primary pathogen can cause disease in a host regardless of the host’s resident microbiota or immune system. An opportunistic pathogen, by contrast, can only cause disease in situations that compromise the host’s defenses, such as the body’s protective barriers, immune system, or normal microbiota. Individuals susceptible to opportunistic infections include the very young, the elderly, people who are pregnant, patients undergoing chemotherapy, people with immunodeficiencies (such as acquired immunodeficiency syndrome [AIDS]), patients who are recovering from surgery, and those who have had a breach of protective barriers (such as a severe wound or burn).

An example of a primary pathogen is enterohemorrhagic E. coli (EHEC), which produces a virulence factor known as Shiga toxin. This toxin inhibits protein synthesis, leading to severe and bloody diarrhea, inflammation, and renal failure, even in patients with healthy immune systems. Staphylococcus epidermidis, on the other hand, is an opportunistic pathogen that is among the most frequent causes of nosocomial disease (M. Otto. “Staphylococcus epidermidis–The ‘Accidental’ Pathogen.” Nature Reviews Microbiology 7 no. 8 (2009):555–567.). S. epidermidis is a member of the normal microbiota of the skin, where it is generally avirulent. However, in hospitals, it can also grow in biofilms that form on catheters, implants, or other devices that are inserted into the body during surgical procedures. Once inside the body, S. epidermidis can cause serious infections such as endocarditis, and it produces virulence factors that promote the persistence of such infections.

Other members of the normal microbiota can also cause opportunistic infections under certain conditions. This often occurs when microbes that reside harmlessly in one body location end up in a different body system, where they cause disease. For example, E. coli normally found in the large intestine can cause a urinary tract infection if it enters the bladder. This is the leading cause of urinary tract infections among females.

Members of the normal microbiota may also cause disease when a shift in the environment of the body leads to overgrowth of a particular microorganism. For example, the yeast Candida is part of the normal microbiota of the skin, mouth, intestine, and vagina, but its population is kept in check by other organisms of the microbiota. If an individual is taking antibacterial medications, however, bacteria that would normally inhibit the growth of Candida can be killed off, leading to a sudden growth in the population of Candida, which is not affected by antibacterial medications because it is a fungus. An overgrowth of Candida can manifest as oral thrush (growth on mouth, throat, and tongue), a vaginal yeast infection, or cutaneous candidiasis. Other scenarios can also provide opportunities for Candida infections. Untreated diabetes can result in a high concentration of glucose in the saliva, which provides an optimal environment for the growth of Candida, resulting in thrush. Immunodeficiencies such as those seen in patients with HIV, AIDS, and cancer also lead to higher incidence of thrush. Vaginal yeast infections can result from decreases in estrogen levels during the menstruation or menopause. The amount of glycogen available to lactobacilli in the vagina is controlled by levels of estrogen; when estrogen levels are low, lactobacilli produce less lactic acid. The resultant increase in vaginal pH allows overgrowth of Candida in the vagina.

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Stages of Pathogenesis

To cause disease, a pathogen must successfully achieve four steps or stages of pathogenesis: exposure (contact), adhesion (colonization), invasion, and infection. The pathogen must be able to gain entry to the host, travel to the location where it can establish an infection, evade or overcome the host’s immune response, and cause damage (i.e., disease) to the host. In many cases, the cycle is completed when the pathogen exits the host and is transmitted to a new host.

Exposure

An encounter with a potential pathogen is known as exposure or contact. The food we eat and the objects we handle are all ways that we can come into contact with potential pathogens. Yet, not all contacts result in infection and disease. For a pathogen to cause disease, it needs to be able to gain access into host tissue. An anatomic site through which pathogens can pass into host tissue is called a portal of entry. These are locations where the host cells are in direct contact with the external environment. Major portals of entry are identified in the figure below and include the skin, mucous membranes, and parenteral routes.

Extended description

On the woman: the eye (conjunctiva), nose, mouth, and ear are labeled on her head, and the placenta (portal of entry for the fetus) and vagina are labeled at her pelvis. On the man: a needle is shown near his raised hand, broken skin is labeled on his forearm, and an insect bite is labeled on his thigh. The urethra and anus are labeled with lines pointing to both figures, since both sexes share these portals.

Mucosal surfaces are the most important portals of entry for microbes; these include the mucous membranes of the respiratory tract, the gastrointestinal tract, and the genitourinary tract. Although most mucosal surfaces are in the interior of the body, some are contiguous with the external skin at various body openings, including the eyes, nose, mouth, urethra, and anus.

Most pathogens are suited to a particular portal of entry. A pathogen’s portal specificity is determined by the organism’s environmental adaptions and by the enzymes and toxins they secrete. The respiratory and gastrointestinal tracts are particularly vulnerable portals of entry because particles that include microorganisms are constantly inhaled or ingested, respectively.

Pathogens can also enter through a breach in the protective barriers of the skin and mucous membranes. Pathogens that enter the body in this way are said to enter by the parenteral route. For example, the skin is a good natural barrier to pathogens, but breaks in the skin (e.g., wounds, insect bites, animal bites, needle pricks) can provide a parenteral portal of entry for microorganisms.

In pregnant people, the placenta normally prevents microorganisms from passing from the pregnant person to the fetus. However, a few pathogens are capable of crossing the blood-placental barrier. The gram-positive bacterium Listeria monocytogenes, which causes the foodborne disease listeriosis, is one example that poses a serious risk to the fetus and can sometimes lead to spontaneous abortion. Other pathogens that can pass the placental barrier to infect the fetus are known collectively by the acronym TORCH (below).

Transmission of infectious diseases to the baby is also a concern at the time of birth when the baby passes through the birth canal. Those who have active chlamydia or gonorrhea infections may expose babies the causative pathogens in the vagina, which can result in eye infections that lead to blindness. To prevent this, it is standard practice to administer antibiotic drops to infants’ eyes shortly after birth.

Pathogens Capable of Crossing the Placental Barrier (TORCH Infections)

The “O” in TORCH stands for “other.”

Adhesion

Following the initial exposure, the pathogen adheres at the portal of entry. The term adhesion refers to the capability of pathogenic microbes to attach to the cells of the body using adhesion factors, and different pathogens use various mechanisms to adhere to the cells of host tissues.

Molecules (either proteins or carbohydrates) called adhesins are found on the surface of certain pathogens and bind to specific receptors (glycoproteins) on host cells. Adhesins are present on the fimbriae and flagella of bacteria, the cilia of protozoa, and the capsids or membranes of viruses. Protozoans can also use hooks and barbs for adhesion; spike proteins on viruses also enhance viral adhesion. The production of glycocalyces (slime layers and capsules), with their high sugar and protein content, can also allow certain bacterial pathogens to attach to cells, as shown in the micrograph below.

Biofilm growth can also act as an adhesion factor. A biofilm is a community of bacteria that produce a glycocalyx, known as extrapolymeric substance (EPS), that allows the biofilm to attach to a surface. Persistent Pseudomonas aeruginosa infections are common in patients suffering from cystic fibrosis, burn wounds, and middle-ear infections (otitis media) because P. aeruginosa produces a biofilm. The EPS allows the bacteria to adhere to the host cells and makes it harder for the host to physically remove the pathogen. The EPS not only allows for attachment but provides protection against the immune system and antibiotic treatments, preventing antibiotics from reaching the bacterial cells within the biofilm. In addition, not all bacteria in a biofilm are rapidly growing; some are in stationary phase. Since antibiotics are most effective against rapidly growing bacteria, portions of bacteria in a biofilm are protected against antibiotics (D. Davies. “Understanding Biofilm Resistance to Antibacterial Agents.” Nature Reviews Drug Discovery 2 (2003):114–122.).

Invasion

Once adhesion is successful, invasion can proceed. Invasion involves the dissemination of a pathogen throughout local tissues or the body. Pathogens may produce exoenzymes or toxins, which serve as virulence factors that allow them to colonize and damage host tissues as they spread deeper into the body. Pathogens may also produce virulence factors that protect them against immune system defenses. A pathogen’s specific virulence factors determine the degree of tissue damage that occurs. The figure below shows the invasion of H. pylori into the tissues of the stomach, causing damage as it progresses.

Extended description

First panel, captioned ‘Contact with stomach acid keeps the mucin lining the epithelial cell layer in a spongy gel-like state. This consistency is impermeable to the bacterium H. pylori’: the labeled H. pylori cell, with three long flagella, sits against the outer face of the purple mucin gel block, unable to penetrate it. Second panel, captioned ‘The bacterium releases urease, which neutralizes the stomach acid. This causes the mucin to liquefy, and the bacterium can swim right through it’: the mucin nearest the bacterium has turned into a blue, translucent liquid, and the bacterium’s body is shown partway inside this liquefied region, having swum through toward the labeled epithelial cells.

Intracellular pathogens achieve invasion by entering the host’s cells and reproducing. Some are obligate intracellular pathogens (meaning they can only reproduce inside of host cells) and others are facultative intracellular pathogens (meaning they can reproduce either inside or outside of host cells). By entering the host cells, intracellular pathogens are able to evade some mechanisms of the immune system while also exploiting the nutrients in the host cell.

Entry to a cell can occur by endocytosis. For most kinds of host cells, pathogens use one of two different mechanisms for endocytosis and entry. One mechanism relies on effector proteins secreted by the pathogen; these effector proteins trigger entry into the host cell. This is the method that Salmonella and Shigella use when invading intestinal epithelial cells. When these pathogens come in contact with epithelial cells in the intestine, they secrete effector molecules that cause protrusions of membrane ruffles that bring the bacterial cell in. This process is called membrane ruffling. The second mechanism relies on surface proteins expressed on the pathogen that bind to receptors on the host cell, resulting in entry. For example, Yersinia pseudotuberculosis produces a surface protein known as invasin that binds to beta-1 integrins expressed on the surface of host cells.

Some host cells, such as white blood cells and other phagocytes of the immune system, actively endocytose pathogens in a process called phagocytosis. Although phagocytosis allows the pathogen to gain entry to the host cell, in most cases, the host cell kills and degrades the pathogen by using digestive enzymes. Normally, when a pathogen is ingested by a phagocyte, it is enclosed within a phagosome in the cytoplasm; the phagosome fuses with a lysosome to form a phagolysosome, where digestive enzymes kill the pathogen (see Pathogen Recognition and Phagocytosis). However, some intracellular pathogens have the ability to survive and multiply within phagocytes. Examples include Listeria monocytogenes and Shigella; these bacteria produce proteins that lyse the phagosome before it fuses with the lysosome, allowing the bacteria to escape into the phagocyte’s cytoplasm where they can multiply. Bacteria such as Mycobacterium tuberculosis, Legionella pneumophila, and Salmonella species use a slightly different mechanism to evade being digested by the phagocyte. These bacteria prevent the fusion of the phagosome with the lysosome, thus remaining alive and dividing within the phagosome.

Infection

Following invasion, successful multiplication of the pathogen leads to infection. Infections can be described as local, focal, or systemic, depending on the extent of the infection. A local infection is confined to a small area of the body, typically near the portal of entry. For example, a hair follicle infected by Staphylococcus aureus infection may result in a boil around the site of infection, but the bacterium is largely contained to this small location. Other examples of local infections that involve more extensive tissue involvement include urinary tract infections confined to the bladder or pneumonia confined to the lungs.

In a focal infection, a localized pathogen, or the toxins it produces, can spread to a secondary location. For example, a dental hygienist nicking the gum with a sharp tool can lead to a local infection in the gum by Streptococcus bacteria of the normal oral microbiota. These Streptococcus spp. may then gain access to the bloodstream and make their way to other locations in the body, resulting in a secondary infection.

When an infection becomes disseminated throughout the body, we call it a systemic infection. For example, infection by the varicella-zoster virus typically gains entry through a mucous membrane of the upper respiratory system. It then spreads throughout the body, resulting in the classic red skin lesions associated with chickenpox. Since these lesions are not sites of initial infection, they are signs of a systemic infection.

Sometimes a primary infection, the initial infection caused by one pathogen, can lead to a secondary infection by another pathogen. For example, the immune system of a patient with a primary infection by HIV becomes compromised, making the patient more susceptible to secondary diseases like oral thrush and others caused by opportunistic pathogens. Similarly, a primary infection by Influenzavirus damages and decreases the defense mechanisms of the lungs, making patients more susceptible to a secondary pneumonia by a bacterial pathogen like Haemophilus influenzae or Streptococcus pneumoniae. Some secondary infections can even develop as a result of treatment for a primary infection. Antibiotic therapy targeting the primary pathogen can cause collateral damage to the normal microbiota, creating an opening for opportunistic pathogens (see the case below).

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Transmission of Disease

For a pathogen to persist, it must put itself in a position to be transmitted to a new host, leaving the infected host through a portal of exit (see the figure below). As with portals of entry, many pathogens are adapted to use a particular portal of exit. Similar to portals of entry, the most common portals of exit include the skin and the respiratory, urogenital, and gastrointestinal tracts. Coughing and sneezing can expel pathogens from the respiratory tract. A single sneeze can send thousands of virus particles into the air. Secretions and excretions can transport pathogens out of other portals of exit. Feces, urine, semen, vaginal secretions, tears, sweat, and shed skin cells can all serve as vehicles for a pathogen to leave the body. Pathogens that rely on insect vectors for transmission exit the body in the blood extracted by a biting insect. Similarly, some pathogens exit the body in blood extracted by needles.

Extended description

On the woman: the eye (tears), mammary glands (milk, secretions), placenta (transmission to fetus), vagina (secretions, blood), urethra (urine), and skin (flakes) are labeled. On the man: the nose (secretions), mouth (saliva, sputum), ear (earwax), a needle (blood) near his raised hand, broken skin on his forearm (labeled both for skin flakes and for blood), an insect bite on his thigh, urethra (urine, semen, secretions), and anus (feces) are labeled.

Summary

• Koch’s postulates are used to determine whether a particular microorganism is a pathogen. Molecular Koch’s postulates are used to determine what genes contribute to a pathogen’s ability to cause disease.
• Virulence, the degree to which a pathogen can cause disease, can be quantified by calculating either the ID₅₀ or LD₅₀ of a pathogen on a given population.
• Primary pathogens are capable of causing pathological changes associated with disease in a healthy individual, whereas opportunistic pathogens can only cause disease when the individual is compromised by a break in protective barriers or immunosuppression.
• Infections and disease can be caused by pathogens in the environment or microbes in an individual’s resident microbiota.
• Infections can be classified as local, focal, or systemic depending on the extent to which the pathogen spreads in the body.
• A secondary infection can sometimes occur after the host’s defenses or normal microbiota are compromised by a primary infection or antibiotic treatment.
• Pathogens enter the body through portals of entry and leave through portals of exit. The stages of pathogenesis include exposure, adhesion, invasion, infection, and transmission.

Key terms

• pathogenicity — ability of a microbial agent to cause disease.
• virulence — degree to which an organism is pathogenic; severity of disease signs and symptoms.
• median infectious dose (ID₅₀) — concentration of pathogen that will produce active infection in 50% of test animals inoculated.
• median lethal dose (LD₅₀) — concentration of pathogen that kills 50% of infected test animals.
• primary pathogen — microorganism that can cause disease in the host regardless of the effectiveness of the host’s immune system.
• opportunistic pathogen — microorganism that can cause disease in individuals with compromised host defenses.
• exposure — contact between potential pathogen and host; also called contamination or contact.
• contact — see exposure.
• portal of entry — anatomical feature of the body through which pathogens can enter host tissue.
• parenteral route — means of entry by a pathogen through skin or mucous membranes when these barriers are breached.
• adhesion — the capability of microbes to attach to host cells.
• adhesins — molecules on the surface of pathogens that promote colonization of host tissue.
• invasion — dissemination of a pathogen through local tissues or throughout the body.
• local infection — infection in one limited area.
• focal infection — infection in which the pathogen causes infection in one location that then spreads to a secondary location.
• systemic infection — infection that has spread to multiple locations or body systems.
• primary infection — initial infection produced by a pathogen.
• secondary infection — second infection that develops after a primary infection as a result of the primary disease compromising immune defenses or antibiotics, thus eliminating protective microbiota.
• portal of exit — anatomical feature of the body through which pathogens can leave diseased individual.

Practice

Summarize Koch’s postulates and molecular Koch’s postulates, respectively, and explain their significance and limitations

Explain the concept of pathogenicity (virulence) in terms of infectious and lethal dose

Distinguish between primary and opportunistic pathogens and identify specific examples of each

Summarize the stages of pathogenesis

Explain the roles of portals of entry and exit in the transmission of disease and identify specific examples of these portals

This section is adapted from Microbiology, Section 15.2: How Pathogens Cause Disease by Nina Parker, Mark Schneegurt, Anh-Hue Thi Tu, Philip Lister, Brian M. Forster, and OpenStax, © OpenStax, licensed under CC BY-NC-SA 4.0. Access the original for free at openstax.org. Changes: all seven source figures re-encoded as WebP and rendered as mediafigures after image and PDF inspection; kind="diagram" set on the Koch’s-postulates, population-curve, portal-of-entry, invasion, and portal-of-exit figures and kind="photo" on the adhesion micrograph and the acupuncture photo, overriding the media manifest’s JPEG-based guess for the four drawn figures; the Koch’s-postulates figure carries eager="true" as the page’s first figure; a longdesc was added for all five diagram figures, walking each in reading order, because their labels and multi-panel narratives are not fully carried by the caption; the population-curve figure’s source alt claim that mortality is “nearly 100%” at $10^5$ agents is corrected against the drawn curve, which is still rising toward roughly 90% at that point and does not visibly level off until nearer $10^8$ — reported to the parent for the errata log — and the alt’s spelled-out “10 to the 5” / “10 to the 4” notation is set as Unicode superscripts throughout, per this run’s new house rule for a subscript or exponent inside an alt or longdesc; feature boxes rendered as callouts, with the Clinical Focus box’s “Jump to the next / Go back to the previous” links replaced by two Markdown links to Sections 15.3 and 15.1 (this run’s own routes, per the parent’s run-facts, even though neither page was yet on disk at authoring time); the case-in-point box’s closing question kept as an unanswered plain bullet, as the Clinical Focus box’s questions are; the cross-reference to “Pathogen Recognition and Phagocytosis” (m58880) left as plain italic text, since that module is not authored in this run; the four footnoted citations (the FDA Bad Bug Book, the Otto 2009 S. epidermidis review, the Davies 2003 biofilm review, and the TORCH “O” gloss) rendered as inline parentheticals at the sentence or table cell they support; the two step-sequence tables (Koch’s Postulates, Molecular Koch’s Postulates Applied to EHEC) and the two data tables (ID₅₀ for Selected Foodborne Diseases, TORCH Infections) transcribed as Markdown from the CNXML cells, checked against the PDF; the TORCH table is transcribed only, with no sortbins built for it, on the parent’s own offered alternative (run-facts C5 correction): the table’s only workable 4-bin, ≥1-item axis is the four single-disease letters (T, R, C, H) with the fifth, heterogeneous “O” (“other”) row of five diseases dropped, but that leaves every bin holding exactly one pathogen, which sorts nothing — it is a disguised 1:1 matching pair, not a categorization task — so the table is left as a transcribed comparison rather than shipped as a degenerate sortbins; the misspelled “Brucellis” is corrected in place to “Brucella” with no inline note, per this book’s one-word-typo rule, and reported for the errata log; the ID₅₀-comparison numeral is set as $1 \times 10^{6}$ and the LD₅₀ example values are set as $10^4$ in body prose and the figure caption, per the house numeric-exponent rule, while ID₅₀/LD₅₀ itself stays a Unicode subscript throughout; key terms compiled from the module’s 19 defined terms and the book’s Glossary appendix (all 19 taken from the glossary; none sentence-derived); all seven of the section’s body Check Your Understanding bullets are rendered as body self-checks at their note’s position, because each needs either several assembled module facts, an open list, or an inference the module does not state outright to answer honestly; of the source’s three unkeyed Critical Thinking questions, none is graded and all three stay self-checks with model answers and rubrics assembled from this section’s own text — the biofilm and molecular-Koch’s-postulates questions each need more than one module sentence, and the acupuncture question (rendered as a mediafigure, with an author-written neutral caption, followed by its self-check) is openly analogical; the source’s three Multiple Choice items keep their source options, order, and key, and its four Fill in the Blank items are rendered as textin, the LD₅₀ item keyed to the plain-ASCII answer LD50 (the grader already folds the Unicode subscript to the same value, so no accept entry is needed); seven filler items (four textin and three multiplechoice) are added across the five objective groups to meet the book’s three-item floor with at least one auto-graded item apiece, each built from a single sentence of this module and disclosed in the ledger; a checker’s page-wide leak read caught three: a summary-sentence cloze keyed “molecular Koch’s postulates” was replaced with a multiple choice on the EHEC/ETEC origin story, because the body self-check immediately above it prints that exact source-verbatim phrase in its own stem; the S. epidermidis filler’s stem was reworded to drop the word “opportunistic,” which is a co-group textin’s key; and the acupuncture self-check’s hint was reworded to drop the phrase “portal of entry,” which is a later textin’s key. Two figure alts are also corrected on that same read: the portal-of-entry and portal-of-exit diagrams both wrongly described the placenta, vagina, or anus as shared between the two figures when the artwork labels the placenta and vagina only on the woman and the anus only on the man (only the urethra, and only in the entry figure, is one label pointing to both). The Koch’s-postulates limitations self-check’s rubric originally merged the H. pylori (human carriers) and Brucella (cattle carriers) examples into one checkpoint; they are now two, since each traces to its own sentence and the two examples are about different hosts. No source exercise item is omitted.