Microfilaria
_Surrounded_by_Neoplastic_Lymphocytes_1.jpg)
The microfilaria (plural microfilariae, sometimes abbreviated mf) is an early stage in the life cycle of certain parasitic nematodes in the family Onchocercidae.[1] In these species, the adults live in a tissue or the circulatory system of vertebrates (the "definitive hosts"). They release microfilariae into the bloodstream of the vertebrate host. The microfilariae are taken up by blood-feeding arthropod vectors (the "intermediate hosts"). In the intermediate host the microfilariae develop into infective larvae that can be transmitted to a new vertebrate host.
The presence of microfilariae in the host bloodstream is called "microfilaraemia". The success of filariasis eradication programs is typically gauged by the reduction in numbers of circulating microfilariae in infested individuals within a geographic area.[2]
Microfilaria may also refer to an informal "collective group" genus name, proposed by Cobbold in 1882. While a convenient category for newly discovered microfilariae which can not be assigned to a known species because the adults are unknown,[3] it is seldom used today.
Escaping the circulatory system
[edit]All parasites need a mechanism for spreading to new individual hosts. Parasites in the lower gastrointestinal tract usually shed eggs in the host feces. Tissue-dwelling parasites, such as Trichinella spiralis (cause of trichinosis), rely on new hosts eating the tissues of their current host. For members of the family Onchocercid whose adults live in the "closed" vertebrate circulatory system, transmission to a new host is achieved by the microfilaria stage, with the help of blood-feeding arthropod vectors.
This system is seen in the life cycle of Elaeophora Schneider.[4] The adults of E. Schneider typically reside in the carotid artery of its parasitic life cycles definitive host, the Mule deer. The female may be up to 12 cm (almost 5 inches) long, and releases microfilariae which measure 207 by 13 μm (or 0.008 by 0.00051 inches) into the bloodstream of the host. The blood flow carries the microfilariae away from the female in the carotid artery, and directly into the branching arteries of the head and face. Because of their size, the microfilariae pass easily through successively smaller vessels, becoming physically lodged in the small capillaries near the skin surface of the face and head.
Attracted by the carbon dioxide exhaled by the mule deer,[1] the blood-feeding female horse fly often lands on the head or face to feed. The horse fly uses its scissor-like mouthparts to cut the surface of the skin, creating a pool of blood which it takes in through its sucking mouthparts. The microfilariae, which were just under the surface of the skin, are small enough to be ingested whole by the horse fly. Once inside the horse fly, the microfilariae bore through the stomach wall, and mature into infective larvae about two weeks later. These larvae migrate to the head and mouthparts of the horse fly, and enter the bloodstream of another vertebrate host when the horse fly feeds again.
Microfilaria as a developmental stage
[edit]Most recent parasitology textbooks consider the microfilariae to be "pre-larvae or advanced embryos" which will develop into the first stage larvae (L1) in the arthropod vector (p. 364[5]). Some consider them to be the first larval stage, such as "microfilariae; i.e. first larva (= L1)" (p. 361[6]).
In either case, the microfilaria is the stage which develops from the egg. In most tissue-dwelling species the eggs hatch in the uterus of the female, and the unsheathed microfilariae are released. In most blood-dwelling species, embryonated eggs (or, microfilariae which are said to be sheathed in the envelope of the egg) are released; and they will only exsheath ("hatch") after being ingested by the arthropod intermediate host. All microfilariae burrow through the stomach wall after being eaten by the arthropod host, and develop into infective third stage (L3) larvae.
Many of the organs of microfilariae are in a very early stage of development. For some species, the developmental fates of individual cells have been followed from the microfilaria stage to the adult worm. The microfilariae of many species undergo a development phase called the "sausage stage", becoming temporarily shorter and thicker, while the first-stage (L1) larval organs develop.
In some species of Onchocercidae, the release of microfilariae by the adult female is periodic - occurring daily at a particular time of the day or night. This timing increases the chance that they will be picked up by a blood-feeding arthropod vector, which are often more active at certain times of the day.
References
[edit]- ^ Anderson, R.C. (2000) Nematode Parasites of Vertebrates: Their Development and Transmission. Second Edition. CABI Publishing: Wallingford, England, pp. 472–475. ISBN 0851997864
- ^ Farid, H.A., Z.S. Morsy, H. Helmy, R.M.R. Ramzy, M. El Setouhy, and G.J. Weil (2007) "A critical appraisal of molecular xenomonitoring as a tool for assessing progress toward elimination of lymphatic filariasis." American Journal of Tropical Medicine and Hygiene 77(4):593-600.
- ^ Purnomo; Bangs, M.J. (1995) "Microfilaria sundaicus sp.n., a Chabfilaria-like parasite (Filarioidea: Onchocerciae) from the blood of the horseshoe bat (Rhinolophus affinis) in Flores, Indonesia". Journal of the Helminthological Society of Washington 62(1):32-34.
- ^ Hibler, C.P. and C.J. Metzger (1974) Morphology of the larval stages of Elaeophora Schneider in the intermediate and definitive hosts with some observations on their pathogenesis in abnormal definitive hosts. Journal of Wildlife Diseases 10(4):361-369.
- ^ Bogitsh, B.J., C.E. Carter and T.N. Oeltmann (2005) Human Parasitology. 3rd Edition. Elsevier: Burlington, MA. ISBN 0-12-088468-2.
- ^ Mehlhorn, H. (ed) (2001) Encyclopedic Reference of Parasitology: Biology, Structure and Function. 2nd Edition. Springer: Berlin
Kolte SS, Satarkar RN, Mane PM. Microfilaria concomitant with metastatic deposits of adenocarcinoma in lymph node fine needle aspiration cytology: A chance finding. J Cytol [serial online] 2010 [cited 2010 Nov 22];27:78-80. Available from: http://www.jcytol.org/text.asp?2010/27/2/78/70759