Template:Short description Template:About Template:Use dmy dates Template:Infobox medical condition (new) Toxocariasis is an illness of humans caused by the dog roundworm (Toxocara canis) and, less frequently, the cat roundworm (Toxocara cati).<ref name=Ye2014>https://academic.oup.com/ajcp/article/142/suppl_1/A104/1771175 Eosinophilic Pseudoleukemia Due to Toxocariasis in a 3-year-old Patient: Report of A Rare Case</ref> These are the most common intestinal roundworms of dogs, coyotes, wolves and foxes and domestic cats, respectively.<ref name=Wu2020>Template:Cite journal</ref> Humans are among the many "accidental" or paratenic hosts of these roundworms.<ref name=afip>Template:Cite book</ref>

While this zoonotic infection is usually asymptomatic, it may cause severe disease. There are three distinct syndromes of toxocariasis: covert toxocariasis is a relatively mild illness very similar to Löffler's syndrome. It is characterized by fever, eosinophilia, urticaria, enlarged lymph nodes, cough, bronchospasm, wheezing, abdominal pain, headaches, and/or hepatosplenomegaly. Visceral larva migrans (VLM) is a more severe form of the disease; signs and symptoms depend on the specific organ system(s) involved. Lung involvement may manifest as shortness of breath, interstitial lung disease, pleural effusion, and even respiratory failure. Brain involvement may manifest as meningitis, encephalitis, or epileptic seizures. Cardiac involvement may manifest as myocarditis. Ocular larva migrans (OLM) is the third syndrome, manifesting as uveitis, endophthalmitis, visual impairment or even blindness in the affected eye.<ref name=Huh>Template:EMedicine</ref>

Signs and symptomsEdit

Physiological reactions to Toxocara infection depend on the host's immune response and the parasitic load. Most cases of Toxocara infection are asymptomatic, especially in adults.<ref name=Huh/><ref name=CDC3>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref name=CDC2>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> When symptoms do occur, they are the result of migration of second-stage Toxocara larvae through the body.<ref name=Markell2006>Template:Cite book</ref>

Covert toxocariasisEdit

Covert toxocariasis is the least serious of the three syndromes and is believed to be due to chronic exposure.<ref name=Sariego2012>Template:Cite journal</ref> Signs and symptoms of covert toxocariasis are coughing, fever, abdominal pain, headaches, and changes in behavior and ability to sleep.<ref name=Holland2006>Template:Cite book</ref> Upon medical examination, wheezing, hepatomegaly, and lymphadenitis are often noted.<ref name=Huh/>

Visceral larva migransEdit

High parasitic loads or repeated infection can lead to visceral larva migrans (VLM).<ref name=CDC3/> VLM is primarily diagnosed in young children because they are more prone to exposure and ingestion of infective eggs.<ref name=Markell2006/> Toxocara infection commonly resolves itself within weeks, but chronic eosinophilia may result. In VLM, larvae migration incites inflammation of internal organs and sometimes the central nervous system. Symptoms depend on the organs affected. Children can present with pallor, fatigue, weight loss, anorexia, fever, headache, urticaria skin rash, cough, asthma, chest tightness, increased irritability, abdominal pain, nausea, and vomiting.<ref name=Markell2006/> Sometimes the subcutaneous migration tracks of the larvae can be seen.<ref name=Markell2006/> Children are commonly diagnosed with pneumonia, bronchospasms, chronic pulmonary inflammation, hypereosinophilia, hepatomegaly, hypergammaglobulinaemia (IgM, IgG, and IgE classes), leukocytosis, and elevated anti-A and anti-B isohaemagglutinins.<ref name=Markell2006/><ref name=Despommier2003>Template:Cite journal</ref><ref name=CDC3/><ref name=Holland2006/> Severe cases have occurred in people who are hypersensitive to allergens; in rare cases, epilepsy, inflammation of the heart, pleural effusion, respiratory failure, and death have resulted from VLM.<ref name=Huh/><ref name=Holland2006/>

File:PMID20029144 03 toxocariasis.png
Retinal granuloma in ocular toxocariasis

Ocular larva migransEdit

Ocular larva migrans (OLM) is rare compared with VLM.<ref name=Markell2006/><ref name=merckvetmanual>Template:Cite book</ref> A light Toxocara burden is thought to induce a low immune response, allowing a larva to enter the host's eye.<ref name=Holland2006/> Although there have been cases of concurrent OLM and VLM, these are extremely exceptional.<ref name=Holland2006/> OLM often occurs in just one eye and from a single larva migrating into and encysting within the orbit.<ref name=Markell2006/><ref name=OLM>Template:Cite book</ref> Loss of vision occurs over days or weeks.<ref name=Holland2006/> Other signs and symptoms are red eye, white pupil, fixed pupil, retinal fibrosis, retinal detachment, inflammation of the eye tissues, retinal granulomas, and strabismus.<ref name=Markell2006/><ref name=Holland2006/><ref name=OLM/><ref name=Stewart2005>Template:Cite journal</ref> Ocular granulomas resulting from OLM are frequently misdiagnosed as retinoblastomas.<ref name=Markell2006/> Toxocara damage in the eye is permanent and can result in blindness.<ref name=CDC3/><ref name=OLM/>

OtherEdit

Skin manifestations commonly include chronic urticaria, chronic pruritus, and miscellaneous forms of eczema.<ref>Template:Cite journal</ref> A case study published in 2008 supported the hypothesis that eosinophilic cellulitis may also be caused by infection with Toxocara: the adult patient presented with eosinophilic cellulitis, hepatosplenomegaly, anemia, and a positive ELISA for T. canis.<ref name=Bassukas2008>Template:Cite journal</ref>

CauseEdit

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TransmissionEdit

Toxocara is usually transmitted to humans through ingestion of infective eggs.<ref name=CDC3/><ref name=CDC1>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> T. canis can lay around 200,000 eggs per day.<ref name=Cheprasov/> These eggs are passed in cat or dog feces, but the defecation habits of dogs cause T. canis transmission to be more common than that of T. cati.<ref name=Markell2006/><ref name=CDC1/> Both Toxocara canis and Toxocara cati eggs require a several week incubation period in moist, humid weather outside a host before becoming infective, so fresh eggs cannot cause toxocariasis.<ref name=Markell2006/><ref name=CDC1/><ref name=Cheprasov/>

Many objects and surfaces can become contaminated with infectious Toxocara eggs. Flies that feed on feces can spread Toxocara eggs to surfaces or foods.<ref name=Holland2006/> Young children who put contaminated objects in their mouths or eat dirt (pica) are at risk of developing symptoms.<ref name=Markell2006/><ref name=Despommier2003/><ref name=Holland2006/> Humans can also contaminate foods by not washing their hands before eating.<ref name=CDC3/>

Humans are not the only accidental hosts of Toxocara.<ref name=Fan2015>Template:Cite journal</ref> Eating undercooked rabbit, chicken, or sheep can lead to infection; encysted larvae in the meat can become reactivated and migrate through a human host, causing toxocariasis.<ref name=Fan2015/> Special attention should be paid to thoroughly cooking giblets and liver to avoid transmission.<ref name=Markell2006/><ref name=Holland2006/>

Incubation periodEdit

The incubation period for Toxocara canis and cati eggs depends on temperature and humidity.<ref name=Markell2006/><ref name=CDC1/> T. canis females, specifically, are capable of producing up to 200,000 eggs a day that require 2–6 weeks minimum up to a couple months before full development into the infectious stage.<ref name=Azam2012>Template:Cite journal</ref> Under ideal summer conditions, eggs can mature to the infective stage after two weeks outside of a host.<ref name=Holland2006/><ref name=CDC1/> Provided sufficient oxygen and moisture availability, Toxocara eggs can remain infectious for years, as their resistant outer shell enables protection from most environmental threats.<ref name="auto789">Template:Cite journal</ref><ref name=Harris/><ref name=Soskolne>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> However, as identified in a case study presented within the journal of helminthology, the second stage of larvae development poses strict vulnerabilities to certain environmental elements. High temperatures and low moisture levels will quickly degrade the larvae during this developmental stage.<ref name="auto789"/> Template:Automatic taxobox

ReservoirEdit

File:2009-08-16 Puppy at Duke East 1.jpg
Puppies are the major source of environmental contamination with roundworm eggs

Dogs and foxes are the reservoir for Toxocara canis, but puppies and cubs pose the greatest risk of spreading the infection to humans.<ref name=CDC3/> Infection in most adult dogs is characterized by encysted second-stage larvae. However, these larvae can reactivate in pregnant females and cross the placental barrier to infect the pups. Vertical transmission can also occur through breast milk.<ref name=Markell2006/><ref name=CDC1/><ref name=CDC4>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Infectious mothers, and puppies under five weeks old, pass eggs in their feces.<ref name=CDC1/><ref name=CDC4/> Approximately 50% of puppies and 20% of adult dogs are infected with T. canis.<ref name=Markell2006/>

Cats are the reservoir for Toxocara cati.<ref name=CDC3/> As with T. canis, encysted second-stage larvae in pregnant or lactating cats reactivate. However, vertical transmission can only occur through breastfeeding.<ref name=CDC1/>

Flies can act as mechanical vectors for Toxocara, but most infections occur without a vector.<ref name=Holland2006/> Most incidents with Toxocariasis result from prokaryotic expression vectors and their transmission through direct physical contact with feces that results in the contraction of the illness.<ref name=Mohamad2009>Template:Cite journal</ref>

MorphologyEdit

Both species produce eggs that are brown and pitted.<ref name=merckvetmanual/><ref name=Harris/><ref name=Soskolne/> T. canis eggs measure 75-90 μm and are spherical, whereas the eggs of T. cati are 65-70 μm in diameter and oblong.<ref name=Markell2006/><ref name=Harris/><ref name=Soskolne/> Second-stage larvae hatch from these eggs and are approximately 0.5mm long and 0.02mm wide.<ref name=Huh/> Adults of both species have complete digestive systems and three lips, each composed of a dentigerous ridge.<ref name=Harris/><ref name=Soskolne/>

Adult T. canis are found only within dogs and foxes and the males are 4–6 cm in length, with a curved posterior end.<ref name=Despommier2003/><ref name=Harris/> The males each have spicules and one “tubular testis.”<ref name=Harris/> Females can be as long as 15 cm, with the vulva stretching one-third of their body length.<ref name=Harris/> The females do not curve at the posterior end.<ref name=Despommier2003/><ref name=Harris/>

T. cati adult females are approximately 10 cm long, while males are typically 6 cm or less. The T. cati adults only occur within cats, and male T. cati are curved at the posterior end.<ref name=Soskolne/>

Life cycleEdit

Cats, dogs, and foxes can become infected with Toxocara through the ingestion of eggs or by transmission of the larvae from a mother to her offspring.<ref name=CDC1/><ref name=CDC4/> Transmission to cats and dogs can also occur by ingestion of infected accidental hosts, such as earthworms, cockroaches, rodents, rabbits, chickens, or sheep.<ref name=Holland2006/><ref name=Soskolne/>

Eggs hatch as second-stage larvae in the intestines of the cat, dog, or fox host (for consistency, this article will assume that second-stage larvae emerge from Toxocara eggs, although there is debate as to whether larvae are truly in their second or third stage of development).<ref name=Despommier2003/><ref name=Holland2006/> Larvae enter the bloodstream and migrate to the lungs, where they are coughed up and swallowed. The larvae mature into adults within the small intestine of a cat, dog, or fox, where mating and egg-laying occurs.<ref name=Holland2006/><ref name=OLM/><ref name=CDC1/><ref name=Harris/> Eggs are passed in the feces and only become infective after three weeks outside of a host.<ref name=Becerril2019>Template:Cite book</ref> During this incubation period, molting from first to second (and possibly third) stage larva takes place within the egg.<ref name=Holland2006/><ref name=Soskolne/> In most adult dogs, cats and foxes, the full lifecycle does not occur, but instead second stage larvae encyst after a period of migration through the body. Reactivation of the larvae is common only in pregnant or lactating cats, dogs and foxes. The full lifecycle usually only occurs in these females and their offspring.<ref name=CDC1/><ref name=CDC4/>

Second-stage larvae will also hatch in the small intestine of an accidental host, such as a human, after ingestion of infective eggs.<ref name=Ahn2014>Template:Cite journal</ref> The larvae will then migrate through the organs and tissues of the accidental host, most commonly the lungs, liver, eyes, and brain.<ref name=Lee2014>Template:Cite journal</ref> Since L2 larvae cannot mature in accidental hosts, after this period of migration, Toxocara larvae will encyst as second stage larvae.<ref name=Markell2006/><ref name=CDC1/>

DiagnosisEdit

Finding Toxocara larvae within a patient is the only definitive diagnosis for toxocariasis; however, biopsies to look for second-stage larvae in humans are generally not very effective.<ref name=Holland2006/> PCR, ELISA, and serological testing are more commonly used to diagnose Toxocara infection.<ref name=Holland2006/> Serological tests are dependent on the number of larvae within the patient, and are unfortunately not very specific.<ref name=Holland2006/> ELISAs are much more reliable and currently have a 78% sensitivity and a 90% specificity.<ref name=Auweerter>Template:Cite bookTemplate:Dead link</ref> A 2007 study announced an ELISA specific to Toxocara canis, which will minimize false positives from cross reactions with similar roundworms and will help distinguish if a patient is infected with T. canis or T. cati.<ref name=pmid17374974>Template:Cite journal</ref> OLM is often diagnosed after a clinical examination.<ref name=Auweerter/> Granulomas can be found throughout the body and can be visualized using ultrasound, MRI, and CT technologies.<ref name=Holland2006/>

PreventionEdit

Actively involving veterinarians and pet owners is important for controlling the transmission of Toxocara from pets to humans. A group very actively involved in promoting a reduction of infections in dogs in the United States is the Companion Animal Parasite Council -- CAPC. Since pregnant or lactating dogs and cats and their offspring have the highest, active parasitic load, these animals should be placed on a deworming program.<ref name=CDC3/><ref name=Holland2006/><ref name=CDC1/> Pet feces should be picked up and disposed of or buried, as they may contain Toxocara eggs.<ref name=CDC3/> Practicing this measure in public areas, such as parks and beaches, is especially essential for decreasing transmission.<ref name=Markell2006/><ref name=Despommier2003/> Up to 20% of soil samples of U.S. playgrounds have found roundworm eggs.<ref name=Cheprasov>Template:Cite journal</ref> Also, sandboxes should be covered when not in use to prevent cats from using them as litter boxes. Hand washing before eating and after playing with pets, as well as after handling dirt will reduce the chances of ingesting Toxocara eggs.<ref name=Markell2006/><ref name=CDC3/><ref name=Holland2006/> Washing all fruits and vegetables, keeping pets out of gardens, and thoroughly cooking meats can also prevent transmission.<ref name=Holland2006/> Finally, teaching children not to place nonfood items, especially dirt, in their mouths will drastically reduce the chances of infection.<ref name=CDC3/>

Toxocariasis has been named one of the neglected diseases of US poverty, because of its prevalence in Appalachia, the southern U.S., inner city settings, and minority populations.<ref name=Hotez>Template:Cite journal</ref>

There is currently no vaccine available or under development.<ref name=CDC2/><ref name=Hotez/> The mitochondrial genomes of both T. cati and T. canis have been sequenced in 2008, which could lead to breakthroughs in treatment and prevention.<ref name=pmid18482460>Template:Cite journal</ref>

TreatmentEdit

Toxocariasis will often resolve itself because the Toxocara larvae cannot mature within human hosts.<ref name=Markell2006/> Corticosteroids are prescribed in severe cases of VLM or if the patient is diagnosed with OLM. Either albendazole (preferred) or mebendazole (“second line therapy”) may be prescribed.<ref name=Markell2006/><ref name=OLM/><ref name=Auweerter/> Granulomas can be surgically removed, or laser photocoagulation and cryoretinopexy can be used to destroy ocular granulomas.<ref name=Holland2006/><ref name=OLM/><ref name=Auweerter/><ref name=Werner1999>Template:Cite journal</ref>

Visceral toxocariasis in humans can be treated with antiparasitic drugs such as albendazole or mebendazole, tiabendazole or diethylcarbamazine usually in combination with anti-inflammatory medications. Steroids have been utilized with some positive results. Anti-helminthic therapy is reserved for severe infections (lungs, brain) because therapy may induce, due to massive larval killing, a strong inflammatory response. Ocular toxocariasis is more difficult to treat and usually consists of measures to prevent progressive damage to the eye.<ref name=CDC2013>"Toxocariasis." Parasites. Centers for Disease Control and Prevention, 10 Jan. 2013. {{#invoke:citation/CS1|citation |CitationClass=web }}. 22 Apr. 2014</ref>

EpidemiologyEdit

Humans are accidental hosts of Toxocara, yet toxocariasis is seen throughout the world. Most cases of toxocariasis are seen in people under the age of twenty.<ref name=CDC2/> Seroprevalence is higher in developing countries but can be considerable in first world countries, as well.<ref name=Holland2006/> In Bali, St. Lucia, Nepal, and other countries, seroprevalence is over fifty percent.<ref name=Holland2006/> Previous to 2007, the U.S. seroprevalence was thought to be around 5% in children.<ref name=Markell2006/> However, Won et al. discovered that U.S. seroprevalence is 14% for the population at large.<ref name=CDC2/> In many countries, toxocariasis is considered very rare. Approximately 10,000 clinical cases are seen a year in the U.S., with ten percent being OLM.<ref name=CDC2/><ref name=OLM/> Permanent vision loss occurs in 700 of these cases.<ref name=OLM/>

Young children are at the greatest risk of infection because they play outside and tend to place contaminated objects and dirt in their mouths.<ref name=Markell2006/><ref name=Despommier2003/><ref name=Holland2006/> Dog ownership is another known risk factor for transmission.<ref name=Despommier2003/> There is also a significant correlation between high Toxocara antibody titers and epilepsy in children.<ref name=Markell2006/><ref name=Luna2018>Template:Cite journal</ref>

Parasitic loads as high as 300 larvae in a single gram of liver have been noted in humans.<ref name=Holland2006/> The "excretory-secretory antigens of larvae ... released from their outer epicuticle coat [and] ... readily sloughed off when bound by specific antibodies" incite the host's immune response.<ref name=Huh/> The tipping point between the development of VLM and OLM is believed to be between 100 and 200 larvae.<ref name=Holland2006/> The lighter infection in OLM is believed to stimulate a lower immune response and allow for the migration of a larva into the eye. Larvae are thought to enter the eye through the optic nerve, central retinal artery, short posterior ciliary arteries, soft tissues, or cerebrospinal fluid.<ref name=Holland2006/><ref name=OLM/> Ocular granulomas that form around a larva typically are peripheral in the retina or optic disc.<ref name=OLM/>

Visceral larva migrans seems to affect children aged 1–4 more often while Ocular larva migrans more frequently affects children aged 7–8. Between 4.6% and 23% of US children have been infected with the dog roundworm egg. This number is much higher in other parts of the world, in tropical countries there is seroprevalence of up to 80–90%, such as Colombia, where up to 81% of children have been infected, or Honduras where seroprevalence among school-age children was reported to be 88%.<ref name=Cheprasov/><ref name=Luna2018/><ref name=Hernandez>Template:Cite journal</ref> In the western part of the world, seroprevalence is lower, around 35–42%.<ref name=Luna2018/>

HistoryEdit

Werner described a parasitic nematode in dogs in 1782 which he named Ascaris canis. Johnston determined that what Werner had described was actually a member of the genus Toxocara established by Stiles in 1905. Fülleborn speculated that T canis larvae might cause granulomatous nodules in humans. In 1947 Perlingiero and Gyorgy described the first case of what was probably toxocariasis. Their patient was a 2-year-old boy from Florida who had classical symptoms and eosinophilic necrotizing granulomas.<ref name=afip/> In 1950, Campbell-Wilder was the first to describe toxocariasis in humans; she published a paper describing ocular granulomas in patients with endophthalmitis, Coat's disease, or pseudoglioma. Two years later, Beaver et al. published the presence of Toxocara larvae in granulomas removed from patients with symptoms similar to those in Wilder's patients.<ref name=Holland2006/><ref name=Despommier2003/> The dangers of toxocariasis were first raised in Britain in the 1970s, leading to a public health scare.<ref name=Pemberton>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Other animalsEdit

CatsEdit

Some treatments for infection with Toxocara cati include drugs designed to cause the adult worms to become partially anaesthetized and detach from the intestinal lining, allowing them to be excreted live in the feces. Such medications include piperazine and pyrantel. These are frequently combined with the drug praziquantel which appears to cause the worm to lose its resistance to being digested by the host animal. Other effective treatments include ivermectin, milbemycin, and selamectin.<ref name=fcp>Template:Cite book</ref> Dichlorvos has also been proven to be effective as a poison, though moves to ban it over concerns about its toxicity have made it unavailable in some areas.Template:Citation needed

Treatment for wild felids, however, is difficult for this parasite, as detection is the best way to find which individuals have the parasite. This can be difficult as infected species are hard to detect. Once detected, the infected individuals would have to be removed from the population, to lower the risk of continual exposure to the parasites. A primary method that has been used to lower the amount of infection is removal through hunting. Removal can also occur through landowners, as Dare and Watkins (2012) discovered through their research on cougars. Both hunters and landowners can provide samples that can be used to detect the presence of feline roundworm in the area, as well as help remove it from the population. This method is more practical than administering medications to wild populations, as wild animals, as mentioned before, are harder to find in order to administer medicinal care.Template:Citation needed

Medicinal care, however, is also another method used in roundworm studies; such as the experiment on managing raccoon roundworm done by Smyser et al. (2013) in which they implemented medical baiting. However, medicine is often expensive and the success of the baiting depends on whether the infected individuals consume the bait. Additionally, it can be costly (in time and resources) to check on baited areas. Removal by hunting allows agencies to reduce costs and gives agencies a more improved chance of removing infected individuals.Template:Citation needed

ReferencesEdit

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External linksEdit

Template:Medical resources Template:Helminthiases Template:Taxonbar