Fasciola hepatica

Last updated

Fasciola hepatica
Fasciola hepatica.JPG
Adult Fasciola hepatica specimen
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Platyhelminthes
Class: Trematoda
Order: Plagiorchiida
Family: Fasciolidae
Genus: Fasciola
Species:
F. hepatica
Binomial name
Fasciola hepatica

Fasciola hepatica, also known as the common liver fluke or sheep liver fluke, is a parasitic trematode (fluke or flatworm, a type of helminth) of the class Trematoda, phylum Platyhelminthes. It infects the livers of various mammals, including humans, and is transmitted by sheep and cattle to humans all over the world. The disease caused by the fluke is called fasciolosis or fascioliasis, which is a type of helminthiasis and has been classified as a neglected tropical disease. [2] Fasciolosis is currently classified as a plant/food-borne trematode infection, often acquired through eating the parasite's metacercariae encysted on plants. [3] F. hepatica, which is distributed worldwide, has been known as an important parasite of sheep and cattle for decades and causes significant economic losses in these livestock species, up to £23 million in the UK alone. [4] Because of its relatively large size and economic importance, it has been the subject of many scientific investigations and may be the best-known of any trematode species. The closest relative of Fasciola hepatica is F. gigantica . These two flukes are sister species; they share many morphological features and can mate with each other. [5]

Contents

Life cycle

Galba truncatula, an amphibious freshwater lymnaeid snail that serves as the main intermediate host of Fasciola hepatica in Europe Galba truncatula shell.png
Galba truncatula , an amphibious freshwater lymnaeid snail that serves as the main intermediate host of Fasciola hepatica in Europe
The lifecycle of Fasciola hepatica Fasciola LifeCycle 2013.png
The lifecycle of Fasciola hepatica

Fasciola hepatica occurs in the liver of a definitive host and its lifecycle is indirect. Definitive hosts of the fluke are cattle, sheep, and buffaloes. Wild ruminants and other mammals, including humans, can act as definitive hosts as well. [6] The life cycle of F. hepatica goes through the intermediate host and several environmental larval stages. [7] Intermediate hosts of F. hepatica are air-breathing freshwater snails from the family Lymnaeidae. Although several lymnaeid species susceptible to F. hepatica have been described, the parasite develops only in one or two major species on each continent. Galba truncatula is the main snail host in Europe, partly in Asia, Africa, and South America. Lymnaea viator , L. neotropica , Pseudosuccinea columella , and L. cubensis are most common intermediate hosts in Central and South America. [5] [8] [6] Several other lymnaeid snails may be naturally or experimentally infected with F. hepatica, but their role in transmission of the fluke is low. [5] The list of lymnaeid snails that may serve as natural or experimental intermediate hosts of F. hepatica include: [9]

The metacercariae are released from the freshwater snail as cercariae, and form cysts on various surfaces including aquatic vegetation. The mammalian host then eats this vegetation and can become infected. Humans can often acquire these infections through drinking contaminated water and eating freshwater plants such as watercress. Inside the duodenum of the mammalian host, the metacercariae are released from within their cysts. From the duodenum, they burrow through the lining of the intestine and into the peritoneal cavity. They then migrate through the intestines and liver, and into the bile ducts. Inside the bile ducts, they develop into an adult fluke. [10] In humans, the time taken for F. hepatica to mature from metacercariae into an adult fluke is roughly 3 to 4 months. The adult flukes can then produce up to 25,000 eggs per fluke per day. [11] These eggs are passed out via stools and into freshwater. Once in freshwater, the eggs become embryonated, allowing them to hatch as miracidia, which then find a suitable intermediate snail host of the Lymnaeidae family. Inside this snail, the miracidia develop into sporocysts, then to rediae, then to cercariae. The cercariae are released from the snail to form metacercariae and the life cycle begins again. [10]

Morphology and anatomy

Fasciola hepatica is one of the largest flukes of the world, reaching a length of 30 mm and a width of 13 mm ( Fasciola gigantica , though, is even bigger and can reach up to 75 mm). [12] It is leaf-shaped, pointed at the back (posteriorly), and wide in the front (anteriorly). The oral sucker is small but powerful and is located at the end of a cone-shape projection at the anterior end. The acetabulum is a larger sucker than the oral sucker and is located at the anterior end. [10]

A simple diagram to show the difference between the teguments of free-living and parasitic flatworms: a. shows the syncytial epithelial tegument found in parasitic flatworms, such as F. hepatica. b. shows the multicellular, nonsyncytial, epithelia, found in nonparasitic, free-living flatworms. Syncytial epithelia.jpg
A simple diagram to show the difference between the teguments of free-living and parasitic flatworms: a. shows the syncytial epithelial tegument found in parasitic flatworms, such as F. hepatica. b. shows the multicellular, nonsyncytial, epithelia, found in nonparasitic, free-living flatworms.

Tegument

The outer surface of the fluke is formed by the tegument. This is composed of scleroprotein, and its primary function is to protect the fluke from the destructive digestive system of the host. [13] Its also used for renewal of the surface plasma membrane and the active uptake of nutrients, and the uptake of some compounds (e.g. taurine) make flukes even more resistant to be killed by the digestive system of host. [14] [15] On the surface of the tegument are also small spines. Initially, these spines are single-pointed, then, just prior to the fluke entering the bile ducts, they become multipointed. At the anterior end of the fluke, the spines have between 10 and 15 points, whereas at the posterior end, they have up to 30 points. [16] The tegument is a syncytial epithelium. This means it is made from the fusion of many cells, each containing one nucleus, to produce a multinucleated cell membrane. In the case of F. hepatica, no nuclei are in the outer cytoplasm between the basal and apical membranes. Thus, this region is referred to as anucleate. Instead, the nuclei are found in the cell bodies, also known as tegumental cells, these connect to the outer cytoplasm via thin cytoplasmic strands. The tegumental cells contain the usual cytoplasmic organelles (mitochondria, Golgi bodies, and endoplasmic reticulum). [17] The tegument plays a key role in the fluke's infection of the host. Studies have shown that certain parts of the tegument (in this case, the antigen named Teg) can actually suppress the immune response of the mammalian host. This means that the fluke is able to weaken the immune response, and increase its chances of a successful infection. A successful infection is needed for the fluke to have enough time to develop into an adult and continue its lifecycle. [18]

Digestive system

Image showing the location of the mouth, labelled mo, and the anterior sucker, as labelled sckr Image from page 174 of "Introduction to zoology; a guide to the study of animals, for the use of secondary schools;" (1900) (14598306110).jpg
Image showing the location of the mouth, labelled mo, and the anterior sucker, as labelled sckr

The alimentary canal of F. hepatica has a single mouth which leads into the blind gut; it has no anus. The mouth is located within the anterior sucker on the ventral side of the fluke. This mouth leads to the pharynx, which is then followed by a narrow oesophagus. The oesophagus, which is lined with a thin layer of epithelial cells, then opens up into the large intestine. As no anus is present, the intestine branches, with each branch ending blindly near the posterior end of the body. [19] Flukes migrate into smaller capillaries and bile ducts when feeding within the host. They use their mouth suckers to pull off and suck up food, bile, lymph, and tissue pieces from the walls of the bile ducts. [19] F. hepatica relies on extracellular digestion which occurs within the intestine of the host. The waste materials are egested through the mouth. The nonwaste matter is adsorbed back in through the tegument and the general surface of the fluke. The tegument facilitates this adsorption by containing many small folds to increase the surface area. [19]

Respiratory system

Diagram of the main organ systems of F. hepatica throughout the progressive life stages of the fluke (1938). A - egg; B - miracidium; C - sporocyst; D - rediae, E - immature cercaria, F - cercaria, G - encysted stage, H - adult fluke (nervous and reproductive systems omitted) Animal biology (1938) (17576890133).jpg
Diagram of the main organ systems of F. hepatica throughout the progressive life stages of the fluke (1938). A - egg; B - miracidium; C - sporocyst; D - rediae, E - immature cercaria, F - cercaria, G - encysted stage, H - adult fluke (nervous and reproductive systems omitted)

F. hepatica has no respiratory organs: the adult flukes respire anaerobically (without oxygen). Glycogen taken from within the host is broken down by glycolysis to produce carbon dioxide and fatty acids. This process provides the fluke with energy. [20] In contrast, the free-living miracidia stages of the parasite generally develop within oxygen-rich environments. The free-living stages of the parasite are thought to respire aerobically, to gain the most energy from their environment. [21]

Excretory system

The excretory system of F. hepatica contains a network of tubules surrounding one main excretory canal. This canal leads to the excretory pore at the posterior end of the fluke. This main canal branches into four sections within the dorsal and ventral regions of the body. The excretory system functions in excretion and osmoregulation. [20] Each tubule within the excretory system is connected to a flame cell, otherwise known as protonephridia. These cells are modified parenchyme cells. In F. hepatica, their role is to perform excretion, but more importantly, osmoregulatory functions. Flame cells are therefore primarily used to remove excess water. [20]

Nervous system and sensory organs

The nerve system of F. hepatica consists of a pair of nerve ganglia, each one is located on either side of the oesophagus. Around the oesophagus is a nerve ring, which connects the two nerve ganglia together. The nerves stem from this ring, reaching the posterior end of the body. At the posterior end, one pair of nerves becomes thicker than the others; these are known as the lateral nerve cords. From these lateral nerve cords, the other nerves branch. Sensory organs are absent from F. hepatica. [22] [23]

Reproductive system

F. hepatica adult flukes are hermaphrodite; each contains both male and female reproductive organs. The male and female reproductive organs open up into the same chamber within the body, which is called the genital atrium. The genital atrium is an ectodermal sac which opens up to the outside of the fluke via a genital pore. [22] The testes are formed of two branched tubules, these are located in the middle and posterior regions of the body. From the epithelium lining of the tubules, sperm is produced. The sperm then passes into the vas deferens and then into the seminal vesicle. From the seminal vesicle projects the ejaculatory duct, and this opens into the genital atrium, and many prostate glands surround this opening. [22] The right side of the anterior testis has a branched, tubular ovary. From here, a short oviduct passes to the vitelline duct. This duct connects, via a junction, the ovaries, the uterus, and the yolk reservoir. From this junction, the uterus opens into the genital atrium; this opening is surrounded by Mehlis glands. In some flukes, the terminal end of the uterus is strengthened with muscles and spines. [22]

F. hepatica reproduces both sexually, via the hermaphrodite adult flukes, and asexually. The miracidia can reproduce asexually within the intermediate snail host. [24]

Genome

With its draft genome sequence published in 2015, F. hepatica is known to have the largest nuclear genome size among trematodes so far sequenced. It is about 1.3 Gb, [25] which is two times that of Opisthorchis viverrini with 634.5 Mb, the second largest genome among trematodes. [26] The genome is contained in 10 pairs of chromosomes. The protein-coding sequence covers about 21.8 Mb and repetitive DNA sequence about 32% of the total genome. [25] The number of genes predicted is 14,642. [27] The mitochondrial genome consists of 14462 bp, containing 12 protein-encoding, 2 ribosomal and 22 transfer RNA genes. [28]

Prevalence

Fasciola hepatica prevalence. The countries in red are those with high prevalence, those in orange have low-medium prevalence. Fasciola hepatica prevalence.jpg
Fasciola hepatica prevalence. The countries in red are those with high prevalence, those in orange have low-medium prevalence.

Currently, F. hepatica has one of the widest geographical spread of any parasitic and vector-borne disease. Originating in Europe, it has expanded to colonize over 50 countries, covering all continents except Antarctica. [31] In contrast, F. gigantica is generally considered more geographically restricted to the tropical regions of Africa, Asia, and the Middle East, with some overlap between the two species. [29]

Climate affects both F. hepatica and its intermediate host, the snail. For example, the development of F. hepatica miracidia and larvae, and the reproduction of Galba truncatula , require a temperature range of 10 to 25 °C. In addition, they both require high levels of moisture in the air, as both are at risk of desiccation. Due to this, the prevalence, along with the intensity of infection, of F. hepatica is primarily dependent on rainfall levels and temperature. [31]

Parasitic adaptations

The left image shows the free-swimming cercariae, the swimming "tail" is clearly visible. The right side of the diagram shows the cysts attached to grass. PSM V23 D765 Free cercaria in water and cysts attached to the grass.jpg
The left image shows the free-swimming cercariae, the swimming "tail" is clearly visible. The right side of the diagram shows the cysts attached to grass.

F. hepatica has a tegument that protects it from the enzymes of the host's digestive system, whilst still allowing water to pass through. [15] Free-swimming larvae have cilia and the cercariae have a muscular tail to help them swim through the aquatic environment and also allow them to reach the plants on which they form a cyst. [30] To attach within the host, F. hepatica has oral suckers and body spines. Their pharynges also help them to suck onto the tissues within the body, particularly within the bile ducts. [32] The adult fluke's respiration is anaerobic; this is ideal, as no oxygen is available in the liver. [20] F. hepatica is adapted to produce a large number of eggs, which increases its chances of survival, as many eggs are destroyed on release into the environment. Also, F. hepatica is hermaphrodite, thus all flukes can produce eggs, increasing the number of offspring produced by the population. [22]

The genome for F. hepatica was published in 2015. [33] At 1.3 Gb, its genome is one of the largest known pathogen genomes. The genome contains many polymorphisms, and this represents the potential for the fluke to evolve and rapidly adapt to changes in the environment, such as host availability and drug or vaccine interventions. [25]

Epidemiology

Infection begins when cyst-covered aquatic vegetation is eaten or when water containing metacercariae is drunk. In the United Kingdom, F. hepatica frequently causes disease in ruminants, most commonly between March and December. [34]

Humans become infected by eating watercress or by drinking emoliente , a Peruvian drink that uses drops of watercress juice. Cattle and sheep are infected when they consume the infectious stage of the parasite from low-lying, marshy pasture. [34]

Human infections have been reported from more than 75 countries around the world. In Asia and Africa, people are infected both by F. hepatica and F. gigantica whereas human fasciolosis is caused only by F. hepatica in South and Central America and Europe. [35]

The presence of F. hepatica can interfere with the detection of bovine tuberculosis in cattle. Cattle co-infected with F. hepatica, compared to those infected with M. bovis alone, react weakly to the single intradermal comparative cervical tuberculin (SICCT) test. [36] Therefore, an infection from F. hepatica can make it difficult to detect bovine tuberculosis; this is, of course, a major problem in the farming industry. [37]

Fasciolosis

Slide showing the internal organs of Fasciola hepatica Fasciola hepatica2.jpg
Slide showing the internal organs of Fasciola hepatica

Both F. hepatica and F. gigantica can cause fasciolosis. Human symptoms vary depending on whether the disease is chronic or acute. During the acute phase, the immature worms begin penetrating the gut, causing symptoms of fever, nausea, swollen liver (caused by Fh8), skin rashes, and extreme abdominal pain. [38] The chronic phase occurs when the worms mature in the bile duct, and can cause symptoms of intermittent pain, jaundice, and anemia. [38] In cattle and sheep, classic signs of fasciolosis include persistent diarrhea, chronic weight loss, anemia, and reduced milk production. [39] Some remain asymptomatic. F. hepatica can cause sudden death in both sheep and cattle, due to internal hemorrhaging and liver damage. [4]

Fasciolosis is an important cause of both production and economic losses in the dairy and meat industries. Over the years, the prevalence has increased and it is likely to continue increasing in the future. [40] Livestock are often treated with flukicides, chemicals toxic to flukes, including bromofenofos, [41] [42] triclabendazole, and bithionol. Ivermectin, which is widely used for many helminthic parasites, has low effectivity against F. hepatica, as does praziquantel. [43] [44] For humans, the type of control depends on the setting. One important method is through the strict control over the growth and sales of edible water plants such as watercress. This is particularly important in highly endemic areas. Some farms are irrigated with polluted water, hence, vegetables farmed from such land should be thoroughly washed and cooked before being eaten. [10]

The best way to prevent fasciolosis is by reducing the lymnaeid snail population or separating livestock from areas with these snails. [39] These two methods are not always the most practical, so control by treating the herd before they are potentially infected is commonly practiced.

Diagnosis

F. hepatica egg in stool sample. Egg of Fasciola hepatica 08G0041 lores.jpg
F. hepatica egg in stool sample.

A diagnosis may be made by finding yellow-brown eggs in the stool. They are indistinguishable from the eggs of Fascioloides magna , although the eggs of F. magna are very rarely passed in sheep, goats, or cattle. If a patient has eaten infected liver, and the eggs pass through the body and out via the faeces, a false positive result to the test can occur. Daily examination during a liver-free diet will unmask this false diagnosis. [45]

An enzyme-linked immunosorbent assay (ELISA) test is the diagnostic test of choice. ELISA is available commercially and can detect antihepatica antibodies in serum and milk; new tests intended for use on faecal samples are being developed. [46] Using ELISA is more specific than using a Western blot or Arc2 immunodiffusion. [34] Proteases secreted by F. hepatica have been used experimentally in immunizing antigens. [47]

See also

Related Research Articles

<span class="mw-page-title-main">Trematoda</span> Class of parasitic flatworms

Trematoda is a class of flatworms known as flukes or trematodes. They are obligate internal parasites with a complex life cycle requiring at least two hosts. The intermediate host, in which asexual reproduction occurs, is usually a snail. The definitive host, where the flukes sexually reproduce, is a vertebrate. Infection by trematodes can cause disease in all five traditional vertebrate classes: mammals, birds, amphibians, reptiles, and fish.

<i>Clonorchis sinensis</i> Species of fluke

Clonorchis sinensis, the Chinese liver fluke, is a liver fluke belonging to the class Trematoda, phylum Platyhelminthes. It infects fish-eating mammals, including humans. In humans, it infects the common bile duct and gall bladder, feeding on bile. It was discovered by British physician James McConnell at the Medical College Hospital in Calcutta (Kolkata) in 1874. The first description was given by Thomas Spencer Cobbold, who named it Distoma sinense. The fluke passes its lifecycle in three different hosts, namely freshwater snail as first intermediate hosts, freshwater fish as second intermediate host, and mammals as definitive hosts.

<span class="mw-page-title-main">Fasciolosis</span> Parasitic worm infection

Fasciolosis is a parasitic worm infection caused by the common liver fluke Fasciola hepatica as well as by Fasciola gigantica. The disease is a plant-borne trematode zoonosis, and is classified as a neglected tropical disease (NTD). It affects humans, but its main host is ruminants such as cattle and sheep. The disease progresses through four distinct phases; an initial incubation phase of between a few days up to three months with little or no symptoms; an invasive or acute phase which may manifest with: fever, malaise, abdominal pain, gastrointestinal symptoms, urticaria, anemia, jaundice, and respiratory symptoms. The disease later progresses to a latent phase with less symptoms and ultimately into a chronic or obstructive phase months to years later. In the chronic state the disease causes inflammation of the bile ducts, gall bladder and may cause gall stones as well as fibrosis. While chronic inflammation is connected to increased cancer rates, it is unclear whether fasciolosis is associated with increased cancer risk.

<span class="mw-page-title-main">Fasciolopsiasis</span> Medical condition

Fasciolopsiasis results from an infection by the trematode Fasciolopsis buski, the largest intestinal fluke of humans, growing up to 7.5 cm (3.0 in) long.

<i>Fasciola</i> Genus of flukes

Fasciola, commonly known as the liver fluke, is a genus of parasitic trematodes. There are three species within the genus Fasciola: Fasciola nyanzae,Fasciolahepatica and Fasciolagigantica. Fasciola hepatica and F. gigantica are known to form hybrids. Both F. hepatica and F. gigantica and their hybrids infect the liver tissue of a wide variety of mammals, including humans, in a condition known as fascioliasis. F. hepatica measures up to 30 mm by 15 mm, while F. gigantica measures up to 75 mm by 15 mm. Fasciola nyanzae is thought to exclusively infect the common hippopotamus, Hippopotamus amphibius.

<i>Fasciola gigantica</i> Species of fluke

Fasciola gigantica is a parasitic flatworm of the class Trematoda, which causes tropical fascioliasis. It is regarded as one of the most important single platyhelminth infections of ruminants in Asia and Africa. The infection is commonly called fasciolosis.

<i>Fascioloides magna</i> Species of fluke

Fascioloides magna, also known as giant liver fluke, large American liver fluke or deer fluke, is trematode parasite that occurs in wild and domestic ruminants in North America and Europe. Adult flukes occur in the liver of the definitive host and feed on blood. Mature flukes measure 4 to 10 centimetres in length × 2 to 3.5 centimetres in width, and have an oval dorso-ventrally flattened body with oral and ventral sucker. The flukes are reddish-brown in colour and are covered by tegument. As with other digenean trematodes, the life cycle includes intramolluscan phase in snails. The parasite is currently distributed in wild ruminants in North America and Europe, including Austria, Canada, the Czech Republic, Croatia, Germany, Hungary, Italy, Poland, Serbia, Slovakia, and the United States.

Opisthorchis viverrini, common name Southeast Asian liver fluke, is a food-borne trematode parasite from the family Opisthorchiidae that infects the bile duct. People are infected after eating raw or undercooked fish. Infection with the parasite is called opisthorchiasis. O. viverrini infection also increases the risk of cholangiocarcinoma, a cancer of the bile ducts.

<i>Galba truncatula</i> Species of gastropod

Galba truncatula is a species of air-breathing freshwater snail, an aquatic pulmonate gastropod mollusk in the family Lymnaeidae, the pond snails.

<span class="mw-page-title-main">Liver fluke</span> Group of liver parasites

Liver fluke is a collective name of a polyphyletic group of parasitic trematodes under the phylum Platyhelminthes. They are principally parasites of the liver of various mammals, including humans. Capable of moving along the blood circulation, they can occur also in bile ducts, gallbladder, and liver parenchyma. In these organs, they produce pathological lesions leading to parasitic diseases. They have complex life cycles requiring two or three different hosts, with free-living larval stages in water.

<i>Lymnaea tomentosa</i> Species of gastropod

Lymnaea tomentosa is a species of freshwater snail, an aquatic gastropod mollusc in the family Lymnaeidae.

<i>Pseudosuccinea columella</i> Species of gastropod

Pseudosuccinea columella, the American ribbed fluke snail, is a species of air-breathing freshwater snail, an aquatic pulmonate gastropod mollusk in the family Lymnaeidae, the pond snails.

<i>Fasciolopsis</i> Genus of flukes

Fasciolopsis is a genus of trematodes. They are also known as giant intestinal flukes.

Lymnaea acuminata is a species of freshwater snail in the family Lymnaeidae. It is native to South Asia, where it occurs in Bangladesh, Burma, India, Nepal, and Pakistan. There it is a widespread and common species.

<i>Radix natalensis</i> Species of gastropod

Radix natalensis is a species of freshwater snail, an aquatic gastropod mollusc in the family Lymnaeidae.

Paramphistomum cervi, the type species of Paramphistomum, is a parasitic flat worm belonging to the class Trematoda. It is a tiny fluke mostly parasitising livestock ruminants, as well as some wild mammals. Uniquely, unlike most parasites, the adult worms are relatively harmless, but it is the developing juveniles that cause serious disease called paramphistomiasis, especially in cattle and sheep. Its symptoms include profuse diarrhoea, anaemia, lethargy, and often result in death if untreated.

Paramphistomum is a genus of parasitic flatworms belonging to the digenetic trematodes. It includes flukes which are mostly parasitising livestock ruminants, as well as some wild mammals. They are responsible for the serious disease called paramphistomiasis, also known as amphistomosis, especially in cattle and sheep. Its symptoms include profuse diarrhoea, anaemia, lethargy, and often result in death if untreated. They are found throughout the world, and most abundantly in livestock farming regions such as Australia, Asia, Africa, Eastern Europe, and Russia.

<span class="mw-page-title-main">Trematodiasis</span> Medical condition

Trematodiasis is a group of parasitic infections due different species of flukes, the trematodes. Symptoms can range from mild to severe depending on the species, number and location of trematodes in the infected organism. Symptoms depend on type of trematode present, and include chest and abdominal pain, high temperature, digestion issues, cough and shortness of breath, diarrhoea and change in appetite.

<span class="mw-page-title-main">Trematoda in Kuwait</span>

Trematoda is a whole-living worm that lives in different parts of the host's body, some of which live in bile ducts. These are called hepatic worms such as Fasciola species, including species that live in the intestines such as the genus Heterophyes, including those living in blood vessels such as the genus that causes schistosomiasis, the genus of Schistosoma. Including what lives in the lung such as the genus of Paragonimus.

<span class="mw-page-title-main">Gastropod-borne parasitic disease</span> Medical condition

Gastropod-borne parasitic diseases (GPDs) are a group of infectious diseases that require a gastropod species to serve as an intermediate host for a parasitic organism that can infect humans upon ingesting the parasite or coming into contact with contaminated water sources. These diseases can cause a range of symptoms, from mild discomfort to severe, life-threatening conditions, with them being prevalent in many parts of the world, particularly in developing regions. Preventive measures such as proper sanitation and hygiene practices, avoiding contact with infected gastropods and cooking or boiling food properly can help to reduce the risk of these diseases.

References

  1. ↑ Linnæi, C. (1758–1759). Systema Naturae per Regna Tria Naturæ, Secundum Classes, Ordines, Genera, Species, cum Haracteribus, Differentiis, Synonymis, Locis. Tomus I. Holmiæ: Impensis Direct. Laurentii Salvii. doi:10.5962/bhl.title.542
  2. ↑ "Neglected Tropical Diseases". cdc.gov. June 6, 2011. Retrieved 28 November 2014.
  3. ↑ Mas-Coma, S; Bargues, MD; Valero, MA (2005). "Fascioliasis and other plant-borne trematode zoonoses". International Journal for Parasitology. 35 (11): 1255–1278. doi:10.1016/j.ijpara.2005.07.010. PMID   16150452.
  4. 1 2 "NADIS - National Animal Disease Information Service -". www.nadis.org.uk. Retrieved 2016-04-30.
  5. 1 2 3 Mas-Coma, Santiago; Valero, María Adela; Bargues, María Dolores (2009). "Fasciola, Lymnaeids and Human Fascioliasis, with a Global Overview on Disease Transmission, Epidemiology, Evolutionary Genetics, Molecular Epidemiology and Control". Advances in Parasitology. Vol. 69. pp. 41–146. doi:10.1016/S0065-308X(09)69002-3. ISBN   978-0-12-374795-2. PMID   19622408.
  6. 1 2 Torgerson, P; Claxton JR (1999). "Epidemiology and Control". In Dalton, JP (ed.). Fasciolosis. Wallingford, Oxon, UK: CABI Pub. pp. 113–149. ISBN   978-0-85199-260-0.
  7. ↑ Andrews, JS (1999). "Life cycle of Fasciola hepatica". In Dalton, JP (ed.). Fasciolosis. Wallingford, Oxon, UK: CABI Pub. pp. 1–30. ISBN   978-0-85199-260-0.
  8. ↑ Bargues, M. D.; Gayo, V.; Sanchis, J.; Artigas, P.; Khoubbane, M.; Birriel, S.; Mas-Coma, S. (2017). "DNA multigene characterization of Fasciola hepatica and Lymnaea neotropica and its fascioliasis transmission capacity in Uruguay, with historical correlation, human report review and infection risk analysis". PLOS Neglected Tropical Diseases. 11 (2): e0005352. doi: 10.1371/journal.pntd.0005352 . PMC   5310921 . PMID   28158188.
  9. ↑ Correa, C. A.; Escobar, J. S.; Durand, P.; Renaud, F.; David, P.; Jarne, P.; Pointier, J.-P.; Hurtrez-Boussès, S. (2010). "Bridging gaps in the molecular phylogeny of the Lymnaeidae (Gastropoda: Pulmonata), vectors of Fascioliasis". BMC Evolutionary Biology . 10 (1): 381. Bibcode:2010BMCEE..10..381C. doi: 10.1186/1471-2148-10-381 . PMC   3013105 . PMID   21143890.
  10. 1 2 3 4 "Parasites – Fascioliasis (Fasciola Infection)". cdc.gov. January 10, 2013. Retrieved 12 March 2016.
  11. ↑ Valero, M. Adela; Panova, Miroslava; Comes, Ana M.; Fons, Roger; Mas-Coma, Santiago (April 2002). "Patterns in size and shedding of Fasciola hepatica eggs by naturally and experimentally infected murid rodents". Journal of Parasitology. 88 (2): 308–313. doi:10.1645/0022-3395(2002)088[0308:PISASO]2.0.CO;2. hdl: 10550/16781 . PMID   12054003. S2CID   41190159.
  12. ↑ Prevention, CDC - Centers for Disease Control and. "CDC - Fasciola - Biology". www.cdc.gov. Retrieved 2016-04-30.
  13. ↑ Bils, R. F.; Martin, W. E. (1966). "Fine Structure and Development of the Trematode Integument". Transactions of the American Microscopical Society. 85 (1): 78–88. doi:10.2307/3224777. JSTOR   3224777. PMID   5908220.
  14. ↑ Wilson, R. Alan; Wright, Janelle M.; de Castro-Borges, William; Parker-Manuel, Sophie J.; Dowle, Adam A.; Ashton, Peter D.; Young, Neil D.; Gasser, Robin B.; Spithill, Terry W. (November 2011). "Exploring the Fasciola hepatica tegument proteome". International Journal for Parasitology. 41 (13–14): 1347–1359. doi:10.1016/j.ijpara.2011.08.003. PMID   22019596.
  15. 1 2 Hamali, Bulut; Kudlacek, Oliver; Sehr, Eva Maria; Molin, Martina; Jaentsch, Kathrin; Freissmuth, Michael; Burger, Melanie; Schicker, Klaus; Wischnitzki, Elisabeth (2018). "Identification and characterization of the Fasciola hepatica sodium- and chloride-dependent taurine transporter". PLOS Neglected Tropical Diseases. 12 (4): e0006428. doi: 10.1371/journal.pntd.0006428 . PMC   5942844 . PMID   29702654.
  16. ↑ Bennett, Clive E. (1975). "Scanning Electron Microscopy of Fasciola hepatica L. during Growth and Maturation in the Mouse". The Journal of Parasitology. 61 (5): 892–8. doi:10.2307/3279230. JSTOR   3279230. PMID   1185431.
  17. ↑ Southgate, V. R. (2009). "Observations on the epidermis of the miracidium and on the formation of the tegument of the sporocyst of Fasciola hepatica". Parasitology. 61 (2): 177–90. doi:10.1017/S0031182000040993. PMID   5483910. S2CID   40452047.
  18. ↑ Hamilton, C. M.; Dowling, D. J.; Loscher, C. E.; Morphew, R. M.; Brophy, P. M.; O'Neill, S. M. (2009). "The Fasciola hepatica Tegumental Antigen Suppresses Dendritic Cell Maturation and Function". Infection and Immunity. 77 (6): 2488–2498. doi:10.1128/IAI.00919-08. PMC   2687350 . PMID   19332532.
  19. 1 2 3 Kotpal, RL (2012). Modern Text Book of Zoology: Invertebrates. New Delhi: Rastogi Publications. p. 338. ISBN   978-81-7133-903-7.
  20. 1 2 3 4 Bhatnagar, MC; Bansal, G (2009). Non-Chordata. Delhi: Krishna Prakashan Media. pp. 153–154. ISBN   978-81-8283-036-3.
  21. ↑ Boyunaga, H.; Schmitz, M.G.J.; Brouwers, J.F.H.M.; Van Hellemond, J.J.; Tielens, A.G.M. (2002). "Fasciola hepatica miracidia are dependent on respiration and endogenous glycogen degradation for their energy generation". Parasitology. 122 (2): 169–73. doi:10.1017/S0031182001007211. PMID   11272647. S2CID   24663107.
  22. 1 2 3 4 5 Puranik, P; Bhate, A (2007). Animal Forms And Functions: Invertebrata. New Delhi: Sarup & Sons. pp. 172–175. ISBN   978-81-7625-791-6.
  23. ↑ Mandal, P; F.B. (2012). Invertebrate Zoology. Delhi: PHI Learning. ISBN   978-81-203-4615-4.
  24. ↑ Hurtrez-Boussès, Sylvie; Meunier, Cécile; Durand, Patrick; Renaud, François (2001). "Dynamics of host–parasite interactions: the example of population biology of the liver fluke (Fasciola hepatica)". Microbes and Infection. 3 (10): 841–849. doi: 10.1016/S1286-4579(01)01442-3 . PMID   11580979.
  25. 1 2 3 Cwiklinski, Krystyna; Dalton, John Pius; Dufresne, Philippe J; La Course, James; Williams, Diana JL; Hodgkinson, Jane; Paterson, Steve (2015). "The Fasciola hepatica genome: gene duplication and polymorphism reveals adaptation to the host environment and the capacity for rapid evolution". Genome Biology. 16 (1): 71. doi: 10.1186/s13059-015-0632-2 . PMC   4404566 . PMID   25887684.
  26. ↑ Young, Neil D.; Nagarajan, Niranjan; Lin, Suling Joyce; Korhonen, Pasi K.; Jex, Aaron R.; Hall, Ross S.; Safavi-Hemami, Helena; Kaewkong, Worasak; et al. (2014). "The Opisthorchis viverrini genome provides insights into life in the bile duct". Nature Communications. 5 (1): 4378. Bibcode:2014NatCo...5.4378Y. doi:10.1038/ncomms5378. PMC   4104445 . PMID   25007141.
  27. ↑ McNulty, Samantha N.; Tort, Jose F.; Rinaldi, Gabriel; Fischer, Kerstin; Rosa, Bruce A.; Smircich, Pablo; Fontenla, Santiago; Choi, Young-Jun; et al. (2017). "Genomes of Fasciola hepatica from the Americas Reveal Colonization with Neorickettsia Endobacteria Related to the Agents of Potomac Horse and Human Sennetsu Fevers". PLOS Genetics. 13 (1): e1006537. doi: 10.1371/journal.pgen.1006537 . PMC   5257007 . PMID   28060841.
  28. ↑ Le, T.H.; Blair, D.; McManus, D.P. (2003). "Complete DNA sequence and gene organization of the mitochondrial genome of the liverfluke, Fasciola hepatica L. (Platyhelminthes; Trematoda)". Parasitology. 123 (6): 609–21. doi:10.1017/S0031182001008733. PMID   11814048. S2CID   41357043.
  29. 1 2 Tolan, Robert W. (February 2011). "Fascioliasis Due to Fasciola hepatica and Fasciola gigantica Infection: An Update on This 'Neglected' Neglected Tropical Disease". Laboratory Medicine. 42 (2): 107–116. doi: 10.1309/LMLFBB8PW4SA0YJI .
  30. 1 2 McManus, DP; Dalton, JP (2007). "Vaccines against the zoonotic trematodes Schistosoma japonicum, Fasciola hepatica and Fasciola gigantica". Parasitology. 133 (S2): S43–61. doi:10.1017/S0031182006001806. hdl: 10453/15032 . PMID   17274848. S2CID   8952857.
  31. 1 2 3 Mas-Coma, S. (September 2005). "Epidemiology of fascioliasis in human endemic areas". Journal of Helminthology. 79 (3): 207–216. doi:10.1079/joh2005296. PMID   16153314. S2CID   20879979.
  32. ↑ Halferty, L.; Brennan, G.P.; Hanna, R.E.B.; Edgar, H.W.; Meaney, M.M.; McConville, M.; Trudgett, A.; Hoey, L.; Fairweather, I. (August 2008). "Tegumental surface changes in juvenile Fasciola hepatica in response to treatment in vivo with triclabendazole". Veterinary Parasitology. 155 (1–2): 49–58. doi:10.1016/j.vetpar.2008.04.011. PMID   18511199.
  33. ↑ "Fasciola hepatica - WormBase ParaSite". parasite.wormbase.org. Archived from the original on 22 March 2016. Retrieved 11 January 2022.
  34. 1 2 3 "Gorgas Case 5 - 2015 Series". The Gorgas Course in Clinical Tropical Medicine. University of Alabama. 2 March 2015. Archived from the original on 15 March 2015.
  35. ↑ "Fascioliasis epidemiology". WHO. Archived from the original on March 13, 2014.
  36. ↑ Skin Test. Animal and Plant Health Agency, UK
  37. ↑ Claridge, Jen; Diggle, Peter; McCann, Catherine M.; Mulcahy, Grace; Flynn, Rob; McNair, Jim; Strain, Sam; Welsh, Michael; Baylis, Matthew; Williams, Diana J.L. (January 2012). "Fasciola hepatica is associated with the failure to detect bovine tuberculosis in dairy cattle". Nature Communications. 3 (1): 853. Bibcode:2012NatCo...3..853C. doi:10.1038/ncomms1840. PMC   3989536 . PMID   22617293.
  38. 1 2 "WHO | Fascioliasis". www.who.int. Archived from the original on May 8, 2013. Retrieved 2016-04-30.
  39. 1 2 Scott, Phil. "Fascioliasis (liver fluke) in cattle" (PDF). NADIS Health Bulletin. Archived from the original (PDF) on 2016-05-31. Retrieved 2016-04-30.
  40. ↑ Howell, Alison; Baylis, Matthew; Smith, Rob; Pinchbeck, Gina; Williams, Diana (2015). "Epidemiology and impact of Fasciola hepatica exposure in high-yielding dairy herds". Preventive Veterinary Medicine. 121 (1–2): 41–48. doi:10.1016/j.prevetmed.2015.05.013. PMC   4528078 . PMID   26093971.
  41. ↑ Virginia P. Studdert; Clive C. Gay; Douglas C. Blood (2011). Saunders Comprehensive Veterinary Dictionary. Elsevier Health Sciences.
  42. ↑ Ruckebusch, Y.; Toutian, P.-L.; Koritz, G.D., eds. (2012). Veterinary Pharmacology and Toxicology. Springer Science & Business Media. p. 762. ISBN   978-94-009-6604-8.
  43. ↑ Sibille, Pierre; Calléja, Cécile; Carreras, Florence; Bigot, Karine; Galtier, Pierre; Boulard, Chantal (2000). "Fasciola hepatica: Influence of Gender and Liver Biotransformations on Flukicide Treatment Efficacy of Rats Infested and Cured with Either Clorsulon/Ivermectin or Triclabendazole". Experimental Parasitology. 94 (4): 227–237. doi:10.1006/expr.2000.4501. PMID   10831390.
  44. ↑ Ortega, YR (2006-11-22). Foodborne Parasites. Georgia, USA: Springer. p. 186. ISBN   978-0387-30068-9.
  45. ↑ Valero, M. Adela; Perez-Crespo, Ignacio; Periago, M. Victoria; Khoubbane, Messaoud; Mas-Coma, Santiago (2009). "Fluke egg characteristics for the diagnosis of human and animal fascioliasis by Fasciola hepatica and F. gigantica". Acta Tropica. 111 (2): 150–159. doi:10.1016/j.actatropica.2009.04.005. PMID   19375410.
  46. ↑ Mezo, Mercedes; González-Warleta, Marta; Carro, Carmen; Ubeira, Florencio M. (2004). "An Ultrasensitive Capture Elisa for Detection of Fasciola Hepatica Coproantigens in Sheep and Cattle Using a New Monoclonal Antibody (MM3)". Journal of Parasitology. 90 (4): 845–852. doi:10.1645/GE-192R. PMID   15357080. S2CID   31734209.
  47. ↑ Cornelissen, Jan B.W.J.; Gaasenbeek, Cor P.H.; Borgsteede, Fred H.M; Holland, Wicher G; Harmsen, Michiel M; Boersma, Wim J.A (2001). "Early immunodiagnosis of fasciolosis in ruminants using recombinant Fasciola hepatica cathepsin L-like protease". International Journal for Parasitology. 31 (7): 728–737. doi:10.1016/S0020-7519(01)00175-8. PMID   11336755.
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.