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Acoelomate Bilateral Animals

   The term worm is loosely employed in
    biology and is applied to very different
    animals including the segmented worms
    (Annelids), roundworms
    (pseudocolomates and a variety of
    acoelomate bilateral animals.
Acoelomate Bilateral Animals
   There are three phyla of acoelomate
    bilateral animals:
       Platyhelminthes: flatworms
       Nemertea: ribbon worms
       Gnathostomulida: jawed worms
Acoelomate Bilateral Animals
   By far the most important in diversity and
    economic importance is the phylum
    Platyhelminthes, which includes a variety
    of parasitic forms such as the flukes and
    tapeworms.
Acoelomate Bilateral Animals
   Unlike the radiate animals all of these organisms
    are mobile and have evolved cephalization with
    their sense organs concentrated at the head
    end. There is also the beginning of a ladder-
    type nervous system.

   In addition, they are bilaterally symmetrical.
Acoelomate Bilateral Animals
   All of these animals are triploblastic, but lack a
    coelom. Instead, they have a solid body filled
    with parenchyma cells.

   They have evolved organs and in some cases
    organ systems. The simplest excretory or
    osmoregulatory systems and circulatory systems
    are found in members of these groups.
Phylum Platyhelminthes
   Members of the Platyhelminthes typically have
    dorsoventrally flattened bodies that are usually
    slender and leaflike or ribbonlike.

   There are four classes in the Platyhelminthes.
    The Turbellaria are free living whereas as
    members of the Monogenea, Trematoda and
    Cestoda are parasitic.
Nutrition
   The digestive system includes a mouth, pharynx,
    and blind intestine.

   In the free-living Turbellarians the pharynx can
    be everted from the mouth.

   Food is sucked into the intestine where a
    combination of extracellular and intracellular
    digestion takes place.
Nutrition
   Undigested food exits via the pharynx.

   In the Cestoda the digestive tract is absent
    and all nutrients are absorbed across the
    tegument (the syncytial membrane/body
    covering found in all parasitic
    Platyhelminthes).
Excretion/Osmoregulation
   The osmoregulatory system consists of a series
    of canals that end in flame cells or
    protonephridia).

   This system appears mainly intended to remove
    excess fluid, but retain essential ions. It is most
    well developed in freshwater Turbellarians, but
    reduced or absent in marine species, which do
    not have to remove excess water.
Nervous system and sense organs
   Flatworms possess a simple brain and one to
    five pairs of longitudinal nerve cords that are
    cross connected to form a ladder-like
    arrangement.

   There has been a tendency towards reduction of
    the number of pairs of nerve cords and
    increased development of the ventral pair. A
    similar evolutionary pathway may have led to
    the development of the ventral nerve cord found
    in annelids and arthropods.
Nervous system and sense organs

   Neurons are specialized for different tasks e.g.
    sensory and motor functions, which is an
    important advance in the evolution of nervous
    systems.

   There are a number of different sensory cells
    (e.g. rheoceptors and statocysts) found in
    flatworms and tactile and chemoreceptive cells
    are abundant.
Nervous system and sense organs

   In freshwater Planarians concentrations of
    sensory cells form two ear-like structures
    (the auricles) found on the side of the
    head.

   Light sensitive eyespots or ocelli are
    common in all classes but Cestoda.
Reproduction
   Reproduction in the Platyhelminthes can
    be asexual or sexual. However, most are
    hermaphroditic and cross fertilize.

   In parasitic forms sexual and asexual
    reproduction may alternate in different
    stages of the life history
Classification of Platyhelminthes
   There are four classes in the
    Platyhelminthes:
       Class Turbellaria: free-living flatworms.
       Class Turbellaria: endoparasitic flukes
       Class Monogenea: parasitic flukes that are
        mainly ectoparasites
       Class Cestoda: tapeworms
Class Turbellaria
   Class Turbellaria contains about 3000 species.
    There is considerable debate about the
    classification of the class and it is likely that the
    class is not monophyletic.

   Most species are marine and benthic. However,
    some are also found in fresh water as well as in
    moist temperate and tropical terrestrial habitats.
Figure 14.10




                             8.2




               Marine turbellarian
Dugesia tigrina, a freshwater turbellarian




                              © Mauricio A. Muñoz
Class Turbellaria
   Most Turbellarians are predators of invertebrates
    smaller than themselves. Other species are
    herbivores or scavengers.

   Turbellarians move by swimming, creeping or
    crawling. They combine muscular contractions
    with ciliary movement to move.
Class Trematoda
   There are about 9000 species of
    trematodes all of which are parasitic.
    Most parasitize vertebrates.

   Adaptations for parasitism include suckers
    and hooks for attachment, glands to
    produce cyst material and increased
    reproductive capacity.
Sheep liver fluke
Class Trematoda
   Structurally trematodes are similar to
    turbellarians having a well developed
    digestive system and similar nervous,
    excretory, and reproductive systems.
    However, a major difference is the
    tegument .
Tegument
   The tegument (found in all parasitic
    Platyhelminthes) is a nonciliated, cytoplasmic
    syncytium that overlays layers of muscle.

   The syncytium represents extensions of cells
    that are located below the muscle in the
    parenchyma.

   The tegument protects the parasite against its
    host (e.g. against digestive enzymes).
Figure 14.05




               8.5
Digenean Trematodes
   There are three subclasses of
    Trematodes, but two are small, poorly
    studied groups.

   The third group, the Digenea, however is a
    large group of major medical and
    economic importance.
Digenean trematodes
   The flukes have a complex life cycle in
    which a snail is the first (or intermediate)
    host and a vertebrate the final (or
    definitive host).

   The definitive host is one in which the
    fluke reproduces sexually.
Digenean trematodes
   In some species there may be 2 or 3
    intermediate hosts before the definitive
    host is reached.

   Trematodes inhabit a variety of sites in
    their hosts including the digestive tract,
    respiratory tract, circulatory system,
    urinary tract, and reproductive tract.
Digenean trematodes
   Digenean life cycles are very complex and
    the fluke passes through numerous
    stages.
Digenean trematodes
   A typical example would include the
    following stages:
       Adult
       Egg (or shelled embryo) shed into water
       Miracidium : a free swimming, ciliated larva
        that finds and penetrates a snail intermediate
        host
Digenean trematodes
   Sporocyst : reproduces asexually in
    intermediate host producing more sporocysts
    or another asexually reproducing stage called
    a redia.
   Redia produce more redia or cercariae.
    Cercariae leave the intermediate host and
    swim. Then they penetrate the skin of
    another intermediate host or the definitive
    host.
Digenean trematodes
   Cercariae that enter an intermediate host
    encyst in muscle and wait to be consumed by
    the definitive host.
   Cercariae that enter the definitive host make
    their way to their desired home and develop
    into an adult fluke which reproduces sexually
    and produces eggs.
Clonorchis liver fluke
   Clonorchis is the most important liver fluke to infect
    humans. Common in much of Asia (including China,
    Japan and southern Asia).

   Adult flukes live in the bile passages and shelled
    miricidia pass out in feces. The miricidia enter snails
    eventually leave the snails as cercariae and find a fish
    where they encyst.

   If fish is eaten raw or poorly cooked the person becomes
    infected
Figure 14.12




               8.8
How do flukes manipulate their
                hosts?
   Many parasites infect an intermediate host that
    needs to be eaten by the definitive host for the
    parasite to complete its lifecycle.

   There are many instances of parasites altering
    their intermediate hosts behavior to make it
    more vulnerable a predator (the definitive host).
    Such behavior is widespread in flukes.
How do flukes manipulate their
                hosts?
   In the Carpenteria Salt Marshes in
    southern California lives the fluke
    Euhaplorchis californiensis.
   It has a life cycle that includes two
    intermediate hosts, first the California
    Horn Snail and then the California killifish
    and a final host which can be any of a
    variety of fish eating birds.
How do flukes manipulate their
                hosts?
   The fluke leaves its definitive host as an egg in
    bird droppings which are eaten by the fluke’s
    first intermediate host the snail. snail host.

   The fluke then castrates the snail (preventing it
    from diverting energy into eggs and away from
    the parasite).

   The fluke then reproduces asexually and sheds
    cercariae into the water.
How do flukes manipulate their
                hosts?
   The cercariae seek out the next
    intermediate host the killifish and latch
    onto the fish’s gills.

   Each cercaria works its way into a blood
    vessel and explores until it finds a nerve
    which it then follows until it reaches the
    fish’s brain.
How do flukes manipulate their
                hosts?
   The cercariae don’t penetrate the brain
    but sit on top of it. Then they wait for the
    fish to be eaten by a bird.

   Once eaten by a bird they break out of the
    fish’s head and move into the bird’s gut
    where they produce eggs that continue
    the cycle
How do flukes manipulate their
                hosts?
   The cercariae sitting on the bird’s brain
    apparently don’t sit passively waiting.

   Killifish when swimming occasionally
    shimmy and jerk around flashing their
    bellies. Those infected with cercariae are
    four times more likely to do so than non-
    infected fish.
How do flukes manipulate their
                hosts?
   In field experiments in which penned fish
    were made available to foraging birds
    infected fish were 30 times (!) more likely
    to be eaten than uninfected fish.
How do flukes manipulate their
                hosts?
   Research on how the flukes alter the fish’s
    behavior has shown that the flukes
    produce powerful molecular signals called
    fibroblast growth factors.

   These interfere with the growth of nerves
    and may be the mechanism the flukes
    use.
Schistosomiasis
   Schsitosomiasis is an infection with blood
    flukes and is one of the most important
    major infectious diseases on the planet.

   More then 200 million people are infected
    worldwide with these flukes which they
    acquire swimming or walking in water in
    which the intermediate snail host lives
Schistosome
life cycle.
Schistosomiasis
   When a schistosome cercaria swims it takes
    care to avoid UV light which can damage it, but
    is very sensitive to the scent of humans.

   When it senses molecules from human skin it
    swims rapidly and jerks around looking for the
    person. When it makes contact it releases
    chemicals that soften the skin and burrows in
    shedding its tail at the same time.
Schistosomiasis
   The fluke searches until it finds a capillary and
    enters it.

   The capillary is only barely wide enough for the
    fluke and it moves along using its pair of
    suckers. Eventually, it reaches a larger blood
    vessel in which it can float until it reaches the
    lungs and enters an artery and eventually makes
    its way to the liver.
Schistosomiasis
   Once in the liver, the fluke feeds on blood
    and begins to mature and develops
    ovaries or testes depending on its sex.

   The fluke grows dozens of times larger in
    the course of a few weeks and then
    begins to search for a mate.
Schistosomiasis
   The fluke produces chemicals to attract
    members of the opposite sex.

   Females are slender and delicate,
    whereas males are much bigger and have
    a spiny trough or groove into which the
    female fits and locks in.
Figure 14.13




               8.9a and b
Schistosomiasis
   Once paired up the pair mature sexually
    and travel from the liver to a permanent
    home that is species-specific.

   In Schistosoma mansoni it is near the
    large intestine, in S. haemotobium it is the
    bladder, and in S. nasale, a blood fluke of
    cows, it is the nose.
Schistosomiasis
   Once established the pair remain in situ
    for the rest of their lives.

   The male consumes blood and feeds the
    female most of it, which she turns into
    eggs, which pass out of the host and can
    begin the life cycle again.
Class Monogenea
   The monogenetic flukes were previously
    classified as on order of the Trematoda, but
    recent work suggests they are more closely
    related to cestodes (tapeworms).

   Monogeneans are typically external parasites of
    fish that clamp onto the gills using a hooked
    organ called an opisthaptor . Some also
    parasitize frogs and turtles.
Figure 14.16




               8.11
Class Monogenea
   Unlike the trematodes Monogeneans have
    only a single host.

   The egg hatches into a ciliated larva which
    seeks out its host in the water.
Class Cestoda (tapeworms)
   Tapeworms are parasites of the vertebrate
    digestive tract and about 4000 species of
    are known.

   Almost all tapeworms require at least two
    hosts with the definitive host being a
    vertebrate although intermediate hosts
    can be invertebrates.
Class Cestoda
   Members of the Class Cestoda (tapeworms) are
    quite different in appearance from the other
    members of the Platyhelminthes.

   They have long, flat, tape-like bodies composed
    of a scolex for attaching to their host and a
    chain of many reproductive units or proglottids
    called a strobila. New proglottids form behind
    the scolex and the strobila may become
    extremely long.
Figure 14.18




               8.12
Tapeworm scolex
                                     Hooks




                                             Suckers



The scolex is equipped with a combination of suckers
and hooks that enable it to grip onto its host’s
intestines.
Class Cestoda
   Tapeworms live in the intestines and
    because they are immersed in digested
    food lack a digestive system of their own
    simply absorbing food across their
    tegument.
Class Cestoda
   To facilitate the absorption of food a
    tapeworm’s tegument has huge numbers
    of tiny projections called microtriches ,
    which are broadly similar to the microvilli
    of the vertebrate intestine.

   They similarly increase the surface area of
    the tegument for absorption.
Figure 14.17




               8.13
Class Cestoda
   Tapeworms are usually monoecious (have both
    male and female reproductive organs).

   A proglottid is fertilized by another proglottid in
    the same or a different strobila.

   Shell-encased embryos form in the uterus and
    exit the proglottid via a uterine pore or the entire
    proglottid may detatch and pass out of the host.
Figure 14.20




               8.14
Human tapeworms
   Humans are definitive hosts to several
    tapeworms including the beef tapeworm
    Taenia saginata, pork tapeworm T. solium,
    and fish tapeworm Diphyllobothrium latum.
Human tapeworms
   The lifecycles of these parasites are similar.

   Shelled larave are shed into the environment.

   These are consumed by the intermediate host
    and the larvae (oncospheres) hatch, bury into
    blood vessels and make their way to skeletal
    muscle where they encyst becoming so called
    “bladder worms” or cysticerci.
Human tapeworms
   The encysted larva develops an invaginated
    scolex and waits, perhaps for years, for its host
    to be eaten.

   If the meat is uncooked the cysticercus extends
    its scolex, attaches to the wall of the intestine
    and within 2-3 weeks matures and begins
    growing and producing eggs. A tapeworm may
    be many meters long and live for years.
Figure 14.19




               8.15
Humans as intermediate hosts
   Humans may become intermediate hosts for
    tapeworms with potentially disastrous
    consequences if they consume shelled larvae in
    contaminated food.

   In an evolutionarily unfamiliar environment,
    cysticerci may encyst in inappropriate locations
    such as the brain which is frequently fatal.
Figure 14.21


 Cysticerci in human brain




                             8.16
Phylum Nemertea (Rhynchocoela)
        Ribbonworms
   The nemerteans (ribbon worms) are long,
    marine predatory worms and there are
    about 1000 species known.

   Unlike members of the Platyhelminthes
    nemerteans have a complete gut with a
    mouth and anus and a true circulatory
    system
Phylum Nemertea (Rhynchocoela)
        Ribbonworms
   Prey is captured using a long muscular proboscis
    armed with a barb called a stylet..

   The proboscis lies in an interior cavity called the
    rhynchocoel and muscular pressure on fluid in the
    rhynchocoel causes the proboscis to be quickly
    everted.

   The prey is wrapped in the sticky, slime-covered,
    proboscis and stabbed repeatedly with the stylet.
    Neurotoxins in the slime incapacitate the prey.
Figure 14.24a




                                            Figure 14.24b




                        8.18



Internal structure of female ribbon worm
(above).

Nemertean with proboscis extended (right)
Figure 14.25




               8.19



                      Baseodiscus mexicanus a nemertean from
                      the Galapagos Islands
Phylum Gnathostomulida
   The first Gnatostomulid was not
    discovered until 1928 and only about 80
    species are known.

   They are tiny (0.5-1mm long) wormlike
    animals that live in the interstitial spaces
    of sand and silt.
Phylum Gnathostomulida
   Because they lack a pseudocoel,
    circulatory system, and anus
    gnathostomulids were first classed as
    turbellarians.

   More recently it has been suggested that
    they are more closely related to the phyla
    Rotifera and Acanthocephala.
Figure 14.27




                     8.20



               Gnathostomula jenneri

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Flatworms

  • 1. Acoelomate Bilateral Animals  The term worm is loosely employed in biology and is applied to very different animals including the segmented worms (Annelids), roundworms (pseudocolomates and a variety of acoelomate bilateral animals.
  • 2. Acoelomate Bilateral Animals  There are three phyla of acoelomate bilateral animals:  Platyhelminthes: flatworms  Nemertea: ribbon worms  Gnathostomulida: jawed worms
  • 3. Acoelomate Bilateral Animals  By far the most important in diversity and economic importance is the phylum Platyhelminthes, which includes a variety of parasitic forms such as the flukes and tapeworms.
  • 4. Acoelomate Bilateral Animals  Unlike the radiate animals all of these organisms are mobile and have evolved cephalization with their sense organs concentrated at the head end. There is also the beginning of a ladder- type nervous system.  In addition, they are bilaterally symmetrical.
  • 5. Acoelomate Bilateral Animals  All of these animals are triploblastic, but lack a coelom. Instead, they have a solid body filled with parenchyma cells.  They have evolved organs and in some cases organ systems. The simplest excretory or osmoregulatory systems and circulatory systems are found in members of these groups.
  • 6. Phylum Platyhelminthes  Members of the Platyhelminthes typically have dorsoventrally flattened bodies that are usually slender and leaflike or ribbonlike.  There are four classes in the Platyhelminthes. The Turbellaria are free living whereas as members of the Monogenea, Trematoda and Cestoda are parasitic.
  • 7. Nutrition  The digestive system includes a mouth, pharynx, and blind intestine.  In the free-living Turbellarians the pharynx can be everted from the mouth.  Food is sucked into the intestine where a combination of extracellular and intracellular digestion takes place.
  • 8. Nutrition  Undigested food exits via the pharynx.  In the Cestoda the digestive tract is absent and all nutrients are absorbed across the tegument (the syncytial membrane/body covering found in all parasitic Platyhelminthes).
  • 9. Excretion/Osmoregulation  The osmoregulatory system consists of a series of canals that end in flame cells or protonephridia).  This system appears mainly intended to remove excess fluid, but retain essential ions. It is most well developed in freshwater Turbellarians, but reduced or absent in marine species, which do not have to remove excess water.
  • 10. Nervous system and sense organs  Flatworms possess a simple brain and one to five pairs of longitudinal nerve cords that are cross connected to form a ladder-like arrangement.  There has been a tendency towards reduction of the number of pairs of nerve cords and increased development of the ventral pair. A similar evolutionary pathway may have led to the development of the ventral nerve cord found in annelids and arthropods.
  • 11. Nervous system and sense organs  Neurons are specialized for different tasks e.g. sensory and motor functions, which is an important advance in the evolution of nervous systems.  There are a number of different sensory cells (e.g. rheoceptors and statocysts) found in flatworms and tactile and chemoreceptive cells are abundant.
  • 12. Nervous system and sense organs  In freshwater Planarians concentrations of sensory cells form two ear-like structures (the auricles) found on the side of the head.  Light sensitive eyespots or ocelli are common in all classes but Cestoda.
  • 13. Reproduction  Reproduction in the Platyhelminthes can be asexual or sexual. However, most are hermaphroditic and cross fertilize.  In parasitic forms sexual and asexual reproduction may alternate in different stages of the life history
  • 14. Classification of Platyhelminthes  There are four classes in the Platyhelminthes:  Class Turbellaria: free-living flatworms.  Class Turbellaria: endoparasitic flukes  Class Monogenea: parasitic flukes that are mainly ectoparasites  Class Cestoda: tapeworms
  • 15. Class Turbellaria  Class Turbellaria contains about 3000 species. There is considerable debate about the classification of the class and it is likely that the class is not monophyletic.  Most species are marine and benthic. However, some are also found in fresh water as well as in moist temperate and tropical terrestrial habitats.
  • 16. Figure 14.10 8.2 Marine turbellarian
  • 17. Dugesia tigrina, a freshwater turbellarian © Mauricio A. Muñoz
  • 18. Class Turbellaria  Most Turbellarians are predators of invertebrates smaller than themselves. Other species are herbivores or scavengers.  Turbellarians move by swimming, creeping or crawling. They combine muscular contractions with ciliary movement to move.
  • 19. Class Trematoda  There are about 9000 species of trematodes all of which are parasitic. Most parasitize vertebrates.  Adaptations for parasitism include suckers and hooks for attachment, glands to produce cyst material and increased reproductive capacity.
  • 21. Class Trematoda  Structurally trematodes are similar to turbellarians having a well developed digestive system and similar nervous, excretory, and reproductive systems. However, a major difference is the tegument .
  • 22. Tegument  The tegument (found in all parasitic Platyhelminthes) is a nonciliated, cytoplasmic syncytium that overlays layers of muscle.  The syncytium represents extensions of cells that are located below the muscle in the parenchyma.  The tegument protects the parasite against its host (e.g. against digestive enzymes).
  • 24. Digenean Trematodes  There are three subclasses of Trematodes, but two are small, poorly studied groups.  The third group, the Digenea, however is a large group of major medical and economic importance.
  • 25. Digenean trematodes  The flukes have a complex life cycle in which a snail is the first (or intermediate) host and a vertebrate the final (or definitive host).  The definitive host is one in which the fluke reproduces sexually.
  • 26. Digenean trematodes  In some species there may be 2 or 3 intermediate hosts before the definitive host is reached.  Trematodes inhabit a variety of sites in their hosts including the digestive tract, respiratory tract, circulatory system, urinary tract, and reproductive tract.
  • 27. Digenean trematodes  Digenean life cycles are very complex and the fluke passes through numerous stages.
  • 28. Digenean trematodes  A typical example would include the following stages:  Adult  Egg (or shelled embryo) shed into water  Miracidium : a free swimming, ciliated larva that finds and penetrates a snail intermediate host
  • 29. Digenean trematodes  Sporocyst : reproduces asexually in intermediate host producing more sporocysts or another asexually reproducing stage called a redia.  Redia produce more redia or cercariae. Cercariae leave the intermediate host and swim. Then they penetrate the skin of another intermediate host or the definitive host.
  • 30. Digenean trematodes  Cercariae that enter an intermediate host encyst in muscle and wait to be consumed by the definitive host.  Cercariae that enter the definitive host make their way to their desired home and develop into an adult fluke which reproduces sexually and produces eggs.
  • 31. Clonorchis liver fluke  Clonorchis is the most important liver fluke to infect humans. Common in much of Asia (including China, Japan and southern Asia).  Adult flukes live in the bile passages and shelled miricidia pass out in feces. The miricidia enter snails eventually leave the snails as cercariae and find a fish where they encyst.  If fish is eaten raw or poorly cooked the person becomes infected
  • 33. How do flukes manipulate their hosts?  Many parasites infect an intermediate host that needs to be eaten by the definitive host for the parasite to complete its lifecycle.  There are many instances of parasites altering their intermediate hosts behavior to make it more vulnerable a predator (the definitive host). Such behavior is widespread in flukes.
  • 34. How do flukes manipulate their hosts?  In the Carpenteria Salt Marshes in southern California lives the fluke Euhaplorchis californiensis.  It has a life cycle that includes two intermediate hosts, first the California Horn Snail and then the California killifish and a final host which can be any of a variety of fish eating birds.
  • 35. How do flukes manipulate their hosts?  The fluke leaves its definitive host as an egg in bird droppings which are eaten by the fluke’s first intermediate host the snail. snail host.  The fluke then castrates the snail (preventing it from diverting energy into eggs and away from the parasite).  The fluke then reproduces asexually and sheds cercariae into the water.
  • 36. How do flukes manipulate their hosts?  The cercariae seek out the next intermediate host the killifish and latch onto the fish’s gills.  Each cercaria works its way into a blood vessel and explores until it finds a nerve which it then follows until it reaches the fish’s brain.
  • 37. How do flukes manipulate their hosts?  The cercariae don’t penetrate the brain but sit on top of it. Then they wait for the fish to be eaten by a bird.  Once eaten by a bird they break out of the fish’s head and move into the bird’s gut where they produce eggs that continue the cycle
  • 38. How do flukes manipulate their hosts?  The cercariae sitting on the bird’s brain apparently don’t sit passively waiting.  Killifish when swimming occasionally shimmy and jerk around flashing their bellies. Those infected with cercariae are four times more likely to do so than non- infected fish.
  • 39. How do flukes manipulate their hosts?  In field experiments in which penned fish were made available to foraging birds infected fish were 30 times (!) more likely to be eaten than uninfected fish.
  • 40. How do flukes manipulate their hosts?  Research on how the flukes alter the fish’s behavior has shown that the flukes produce powerful molecular signals called fibroblast growth factors.  These interfere with the growth of nerves and may be the mechanism the flukes use.
  • 41. Schistosomiasis  Schsitosomiasis is an infection with blood flukes and is one of the most important major infectious diseases on the planet.  More then 200 million people are infected worldwide with these flukes which they acquire swimming or walking in water in which the intermediate snail host lives
  • 43. Schistosomiasis  When a schistosome cercaria swims it takes care to avoid UV light which can damage it, but is very sensitive to the scent of humans.  When it senses molecules from human skin it swims rapidly and jerks around looking for the person. When it makes contact it releases chemicals that soften the skin and burrows in shedding its tail at the same time.
  • 44. Schistosomiasis  The fluke searches until it finds a capillary and enters it.  The capillary is only barely wide enough for the fluke and it moves along using its pair of suckers. Eventually, it reaches a larger blood vessel in which it can float until it reaches the lungs and enters an artery and eventually makes its way to the liver.
  • 45. Schistosomiasis  Once in the liver, the fluke feeds on blood and begins to mature and develops ovaries or testes depending on its sex.  The fluke grows dozens of times larger in the course of a few weeks and then begins to search for a mate.
  • 46. Schistosomiasis  The fluke produces chemicals to attract members of the opposite sex.  Females are slender and delicate, whereas males are much bigger and have a spiny trough or groove into which the female fits and locks in.
  • 47. Figure 14.13 8.9a and b
  • 48. Schistosomiasis  Once paired up the pair mature sexually and travel from the liver to a permanent home that is species-specific.  In Schistosoma mansoni it is near the large intestine, in S. haemotobium it is the bladder, and in S. nasale, a blood fluke of cows, it is the nose.
  • 49. Schistosomiasis  Once established the pair remain in situ for the rest of their lives.  The male consumes blood and feeds the female most of it, which she turns into eggs, which pass out of the host and can begin the life cycle again.
  • 50. Class Monogenea  The monogenetic flukes were previously classified as on order of the Trematoda, but recent work suggests they are more closely related to cestodes (tapeworms).  Monogeneans are typically external parasites of fish that clamp onto the gills using a hooked organ called an opisthaptor . Some also parasitize frogs and turtles.
  • 51. Figure 14.16 8.11
  • 52. Class Monogenea  Unlike the trematodes Monogeneans have only a single host.  The egg hatches into a ciliated larva which seeks out its host in the water.
  • 53. Class Cestoda (tapeworms)  Tapeworms are parasites of the vertebrate digestive tract and about 4000 species of are known.  Almost all tapeworms require at least two hosts with the definitive host being a vertebrate although intermediate hosts can be invertebrates.
  • 54. Class Cestoda  Members of the Class Cestoda (tapeworms) are quite different in appearance from the other members of the Platyhelminthes.  They have long, flat, tape-like bodies composed of a scolex for attaching to their host and a chain of many reproductive units or proglottids called a strobila. New proglottids form behind the scolex and the strobila may become extremely long.
  • 55. Figure 14.18 8.12
  • 56. Tapeworm scolex Hooks Suckers The scolex is equipped with a combination of suckers and hooks that enable it to grip onto its host’s intestines.
  • 57. Class Cestoda  Tapeworms live in the intestines and because they are immersed in digested food lack a digestive system of their own simply absorbing food across their tegument.
  • 58. Class Cestoda  To facilitate the absorption of food a tapeworm’s tegument has huge numbers of tiny projections called microtriches , which are broadly similar to the microvilli of the vertebrate intestine.  They similarly increase the surface area of the tegument for absorption.
  • 59. Figure 14.17 8.13
  • 60. Class Cestoda  Tapeworms are usually monoecious (have both male and female reproductive organs).  A proglottid is fertilized by another proglottid in the same or a different strobila.  Shell-encased embryos form in the uterus and exit the proglottid via a uterine pore or the entire proglottid may detatch and pass out of the host.
  • 61. Figure 14.20 8.14
  • 62. Human tapeworms  Humans are definitive hosts to several tapeworms including the beef tapeworm Taenia saginata, pork tapeworm T. solium, and fish tapeworm Diphyllobothrium latum.
  • 63. Human tapeworms  The lifecycles of these parasites are similar.  Shelled larave are shed into the environment.  These are consumed by the intermediate host and the larvae (oncospheres) hatch, bury into blood vessels and make their way to skeletal muscle where they encyst becoming so called “bladder worms” or cysticerci.
  • 64. Human tapeworms  The encysted larva develops an invaginated scolex and waits, perhaps for years, for its host to be eaten.  If the meat is uncooked the cysticercus extends its scolex, attaches to the wall of the intestine and within 2-3 weeks matures and begins growing and producing eggs. A tapeworm may be many meters long and live for years.
  • 65. Figure 14.19 8.15
  • 66. Humans as intermediate hosts  Humans may become intermediate hosts for tapeworms with potentially disastrous consequences if they consume shelled larvae in contaminated food.  In an evolutionarily unfamiliar environment, cysticerci may encyst in inappropriate locations such as the brain which is frequently fatal.
  • 67. Figure 14.21 Cysticerci in human brain 8.16
  • 68. Phylum Nemertea (Rhynchocoela) Ribbonworms  The nemerteans (ribbon worms) are long, marine predatory worms and there are about 1000 species known.  Unlike members of the Platyhelminthes nemerteans have a complete gut with a mouth and anus and a true circulatory system
  • 69. Phylum Nemertea (Rhynchocoela) Ribbonworms  Prey is captured using a long muscular proboscis armed with a barb called a stylet..  The proboscis lies in an interior cavity called the rhynchocoel and muscular pressure on fluid in the rhynchocoel causes the proboscis to be quickly everted.  The prey is wrapped in the sticky, slime-covered, proboscis and stabbed repeatedly with the stylet. Neurotoxins in the slime incapacitate the prey.
  • 70. Figure 14.24a Figure 14.24b 8.18 Internal structure of female ribbon worm (above). Nemertean with proboscis extended (right)
  • 71. Figure 14.25 8.19 Baseodiscus mexicanus a nemertean from the Galapagos Islands
  • 72. Phylum Gnathostomulida  The first Gnatostomulid was not discovered until 1928 and only about 80 species are known.  They are tiny (0.5-1mm long) wormlike animals that live in the interstitial spaces of sand and silt.
  • 73. Phylum Gnathostomulida  Because they lack a pseudocoel, circulatory system, and anus gnathostomulids were first classed as turbellarians.  More recently it has been suggested that they are more closely related to the phyla Rotifera and Acanthocephala.
  • 74. Figure 14.27 8.20 Gnathostomula jenneri