Volume 20, Number 5—May 2014
Perspective
Bat Flight and Zoonotic Viruses
Table 2
Enhanced neutrophil and monocyte motility and emigration |
Enhanced phagocytosis and pinocytosis |
Increased oxygen radical production by phagocytes |
Increased interferon production |
Increased antiviral, antitumor, or antiproliferative, and natural killer cell stimulating activities of interferon |
Potentiated interferon-induced anti-anaphylaxis (anergy) |
Enhanced natural killer complement activation |
Enhanced expression of Fc receptors |
Increased T-helper cell activation, expression, recruitment, and cytotoxic activity |
Blocked T-suppressor cell activity |
Increased antibody production |
Enhanced tumor necrosis factor-α |
Increased T-cell proliferative response to nonspecific mitogens, interleukin-1 and −2, and allogeneic lymphocytes |
Increased killing of intracellular bacteria |
Increased bactericidal effect of antimicrobial agents |
Induced cytoprotective heat-shock proteins in host cells |
Induced pathogen heat-shock proteins, which activate host defenses |
Induced cytoprotective heat-shock proteins in host cells |
References
- Calisher CH, Childs JE, Field HE, Holmes KV, Schountz T. Bats: important reservoir hosts of emerging viruses. Clin Microbiol Rev. 2006;19:531–45 . DOIPubMedGoogle Scholar
- Dobson AP. What links bats to emerging infectious diseases? Science. 2005;310:628–9. DOIPubMedGoogle Scholar
- Luis AD, Hayman DTS, O’Shea TJ, Cryan PM, Gilbert AT, Pulliam JRC, A comparison of bats and rodents as reservoirs of zoonotic viruses: are bats special? Proc Royal Soc B Biol Sci. 2013;280:20122753.
- Ge XY, Li JL, Yang XL, Chmura AA, Zhu G, Epstein JH, Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor. Nature. 2013;503:535–8. DOIPubMedGoogle Scholar
- Leroy EM, Kumulungui B, Pourrut X, Rouquet P, Hassanin A, Yaba P, Fruit bats as reservoirs of Ebola virus. Nature. 2005;438:575–6. DOIPubMedGoogle Scholar
- Towner JS, Amman BR, Sealy TK, Carroll SA, Comer JA, Kemp A, Isolation of genetically diverse Marburg viruses from Egyptian fruit bats. PLoS Pathog. 2009;5:e1000536. DOIPubMedGoogle Scholar
- Halpin K, Young PL, Field HE, Mackenzie JS. Isolation of Hendra virus from pteropid bats: a natural reservoir of Hendra virus. J Gen Virol. 2000;81:1927–32 .PubMedGoogle Scholar
- Chua KB, Koh CL, Hooi PS, Wee KF, Khong JH, Chua BH, Isolation of Nipah virus from Malaysian Island flying foxes. Microbes Infect. 2002;4:145–51. DOIPubMedGoogle Scholar
- Drexler JF, Corman VM, Müller MA, Maganga GD, Vallo P, Binger T, Bats host major mammalian paramyxoviruses. Nat Commun. 2012;3:796.
- Baker ML, Schountz T, Wang LF. Antiviral immune responses of bats: a review. Zoonoses Public Health. 2013;60:104–16. DOIPubMedGoogle Scholar
- Wang LF, Walker PJ, Poon LLM. Mass extinctions, biodiversity and mitochondrial function: are bats ‘special’ as reservoirs for emerging viruses? Curr Opin Virol. 2011;1:649–57.
- Sohayati AR, Hassan L, Sharifah SH, Lazarus K, Zaini CM, Epstein JH, Evidence for Nipah virus recrudescence and serological patterns of captive Pteropus vampyrus. Epidemiol Infect. 2011;139:1570–9. DOIPubMedGoogle Scholar
- Zhang G, Cowled C, Shi Z, Huang Z, Bishop-Lilly KA, Fang X, Comparative analysis of bat genomes provides insight into the evolution of flight and immunity. Science. 2013;339:456–60. DOIPubMedGoogle Scholar
- Blatteis CM. Fever: pathological or physiological, injurious or beneficial? J Therm Biol. 2003;28:1–13. DOIGoogle Scholar
- Hasday JD, Fairchild KD, Shanholtz C. The role of fever in the infected host. Microbes Infect. 2000;2:1891–904. DOIPubMedGoogle Scholar
- Speakman JR, Thomas DW. Physiological ecology and energetics of bats. In: Kunz TH, Fenton MB, editors. Bat ecology. Chicago: University of Chicago Press; 2003. p. 430–90.
- Thomas SP, Suthers RA. The physiology and energetics of bat flight. J Exp Biol. 1972;57:317–35.
- Bundle MW, Hansen KS, Dial KP. Does the metabolic rate–flight speed relationship vary among geometrically similar birds of different mass? J Exp Biol. 2007;210:1075–83. DOIPubMedGoogle Scholar
- Książek A, Konarzewski M. Effect of dietary restriction on immune response of laboratory mice divergently selected for basal metabolic rate. Physiol Biochem Zool. 2012;85:51–61. DOIPubMedGoogle Scholar
- Cutrera AP, Zenuto RR, Luna F, Antenucci CD. Mounting a specific immune response increases energy expenditure of the subterranean rodent Ctenomys talarum (tuco-tuco): implications for intraspecific and interspecific variation in immunological traits. J Exp Biol. 2010;213:715–24. DOIPubMedGoogle Scholar
- Martin LB, Weil ZM, Nelson RJ. Seasonal changes in vertebrate immune activity: mediation by physiological trade-offs. Philos Trans R Soc Lond B Biol Sci. 2008;363:321–39. DOIPubMedGoogle Scholar
- Canale CI, Henry PY. Energetic costs of the immune response and torpor use in a primate. Funct Ecol. 2011;25:557–65. DOIGoogle Scholar
- Carpenter RE. Flight physiology of intermediate-sized fruit bats (Pteropodidae). J Exp Biol. 1986;120:79–103.
- Burbank RC, Young JZ. Temperature changes and winter sleep of bats. J Physiol. 1934;82:459–67 .PubMedGoogle Scholar
- Morrison P. Body temperatures in some Australian mammals. I. Chiroptera. Biol Bull. 1959;116:484–97. DOIGoogle Scholar
- Voigt CC, Lewanzik D. Trapped in the darkness of the night: thermal and energetic constraints of daylight flight in bats. Proc Biol Sci. 2011;278:2311–7. DOIPubMedGoogle Scholar
- Morrison P, McNab BK. Temperature regulation in some Brazilian phyllostomid bats. Comp Biochem Physiol. 1967;21:207–21. DOIPubMedGoogle Scholar
- Roverud RC, Chappell MA. Energetic and thermoregulatory aspects of clustering behavior in the neotropical bat Noctilio albiventris. Physiol Zool. 1991;64:1527–41.
- Reeder WG, Cowles RB. Aspects of thermoregulation in bats. J Mammal. 1951;32:389–403. DOIGoogle Scholar
- Willis CKR, Brigham RM. Defining torpor in free-ranging bats: experimental evaluation of external temperature-sensitive radiotransmitters and the concept of active temperature. J Comp Physiol B. 2003;173:379–89. DOIPubMedGoogle Scholar
- Bronner GN, Maloney SK, Buffenstein R. Survival tactics within thermally-challenging roosts: heat tolerance and cold sensitivity in the Angolan free-tailed bat, Mops condylurus. S Afr J Zool. 1999;34:1–10.
- Herreid CF II. Temperature regulation and metabolism in Mexican freetail bats. Science. 1963;142:1573–4. DOIPubMedGoogle Scholar
- Leitner P. Body temperature, oxygen consumption, heart rate and shivering in the California mastiff bat, Eumops perotis. Comp Biochem Physiol. 1966;19:431–43. DOIGoogle Scholar
- O’Farrell MJ, Bradley WG. Comparative thermal relationships of flight for some bats in southwestern United States. Comp Biochem Physiol A. 1977;58:223–7. DOIGoogle Scholar
- Thomas DW. The physiological ecology of hibernation in vespertilionid bats. In: Racey PA, Swift, SM, editors. Ecology, evolution, and behaviour of bats. Oxford (UK): Clarendon Press; 1995. p. 233–44.
- Long GH, Boots M. How can immunopathology shape the evolution of parasite virulence? Trends Parasitol. 2011;27:300–5. DOIPubMedGoogle Scholar
- Meteyer CU, Barber D, Mandl JN. Pathology in euthermic bats with white nose syndrome suggests a natural manifestation of immune reconstitution inflammatory syndrome. Virulence. 2012;3:583–8. DOIPubMedGoogle Scholar
- Graham AL, Allen JE, Read AF. Evolutionary causes and consequences of immunopathology. Annu Rev Ecol Evol Syst. 2005;36:373–97. DOIGoogle Scholar
- Clark DW Jr. Bats and environmental contaminants: a review. US Fish and Wildlife Service Special Scientific Report—Wildlife 1981; 235:1–27.
- LeGrand EK, Alcock J. Turning up the heat: immune brinksmanship in the acute-phase response. Q Rev Biol. 2012;87:3–18. DOIPubMedGoogle Scholar
Page created: April 16, 2014
Page updated: April 16, 2014
Page reviewed: April 16, 2014
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.