Infrared sensing in vampire bats

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Vampire bat Desmodus rotundus. Desmodus Upclose Image of Face.jpeg
Vampire bat Desmodus rotundus.

Vampire bats have developed a specialized system using infrared-sensitive receptors on their nose-leaf to prey on homeothermic (warm-blooded) vertebrates. [1] Trigeminal nerve fibers that innervate these IR-sensitive receptors may be involved in detection of infrared thermal radiation emitted by their prey. This may aid bats in locating blood-rich areas on their prey. [1] [2] In addition, neuroanatomical and molecular research has suggested possible similarities of IR-sensing mechanisms between vampire bats and IR-sensitive snakes. [2] [3] [4] [5] Infrared sensing in vampire bats has not yet been hypothesized to be image forming, as it was for IR-sensitive snakes. [6] While the literature on IR-sensing in vampire bats is thin, progress continues to be made in this field to identify how vampire bats can sense and use infrared thermal radiation.

Contents

Vampire bats are the only known mammals whose entire nutrition relies on blood from mammals or birds. In the family Phyllostomidae and the subfamily Desmodontinae, there are three known species of vampire bats: Desmodus rotundus (common vampire bat), Diphylla ecaudata (hairy-legged vampire bat), and Diaemus youngi (white-winged vampire bat). [7] Most of the referenced research on infrared sensing in vampire bats has been done on the common vampire bat because this is the most commonly found species. [8]

Behavior

Vampire bats were not studied in their natural habitats until about 1935. During predation, bats first spend a few minutes in the air circling the target prey, eventually landing on the back or neck crest of the animal, and sometimes the ground. They then proceed to search for a suitable spot to bite, which can take seconds to minutes, and usually will feed on the neck or flank. The same spot may be fed on multiple times by different bats. [9] Kürten and Schmidt (1982) were the first to suggest that infrared perception in vampire bats is possibly used in detecting regions of maximal blood flow on targeted prey. Although warm receptors are also found in the facial regions of species such as mice, humans, and dogs, the extreme low-temperature sensitivity of these receptors on vampire bats suggest specialization for sensing infrared. (see section on Physiology). [10]

In 1982, Kürten and Schmidt performed behavioral studies to examine the ability of vampire bats to detect infrared radiation. Their study showed that when given a choice between a warm and cold object, vampire bats can be trained to choose the infrared emitting signal unit (SU). Two SUs made of a heating element with a copper plate backing were mounted on a wall. For each trial, one SU was warmed while the other was maintained at room temperature. The heating and warming of the SUs were interchanged at random between trials. If bats chose the warm SU correctly, they were rewarded with food through a feeding tube below each SU. In this study, olfactory and visual stimuli were minimized to ascertain that only thermal cues affected behavioral learning. Olfactory cues were eliminated by the full feeding tube attached behind the opening from which the bats received their rewards. Dim lighting minimized visual cues of the two SUs. [1]

Anatomy

Head of Desmodus rotundus: Indicated is position of nasal pits (*), apical pad (aP) and lateral pad (lP). Vampir-Head.jpg
Head of Desmodus rotundus: Indicated is position of nasal pits (*), apical pad (aP) and lateral pad (lP).
Nasal structure of Desmodus rotundus: Stars indicate position of nasal pits and red outlines the nose-leaf. Sketch of Desmodus Noseleaf.png
Nasal structure of Desmodus rotundus: Stars indicate position of nasal pits and red outlines the nose-leaf.

The central nose-leaf and a semicircular ring of pads construct the nasal structure of the vampire bat. There are also three depressions known as nasal or leaf pits, located between the nose-leaf and pads. Two lateral pits, one on each side of the nose-leaf, are situated at 45° angles towards the nose-leaf. The apical pit is slightly raised and directed upward and forward relative to the nose-leaf. The pits are about 1 millimeter wide and 1 millimeter deep, hairless, and glandless. A layer of dense connective-tissue with sparsely distributed blood vessels insulates the nasal structure. Based on structure alone, these pits were first suggested to house IR-receptors. [1]

Neuroanatomy

Kürten and Schmidt (1982) [1] first suggested that the location and orientation of each pit structure provided directional information in infrared radiation detection. From their initial studies, the nasal pits seemed to be ideal for purposes of IR-perception. Later in 1984, Kürten and collaborators made electrophysiological recordings from nerve fibers of temperature-sensitive infrared thermoreceptors located on the central nose-leaf and upper lip, but did not find such receptors in the nasal pits (see Physiology). This revoked their earlier hypothesis and established that the infrared-sensitive receptors are located on the central nose-leaf. [3] Schäfer and collaborators confirmed this by recording impulses from thermoreceptors on the nose-leaf as well. [10]

Klüver-Barrera and Nissl staining of vampire bat brain sections uncovered a unique nucleus located lateral to the descending trigeminal tract (dv). The nucleus is composed of neuropils and medium-sized cells, which is very similar to the nucleus (DLV) in the lateral descending trigeminal system in IR-sensitive snakes. This special nucleus is found in all three species of vampire bats and no other bats, but does not necessarily indicate a direct connection with infrared sensing. [2] More recent studies using in situ hybridization studies have located large diameter neurons in the trigeminal ganglia (TG) that are unique to vampire bats and extremely similar to those found in IR-sensitive snakes. [5] Although the morphological organization of neurons suggests convergent evolution with IR-sensing snakes lineages, it remains unclear what the exact neural pathway is for infrared sensing in vampire bats. [2] [5]

Physiology

Thermography, a method which produces pictures of the distribution of temperatures on an object, was used to investigate temperature variation across facial structures of the common vampire bat. The nasal structure has a temperature of 9 °C lower than the rest of the face. The thermal insulation of the nasal structure and maintained temperature difference may possibly prevent interference of self-emitted thermal radiation. Warm receptors located in the nose may then optimally detect outside sources of infrared radiation. [1]

Vampire bats are sensitive to power densities (a measure of emitted energy) greater than 50 μW/cm2 at distances between 13 and 16 cm (a power density of 1.8x10−4W/cm2 corresponds to 50 °C). This was first determined by quantifying the temperature at which vampire bats could not behaviorally distinguish between heat emitting and room temperature SUs. A positive linear relationship exists between the energy-threshold of heat detection and distance from stimuli. Through mathematical calculations, at a distance of 8 cm, vampire bats should be able to detect humans who emit radiation of 80 μW/cm2. [1] Temperature threshold measurements were directly measured by stimulating nerve fibers of thermoreceptors in the nose-leaf and upper lip with a water-circulated brass thermode and recording the impulses/second at every 5 °C shift in temperature from 10 to 40 °C. These receptors have a threshold of 28 °C and a maximum temperature response to 40 °C, beyond which there was either no firing or an irregular firing pattern. [3] [10] This threshold is 8 °C lower compared to those of warm receptor in other species of mammals, which implies extreme sensitivity to heat. After stimulation of these receptors, there is a transient increase in impulse activity which quickly decays due to adaptation and thus strengthens temporal acuity. [10]

Molecular mechanism of infrared detection

A family of TRP (transient receptor potential) channels, including TRPV1 (transient receptor potential vanilloid) and TRPA1 (transient receptor potential cation channel A1), is important in thermal and pain detection. [4] TRPV1 channels are activated by capsaicin (a chemical which can be extracted from chili peppers), noxious temperature ranges (>43 °C), membrane-derived lipids, low pH, and voltage changes. [11] Activation of TRPV1 by capsaicin results in calcium and sodium influx, and functionally allows for detection of painful thermal stimuli. [11] [12] TRPV1 may also act as a molecular thermometer in response to temperatures greater than 43 °C. The result is an inward calcium and sodium current similar to capsaicin-evoked currents. TRPV1 channels may also have voltage-sensitive properties responsible for its activation. [13] Phosphorylation and mutations, especially at the C-terminus (carboxylic acid end of primary amino acid sequence), can alter the threshold temperature of heat-activation. [11] The specific mechanism behind heat-activation of TRPV1 channels has yet to be deciphered.

TRPV1-S

TRPV1-S (TRPV1 short) is an isoform of the capsaicin receptor TRPV1 and comprises 35-46% of TRPV1 transcripts in the trigeminal ganglia of common vampire bats. Deep sequencing of complementary DNA of these receptor channels shows that this is not true for closely related fruit bats Carollia brevicauda (< 6% TRPV1-S) and other fruit, nectar, or insect feeding bats (Uroderma bilobatum, Sturnira lilium, and Anoura cultrata) (<1% TRPV1-S). TRPA1 channels in pit-bearing snakes, such as the western diamondback rattlesnake ( Crotalus atrox ), are sensitive to infrared thermal radiation as well. TRPA1 transcripts are mostly found in the TG of IR-sensitive snake lineages as was for bats. [4]

TRPV1-S isoform results from alternative splicing during post-transcriptional regulation, a variation of the TRPV1 C-terminus due to insertion of 23-base-pair sequence, exon14a, that contains a stop codon. The inserted sequence is flanked by two introns marked with G T/AG donor-acceptor sites that are necessary for U2-dependent splicing. Consequently, incorporation or bypass of exon14a results in the short or long isoforms, respectively. It is suggested that efficient splicing of the exon14a segment necessitates the specialized environment of TG in vampire bats. [5] Compared to the long isoform (threshold ~ 40 °C), the temperature threshold of channel activation is much lower for TRPV1-S. TRPV1-S channels expressed in HEK293 cells and Xenopus oocytes (cells commonly used for manipulation of expressing certain genes) have a threshold of 30 °C. [5] This is highly consistent with in vitro studies pertaining to temperature thresholds of IR-sensitive receptors in vampire bats (28 °C). [1] Activation of TRPV1-S channels in the TG may then suggest a similar mechanism (as seen in IR-sensing snakes) for how infrared sensing may work in vampire bats. Trigeminal nerves which innervate specialized temperature sensitive receptors on the nose-leaf may in turn activate TRPV1-S channels in the TG in response to infrared thermal radiation. [5]

See also

Related Research Articles

<span class="mw-page-title-main">Infrared</span> Form of electromagnetic radiation

Infrared is electromagnetic radiation (EMR) with wavelengths longer than that of visible light but shorter than microwaves. The infrared spectral band begins with waves that are just longer than those of red light, the longest waves in the visible spectrum, so IR is invisible to the human eye. IR is generally understood to include wavelengths from around 750 nm to 1 mm. IR is commonly divided between longer-wavelength thermal IR, emitted from terrestrial sources, and shorter-wavelength IR or near-IR, part of the solar spectrum. Longer IR wavelengths (30–100 μm) are sometimes included as part of the terahertz radiation band. Almost all black-body radiation from objects near room temperature is in the IR band. As a form of electromagnetic radiation, IR carries energy and momentum, exerts radiation pressure, and has properties corresponding to both those of a wave and of a particle, the photon.

In physiology, thermoception or thermoreception is the sensation and perception of temperature, or more accurately, temperature differences inferred from heat flux. It deals with a series of events and processes required for an organism to receive a temperature stimulus, convert it to a molecular signal, and recognize and characterize the signal in order to trigger an appropriate defense response.

<span class="mw-page-title-main">Vampire bat</span> Subfamily of bats

Vampire bats, members of the subfamily Desmodontinae, are leaf-nosed bats currently found in Central and South America. Their food source is the blood of other animals, a dietary trait called hematophagy. Three extant bat species feed solely on blood: the common vampire bat, the hairy-legged vampire bat, and the white-winged vampire bat. Two extinct species of the genus Desmodus have been found in North America.

<span class="mw-page-title-main">Leaf-nosed bat</span> Family of bats

The New World leaf-nosed bats (Phyllostomidae) are bats found from southern North America to South America, specifically from the Southwest United States to northern Argentina. They are ecologically the most varied and diverse family within the order Chiroptera. Most species are insectivorous, but the phyllostomid bats include within their number true predatory species and frugivores. For example, the spectral bat, the largest bat in the Americas, eats vertebrate prey, including small, dove-sized birds. Members of this family have evolved to use food groups such as fruit, nectar, pollen, insects, frogs, other bats, and small vertebrates, and in the case of the vampire bats, even blood.

<i>Desmodus</i> Genus of bats

Desmodus is a genus of bats which—along with the genera Diaemus and Diphylla—are allied as the subfamily Desmodontinae, the carnivorous, blood-consuming vampire bats of the New World leaf-nosed bat family Phyllostomidae.

<span class="mw-page-title-main">Thermoreceptor</span> Receptive portion of a sensory neuron

A thermoreceptor is a non-specialised sense receptor, or more accurately the receptive portion of a sensory neuron, that codes absolute and relative changes in temperature, primarily within the innocuous range. In the mammalian peripheral nervous system, warmth receptors are thought to be unmyelinated C-fibres, while those responding to cold have both C-fibers and thinly myelinated A delta fibers. The adequate stimulus for a warm receptor is warming, which results in an increase in their action potential discharge rate. Cooling results in a decrease in warm receptor discharge rate. For cold receptors their firing rate increases during cooling and decreases during warming. Some cold receptors also respond with a brief action potential discharge to high temperatures, i.e. typically above 45 °C, and this is known as a paradoxical response to heat. The mechanism responsible for this behavior has not been determined.

<span class="mw-page-title-main">Nociceptor</span> Sensory neuron that detects pain

A nociceptor is a sensory neuron that responds to damaging or potentially damaging stimuli by sending "possible threat" signals to the spinal cord and the brain. The brain creates the sensation of pain to direct attention to the body part, so the threat can be mitigated; this process is called nociception.

<span class="mw-page-title-main">Common vampire bat</span> South and Central American bat

The common vampire bat is a small, leaf-nosed bat native to the Neotropics. It is one of three extant species of vampire bat, the other two being the hairy-legged and the white-winged vampire bats. The common vampire bat practices hematophagy, mainly feeding on the blood of livestock. The bat usually approaches its prey at night while they are sleeping. It then uses its razor-sharp teeth to cut open the skin of its hosts and lap up their blood with its long tongue.

Chemesthesis is the detection of potentially harmful chemicals by the skin and mucous membranes. Chemesthetic sensations arise when chemical compounds activate receptors associated with other senses that mediate pain, touch, and thermal perception. These chemical-induced reactions do not fit into the traditional sense categories of taste and smell.

<span class="mw-page-title-main">TRPV1</span> Human protein for regulating body temperature

The transient receptor potential cation channel subfamily V member 1 (TRPV1), also known as the capsaicin receptor and the vanilloid receptor 1, is a protein that, in humans, is encoded by the TRPV1 gene. It was the first isolated member of the transient receptor potential vanilloid receptor proteins that in turn are a sub-family of the transient receptor potential protein group. This protein is a member of the TRPV group of transient receptor potential family of ion channels. Fatty acid metabolites with affinity for this receptor are produced by cyanobacteria, which diverged from eukaryotes at least 2000 million years ago (MYA). The function of TRPV1 is detection and regulation of body temperature. In addition, TRPV1 provides a sensation of scalding heat and pain (nociception). In primary afferent sensory neurons, it cooperates with TRPA1 to mediate the detection of noxious environmental stimuli.

<span class="mw-page-title-main">TRPV</span> Subgroup of TRP cation channels named after the vanilloid receptor

TRPV is a family of transient receptor potential cation channels in animals. All TRPVs are highly calcium selective.

<span class="mw-page-title-main">Capsazepine</span> Chemical compound

Capsazepine is a synthetic antagonist of capsaicin. It is used as a biochemical tool in the study of TRPV ion channels.

<span class="mw-page-title-main">TRPV2</span> Protein-coding gene in the species Homo sapiens

Transient receptor potential cation channel subfamily V member 2 is a protein that in humans is encoded by the TRPV2 gene. TRPV2 is a nonspecific cation channel that is a part of the TRP channel family. This channel allows the cell to communicate with its extracellular environment through the transfer of ions, and responds to noxious temperatures greater than 52 °C. It has a structure similar to that of potassium channels, and has similar functions throughout multiple species; recent research has also shown multiple interactions in the human body.

<span class="mw-page-title-main">Infrared sensing in snakes</span> Sensory abilities in snakes

The ability to sense infrared thermal radiation evolved independently in two different groups of snakes, one consisting of the families Boidae (boas) and Pythonidae (pythons), the other of the family Crotalinae. What is commonly called a pit organ allows these animals to essentially "see" radiant heat at wavelengths between 5 and 30 μm. The more advanced infrared sense of pit vipers allows these animals to strike prey accurately even in the absence of light, and detect warm objects from several meters away. It was previously thought that the organs evolved primarily as prey detectors, but recent evidence suggests that it may also be used in thermoregulation and predator detection, making it a more general-purpose sensory organ than was supposed.

A sense is a biological system used by an organism for sensation, the process of gathering information about the surroundings through the detection of stimuli. Although, in some cultures, five human senses were traditionally identified as such, many more are now recognized. Senses used by non-human organisms are even greater in variety and number. During sensation, sense organs collect various stimuli for transduction, meaning transformation into a form that can be understood by the brain. Sensation and perception are fundamental to nearly every aspect of an organism's cognition, behavior and thought.

Relief from chronic pain remains a recognized unmet medical need. Consequently, the search for new analgesic agents is being intensively studied by the pharmaceutical industry. The TRPV1 receptor is a ligand gated ion channel that has been implicated in mediation of many types of pain and therefore studied most extensively. The first competitive antagonist, capsazepine, was first described in 1990; since then, several TRPV1 antagonists have entered clinical trials as analgesic agents. Should these new chemical entities relieve symptoms of chronic pain, then this class of compounds may offer one of the first novel mechanisms for the treatment of pain in many years.

<span class="mw-page-title-main">David Julius</span> American physiologist and Nobel laureate 2021

David Jay Julius is an American physiologist and Nobel Prize laureate known for his work on molecular mechanisms of pain sensation and heat, including the characterization of the TRPV1 and TRPM8 receptors that detect capsaicin, menthol, and temperature. He is a professor at the University of California, San Francisco.

Zucapsaicin (Civanex) is a medication used to treat osteoarthritis of the knee and other neuropathic pain. Zucapsaicin is a member of phenols and a member of methoxybenzenes. It is a modulator of transient receptor potential cation channel subfamily V member 1 (TRPV-1), also known as the vanilloid or capsaicin receptor 1 that reduces pain, and improves articular functions. It is the cis-isomer of capsaicin. Civamide, manufactured by Winston Pharmaceuticals, is produced in formulations for oral, nasal, and topical use.

<span class="mw-page-title-main">Vanillotoxin</span> Chemical compound

Vanillotoxins are neurotoxins found in the venom of the tarantula Psalmopoeus cambridgei. They act as agonists for the transient receptor potential cation channel subfamily V member 1 (TRPV1), activating the pain sensory system. VaTx1 and 2 also act as antagonists for the Kv2-type voltage-gated potassium channel (Kv2), inducing paralytic behavior in small animals.

RhTx is a small peptide toxin from Scolopendra subspinipes mutilans, also called the Chinese red-headed centipede. RhTx binds to the outer pore region of the temperature regulated TRPV1 ion channel, preferably in activated state, causing a downwards shift in the activation threshold temperature, which leads to the immediate onset of heat pain.

References

  1. 1 2 3 4 5 6 7 8 9 10 Kürten, Ludwig; Schmidt, Uwe (1982). "Thermoperception in the Common Vampire Bat (Desmodus rotundus)". Journal of Comparative Physiology. 146 (2): 223–228. doi:10.1007/BF00610241.
  2. 1 2 3 4 Kishida, Reiji; Goris, Richard C.; Terashima, Shin-Ichi; Dubbeldam, Jacob L. (1984). "A suspected infrared-recipient nucleus in the brainstem of the vampire bat,Desmodus rotundus". Brain Research. 322 (2): 351–355. doi:10.1016/0006-8993(84)90132-x. PMID   6509324.
  3. 1 2 3 Kürten, Ludwig; Schmidt, Uwe; Schäfer, Klaus (1984). "Warm and Cold Receptors in the Nose of the Vampire Bat Desmodus rotundus". Naturwissenschaften. 71 (6): 327–328. doi:10.1007/BF00396621. PMID   6472483.
  4. 1 2 3 Gracheva, Elena O.; Ingolia, Nicholas T.; Kelly, Yvonne M.; Cordero-Morales, Julio F.; Hollopeter, Gunther; Chesler, Alexander T.; Sánchez, Elda E.; Perez, John C.; Weissman, Jonathan S.; Julius, David (2010). "Molecular basis of infrared detection by snakes". Nature. 464 (7291): 1006–11. doi:10.1038/nature08943. PMC   2855400 . PMID   20228791.
  5. 1 2 3 4 5 6 Gracheva, Elena O.; Codero-Morales, Julio F.; González-Carcaía, José A.; Ingolia, Nicholas T.; Manno, Carlo; Aranguren, Carla I.; Weissman, Jonathan S.; Julius, David (2011). "Ganglion-specific splicing of TRPV1 underlies infrared sensation in vampire bats". Nature. 476 (7358): 88–91. doi:10.1038/nature10245. PMC   3535012 . PMID   21814281.
  6. Newman, E.A.; Hartline, P.H. (1982). "The Infrared 'vision' of snakes". Scientific American. 20: 116–127.
  7. Tellgren-Roth, Åsa; Dittmar, Katharina; Massey, Steven E.; Kemi, Cecillia; Tellgren-Roth, Christian; Savolainen, Peter; Lyons, Leslie A.; Liberles, David A. (2009). "Keeping the blood flowing – plasminogen activator genes and feeding behavior in vampire bats". Naturwissenschaften. 96 (1): 39–47. doi:10.1007/s00114-008-0446-0.
  8. Mulheisen, M. and R. Anderson. 2001. Animal Diversity Web. "Desmodus rotundus." Accessed November 14, 2011 http://animaldiversity.ummz.umich.edu/site/accounts/information/Desmodus_rotundus.html.
  9. Greenhall, Arthur M.; Schmidt, Uwe; Lopez-Forment, William (1971). "Attacking Behavior of the Vampire Bat, Desmodus rotundus, Under Field Conditions in Mexico". Biotropica. 3: 136–41. JSTOR   2989817.
  10. 1 2 3 4 Schäfer, Klaus; Braun, Hans A.; Kürten, Ludwig (1988). "Analysis of cold and warm receptor activity in vampire bats and mice". Pflügers Arch. 412: 188–194. doi:10.1007/BF00583749.
  11. 1 2 3 Rosenbaum, Tamara, and Sidney A. Simon. "TRPV1 Receptors and Signal Transduction." In TRP Ion Channel Function in Sensory Transduction and Cellular Signaling Cascades, edited by Wolfgang B. Liedtke and Stefan Heller. Boca Ranton: CRC Press, 2007. Available online.
  12. Caterina, Michael J.; Schumacher, Mark A.; Tominaga, Makoto; Rosen, Tobias A.; Levine, Jon D.; Julius, David (1997). "The capsaicin receptor: a heat-activated ion channel in the pain pathway". Nature. 389 (6653): 816–824. doi: 10.1038/39807 . PMID   9349813.
  13. Matta, José A.; Ahern, Gerard P. (2007). "Voltage is a partial activator of rat thermosensitive TRP channels". J Physiol. 582: 469–82.

Further reading

  1. Bullock, Theodore H. and Raymond B. Cowles. "Physiology of an infrared receptor: the facial pit of pit vipers." Science115 (1952), 541–543.
  2. Schutt, Bill. Dark Banquet: Blood and the Curious Lives of Blood-Feeding Creatures. New York: Three Rivers Press, 2008.