Hostname: page-component-8448b6f56d-wq2xx Total loading time: 0 Render date: 2024-04-23T07:51:52.669Z Has data issue: false hasContentIssue false

Variation within and among host species in engorgement of larval trombiculid mites

Published online by Cambridge University Press:  15 October 2010

C.-C. KUO*
Affiliation:
Department of Wildlife, Fish, & Conservation Biology, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA Research and Diagnostic Center, Centers for Disease Control, Department of Health, No. 6, Linsen S. Road, Taipei, Taiwan, ROC
H.-C. WANG
Affiliation:
Research and Diagnostic Center, Centers for Disease Control, Department of Health, No. 6, Linsen S. Road, Taipei, Taiwan, ROC
C.-L. HUANG
Affiliation:
Research and Diagnostic Center, Centers for Disease Control, Department of Health, No. 6, Linsen S. Road, Taipei, Taiwan, ROC
*
*Corresponding author: Department of Wildlife, Fish, & Conservation Biology, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA. Tel: +886-4-23226940. Fax: +886-4-23232146. E-mail: ccckuo@ucdavis.edu

Summary

We recovered larval trombiculid mites (i.e. chiggers), vectors of scrub typhus, from small mammal hosts in Taiwan, and compared the relative degree of engorgement (RDE) of the dominant chigger (Leptotrombidium imphalum) from different hosts. Naturally occurring chiggers recovered from Rattus losea and Bandicota indica were 1·4x and 1·3x as engorged as those from Apodemus agrarius. Within each host species, RDE was negatively related to chigger loads, but was mostly unrelated to gender or to body or reproductive condition of hosts. We documented significant variation in chigger engorgement both within and among host species; to the extent that RDE is a proxy for fitness, this contradicts predictions of the Ideal Free Distribution (IFD) that the per capita fitness of vectors should be similar among hosts. Failure to meet predictions of the IFD may reflect the limited mobility of chiggers, which consequently must be less selective in the hosts on which they feed. Further disease control efforts should consider vector feeding success in addition to vector abundance and may be able to capitalize on the unsuitability of certain hosts in supporting disease vectors.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Balashov, Y. S. (1972). Bloodsucking ticks (Ixodoidea)- vectors of diseases of man and animals. Miscellaneous Publications of the Entomological Society of America 8, 163376.Google Scholar
CDC, Centers for Disease Control, Taiwan. Notifiable Infectious Disease Statistics System. [online] URL: http://nidss.cdc.gov.tw/. Accessed 12–6–2008Google Scholar
Combes, C. (2001). Parasitism: the Ecology and Evolution of Intimate Interactions. The University of Chicago Press, Chicago, IL, USA and London, UK.Google Scholar
Conover, W. J. and Iman, R. L. (1981). Rank transformations as a bridge between parametric and nonparametric statistics. American Statistician 35, 124129.Google Scholar
CWB, Central Weather Bureau, Taiwan. Statistical Data. [online] URL: http://www.cwb.gov.tw/V6/index.htm. Accessed 5–11–2009Google Scholar
Fretwell, S. D. and Lucas, H. L. Jr. (1970). On the territorial behavior and other factors influencing habitat distribution in birds. Acta Biotheoretica 19, 1636.CrossRefGoogle Scholar
Gannon, W. L., Sikes, R. S., and the Animal Care and Use Committee of the American Society of Mammalogists. (2007). Guidelines of the American Society of Mammalogists for the use of wild mammals in research. Journal of Mammalogy 88, 809823. doi: 10.1644/06-MAMM-F-185R1.1.CrossRefGoogle Scholar
Gürtler, R. E., Ceballos, L. A., Ordóñez-Krasnowski, P., Lanati, L. A., Stariolo, R. and Kitron, U. (2009). Strong host-feeding preferences of the vector Triatoma infestans modified by vector density: implications for the epidemiology of Chagas disease. PloS Neglected Tropical Diseases 3, e447. doi:10.1371/journal.pntd.0000447.Google Scholar
Hart, B. L., Hart, L. A., Mooring, M. S. and Olubayo, R. (1992). Biological basis of grooming behaviour in antelope: the body-size, vigilance and habitat principles. Animal Behaviour 44, 615631.Google Scholar
Hawlena, H., Abramsky, Z. and Krasnov, B. R. (2007 a). Ultimate mechanisms of age-biased flea parasitism. Oecologia 154, 601609. doi: 10.1007/s00442-007-0851-7.CrossRefGoogle ScholarPubMed
Hawlena, H., Abramsky, Z., Krasnov, B. R. and Saltz, D. (2007 b). Host defence versus intraspecific competition in the regulation of infrapopulations of the flea Xenopsylla conformis on its rodent host Meriones crassus. International Journal for Parasitology 37, 919925. doi: 10.1016/j.ijpara.2007.01.015.CrossRefGoogle ScholarPubMed
Hawlena, H., Bashary, D., Abramsky, Z. and Krasnov, B. R. (2007 c). Benefits, costs and constraints of anti-parasitic grooming in adult and juvenile rodents. Ethology 113, 394402. doi: 10.1111/j.1439-0310.2007.01332.x.Google Scholar
Kawamura, A., Tanaka, H. and Takamura, A. (1995). Tsutsugamushi Disease: an Overview. University of Tokyo Press. Tokyo, Japan.Google Scholar
Keesing, F., Brunner, J., Duerr, S., Killilea, M., LoGiudice, K., Schmidt, K., Vuong, H. and Ostfeld, R. S. (2009). Hosts as ecological traps for the vector of Lyme disease. Proceedings of the Royal Society of London, B 276, 39113919. doi: 10.1098/rspb.2009.1159.Google Scholar
Kelly, D. W. (2001). Why are some people bitten more than others? Trends in Parasitology 17, 578581. doi: 10.1016/S1471-4922(01)02116-X.CrossRefGoogle ScholarPubMed
Kelly, D. W. and Thompson, C. E. (2000). Epidemiology and optimal foraging: modelling the ideal free distribution of insect vectors. Parasitology 120, 319327. doi: 10.1017/S0031182099005442.Google Scholar
Kelly, D. W., Mustafa, A. and Dye, C. (1996). Density-dependent feeding success in a field population of the sandfly, Lutzomyia longipalpis. Journal of Animal Ecology 65, 517527.Google Scholar
Khokhlova, I. S., Serobyan, V., Krasnov, B. R. and Degen, A. A. (2009). Is the feeding and reproductive performance of the flea, Xenopsylla ramesis, affected by the gender of its rodent host, Meriones crassus? Journal of Experimental Biology 212, 14291435. doi: 10.1242/jeb.029389.Google Scholar
Khokhlova, I. S., Ghazaryan, L., Krasnov, B. R. and Degen, A. A. (2008). Effects of parasite specificity and previous infestation of hosts on the feeding and reproductive success of rodent-infesting fleas. Functional Ecology 22, 530536. doi: 10.1111/j.1365-2435.2008.01393.x.Google Scholar
Krasnov, B. R., Khokhlova, I. S., Arakelyan, M. S. and Degen, A. A. (2005). Is a starving host tastier? Reproduction in fleas parasitizing food-limited rodents. Functional Ecology 19, 625631. doi: 10.1111/j.1365-2435.2005.01015.x.CrossRefGoogle Scholar
Krasnov, B. R., Khokhlova, I. S., Burdelova, N. V., Mirzoyan, N. S. and Degen, A. A. (2004). Fitness consequences of host selection in ectoparasites: testing reproductive patterns predicted by isodar theory in fleas parasitizing rodents. Journal of Animal Ecology 73, 815820. doi: 10.1111/j.0021-8790.2004.00860.x.CrossRefGoogle Scholar
Kuo, C. C. (2010). Ecology of scrub typhus in Taiwan: the impact of environment, rodent community, and socio-economy. Ph.D. dissertation. University of California, Davis, CA, USA.Google Scholar
Li, J., Wang, D. and Chen, X. (1997). Trombiculid Mites of China: Studies on Vector and Pathogen of Tsutsugamushi Disease. Guangdong Science and Technology Publishing, Guangzhou, China.Google Scholar
LoGiudice, K., Ostfeld, R. S., Schmidt, K. A. and Keesing, F. (2003). The ecology of infectious disease: effects of host diversity and community composition on Lyme disease risk. Proceedings of the National Academy of Sciences, USA 100, 567571. doi: 10.1073/pnas.0233733100.CrossRefGoogle ScholarPubMed
Lyimo, I. N. and Ferguson, H. M. (2009). Ecological and evolutionary determinants of host species choice in mosquito vectors. Trends in Parasitology 25, 189196. doi: 10.1016/j.pt.2009.01.005.CrossRefGoogle ScholarPubMed
Olubayo, R. O., Jono, J., Orinda, G., Groothenhuis, J. G. and Hart, B. L. (1993). Comparative differences in densities of adult ticks as a function of body size on some East African antelopes. African Journal of Ecology 31, 2634. doi: 10.1111/j.1365-2028.1993.tb00515.x.Google Scholar
Ostfeld, R. S. and Keesing, F. (2000). The function of biodiversity in the ecology of vector-borne zoonotic diseases. Canadian Journal of Zoology 78, 20612078. doi: 10.1139/cjz-78-12-2061.Google Scholar
Philip, C. B., Traub, R. and Smadel, J. E. (1949). Chloramphenicol (chloromycetin) in the chemoprophylaxis of scrub typhus (tsutsugamushi disease): epidemiological observations on hyperendemic areas of scrub typhus in Malaya. American Journal of Hygiene 50, 6374.Google ScholarPubMed
Randolph, S. E. (2004). Tick ecology: processes and patterns behind the epidemiological risk posed by ixodid ticks as vectors. Parasitology 129 (Suppl.) S37S65. doi: 10.1017/S0031182004004925.Google Scholar
Schulte-Hostedde, A. I., Zinner, B., Millar, J. S. and Hickling, G. J. (2005). Restitution of mass/size residuals: validating body condition indices. Ecology 86, 155163. doi: 10.1890/04-0232.CrossRefGoogle Scholar
Slowik, T. J. and Lane, R. S. (2009). Feeding preferences of the immature stages of three western north American ixodid ticks (Acari) for avian, reptilian, or rodent hosts. Journal of Medical Entomology 46, 115122. doi: 10.1603/033.046.0115.Google Scholar
Sonenshine, D. E. (1991). Biology of Ticks, Vol. 1. Oxford University Press. Oxford, UK.Google Scholar
Takken, W., Klowden, M. J. and Chambers, G. M. (1998). Effect of body size on host seeking and blood meal utilization in Anopheles gambiae sensu stricto (Diptera: Culicidae): the disadvantage of being small. Journal of Medical Entomology 35, 639645.CrossRefGoogle ScholarPubMed
Traub, R. and Wisseman, C. L. Jr. (1974). The ecology of chigger-borne rickettsiosis (scrub typhus). Journal of Medical Entomology 11, 237303.CrossRefGoogle ScholarPubMed
Wang, D. Q. and Yu, Z. Z. (1992). Chigger mites of the genus Leptotrombidium: key to species and their distribution in China. Medical and Veterinary Entomology 6, 389395.Google Scholar
Supplementary material: Image

Kuo supplementary material

Figure S1.tif

Download Kuo supplementary material(Image)
Image 322.4 KB
Supplementary material: Image

Kuo supplementary material

Figure S2.tif

Download Kuo supplementary material(Image)
Image 681 KB
Supplementary material: Image

Kuo supplementary material

Figure S3.tif

Download Kuo supplementary material(Image)
Image 838.9 KB