Summary
Parasites are symbiotic organisms that live on or in a larger organism (host) in order to feed, develop, and/or multiply, causing harm to the host in the process. Parasitism is distinguished from commensalism, in which the symbiont benefits from the relationship without harming or benefiting the host in return, and mutualism, in which the symbiont and the host equally benefit from the relationship. A definitive host is a host in whom a parasite reaches its adult form and/or undergoes a sexual phase of development; an intermediate host is a host in whom a parasite passes one or more phases of its asexual development. Intermediate hosts often function as vectors that carry the parasite from one host to the next, but parasites themselves can also function as vectors for viruses, bacteria, and other parasites. Parasites can be classified by size as microparasites (unicellular) or macroparasites (multicellular); by the class of organism as protozoans, helminths, and arthropods; by dependency on a host for survival as obligate (require a definitive host and may go through one or more intermediate hosts to complete their life cycle) or facultative (do not rely on a host to complete their life cycle but may adopt parasitic activity); and by their relation to the host as endoparasites, which “infect” the host and live inside their body (mostly protozoa and helminths), and ectoparasites, which “infest” the host and attach to, burrow into, or temporarily feed off a host's integumentary system (mostly arthropod macroparasites). Arthropod infestations are clinically significant in their own right, but play a far greater role in the transmission of other pathogens (e.g., Plasmodium by mosquitoes and Borrelia by ticks).
Basics of parasitology
Symbiosis
- Definition: a long-term interaction between dissimilar species living together in biological association
- Depending on the degree of dependence and the advantages or disadvantages derived from the relationship, symbiosis can be classified as:
- Parasitism
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Commensalism
- A relationship between a symbiont (commensal) and its host, in which the commensal benefits from the relationship and the host derives neither benefit nor harm
- Some organisms can be commensal under certain conditions (e.g., as intestinal or skin microbiota in a healthy individual) but become pathogenic if these conditions change (e.g., host immune deficiency, colonization of other sites, changes in temperature or humidity).
- Example: E. Coli, which is part of the physiological intestinal flora, but can cause infections when it colonizes, for example, the urinary tract
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Mutualism
- A relationship between a symbiont and its host that benefits both parties
- Like commensals, mutualism can become pathogenic under certain conditions.
- Example: symbiosis between humans and intestinal Enterobacter agglomerans, in which the bacteria benefit from the nutrient supply and the human benefits from the menaquinones (vitamin K) that the bacteria produce
Classification of parasites [1][2]
Parasites can be categorized by location, dependence on host for survival, size, and type of organism.
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Location
- Ectoparasites: live and/or feed on the integumentary system of the host (e.g., ticks, mosquitoes)
- Endoparasites: live inside the host (e.g., helminths)
- Class of organism
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Host dependence
- Obligate parasites: cannot complete their life cycle without a host (e.g., Plasmodium, Toxoplasma)
- Facultative parasites: do not require a host to complete their life cycle and adopt parasitic behavior only if necessary or opportunity presents itself (e.g., Naegleria fowleri)
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Size
- Macroparasite: multicellular organisms
- Microparasite: unicellular organisms
Life cycle [1]
The life-cycle of obligate parasites can be divided into a parasitic stage, during which the organism lives in or feeds on the host, and a free-living stage, during which it lives outside the host and is not dependent on the host. Transmission generally occurs during the free-living stage.
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Microparasites (protozoa):
- The life cycles of microparasites vary greatly from species to species, but for most clinically relevant protozoans a simple division into two stages applies:
- Trophozoite
- Cyst
- The life cycles of microparasites vary greatly from species to species, but for most clinically relevant protozoans a simple division into two stages applies:
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Helminths
- Ovum
- Larva
- Adult
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Arthropods
- Ovum
- Larva
- Nymph/pupa
- Adult
- Some arthropods adopt parasitic behavior only during specific phases of development (e.g., adult female mosquitoes, who require a blood meal to produce eggs, or ticks, who require a blood meal to transition from one stage of development to the next)
Diagnostic and infective stage [3]
- For clinical purposes, the life cycle of endoparasites can be divided into two stages:
- Infective stage: the stage during which the parasite assumes a form in which it can invade its host.
- Diagnostic stage: the stage during which the parasite can be detected using the naked eye or laboratory methods. The diagnostic stage typically coincides with the stage during which the parasite leaves the host (via stool, urine, or sputum) to proliferate.
- Protozoans are typically infective while encysted and noninfective while in trophozoite form, while helminths are typically infective in the oval or larval form and noninfective as adults. However, the diagnostic stage varies greatly between the species of both classes.
Hosts and vectors
Host
A host is an organism that harbors a smaller parasitic, commensal, or mutualistic organism. The life cycle of any obligate parasite involves at least one host. The parasite uses a host for nutrition, protection, and/or conditions for reproduction.
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Reservoir host
- A host (e.g., dogs and cats for Leishmania) that can carry the pathogen indefinitely without any ill effects (i.e., asymptomatic/latent infection)
- Provides an ecological niche for the pathogen when active transmission to a definite or intermediate host is not possible
- Transport host: a host that mechanically transfers a parasite to another host (e.g., rodents that transport certain helminths to cats and dogs)
- Dead-end host: a host that can be affected by a parasite but cannot act as a vector (e.g., humans for the West Nile virus)
- Intermediate host: a host in which the parasite undergoes one or several asexual phases of its development (e.g., humans for Plasmodium)
- Definitive host: a host in which a parasite undergoes development into its adult form and, in some cases, undergoes the sexual phase of its development (e.g., humans for Wuchereria bancrofti)
Vector
Vectors are organisms that can carry a pathogen and transmit it to another organism. They can be intermediate or transport hosts.
Pathological effects of parasites
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Direct
- Mechanical destruction of tissue
- Production of substances (e.g., debris, feces) that can cause allergic reactions/diseases
- Metabolic/nutritional interference (e.g., tapeworms such as Diphyllobothrium latum can cause vitamin B12 deficiencies by interfering with the vitamin B12-intrinsic factor complex)
- Indirect: immune response to the parasite
Overview of clinically significant parasites
Overview [4] | |||
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Characteristics | Endoparasites | Ectoparasites | |
Microparasites (protozoa) | Macroparasites | ||
Helminths | Arthropods | ||
Pathogens/vectors |
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Life cycle |
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Blood changes |
Overview of protozoa
Definition
Protozoa are microscopic, single-celled nucleated organisms with complex life cycles, involving multiple stages and forms of development. Protozoa can cause a variety of gastrointestinal, visceral, hematological, neurological, genitourinary, and ocular diseases.
Classification
Clinically significant protozoa can be classified into four groups, depending on their means of movement.
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Mastigophora (flagellates)
- Means of motion: flagella
- Examples: Giardia, Trichomonas, Leishmania, Trypanosoma
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Sarcodina (amoeba)
- Means of motion: pseudopodia formed by cell protoplasm
- Examples: Entamoeba, Acanthamoeba, Naegleria
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Ciliophora (ciliates)
- Means of motion: cilia
- Example: Balantidium
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Sporozoa
- Means of motion: gliding motility
- Possess an apical complex that allows them to enter the host cells
- Examples: Plasmodium, Toxoplasma, Babesia
Intestinal protozoa
Overview [1][5]
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Population at risk
- Travelers to the endemic regions
- Individuals with close contact to persons with a recent history of living in endemic regions (e.g., migrant workers, recently immigrated individuals)
- Individuals in crowded conditions
- Individuals at potential risk of fecal-oral zoonotic transmission (e.g., via contaminated soil, sandboxes, or close contact with animals)
- Individuals living in crowded conditions (e.g., residential institutions, barracks, correctional facilities, orphanages)
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Transmission
- Fecal-oral (waterborne, foodborne, hand-to-mouth)
- Intestinal protozoa may also be transmitted sexually to the insertive partner during anal intercourse.
- Diagnostics
Overview of clinically significant intestinal protozoa | ||||
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Feature | Entamoeba histolytica | Giardia lamblia | Cryptosporidium parvum | Cystoisospora belli |
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Morphology |
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Disease |
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Features in special populations |
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Treatment |
Tissue and blood protozoa
All tissue and blood protozoa require a vector for transmission.
Sporozoa
Overview of clinically significant Sporozoa | |||||||
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Characteristics | Plasmodium spp. | Babesia spp. [6] | |||||
P. vivax | P. ovale | P. malariae | P. falciparum | ||||
Distribution |
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Factors affecting risk of infection and disease |
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Vector (definitive host) |
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Intermediate hosts |
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Morphology [1] | Trophozoite |
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Schizont/merozoite |
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Gametocytes |
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Persistence in liver |
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Disease | |||||||
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Fever spikes |
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Treatment |
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Hemoflagellates [1][5][7]
All hemoflagellates have similar morphological stages.
- Trypomastigote
- Amastigote: round or oval with a peripherally located nucleus
- Epimastigote: resembles trypomastigotes, but smaller and with undulating membrane only along half of one side of the body
- Promastigote: resembles epimastigote without the undulating membrane
Overview of clinically significant Hemoflagellates | ||||
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Characteristics | Trypanosoma brucei | Trypanosoma cruzi | Leishmania | |
Species and subspecies |
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Distribution |
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Vector (definitive host) |
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Intermediate hosts |
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Infective stage | ||||
Disease | ||||
Clinical features |
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Diagnostics |
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Treatment |
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Protozoa that cause ocular and neurological disease
Overview of protozoa affecting CNS and eyes | |||
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Feature | Naegleria fowleri [8] | Acanthamoeba spp. [9][10] | Toxoplasma gondii |
Distribution |
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Affected population |
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Transmission |
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Hosts |
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Morphology |
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Pathophysiology |
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Disease |
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Treatment |
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Urogenital protozoa
Trichomonas vaginalis
- Taxonomy: flagellate
- Life cycle: only has trophozoite stage (cannot live outside a host); trophozoite morphology is characterized by the following features:
- Other properties: motile, anaerobic
- Transmission: sexual
- Disease: trichomoniasis
- Diagnosis: detection of motile trophozoites of T. vaginalis on wet mount preparation
- Treatment: oral metronidazole or tinidazole
Antiprotozoal agents
Overview of antiprotozoal agents | |||||
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Indications | Mechanism of action [11][12] | CNS penetration | Adverse effects | ||
Pentamidine |
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Suramin |
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Nifurtimox |
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Melarsoprol |
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Eflornithine |
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Miltefosine |
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Metronidazole |
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Paromomycin |
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Diloxanide |
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Iodoquinol |
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Sodium stibogluconate |
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Overview of helminths
Introduction
Helminths, i.e., parasitic worms, are a group of macroparasites encompassing a variety of species that can infect their hosts in three different ways: ingestion of eggs or larvae (e.g., via contaminated food and water or fecal-oral route), direct penetration of the skin, and via the bite of vectors (e.g., certain species of flies and mosquitoes). Most helminth species colonize the gastrointestinal tract of their hosts, provoking symptoms such as abdominal pain, nausea, and diarrhea. The larvae of certain helminth species, such as those of the Ascaris and Ancylostoma genus, migrate from the intestines via the portal vein to the lungs, potentially causing asthma-like symptoms (e.g., dry cough, wheezing). Other species, such as Taenia solium, are capable of colonizing other human tissue, such as the brain or the liver, which can lead to life-threatening complications (e.g., neurocysticercosis). Diagnosis of helminth infection is made primarily via evidence of eosinophilia in the blood and direct detection of worms, eggs, or larvae in stool samples. Serum IgE levels are often elevated. Treatment consists of anthelmintic agents, such as albendazole or praziquantel. For helminth infection prevention, see “Food and water safety.”
Classification
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Platyhelminths
- Trematodes (e.g., Fasciola, Schistosoma)
- Cestodes (e.g., Taenia, Diphyllobothrium, Echinococcus)
- Acanthocephala
- Nematodes (e.g., Enterobius, Ascaris, Trichinella)
Trematodes (flukes)
Trematodes (flukes) are small, flat, oval worms with two suckers (one located at the mouth and the other ventrally) and a blind-ending gut. Most species are hermaphroditic, but some also form separate male and female adults.
Overview of trematode infections | ||||||
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Disease | Pathogen | Mode of transmission | Clinical features | Diagnosis | Treatment | |
Schistosomiasis |
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Clonorchiasis |
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Paragonimisias |
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Fascioliasis |
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Cestodes (tapeworms)
Cestodes (tapeworms) are long, flat, ribbon-like worms composed of numerous segments and a single scolex at the head with which they anchor themselves to the intestine. Since they do not have a digestive tract, all nutrients are absorbed through the tegument. Cestodes are hermaphroditic (they contain both male and female organs).
Overview of cestode infections | ||||||
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Disease | Pathogen | Mode of transmission | Clinical features | Diagnosis | Treatment | |
Taeniasis |
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Cysticercosis |
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Diphyllobothriasis |
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Echinococcosis |
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Hymenolepiasis |
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Nematodes (roundworms)
Nematodes (roundworms) are long, thin, unsegmented, tube-like worms with a longitudinal digestive tract opening at both ends. Adult worms form separate sexes, with the males usually being smaller than the females. Filarial Nematodes are thread-like nematodes. They are transmitted by arthropod vectors.
Nematodes (roundworms) | ||||||
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Disease | Pathogen | Mode of transmission | Clinical features | Diagnosis | Treatment | |
Ascariasis |
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Enterobiasis (pinworm) |
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Trichuriasis |
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Toxocariasis |
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Trichinellosis |
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Hookworm (ancylostomiasis, necatoriasis) |
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Strongyloidiasis |
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Filariasis | Loiasis |
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Onchocerciasis |
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Lymphatic filariasis |
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eating a Toxic TrEAT: Toxocara, Trichiniella, Enterobius, Ascaris, and Trichiuris are transmitted by ingestion.
SANd on your Shins, Ancles, and Neck: Strongyloides, Ancylostoma, and Necator penetrate the skin while walking on sand.
The OWL bites: Onchocera, Loa loa, and Wucheria are transmitted by bites.
Antihelminthic agents
Overview of antihelminthic agents | |||
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Drug | Indications | Mechanism of action | Adverse effects |
Bendazoles (e.g., albendazole, mebendazole) [18][19] |
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Pyrantel pamoate [20] |
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Praziquantel [21] |
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Ivermectin [22] |
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Diethylcarbamazine [23] |
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Most important antihelminthics (Pyrantel pamoate, Praziquantel, Ivermectin, Mebendazole, and Diethylcarbamazine:Pesky Parasites Inevitably Meet their Doom.
Arthropods
General characteristics
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Overview
- Arthropods are a group of ectoparasites that comprises arachnids and insects.
- Feed on the blood, skin cells and oils, and/or organic debris of their hosts
- Infestation is a disease in its own right, but the role of ectoparasites as vectors for other diseases is generally more clinically significant.
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Morphological features
- Common features include a chitin exoskeleton and segmented bodies with paired appendages (e.g., legs, wings, antennae)
- Life cycle involves several stages and may involve molting and metamorphosis.
- Most arthropods undergo a transformation from larva to an adult organism through several life stages characterized by distinct morphology.
Arachnids
Ticks [1]
Ticks play a clinically significant role as vectors for pathogenic bacteria. The only clinically significant direct effect of tick bites is tick paralysis, a rare response to neurotoxins in the tick's saliva characterized by tingling and numbness throughout the body. See “Lyme disease” for a full discussion of tick-borne diseases.
Overview of clinically significant tick species | ||||
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Species | Distribution | Associated pathogen | Vector-borne diseases | |
Ixodes spp. | I. scapularis |
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I. pacificus |
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I. ricinus |
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I. persculatus |
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Dermacentor spp. |
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Ornithodoros spp. |
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Amblyomma americanum |
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Mites [1]
Overview of clinically significant mite species | |||
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Species | Associated condition | Pathophysiology | |
Parasitic | Sarcoptes scabiei | ||
Nonparasitic | Dermatophagoides farinae (house dust mite) |
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Demodex spp. [24] |
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Trombicula spp. |
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Insects
Lice [1]
For more information on the various species of lice, see “Lice infestation.”
- Examples
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Life cycle
- Adult lice lay eggs (nits) at the base of the hair shaft.
- Hatched larvae undergo three nymph stages (N1–N3) before reaching adulthood after 3 to 4 weeks.
- Lice can be transmitted through direct contact with the host and their personal belongings (e.g., combs, clothes, bedsheets).
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Associated conditions
- Infestation causes pediculosis.
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Pediculus humanus corporis also serves as a vector for the following pathogens:
- Bartonella quintana: causes trench fever
- Rickettsia prowazekii: causes epidemic typhus
- Borrelia recurrentis: causes louse-borne relapsing fever
Fleas [1]
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Examples
- Xenopsylla cheopis
- Tunga penetrans (jigger flea)
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Life cycle
- Usually involves 4 stages of development: egg → larva → pupa → adult
- After adult fleas have found a host and have taken a blood meal, they mate and lay eggs
- Hatching of eggs takes 1–10 day
- Larvae feed on blood and flea feces (“flea dirt”) and will spin a cocoon within 5–20 days to enter the pupa stage
- After several days/weeks, adult fleas are ready to emerge from the cocoon following the detection of a host (e.g., via movement or body heat)
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Associated conditions
- A flea bite can cause pruritus and dermatitis and may be followed by secondary bacterial infections
- Can serve as vectors for the following pathogens:
- Rickettsia typhi, Rickettsia felis
- Yersinia pestis
- Hymenolepis nana
Flies [1]
Parasitic flies are clinically relevant mainly as vectors for pathogens, which they transmit during a blood meal.
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Main types of parasitic flies
- Tsetse flies (e.g., Glossina spp.)
- Sandflies (e.g., Phlebotomus spp.)
- Black flies (e.g., Simulium spp.)
- Deer flies (e.g., Chrysops spp.)
- Botflies (e.g., Dermatobia hominis)
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Associated conditions
- Flies serve as vectors for a range of pathogens (see the table below).
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Myiasis: infestation of human tissue by fly larvae
- Female fly lays eggs onto a hematophagous insect, which acts as intermediate host, or onto the host directly (e.g., into uncovered wounds). → The larvae hatch and penetrate the skin, digging tunnels into the host's subcutaneous tissue. → Once mature, the larvae drop from host to pupate.
- D. hominis is the only species of fly that routinely parasitizes humans, causing myiasis.
- However, other species of the family Oestridae (botflies) as well as the families Calliphoridae (blowflies) and Sarcophagidae (fleshflies) may infest humans if the opportunity presents itself (e.g., uncovered wounds).
- Obligatory myiasis is most common in species found in Central and South America and sub-Saharan Africa, where humans are most commonly affected.
- Treatment involves the removal of larvae and surgical debridement of the wound.
- Complications: Bacterial infection, potentially leading to sepsis, is common.
Overview of clinically significant fly species | |||
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Type | Distribution | Associated pathogen | Disease |
Tsetse fly |
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Sandfly |
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Black fly |
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Bot fly |
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Heteroptera
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Examples
- Triatoma spp. (kissing bug): found predominantly in Central and South America
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Cimex lectularius (bed bug)
- Populates facilities with a high guest turnaround (e.g., hostels, correctional facilities)
- Feeds on human blood
- Life cycle: simple metamorphosis
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Associated conditions
- Bed bug bites can cause a pruritic maculopapular rash.
- Triatoma serve as vectors for Trypanosoma cruzi, which causes Chagas disease
Ectoparasiticides
Overview of ectoparasiticides | ||||
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Drug | Indications | Mechanism of action | Application | Adverse effects |
Permethrin |
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Malathion |
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Dimeticone |
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