A human pathogen is a pathogen (microbe or microorganism such as a virus, bacterium, prion, or fungus) that causes disease in humans.
The spread of human pathogens can be described using the chain of infection. The human physiological defense against common pathogens (such as Pneumocystis) is mainly the responsibility of the immune system with help by some of the body's normal microbiota. However, if the immune system or "good" microbiota are damaged in any way (such as by chemotherapy, human immunodeficiency virus (HIV), or antibiotics being taken to kill other pathogens), pathogenic bacteria that were being held at bay can proliferate and cause harm to the host. Such cases are called opportunistic infections.
Some pathogens (such as the bacterium Yersinia pestis, which may have caused the Black Plague, the Variola virus, and the malaria protozoa) have been responsible for massive numbers of casualties and have had numerous effects on affected groups. Of particular note in modern times is HIV, which is known to have infected several million humans globally, along with the influenza virus. Today, while many medical advances have been made to safeguard against infection by pathogens, through the use of vaccination, antibiotics, and fungicide, pathogens continue to threaten human life. Social advances such as food safety, hygiene, and water treatment have reduced the threat from some pathogens.
Types
Viral
Pathogenic viruses are mainly those of the families of: Adenoviridae, Picornaviridae, Herpesviridae, Hepadnaviridae, Coronaviridae, Flaviviridae, Retroviridae, Orthomyxoviridae, Paramyxoviridae, Papovaviridae, Polyomavirus, Poxviridae, Rhabdoviridae, and Togaviridae. Some notable pathogenic viruses cause smallpox, influenza, mumps, measles, chickenpox, ebola, and rubella. Viruses typically range between 20 and 300 nanometers in length. [1]
This type of pathogen is not cellular; instead a protein shell (the capsid) encases either RNA (Ribonucleic acid) or DNA (Deoxyribonucleic acid). Pathogenic viruses infiltrate host cells and manipulate the organelles within the cell such as the Ribosomes, Golgi Apparatus, and Endoplasmic Reticulum in order to multiply which commonly results in the death of the host cell via cellular decay. All the viruses that were contained within the lipid bilayer of the cell membrane are then released into the intercellular matrix to infect neighboring cells to continue the viral life cycle.
White blood cells surround and consume the virus using a mechanism known as phagocytosis[2] (a type of endocytosis)[3] within the extracellular matrix to reduce and fight the infection. The components within the white blood cell are responsible for destroying the virus and recycling its components for the body to use.[4]
Bacterial

Although the vast majority of bacteria are harmless or beneficial to one's body, a few pathogenic bacteria can cause infectious diseases. The most common bacterial disease is tuberculosis,[citation needed] caused by the bacterium Mycobacterium tuberculosis, which affects about 2 million people mostly in sub-Saharan Africa. Pathogenic bacteria contribute to other globally important diseases, such as pneumonia, which can be caused by bacteria such as Streptococcus and Pseudomonas, and foodborne illnesses, which can be caused by bacteria such as Shigella, Campylobacter, and Salmonella. Pathogenic bacteria also cause infections such as tetanus, typhoid fever, diphtheria, syphilis, and Hansen's disease. They typically range between 1 and 5 micrometers in length.[5]
Fungal
Fungi are a eukaryotic kingdom of microbes that are usually saprophytes, but can cause diseases in humans. Life-threatening fungal infections in humans most often occur in immunocompromised patients or vulnerable people with a weakened immune system, although fungi are common problems in the immunocompetent population as the causative agents of skin, nail, or yeast infections. Most antibiotics that function on bacterial pathogens cannot be used to treat fungal infections because fungi and their hosts both have eukaryotic cells. Most clinical fungicides belong to the azole group. The typical fungal spore size is 1-40 micrometers in length.[6]
Other parasites
Protozoans are single-celled eukaryotes that feed on microorganisms and organic tissues. Considered as "one-celled animal" as they have animal like behaviors such as motility, predation, and a lack of a cell wall. Many protozoan pathogens are considered human parasites as they cause a variety of diseases such as: malaria, amoebiasis, babesiosis, giardiasis, toxoplasmosis, cryptosporidiosis, trichomoniasis, Chagas disease, leishmaniasis, African trypanosomiasis (sleeping sickness), Acanthamoeba keratitis, and primary amoebic meningoencephalitis (naegleriasis).

Parasitic worms (Helminths) are macroparasites that can be seen by the naked eye. Worms live and feed in their living host, receiving nourishment and shelter while affecting the host's way of digesting nutrients. They also manipulate the host's immune system by secreting immunomodulatory products[7] which allows them to live in their host for years. Many parasitic worms are more commonly intestinal that are soil-transmitted and infect the digestive tract; other parasitic worms are found in the host's blood vessels. Parasitic worms living in the host can cause weakness and even lead to many diseases. Parasitic worms can cause many diseases to both humans and animals. Helminthiasis (worm infection), Ascariasis, and enterobiasis (pinworm infection) are few that are caused by various parasitic worms.[citation needed]
Prionic

Prions are misfolded proteins that are transmissible and can influence abnormal folding of normal proteins in the brain. They do not contain any DNA or RNA and cannot replicate other than to convert already existing normal proteins to the misfolded state. These abnormally folded proteins are found characteristically in many neurodegenerative diseases as they aggregate the central nervous system and create plaques that damages the tissue structure. This essentially creates "holes" in the tissue. It has been found that prions transmit three ways: obtained, familial, and sporadic. It has also been found that plants play the role of vector for prions. There are eight different diseases that affect mammals that are caused by prions such as scrapie, bovine spongiform encephalopathy (mad cow disease) and Feline spongiform encephalopathy (FSE). There are also ten diseases that affect humans such as, Creutzfeldt–Jakob disease (CJD).[8] and Fatal familial insomnia (FFI).
Animal pathogens
Animal pathogens are disease-causing agents of wild and domestic animal species, at times including humans.[9]
Virulence
Virulence (the tendency of a pathogen to cause damage to a host's fitness) evolves when that pathogen can spread from a diseased host, despite that host being very debilitated. An example is the malaria parasite, which can spread from a person near death, by hitching a ride to a healthy person on a mosquito that has bitten the diseased person. This is called horizontal transmission in contrast to vertical transmission, which tends to evolve symbiosis (after a period of high morbidity and mortality in the population) by linking the pathogen's evolutionary success to the evolutionary success of the host organism.
Evolutionary medicine has found that under horizontal transmission, the host population might never develop tolerance to the pathogen.
Transmission
Chain of Infection
The chain of infection is a method of describing how a pathogen can spread and infect hosts in 6 stages. It starts with the pathogen, then describes the reservoir where that specific pathogen can multiply. The next step is the portal of exit, alluding to the method the pathogen leaves its reservoir. The mode of transport is how the pathogen is transmitted, which can occur through many different routes, including airborne, direct or indirect contact, sexual contact, through blood, breast milk, or other body fluids, and through the fecal-oral route. One example of direct contact is with contaminated bodily secretions, such as mucus. An indirect contact could be with a contaminated inanimate surface.[10] Food and water can also become contaminated from the release of untreated sewage into a drinking water supply or onto cropland, with the result that people who eat or drink contaminated sources become infected. In developing countries, most sewage is discharged into the environment or on cropland; even in developed countries, some locations have periodic system failures that result in sanitary sewer overflows.[11] The last two phases of the chain are the portal of entry that the pathogen takes and the susceptible host, also known as a susceptible individual, which is a person at risk of developing disease.[12] An example of a reservoir in humans is the skin or gastrointestinal tract, as bacteria can normally be found there. Animals can also be reservoirs for many human pathogens. A portal of entry or exit for a pathogen could be through the mouth or nose. Coughing or sneezing, for instance, would allow a microorganism to exit the human body.[13] Prions differ from other human pathogens, as they lack nucleic acids, like DNA or RNA, and are not transmitted through the same mechanisms. Often, they cause sporadic diseases, as they can arise due to an incorrectly folded protein.[14]
| Human Pathogen | Type of Pathogen | Reservoir | Portal of Exit | Mode of Transport | Portal of Entry | Susceptible Host |
|---|---|---|---|---|---|---|
| SARS-CoV-2 | Virus | Bats | Nose, mouth, eyes | Airborne (coughing, sneezing), contaminated fomites | Nose, mouth, eyes | Humans[15][16][17] |
| Plasmodium falciparum (Malaria) | Parasite | Humans | Bloodstream | Mosquito bite, contaminated needle or syringe, blood transfusion | Bloodstream | Humans[18][19] |
| Mycobacterium tuberculosis (Tuberculosis) | Bacteria | Humans | Nose, mouth | Airborne (coughing, sneezing) | Nose, mouth | Humans[20] |
| Trichophyton rubrum (Ringworm) | Fungi | Humans, animals | Skin, scalp, nails | Direct skin contact, contaminated animals, contaminated fomites | Skin, scalp, nails | Humans, animals[21] |
Immune System Response
After a pathogen is introduced into a human body, it is recognized by a human's immune system as foreign, triggering a response in the form of an innate and adaptive mechanisms. The innate response is a general non-specific defense that recognizes common structural features present in many different microorganisms. However, it can still vary between pathogens. For instance, causing inflammation is a common innate response to decrease replication of a virus, but SARS-CoV-2 has evolved a mechanism to prevent this response.[22] In contrast, the adaptive response is more specific, involving T Cells and B Cells.
Often times, human pathogens rely on their host for nutrients to survive and multiply. Actions of the immune system can prevent the pathogen from receiving required nutrients, however, which allows humans to fight off infection.[23]
Examples
- Bacillus anthracis — the causative agent of anthrax in humans and animals
- Clostridium botulinum — releases the most powerful neurotoxin leading to death from botulism
- Mycobacterium tuberculosis — the causative agent of most cases of tuberculosis
- Mycobacterium leprae — the bacterium that causes leprosy (Hansen's disease)
- Yersinia pestis — pneumonic, septicemic, and the notorious bubonic plagues (Black Death)
- Rickettsia prowazekii — the etiologic agent of typhus fever
- Bartonella spp.
- Spanish influenza virus
- Entamoeba histolytica virus amoeba or amoebiasis
See also
- Cancer bacteria
- Emerging Pathogens Institute
- Oncovirus
- List of clinically important bacteria
- Lists of diseases
- List of human diseases associated with infectious pathogens
- List of infectious diseases
- List of parasites of humans
References
- ^ "Questions and Answers about Ebola Hemorrhagic Fever". U.S. Centers for Disease Control and Prevention. Archived from the original on 2009-05-06. Retrieved 2017-09-09.
- ^ Nainu, Firzan; Shiratsuchi, Akiko; Nakanishi, Yoshinobu (2017-09-28). "Induction of Apoptosis and Subsequent Phagocytosis of Virus-Infected Cells As an Antiviral Mechanism". Frontiers in Immunology. 8 (1220): 954. doi:10.3389/fimmu.2017.01220. PMC 5624992. PMID 29033939.
- ^ Alberts, B.; Johnson, A.; Lewis, J. (2002). SMolecular Biology of the Cell. 4th edition. New York, USA: Garland Science. ISBN 978-0-8153-3218-3.
- ^ Melloy, Patricia G. (2022-07-25). Viruses and Society. Boca Raton: CRC Press. doi:10.1201/9781003172260. ISBN 978-1-003-17226-0.
- ^ Niedzwiecki, Brigitte; Pepper, Julie (2022-11-20). Kinn's The Medical Assistant - E-Book: Kinn's The Medical Assistant - E-Book. Elsevier Health Sciences. p. 1227. ISBN 978-0-323-88301-6.
- ^ Köhler JR, Casadevall A, Perfect J (November 2014). "The spectrum of fungi that infects humans". Cold Spring Harbor Perspectives in Medicine. 5 (1) a019273. doi:10.1101/cshperspect.a019273. PMC 4292074. PMID 25367975.
- ^ Jirillo E, Magrone T, Miragliotta G, eds. (2014). Immune Response to Parasitic Infections. Vol. 2. Bentham Science Publishers. doi:10.2174/97816080598501140201. ISBN 978-1-60805-989-8. S2CID 78737083.
- ^ Prusiner SB (January 1995). "The prion diseases". Scientific American. 272 (1): 48–51, 54–7. Bibcode:1995SciAm.272a..48P. doi:10.1038/scientificamerican0195-48. PMID 7824915. Archived from the original on 25 January 2012.
- ^ Hickling GJ (2011). "Pathogens, animal". In Simberloff D, Rejmánek M (eds.). Encyclopedia of biological invasions. Berkeley: University of California Press. ISBN 978-0-520-26421-2.
Animal pathogens are disease-causing agents of wild and domestic animal species, at times including humans. In the context of invasion biology, the term usually ..
- ^ Rodger, Daniel, ed. (2022). Fundamentals of operating department practice. Cambridge medicine (Second ed.). Cambridge: Cambridge University Press. doi:10.1017/9781108876902. ISBN 978-1-108-87690-2.
- ^ Hrudey, Steve E.; Hrudey, Elizabeth J.; Pollard, Simon J. T. (2006-12-01). "Risk management for assuring safe drinking water". Environment International. 32 (8): 948–957. Bibcode:2006EnInt..32..948H. doi:10.1016/j.envint.2006.06.004. hdl:1826/1519. ISSN 0160-4120. PMID 16839605.
- ^ "Chain of Infection Components". www.cdc.gov. 2023-05-22. Retrieved 2026-09-23.
- ^ Rodger, Daniel, ed. (2022). Fundamentals of operating department practice. Cambridge medicine (Second ed.). Cambridge: Cambridge University Press. doi:10.1017/9781108876902. ISBN 978-1-108-87690-2.
- ^ Zerr, Inga; Ladogana, Anna; Mead, Simon; Hermann, Peter; Forloni, Gianluigi; Appleby, Brian S. (2024-02-29). "Creutzfeldt–Jakob disease and other prion diseases". Nature Reviews Disease Primers. 10 (1). Nature Publishing Group: 14. doi:10.1038/s41572-024-00497-y. ISSN 2056-676X. PMID 38424082.
- ^ Falahi, S.; Kenarkoohi, A. (November 2020). "Transmission routes for SARS-CoV-2 infection: review of evidence". New Microbes and New Infections. 38 100778. doi:10.1016/j.nmni.2020.100778. PMC 7537649. PMID 33042554.
- ^ Oh, Myoung-don (2021-02-05). "Airborne transmission of coronavirus disease 2019: a clinician's perspective". The Korean Journal of Internal Medicine. 36 (2). Korean Association of Internal Medicine: 467–470. doi:10.3904/kjim.2020.461. ISSN 1226-3303. PMC 7969067. PMID 32872727.
- ^ Valencak, Teresa G.; Csiszar, Anna; Szalai, Gabor; Podlutsky, Andrej; Tarantini, Stefano; Fazekas-Pongor, Vince; Papp, Magor; Ungvari, Zoltan (October 2021). "Animal reservoirs of SARS-CoV-2: calculable COVID-19 risk for older adults from animal to human transmission". GeroScience. 43 (5): 2305–2320. doi:10.1007/s11357-021-00444-9. ISSN 2509-2715. PMC 8404404. PMID 34460063.
- ^ Ouédraogo, D. Florence; Kühne, Vera; Toussaint, Rouamba; Guetens, Pieter; Millogo, Aida; Moreno-Murillo, Ana; Drissi-El Boukili, Yasmina; Chopo-Pizarro, Ana; Ràfols, Neus (2026-01-11), Dynamics of Plasmodium falciparum asymptomatic asexual and sexual stages across transmission seasons in a rural and high-transmission setting in Burkina Faso: a two-year longitudinal cohort study with cross-sectional surveys, doi:10.64898/2026.01.09.26343521, retrieved 2026-09-25
- ^ CDC (2026-09-03). "How Malaria Spreads". Malaria. Retrieved 2026-09-25.
- ^ CDC (2025-01-06). "Clinical Overview of Tuberculosis". Tuberculosis (TB). Retrieved 2026-09-30.
- ^ CDC (2026-02-09). "Ringworm Basics". Ringworm. Retrieved 2026-09-30.
- ^ Diamond, Michael S.; Kanneganti, Thirumala-Devi (February 2022). "Innate immunity: the first line of defense against SARS-CoV-2". Nature Immunology. 23 (2). Nature Publishing Group: 165–176. doi:10.1038/s41590-021-01091-0. ISSN 1529-2916. PMC 8935980. PMID 35105981.
- ^ Murdoch, Caitlin C.; Skaar, Eric P. (November 2022). "Nutritional immunity: the battle for nutrient metals at the host–pathogen interface". Nature Reviews Microbiology. 20 (11). Nature Publishing Group: 657–670. doi:10.1038/s41579-022-00745-6. ISSN 1740-1534. PMC 9153222. PMID 35641670.