词条 | Clonorchis sinensis |
释义 |
| image = Clonorchis sinensis 2.png | image_caption = An adult Clonorchis sinensis has these main body parts: oral sucker, pharynx, caecum, ventral sucker, vitellaria, uterus, ovary, Mehlis' gland, testes, excretory bladder. (H&E stain) | taxon = Clonorchis sinensis | authority = Looss, 1907 }}Clonorchis sinensis, the Chinese liver fluke, is a human liver fluke belonging to the class Trematoda, phylum Platyhelminthes. This parasite lives in the liver of humans, and is found mainly in the common bile duct and gall bladder, feeding on bile. These animals, which are believed to be the third-most prevalent worm parasite in the world, are endemic to Japan, China, Taiwan, and Southeast Asia, currently infecting an estimated 30,000,000 humans.[1] About 85% of cases are found in China. The infection, called clonorchiasis, generally appears as jaundice, indigestion, biliary inflammation, bile duct obstruction, even liver cirrhosis, cholangiocarcinoma, and hepatic carcinoma.[2] It is the most prevalent human trematode in Asia, and is still transmitted in Korea, China, Vietnam, and Russia, with 200 million people at constant risk. Recent studies have proved that it is definite cancer-causing agent in the liver (carcinoma) and bile duct (cholangiocarcinoma). For this reason, the International Agency for Research on Cancer has classed it as a group 1 biological carcinogen in 2009.[3][4][5] DiscoveryThe symptoms of C. sinensis infection (clonorchiasis) have been known from ancient times in China. The earliest record is from corpses buried in 278 BCE at Jiangling County of Hubei Province and the Warring States tomb of the western Han Dynasty, but the parasite was discovered only in 1874 by James McConnell, a professor of pathology and resident physician at the Medical College Hospital in Calcutta. He recovered the fluke from a 20-year-old Chinese carpenter who died on 8 September 1874. On autopsy, he observed that the corpse had a swollen liver (hepatomegaly) and distended bile ducts, which he noted were blocked by "small, dark, vermicular-looking bodies." He recovered the vermicules (worms) and compared them with known flukes Fasciola hepatica and Distoma lanceolatum. He concluded that the new fluke was significantly different. He published his observations in the 21 August 1875 issue of The Lancet.[6] The formal scientific description was published in 1875 by Thomas Spencer Cobbold, who named it Distoma sinense. In 1876, Rudolf Leuckart, named it Distomum spithulatum. Kenso Ishisaka recorded the first case of clonorchiasis in Japan in 1877. McConnell identified another infection in a Chinese cook from Hong Kong in 1878. Erwin von Baelz reported the presence of similar flukes from an autopsy of a Japanese patient at Tokyo University in 1883. He recorded two different forms, naming the smaller, more pathogenic form as Distoma hepatis endemicum sive perniciosum, and the larger, less pathogenic form as D.h.e.s. innocuum. Isao Ijima correctly redescribed them as the same species, but still wrongly renamed it Distoma endemicum in 1886. When a new genus Opisthorchis was created by Émile Blanchard in 1895, Cobbold's species name D. sinense was moved to the new genus because of close similarities with the other members. Further analyses by Arthur Looss, though, showed significant differences from the general features of Opisthorchis, particularly on the highly branched testes. He created a new genus Clonorchis (from Greek klon meaning "twig/branch", orkhis meaning "testis") in 1907. Similar to Baelz, he differentiated the larger species as Clonorchis sinensis, which is mostly found in China, and the smaller species as C. endemicum, found mostly in Japan. In 1912, Harujiro Kobayashi corrected the classification that the differences in sizes were due to the nature of the host and intensity of infection, and had nothing to do with the biology.[7] Hence, he supported only C. sinensis. Kobayashi was also the first to discover fish as the second intermediate host in 1911. Masatomo Muto discovered snails as the first intermediate host in 1918.[8][9] DescriptionAn adult C. sinensis is a flattened (dorsoventrally) and leaf-shaped fluke. The body is slightly elongated and slender, measuring 15–20 mm in length and 3–4 mm in width.[10] It narrows at the anterior region into a small opening called the oral sucker, which act as the mouth. From the mouth, two tubes called caeca run the length of body. They are the digestive and excretory tracts. The posterior end is broad and blunt. A poorly developed ventral sucker lies behind the oral sucker, at about one-fourth of the body length from the anterior end. A common genital pore opens just in front of it. As a hermaphrodite, it has both male and female reproductive organs. A single rounded ovary is at the centre of the body, and two testes are towards the posterior end. The uterus from the ovary, and seminal ducts from the testes, meet and open at the genital pore. The testes are highly branched. Other highly branched organs called vitellaria (or vitelline glands) are distributed on either side of the body.[11][12] The eggs are similar to those of other related flukes such as Opisthorchis viverrini and O. felineus, and are often confused during diagnosis. They small and oval in shape, measuring about 30 x 15 μm in diameter. They are sharply curved and with a clear convex operculum towards the narrower end. At the broader end is a stem-shaped knob. The miracidium can be seen inside the fertilised egg.[13] LifecycleProduction of eggsThe eggs of a C. sinensis are released through the biliary tract, and excreted out along with the faeces. The eggs are embryonated and contain the larvae called miracidia. Unlike most other flukes in which the miracidia undergo development and swim in water to infect suitable host, the eggs of C. sinensis are simply deposited in water. The eggs are then eaten by snails.[12] First intermediate hostFreshwater snail Parafossarulus manchouricus often serves as a first intermediate host for C. sinensis in China, Japan, Korea, and Russia.[14][15] Other snail hosts include Alocinma longicornis Bithynia longicornis, Bithynia fuchsiana, Bithynia misella, Parafossarulus anomalospiralis, Melanoides tuberculata, Semisulcospira cancellata, Koreoleptoxis amurensis, Semisulcospira libertina, and Assiminea lutea in China;[15] and Melanoides tuberculata in Vietnam.[16][17]Once inside of the snail body, the embryonic membrane is dissolved by the snail's digestive enzymes, so the miracidium hatches from the egg. The ciliated miracidium can move about, penetrating the intestine, and enters the haemocoel and digestive gland. Here, it undergoes metamorphosis into a sporocyst. The sporocyst gives rise to small larvae called rediae. The rediae burst out from the sporocyst to become the next-stage larvae called cercaria. This system of asexual reproduction allows for an exponential multiplication of cercaria individuals from one miracidium. This aids the Clonorchis in reproduction, because it enables the miracidium to capitalize on one-chance occasion of passively being eaten by a snail before the egg dies. The mature cercariae bore out of the snail body into the freshwater environment. However, they are nonfeeding and must find a fish host within 2–3 days, otherwise they die.[12] The ceraciae of C. sinensis are different from those of other flukes in that they do not swim. Instead, they initially hang upside down in the water, and then sink to the bottom. They rise to the water surface to resume their initial position, and the movement is repeated again. They attack fish when they feel any disturbance.[11] Second intermediate hostWhen they detect fish, they attached themselves on the scales using their suckers. Boring their way into the fish's body, they penetrate into the fish muscle within 6 to 13 minutes. Within an hour of penetration, they develop hard coverings called cysts, and become metacercariae. This protective cyst is useful when the fish muscle is consumed. The metacercariae gradually develop and become infective to their next hosts after 3 to 4 weeks.[11] The common second intermediate hosts are freshwater fish: common carp (Cyprinus carpio), grass carp (Ctenopharyngodon idellus), crucian carp (Carassius carassius), goldfish (Carassius auratus), Pseudorasbora parva, Abbottina rivularis, Hemiculter spp., Opsariichthys spp., Rhodeus spp., Sarcocheilichthys spp., Zacco platypus, Nipponocypris temminckii, and pond smelt (Hypomesus olidus).[18] In China, 102 species of fish and four species of shrimp are known to be the intermediate hosts.[17] In Korea, 40 species of freshwater fish are recorded as hosts.[19] Seven species of fish are known as hosts in Russia.[20] Definitive hostThe metacercariae are eaten along with raw or undercooked fish. The cysts of the metacercariae are gradually digested by the human gastric acids, and upon reaching the small intestines, the entire cyst is lost. The free metacercariae penetrate the intestinal mucosa and enter the bile ducts. Migration into the bile ducts takes 1-2 days. They start feeding on the bile secreted from the liver, and gradually grow.[13] They become adults in about a month, and start laying eggs. The average lifespan of an adult fluke is 30 years.[11] An individual fluke can produce 4,000 eggs in a day.[21] The definitive hosts are fish-eating mammals such as dogs, cats, rats, pigs, badgers, weasels, camels, and buffaloes.[18] Effects on human health{{Main|Clonorchiasis}}Dwelling in the bile ducts, C. sinensis induces an inflammatory reaction, epithelial hyperplasia and sometimes even cholangiocarcinoma, the incidence of which is raised in fluke-infested areas.[22] One adverse effect of Clonorchis spp. is the possibility for the adult metacercaria to consume all bile created in the liver, which would inhibit the host human from digesting food, especially fats. Another possibility is obstruction of the bile duct by the parasite or its eggs, leading to biliary obstruction and cholangitis (specifically oriental cholangitis). Unusual cases of liver abscesses due to clonorchiasis have been reported. Liver abscesses may be seen even without dilatation of intrahepatic bile ducts.[23] SymptomsWhile normally asymptomatic, most pathological manifestations result from inflammation and intermittent obstruction of the biliary ducts. The acute phase consists of abdominal pain with associated nausea and diarrhea. Long-standing infections consist of fatigue, abdominal discomfort, anorexia, weight loss, diarrhea, and jaundice. The pathology of long-standing infections consist of bile stasis, obstruction, bacterial infections, inflammation, periductal fibrosis, and hyperplasia. Development of cholangiocarcinoma is progressive.[24] Diagnosis and treatmentInfection is detected mainly on identification of eggs by microscopic demonstration in faeces or in duodenal aspirate, but other sophisticated methods have been developed, such as ELISA, which has become the most important clinical technique. Diagnosis by detecting DNAs from eggs in faeces are also developed using PCR, real-time PCR, and LAMP, which are highly sensitive and specific. Typical imaging features center around imaging of the liver with CT, ultrasound or MRI for detection of primary biliary cirrhosis. Traits that raise suspicion for the infection include intra- and extra- hepatic dilatation and strictures with intraductal pigmented stones, usually in the absence of gallstones and with regions of segmental liver atrophy, particularly the lateral aspect of the left hepatic lobe. There is also reduced arborization of peripheral ducts. A full 5% of chronic infections go on to develop cholangiocarcinoma.[25] Drugs used to treat infestation include triclabendazole, praziquantel, bithionol, albendazole, levamisole, and mebendazole. However, benzimidazoles are very weak as a vermicide. As with other trematodes, praziquantel is the drug of choice. Lately, tribendimidine has been acknowledged as an effective and safe drug.[3][26] GeneticsThe draft genome sequence of C. sinensis was published in 2011.[27] The total genome size is estimated to be 580 Mb, and the GC content was calculated as approximately 43.85%. About 16,000 genes are predicted, out of which 13,634 genes have been identified.[28] See also
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External links{{Commons category|Clonorchis sinensis}}
5 : Plagiorchiida|IARC Group 1 carcinogens|Infectious causes of cancer|Parasitic helminths of humans|Animals described in 1907 |
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