Lack of seasonal variation in the life-history strategies of the trematode Coitocaecum parvum: no apparent environmental effect

Parasitology ◽  
2008 ◽  
Vol 135 (10) ◽  
pp. 1243-1251 ◽  
Author(s):  
C. LAGRUE ◽  
R. POULIN
Keyword(s):  
Life History ◽  
Seasonal Variation ◽  
Life Cycle ◽  
Water Temperature ◽  
Intermediate Host ◽  
Definitive Host ◽  
Natural Environment ◽  
Life History Strategy ◽  
Life Cycles ◽  
Coitocaecum Parvum

SUMMARYParasites with complex life cycles have developed numerous and very diverse adaptations to increase the likelihood of completing this cycle. For example, some parasites can abbreviate their life cycles by skipping the definitive host and reproducing inside their intermediate host. The resulting shorter life cycle is clearly advantageous when definitive hosts are absent or rare. In species where life-cycle abbreviation is facultative, this strategy should be adopted in response to seasonally variable environmental conditions. The hermaphroditic trematode Coitocaecum parvum is able to mature precociously (progenesis), and produce eggs by selfing while still inside its amphipod second intermediate host. Several environmental factors such as fish definitive host density and water temperature are known to influence the life-history strategy adopted by laboratory raised C. parvum. Here we document the seasonal variation of environmental parameters and its association with the proportion of progenetic individuals in a parasite population in its natural environment. We found obvious seasonal patterns in both water temperature and C. parvum host densities. However, despite being temporally variable, the proportion of progenetic C. parvum individuals was not correlated with any single parameter. The results show that C. parvum life-history strategy is not as flexible as previously thought. It is possible that the parasite's natural environment contains so many layers of heterogeneity that C. parvum does not possess the ability to adjust its life-history strategy to accurately match the current conditions.

Smelling the future: subtle life-history adjustments in response to environmental conditions and perceived transmission opportunities in a trematode

Parasitology ◽  
2016 ◽  
Vol 144 (4) ◽  
pp. 464-474 ◽  
Author(s):  
C. LAGRUE ◽  
R. RINNEVALLI ◽  
R. POULIN
Keyword(s):  
Life History ◽  
Life Cycle ◽  
Intermediate Host ◽  
Definitive Host ◽  
Environmental Conditions ◽  
Life History Strategy ◽  
Host Density ◽  
Life Cycles ◽  
Life History Strategies ◽  
Priming Effects

SUMMARYA number of parasites with complex life cycles can abbreviate their life cycles to increase the likelihood of reproducing. For example, some trematodes can facultatively skip the definitive host and produce viable eggs while still inside their intermediate host. The resulting shorter life cycle is clearly advantageous when transmission probabilities to the definitive hosts are low. Coitocaecum parvum can mature precociously (progenesis), and produce eggs by selfing inside its amphipod second intermediate host. Environmental factors such as definitive host density and water temperature influence the life-history strategy adopted by C. parvum in their crustacean host. However, it is also possible that information about transmission opportunities gathered earlier in the life cycle (i.e. by cercariae-producing sporocysts in the first intermediate host) could have priming effects on the adoption of one or the other life strategy. Here we document the effects of environmental parameters (host chemical cues and temperature) on cercarial production within snail hosts and parasite life-history strategy in the amphipod host. We found that environmental cues perceived early in life have limited priming effects on life-history strategies later in life and probably account for only a small part of the variation among conspecific parasites. External cues gathered at the metacercarial stage seem to largely override potential effects of the environmental conditions experienced by early stages of the parasite.

The effect of Toxoplasma gondii and other parasites on activity levels in wild and hybrid Rattus norvegicus

Parasitology ◽  
1994 ◽  
Vol 109 (5) ◽  
pp. 583-589 ◽  
Author(s):  
J. P. Webster
Keyword(s):  
Life Cycle ◽  
Toxoplasma Gondii ◽  
Intermediate Host ◽  
Definitive Host ◽  
Rattus Norvegicus ◽  
Parasite Load ◽  
Life Cycles ◽  
Parasitic Infections ◽  
Activity Levels ◽  
In The Wild

Using both correlational and experimental evidence, the relationship between parasite load and host activity was assessed in brown rats, Rattus norvegicus. Two hypotheses were tested – (1) that parasites with indirect life-cycles, involving transmission between a prey and its predator, will alter the activity of the intermediate host so as to increase its susceptibility to predation by the definitive host and (2) that activity levels in parasitized rats would be increased rather than decreased. Four groups of rats (n = 140) were examined. One group (n = 50) were wild brown rats trapped from 3 UK farmsteads, with naturally occurring parasites. The others were purpose-bred wild/laboratory hybrid rats with experimentally induced parasitic infections of either (n = 15) adult-acquired or (n = 15) congenitally-acquired Toxoplasma gondii (an indirect life-cycle parasite), or (n = 15) Syphacia muris (a direct life-cycle parasite). Uninfected hybrid rats (n = 45), matched for sex, age and weight, served as controls. Rats were housed individually in outdoor cages, and their activities were recorded on video-tapes for 6 non-consecutive 10 h nights. Exercise wheels were also available for the hybrid rats. Out of 6 parasite species detected in the wild rats, T. gondii was the only one which required predation by a definitive host to complete its life-cycle, and was also the only parasite to be associated with higher activity levels in infected than uninfected rats. Hybrid rats infected with T. gondii were also more active than those uninfected, whereas there were no differences in activity levels between S. muris infected and uninfected rats. This study shows that the indirect life-cycle parasite T. gondii can influence the activity of its intermediate host the rat. I suggest that this may facilitate its transmission to the cat definitive host.

The Life History of Gastrodiscoides hominis (Lewis and McConnel, 1876) Leiper, 1913– the Amphistome Parasite of Man and Pig

1972 ◽  
Vol 46 (1) ◽  
pp. 35-46 ◽  
Author(s):  
S. C. Dutt ◽  
H. D. Srivastava
Keyword(s):  
Life History ◽  
Life Cycle ◽  
Intermediate Host ◽  
Definitive Host ◽  
Growth And Development ◽  
Snail Host ◽  
Adult Fluke ◽  
History Of

The life cycle of Gastrodiscoidcs hominis has been described using Helicorbis coenosus as the experimental intermediate host and the pig as the definitive host.The morphology of the miracidium, redia and metacercaria has been described. Data have been furnished on the infection and longevity, of and production of cercariae by the snail host, and the growth and development of the adult-fluke in the definitive host.

The Life Cycles of Dipetalonematid Nematodes (Filarioidea, Dipetalonematidae): The Problem of Their Evolution

1957 ◽  
Vol 31 (4) ◽  
pp. 203-224 ◽  
Author(s):  
Roy C. Anderson
Keyword(s):  
Life Cycle ◽  
Skin Lesion ◽  
Intermediate Host ◽  
Definitive Host ◽  
Life Cycles ◽  
The Body ◽  
Intermediate Hosts ◽  
Cutaneous Lesions ◽  
The Family ◽  
Subcutaneous Tissues

The evolution of the life cycles of the members of the family Dipetalonematiidae Wehr, 1935 (Filarioidea) is considered in the light of existing knowledge of spirurid nematodes. The hypothesis that the life cycles of the dipetalonematids originated from life cycles similar to those of Draschia megastoma, Habronema muscae and H. microstoma is considered to be incorrect. Alternatively, it is pointed out that in the primitive subfamily Thelaziinae Baylis and Daubney, 1926 there are forms with typical spiruroid life cycles (Rhabdochona ovifilamenta), forms with life cycles approaching those of the dipetalonematids (Thelazia spp.), and forms with life cycles intermediate between these two (Oxyspirura spp.). It is suggested that intestinal species similar to Rhabdochona gave rise to the more specialized spiruroids and forms that left the gut (Oxyspirura, Thelazia) gave rise to the dipetalonematids.The dipetalonematids are believed to have originated from nematodes resembling the species of Thelazia and having life cycles like those of T. rhodesii, T. skrjabini and T. gulosa. Some of these worms established themselves in subcutaneous tissues. Like Parafilaria multipapillosa, they released their eggs through a break in the skin of the definitive host, thus causing a skin lesion that attracted various haematophagous arthropods which finally became involved as intermediate hosts in the life cycle. Certain species like the members of Parafilaria and Stephanofilaria (?) came to rely upon intermediate hosts that were unable to break the skin of the definitive host (Musca) and cutaneous lesions became permanent features of their life cycles. Other species became dependent upon intermediate hosts that could puncture the skin (mosquitoes, simuliids etc.) and skin lesions became unnecessary to the life cycle. The larvae of these worms then began to spread into the tissues of the skin, as found in Stephanofilaria, Onchocerca, and some species of Dipetalonema, and the infective larvae developed the ability to penetrate into the wound made by the intermediate host and perhaps, in some cases, the intact skin. Ultimately the larvae of some species habitually entered, or were deposited into, the blood stream and the adult worms were then free to colonize the vertebrate body as their larvae would then be available to the intermediate host no matter where the latter fed on the body of the definitive host; this group of worms gave rise to the many members of the family Dipetalonematidae.The family Filariidae Claus, 1883 is briefly reviewed in the light of the above hypothesis. It is pointed out that many species, e.g. Diplotriaeninae Skrjabin, 1916, live in the air sacs of reptiles and birds and probably have life cycles similar to that of Diplotriaenoides translucidus, i.e. the eggs pass through the lungs, up the trachea and out in the faeces. It is thought that these forms may represent a separate line of evolution from that which gave rise to the Dipetalonematidae. Certain genera (Lissonema, Aprocta), occurring in the orbits of birds, probably have life cycles like Thelazia or Oxyspirura. Many other genera occurring in superficial muscles and subcutaneous tissues (Squamofilaria, Ularofilaria, Tetracheilonema, Pelecitus, Monopetalonema) may release their eggs through some sort of skin lesion. Studies on these forms are urgently needed as the details of their life cycles may shed fresh light on the origins of the more specialized filarioids.

scholarly journals Endocrine Control of Life-Cycle Stages: A Constraint on Response to the Environment?

The Condor ◽  
2000 ◽  
Vol 102 (1) ◽  
pp. 35-51 ◽  
Author(s):  
Jerry D. Jacobs ◽  
John C. Wingfield
Keyword(s):  
Life History ◽  
Life Cycle ◽  
Control Systems ◽  
Life Cycles ◽  
Environmental Cues ◽  
Endocrine Control ◽  
Theoretical Approaches ◽  
Life Cycle Stages ◽  
Wide Range ◽  
Breeding Seasons

Abstract Most organisms live in seasonal environments that fluctuate on a predictable schedule and sometimes unpredictably. Individuals must, therefore, adjust so as to maximize their survival and reproductive success over a wide range of environmental conditions. In birds, as in other vertebrates, endocrine secretions regulate morphological, physiological, and behavioral changes in anticipation of future events. The individual thus prepares for predictable fluctuations in its environment by changing life-cycle stages. We have applied finite-state machine theory to define and compare different life-history cycles. The ability of birds to respond to predictable and unpredictable regimes of environmental variation may be constrained by the adaptability of their endocrine control systems. We have applied several theoretical approaches to natural history data of birds to compare the complexity of life cycles, the degree of plasticity of timing of stages within the cycle, and to determine whether endocrine control mechanisms influence the way birds respond to their environments. The interactions of environmental cues on the timing of life-history stages are not uniform in all populations. Taking the reproductive life-history stage as an example, arctic birds that have short breeding seasons in severe environments appear to use one reliable environmental cue to time reproduction and they ignore other factors. Birds having longer breeding seasons exhibit greater plasticity of onset and termination and appear to integrate several environmental cues. Theoretical approaches may allow us to predict how individuals respond to their environment at the proximate level and, conversely, predict how constraints imposed by endocrine control systems may limit the complexity of life cycles.

Some Aspects of the Ecology and Life Cycle of Three Species of Subtidal Sand-Burrowing Amphipods (Crustacea: Haustoriidae)

1969 ◽  
Vol 26 (5) ◽  
pp. 1321-1345 ◽  
Author(s):  
D. D. Sameoto
Keyword(s):  
Life Cycle ◽  
Water Temperature ◽  
Life Cycles ◽  
Cape Cod

The life cycles and some aspects of the ecology of the subtidal haustoriid amphipods Acanthohaustorius millsi Bousfield, Parahaustorius longimerus Bousfield, and Protohaustorius deichmannae Bousfield, found on Cape Cod, Massachusetts, are described. All species are annual breeders, the first two species having one brood of eggs and the last species more than one brood. The first ovigerous females appear when the water temperature reaches 5.5–10 C. All species migrate into the sands just below the low tide zone in May and remain there until late August when they start to migrate into deeper waters. The growth of populations of the three species found at Nobska Beach and Barnstable Harbor are discussed.

Encystment site affects the reproductive strategy of a progenetic trematode in its fish intermediate host: is host spawning an exit for parasite eggs?

Parasitology ◽  
2011 ◽  
Vol 138 (9) ◽  
pp. 1183-1192 ◽  
Author(s):  
KRISTIN K. HERRMANN ◽  
ROBERT POULIN
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Body Cavity ◽  
Life Cycles ◽  
Temperature Changes ◽  
Fish Spawning ◽  
Second Intermediate Host ◽  
Host Life ◽  
Major Factors ◽  
Fish Hosts

SUMMARYEach transmission event in complex, multi-host life cycles create obstacles selecting for adaptations by trematodes. One such adaptation is life cycle abbreviation through progenesis, in which the trematode precociously matures and reproduces within the second intermediate host. Progenesis eliminates the need for the definitive host and increases the chance of life cycle completion. However, progenetic individuals face egg-dispersal challenges associated with reproducing within metacercarial cysts in the tissues or body cavity of the second intermediate host. Most progenetic species await host death for their eggs to be released into the environment. The present study investigated temporal variation of progenesis in Stegodexamene anguillae in one of its second intermediate fish hosts and the effect of the fish's reproductive cycle on progenesis. The study involved monthly sampling over 13 months at one locality. A greater proportion of individuals became progenetic in the gonads of female fish hosts. Additionally, progenesis of worms in the gonads was correlated with seasonal daylight and temperature changes, major factors controlling fish reproduction. Host spawning events are likely to be an avenue of egg dispersal for this progenetic species, with the adoption of progenesis being conditional on whether or not the parasite can benefit from fish spawning.

Coevolutionary interactions between host life histories and parasite life cycles

Parasitology ◽  
1998 ◽  
Vol 116 (S1) ◽  
pp. S47-S55 ◽  
Author(s):  
J. C. Koella ◽  
P. Agnew ◽  
Y. Michalakis
Keyword(s):  
Life History ◽  
Life Cycle ◽  
Life Histories ◽  
Life History Traits ◽  
Evolutionary Ecology ◽  
Life Cycles ◽  
Microsporidian Parasite ◽  
History Of ◽  
Host Life ◽  
Host Parasite

SummarySeveral recent studies have discussed the interaction of host life-history traits and parasite life cycles. It has been observed that the life-history of a host often changes after infection by a parasite. In some cases, changes of host life-history traits reduce the costs of parasitism and can be interpreted as a form of resistance against the parasite. In other cases, changes of host life-history traits increase the parasite's transmission and can be interpreted as manipulation by the parasite. Alternatively, changes of host's life-history traits can also induce responses in the parasite's life cycle traits. After a brief review of recent studies, we treat in more detail the interaction between the microsporidian parasite Edhazardia aedis and its host, the mosquito Aedes aegypti. We consider the interactions between the host's life-history and parasite's life cycle that help shape the evolutionary ecology of their relationship. In particular, these interactions determine whether the parasite is benign and transmits vertically or is virulent and transmits horizontally.Key words: host-parasite interaction, life-history, life cycle, coevolution.

Transmission dynamics of Echinococcus multilocularis; its reproduction number, persistence in an area of low rodent prevalence, and effectiveness of control

Parasitology ◽  
2005 ◽  
Vol 131 (1) ◽  
pp. 133-140 ◽  
Author(s):  
K. TAKUMI ◽  
J. VAN DER GIESSEN
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Central Europe ◽  
Definitive Host ◽  
Echinococcus Multilocularis ◽  
Reproduction Number ◽  
Parasite Burden ◽  
Host Population ◽  
Total Biomass ◽  
Control Campaign

On the basis of high prevalences of Echinococcus multilocularis in the growing fox populations in Central Europe, its total biomass may have increased significantly in the past 20 years. E. multilocularis is now also found in areas outside the known endemic area in Central Europe. Therefore, E. multilocularis, the causative agent of a serious parasitic zoonosis, might be of major concern for public health and a challenge to control. Some experimental field trials to control E. multilocularis using an anti-worm drug reduced parasite burden in a contaminated region during the control campaign, but failed to eradicate the parasite completely. It was our aim to develop a mathematical model describing the biomass of egg, larval, and adult worm stages of the E. multilocularis life-cycle, and simulate a hypothetical control campaign. Additionally, we derived the reproduction number of this parasite and explored conditions for the persistence of the parasite's life-cycle. Our model shows that while control campaigns rapidly reduce the worm burden in the definitive host, and consequently eggs in the environment, the pool of larvae in the intermediate host remains large. The parasite's life-cycle persists in a region where prevalence in the intermediate host is low (∼1%). Therefore, we conclude that the parasite is likely to re-emerge if control is discontinued on the basis of reduced worm population. Continued treatment of the definitive host is required to eradicate the larval stage of the parasite from the intermediate host population.

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