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Journal of Parasitic Diseases: Official Organ of the Indian Society for Parasitology logoLink to Journal of Parasitic Diseases: Official Organ of the Indian Society for Parasitology
. 2013 Jan 26;38(3):307–310. doi: 10.1007/s12639-013-0249-x

Seasonal changes in the population of Menacanthus cornutus (Phthiraptera: Amblycera)

Adesh Kumar 1,, Rakesh Kumar 1
PMCID: PMC4087304  PMID: 25035591

Abstract

The chicken body louse, Menacanthus cornutus (Menoponidae s.l.) completes its whole life cycle on the body of Gallus gallus domesticus. The louse exploits the microclimate developed by host skin temperature and feather cover. The weekly visual examination has demonstrated the pronounced response on the population fluctuation of M. cornutus to the seasonal changes in the environment despite all favourable condition on the body of homothermic host. The experiments commences from April 2008. The peak index was obtained in the month of August followed by drastically decline in succeeding 5 months. Lice index begins building up slowly from the months of February and March. The correlation between mean monthly lice indices with temperature and photoperiod were analyses as strong positive. The moderate positive correlation was found with relative humidity and it remained insignificant with rainfall.

Keywords: Phthiraptera, Ectoparasite, Mallophaga, Domestic fowl, Menoponidae

Introduction

Phthirapteran ectoparasites are adapted to warm and humid microclimate developed by the host feather or hair or coat of wooly mammals. The change in environmental factor (i.e. temperature, relative humidity, rainfall, photoperiod etc.) is reflected by population build up on parasitizing host body (Von Keler 1969). Thorough look on literature have revealed that study on avian lice population response to seasonality have been documented by Boyd (1951), Woodman and Dicke (1954), Ash (1960), Touleshkov (1965), Baum (1968), Foster (1969), Eveleigh and Threlfall (1976), Agarwal and Saxena (1979) and Chandra et al. (1988, 1990). Furthermore, seasonal changes in mammalian phthirapteran have been studied by Craufurd-Benson (1941), Matthysse (1946), Cowan (1946), Scott (1952), Allen and Dicke (1954), Murray (1957, 1960, 1963, 1968), Anderson (1962), Murray and Gordon (1969), Samuel and Trainer (1971), Amin and Madbouly (1973), Rust (1974), Rawat and Saxena (1990, 1992) and Kumar et al. (1993). A majority of above workers have noted that mammalian lice are generally exhibited peak intensity of infestation in the winter months while the avian lice are found maximum in the summer months. Menacanthus cornutus is haematophagous and very fast runner on the skin. This poultry louse is least encountered by phthirapterists of the world. The seasonal changes in the population of M. cornutus have been unstudied so far. Keeping in view, authors have made an attempt to record the population fluctuation of M. cornutus on domestic fowl (Gallus gallus domesticus).

Materials and methods

The study was conducted on a flock of six fowls (one male and five females) having age group of 7–9 months at the commencement of the experiment. The experiments were accomplished from April 2008 to March 2009 at Purola (Uttarkashi, India). The flock had only infestation of M. cornutus. The birds were maintaining ad-labitum throughout the year in changing climatic conditions in wooden cage. The feed (wheat, rice, grinded maize etc.), water and similar hygienic condition have been provided to fowls till the completion of experiment. The domestic fowls were of brown leg horn breed.

Each bird was examined weekly with the help of magnifying torch, to record the lice index by gently deflecting feathers so that birds do not get any injury. The counting of lice on each bird have been made for 5 min and selected body parts were searched out for lice which were far visited by M. cornutus. The degree of correlation between mean monthly lice indices and four ecofactors (i.e. Temperature, relative humidity, rainfall and photoperiod) have been analysed.

Results

The chicken body louse, M. cornutus is a very fast runner over the skin of host among all amblyceran species infesting domestic fowl and seldom visited the feathers of host. The mean monthly lice index was recorded 23.67 in the month April 2008 (Fig. 1). Thereafter, sharp decline was recorded in the month of May (15.88), when least humidity was recorded in and around Purola. Furthermore, lice index increases in next 2 months (June-23.25 and July-28.39). The peak index was obtained in the month of August (41) when humidity and temperature might be optimum. The lice index in next 4 months (e.g. September, October, November and December) showed regular decreasing trend (23.8, 21.75, 17.35 and 14.05 respectively) (Fig. 1). This ectoparasite found to be very sensitive to low environmental temperature. The lowest lice index was recorded in the month of January (1.95) while the mean monthly temperature was also least and had sufficient humidity. Lice index begins building up slowly from the months of February and March (3.87, 9.7) (Fig. 1). These months exhibited little increase in temperature and fast decrease in humidity, which support the population build up. The correlation between mean monthly lice indices and four ecofactors were also analyses statistically. The strong positive correlation existed between lice indices and mean monthly temperature as well as lice index and photoperiod (r12 = +0.77 and r15 = +80). The correlation between lice indices and R.H. remain insignificant r13 = +0.19). While the moderate positive correlation recorded between lice indices and rainfall (r14 = +0.57).

Fig. 1.

Fig. 1

Showing the seasonal changes in the population of M. cornutus in relation to four ecofactors during 2008 –09

Discussion

The present study has made it more affirmed that population of M. cornutus respond profoundly to change in environmental factors. The temperature is the vital abiotic factor responsible for the abundance of M. cornutus. The rain might change the ambient humidity of birds and affect the population of M. cornutus. Kettle and Luckies (1982) have documented that heavy rain fall causing saturation of fleece in the autumn which reduce the louse population and also keep a check on winter infestation.

Baum (1968) has pointed out that there is no variation in population density of amblyceran as well as of ischnoceran species with the change in environmental factor (e.g. temperature, RH, rainfall and day light). Moreover, Von Keler (1969) has clearly cited the change in mallophagan population density (highest in summer and lowest in spring as well as in winter). Conversely to avian lice, mammalian lice infestation is peak in winter. Murray (1960, 1968) has reported that atmospheric temperature, shearing, solar radiation and thunderstorms are responsible for the summer decline in the population of sheep louse, Bovicola ovis. Furthermore, the shedding of winter coat and higher temperature in summer play critical role in reducing the number of B. equi on horses (Murray 1957, 1963). The infestation intensity of Tricholipurus parallelus on white tailed knock down in summer due to moulting, higher summer temperature and thunderstorms (Samuel and Trainer 1971). The temperature and ambient humidity (microclimate) of host’s body and sunlight considered as important factor for shaping the population build up of B. bovis on cattles (Craufurd-Benson 1941; Matthysse 1946). Birds and mammals in summer have often seen bathing with water and this might have caused delousing effect. Felso and Rozsa (2006, 2007) have documented that birds and mammals dividing behaviour reduces genera richness of avian and mammalian lice. The birds preening behaviour has also affect the lice population (Brown 1972; Clayton et al. 1999). Those birds cannot preen significantly having huge increase in their louse population (Moyer and Clayton 2004).

In the present study it has been noted that allopreening has important effect on controlling amblyceran lice on domestic fowl. The amblyceran lice, M. cornutus and M. stramineaus lays eggs mostly in the neck region. The small contour feather of neck and nape are fully covered with eggs. The pen mates peck the egg containing feathers of each other and feed them. Furthermore, the population density of lice varied with the host health aspect. Those birds can’t scratch head and neck region due to serious leg injury, the number of lice and nits increases on these regions. However, other parts of body were unaffected which can still preen (Clayton et al. 1999). The birds bear cumbersome lice load because of deformities in their beak than to birds with normal beak (Pomeroy 1962; Clayton et al. 1999). Bell et al. (1962) have presented that the fore parts of mice have huge lice density due to non significant scratching because mice has missed toe of hind legs. James et al. (1998) demonstrated that a crippled lamb (bottle fed) acts as major source of lice on a particular property. Bates (2001) has noted in United Kingdom the high louse count on the sheep which had liver fluke (Faciola hepatica) infestation. James et al. (1998) reported that group of ewes clinically diagnosed with ovine progressive pneumonia serving as rich source of lice to healthier one.

Through scrutiny of literature has possessed that some lice shows synchronization with host (Marshall 1981). The population increase of haematophagous species triggered with the host breeding seasons (Foster 1969). She further postulated that this increases in louse population may be due to host reproductive hormones. Srivastava et al. (2003) have analysed path coefficient of correlation between the breeding cycle of common myna (Acridotheris tristis) and its three phthirapteran ectoparasites (Menacanthus eurysturnus, Brueelia sp. and Sternedoecus sp.). However, there is no particular breeding season in case of Gallus gallus domesticus but incubating hen might exhibit higher population level. The lice population of domestic birds may also be affected by predatory mites and hyperparasites (bacteria and fungi) (Marshall 1981).

The present observation are more or less similar to Woodman and Dicke (1954) for Brueelia vulgata infesting sparrows, Touleshkov (1965) on few mallophagan species infesting Sturnus vulgaris, Eveleigh and Threlfall (1976) on several species of Saemundssonia cummingsiella and Astromenopon infesting auks and by Agarwal and Saxena (1979) on Lipeurus lawrensis tropicalis parasitizing G. gallus domesticus. In the present study it is quite clear from Fig. 1 that lice population increases seasonally. The population of M. cornutus builds up in spring, reaching peak in summer to autumn thereafter, decline and remaining low throughout the winter investigation. Thus high temperature and humid climate are favorable for the lice fluctuation. Such condition occurs in the months of July and August at Purola (India) and its adjoining areas. So, such lice may increase above economic injury level in the summer month. Keeping in view, one should be careful about higher population level of this injurious pest and they should be suggested for proper eradication of M. cornutus. Finally, present investigation and earlier workers agree that strong positive correlation (+0.75) existed between lice index and temperature. So, it might be predicted that global warming might increase the population on domestic and wild birds which would be most menacing for the avian biodiversity in future.

Acknowledgments

Authors are thankful to the Principal, B. L. J. Government Degree College, Purola (Uttarkashi) for providing laboratory facilities, and to Uttarakhand Council for Science and Technology (UCOST), Dehradun, India for providing financial help to Dr. Adesh Kumar in form of project No. UCS&T/R&D/LS/10/06/405.

References

  1. Agarwal GP, Saxena AK. Studies on seasonal dynamics of Lipeurus lawrensis tropicalis Peters (Phthiraptera: Ischnocera) infesting poultry birds. Z ang Ent. 1979;8:470–476. [Google Scholar]
  2. Allen NN, Dicke RJ. Cattle lice control by clipping. J Econ Entomol. 1954;45(6):970–973. [Google Scholar]
  3. Amin OM, Madbouly MH. Distribution and seasonal dynamics of a tick, a louse fly and a louse infesting dogs in the Nile valley and Delta of Egypt. J Med Entomol. 1973;10:295–298. doi: 10.1093/jmedent/10.3.295. [DOI] [PubMed] [Google Scholar]
  4. Anderson RC. The Helminthes and arthropod parasites of the white-tailed deer (Odocoilleus virginianus): a general review. Trans Roy Can Inst. 1962;34:57–92. [Google Scholar]
  5. Ash JS. A study of the Mallophaga of the birds with particular reference to their ecology. Ibis. 1960;102(1):93–110. doi: 10.1111/j.1474-919X.1960.tb05095.x. [DOI] [Google Scholar]
  6. Bates PG. Sheep chewing lice: an update. Proceedings of the Sheep Veterinary Society. 2001;24:163–168. [Google Scholar]
  7. Baum H. Biologie und Okologie der Amselfederlouse. Angew Parasitol. 1968;9:129–175. [Google Scholar]
  8. Bell JF, Jellison WL, Owen CR. Effect of limb disability on lousiness in mice. I. Preliminary studies. Exp Parasitol. 1962;12:176–183. doi: 10.1016/0014-4894(62)90055-3. [DOI] [PubMed] [Google Scholar]
  9. Boyd EM. A survey of parasitism of the starling, Sturnus vulgaris L. in North America. J Parasitol. 1951;37:56–84. doi: 10.2307/3273522. [DOI] [PubMed] [Google Scholar]
  10. Brown NS. The effect of host beak condition on the size of Menacanthus stramineus population of domestic chickens. Poultry Sci. 1972;51:162–164. doi: 10.3382/ps.0510162. [DOI] [PubMed] [Google Scholar]
  11. Chandra S, Agarwal GP, Singh SP, Saxena AK. Seasonal variation in the population of two ischnoceran phthirapteran infesting common myna, Acridotheris tristis (Aves) Angew Parasitol. 1988;30:39–42. [Google Scholar]
  12. Chandra S, Agarwal GP, Singh SP, Saxena AK. Seasonal changes in a population of Menacanthus eurysternus (Mallophaga: Amblycera) on the common myna Acridotheris tristis. Int J Parasitol. 1990;20(8):1063–1065. doi: 10.1016/0020-7519(90)90050-W. [DOI] [PubMed] [Google Scholar]
  13. Clayton DH, Lee PLM, Tompkins DM, Brodie ED., III Reciprocal natural selection on host-parasite phenotypes. Am Nat. 1999;154:261–270. doi: 10.1086/303237. [DOI] [PubMed] [Google Scholar]
  14. Cowan IM. Parasites, disease, injuries and anomalies of the Columbian black tailed deer, Odocoileus hemionus columbianus (Richardson), in British Columbia. Can J Res. 1946;24:71–103. doi: 10.1139/cjr46d-007. [DOI] [PubMed] [Google Scholar]
  15. Craufurd-Benson HJ. The cattle lice of Great Britain. Parasitology. 1941;33:331–358. doi: 10.1017/S0031182000024525. [DOI] [Google Scholar]
  16. Eveleigh ES, Threlfall W. Population dynamics of lice (Mallophaga) on auks (alcidae) from Newfoundland. Can J Zool. 1976;54:1694–1711. doi: 10.1139/z76-197. [DOI] [PubMed] [Google Scholar]
  17. Felso B, Rozsa L. Reduced taxonomic richness of lice (Insecta: Phthiraptera) in diving birds. J Parasitol. 2006;92:867–869. doi: 10.1645/GE-849.1. [DOI] [PubMed] [Google Scholar]
  18. Felso B, Rozsa L. Diving behavior reduces genera richness of lice (Insecta: Phthiraptera) of mammals. Acta Parasitol. 2007;52(1):82–85. doi: 10.2478/s11686-007-0006-3. [DOI] [Google Scholar]
  19. Foster MS. The eggs of three species of Mallophaga and their significance in ecological studies. J Parasitol. 1969;55(2):453–456. doi: 10.2307/3277435. [DOI] [PubMed] [Google Scholar]
  20. James PJ, Moon RD, Brown DR. Seasonal dynamics and variation among sheep biting louse, Bovicola ovis. Int J Parasitol. 1998;28:283–292. doi: 10.1016/S0020-7519(97)00188-4. [DOI] [PubMed] [Google Scholar]
  21. Kettle PR, Luckies JM. Effect of sheep lice (Damalinia ovis) on wool colour. N Z J Exp Agri. 1982;10:15–17. [Google Scholar]
  22. Kumar A, Rawat BS, Saxena AK. Seasonal dynamics of goat biting louse, Bovicola caprae (Phthiraptera: Ischnocera: Tricodectidae) Rudolstad Nat Hist Schr. 1993;5:75–78. [Google Scholar]
  23. Marshall AG. The ecology of ectoparasitic insects. London: Academic Press; 1981. [Google Scholar]
  24. Matthysse JG. Cattle lice, their biology and control. Cornell Univ Agric Exp Sta Bull. 1946;832:1–67. [Google Scholar]
  25. Moyer BR and Clayton DH (2004) Avian defences against ectoparasites. In: HF Van Emden, M Rothschild (eds) Insect and bird interactions, vol 18. Andover, UK , pp 243–259
  26. Murray MD. The distribution of eggs of mammalian lice on their hosts. I. Description of oviposition behaviour. Aust J Zool. 1957;5:13–18. doi: 10.1071/ZO9570013. [DOI] [Google Scholar]
  27. Murray MD. The ecology of lice on sheep. I: the influence of skin temperature on populations of L. pedalis (Osborne) Aust J Zool. 1960;8:349–356. doi: 10.1071/ZO9600349. [DOI] [Google Scholar]
  28. Murray MD. The ecology of lice on sheep IV. The establishment and maintenance of population of Linognathus ovillus (Neumann) Aust J Zool. 1963;11(2):153–156. doi: 10.1071/ZO9630153. [DOI] [Google Scholar]
  29. Murray MD. Ecology of lice on sheep VI: the influence of sheering and solar radiation on population and transmission of Damalinia ovis. Aust J Zool. 1968;16:725–738. doi: 10.1071/ZO9680725. [DOI] [Google Scholar]
  30. Murray MD, Gordon G. Ecology of lice on sheep VII: population dynamics of Damalinia ovis (Schrank) Aust J Zool. 1969;16:179–186. doi: 10.1071/ZO9690179. [DOI] [Google Scholar]
  31. Pomeroy DE. Birds with abnormal bills. British Birds. 1962;55:49–72. [Google Scholar]
  32. Rawat BS and Saxena AK (1990) A note on the natural population levels of short-nosed cattle louse, Linognathus vituli (Linn. 1758). Rivista di Parassitol VII (LI) N 2:183–188
  33. Rawat BS, Saxena AK. Studies on the population of cattle biting louse, Bovicola bovis (L.) (Phthiraptera: Ischnocera) J Zool Res. 1992;5(1&2):17–20. [Google Scholar]
  34. Rust RW. The population dynamics and host utilization of Geomydoecus oreogonus, a parasite of Thomomys bottae. Oecologia. 1974;15:287–304. doi: 10.1007/BF00345184. [DOI] [PubMed] [Google Scholar]
  35. Samuel WM, Trainer DO. Seasonal fluctuations of Tricholipeurus parallelus Osborn 1896) (Mallophaga: Trichodectidae) on white-tailed deer (Odocoileus virginianus, Zimmermann 1780) from South Texas. Am Midl Nat. 1971;85:507–513. doi: 10.2307/2423772. [DOI] [Google Scholar]
  36. Scott MT. Observations on the bionomics of the sheep body louse (Damalinia ovis) Aust J Agric Res. 1952;3:60–67. doi: 10.1071/AR9520060. [DOI] [Google Scholar]
  37. Srivastava R, Kumar S, Gupta N, Singh SK, Saxena AK. Path coefficient analysis of correlation between breeding cycle of common myna, Acridotheres trisitis) and its phthirapteran ectoparasites. Folia Parasitol. 2003;50:315–316. doi: 10.14411/fp.2003.052. [DOI] [PubMed] [Google Scholar]
  38. Touleshkov K. Mallophaga (Insecta) ectoparasites on starling (Sturnus vulgaris L) Izv. Zool Inst (Sofia) 1965;19:175–187. [Google Scholar]
  39. Von Keler S (1969) 17. Ordnung Mallophaga (Federlinge and Haarlinge). In: Helmcke JG, Starck D, Wermuth H (eds) Handbuch der Zoologie 4 (2) Lfg. 10:1–72
  40. Woodman WJ, Dicke RJ. Population fluctuations of the mallophagan parasite Bruellia vulgata (Kellogg) upon the sparrow. Trans Wisconsin Acad Sci. 1954;43:133–135. [Google Scholar]

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