Ammonia excretion and acid–base regulation in the American horseshoe crab, Limulus polyphemus

ABSTRACT Many studies have investigated ammonia excretion and acid–base regulation in aquatic arthropods, yet current knowledge of marine chelicerates is non-existent. In American horseshoe crabs (Limulus polyphemus), book gills bear physiologically distinct regions: dorsal and ventral half-lamellae, a central mitochondria-rich area (CMRA) and peripheral mitochondria-poor areas (PMPAs). In the present study, the CMRA and ventral half-lamella exhibited characteristics important for ammonia excretion and/or acid–base regulation, as supported by high expression levels of Rhesus-protein 1 (LpRh-1), cytoplasmic carbonic anhydrase (CA-2) and hyperpolarization-activated cyclic nucleotide-gated K+ channel (HCN) compared with the PMPA and dorsal half-lamella. The half-lamellae displayed remarkable differences; the ventral epithelium was ion-leaky whereas the dorsal counterpart possessed an exceptionally tight epithelium. LpRh-1 was more abundant than Rhesus-protein 2 (LpRh-2) in all investigated tissues, but LpRh-2 was more prevalent in the PMPA than in the CMRA. Ammonia influx associated with high ambient ammonia (HAA) treatment was counteracted by intact animals and complemented by upregulation of branchial CA-2, V-type H+-ATPase (HAT), HCN and LpRh-1 mRNA expression. The dorsal epithelium demonstrated characteristics of active ammonia excretion. However, an influx was observed across the ventral epithelium as a result of the tissue's high ion conductance, although the influx rate was not proportionately high considering the ∼3-fold inwardly directed ammonia gradient. These novel findings suggest a role for the coxal gland in excretion and in the maintenance of hemolymph ammonia regulation under HAA. Hypercapnic exposure induced compensatory respiratory acidosis and partial metabolic depression. Functional differences between the two halves of a branchial lamella may be physiologically beneficial in reducing the backflow of waste products into adjacent lamellae, especially in fluctuating environments where ammonia levels can increase. Summary: First insight into a marine chelicerate's ammonia and acid-base regulatory strategies as assessed via changes in mRNA expression levels and physiological responses to elevated ambient ammonia and CO2.

[1]  A. Donini,et al.  An animal homolog of plant Mep/Amt transporters promotes ammonia excretion by the anal papillae of the disease vector mosquito Aedes aegypti , 2016, Journal of Experimental Biology.

[2]  D. Weihrauch,et al.  The role of an ancestral hyperpolarization-activated cyclic nucleotide-gated K+ channel in branchial acid-base regulation in the green crab, Carcinus maenas , 2016, Journal of Experimental Biology.

[3]  D. Weihrauch,et al.  Mechanisms of acid–base regulation in seawater-acclimated green crabs (Carcinus maenas) , 2016 .

[4]  J. Treberg,et al.  Mechanism of ammonia excretion in the freshwater leech Nephelopsis obscura: characterization of a primitive Rh protein and effects of high environmental ammonia. , 2015, American journal of physiology. Regulatory, integrative and comparative physiology.

[5]  A. Marini,et al.  Ammonia excretion in Caenorhabditis elegans: mechanism and evidence of ammonia transport of the Rhesus protein CeRhr-1 , 2015, The Journal of Experimental Biology.

[6]  R. J. Pitts,et al.  Antennal-Expressed Ammonium Transporters in the Malaria Vector Mosquito Anopheles gambiae , 2014, PloS one.

[7]  J. Treberg,et al.  Acid–base regulation in the Dungeness crab (Metacarcinus magister) , 2014 .

[8]  J. Treberg,et al.  Cutaneous nitrogen excretion in the African clawed frog Xenopus laevis: effects of high environmental ammonia (HEA). , 2013, Aquatic toxicology.

[9]  K. Gilmour New insights into the many functions of carbonic anhydrase in fish gills , 2012, Respiratory Physiology & Neurobiology.

[10]  Heiko Meyer,et al.  Ammonia excretion in the freshwater planarian Schmidtea mediterranea , 2012, Journal of Experimental Biology.

[11]  M. Wahl,et al.  Sour times: seawater acidification effects on growth, feeding behaviour and acid-base status of Asterias rubens and Carcinus maenas , 2012 .

[12]  C. Rangel,et al.  The hyperpolarization-activated cyclic nucleotide-gated HCN2 channel transports ammonium in the distal nephron. , 2011, Kidney international.

[13]  D. Weihrauch,et al.  Effects of high environmental ammonia on branchial ammonia excretion rates and tissue Rh-protein mRNA expression levels in seawater acclimated Dungeness crab Metacarcinus magister. , 2011, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

[14]  S. Dupont,et al.  Physiological basis for high CO2 tolerance in marine ectothermic animals: pre-adaptation through lifestyle and ontogeny? , 2009 .

[15]  C. Wood,et al.  A new paradigm for ammonia excretion in aquatic animals: role of Rhesus (Rh) glycoproteins , 2009, Journal of Experimental Biology.

[16]  P. Walsh,et al.  Ammonia and urea transporters in gills of fish and aquatic crustaceans , 2009, Journal of Experimental Biology.

[17]  H. Onken,et al.  A structure-function analysis of ion transport in crustacean gills and excretory organs. , 2008, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

[18]  Jonathan M. Wilson,et al.  Ammonia excretion in rainbow trout (Oncorhynchus mykiss): evidence for Rh glycoprotein and H+-ATPase involvement. , 2007, Physiological genomics.

[19]  J. Spicer,et al.  Influence of CO2-related seawater acidification on extracellular acid–base balance in the velvet swimming crab Necora puber , 2007 .

[20]  I. McGaw Burying behaviour of two sympatric crab species: Cancer magister and Cancer productus , 2005 .

[21]  Ken Caldeira,et al.  Ocean model predictions of chemistry changes from carbon dioxide emissions to the atmosphere and ocean , 2005 .

[22]  James M. Russell,et al.  Validation of stratospheric temperatures measured by Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on Envisat , 2005 .

[23]  H. Pörtner,et al.  Biological Impact of Elevated Ocean CO2 Concentrations: Lessons from Animal Physiology and Earth History , 2004 .

[24]  R. Butterworth Pathophysiology of Hepatic Encephalopathy: A New Look at Ammonia , 2002, Metabolic Brain Disease.

[25]  D. Towle,et al.  Active ammonia excretion across the gills of the green shore crab Carcinus maenas: participation of Na(+)/K(+)-ATPase, V-type H(+)-ATPase and functional microtubules. , 2002, The Journal of experimental biology.

[26]  F. A. Leone,et al.  Modulation by ammonium ions of gill microsomal (Na+,K+)-ATPase in the swimming crab Callinectes danae: a possible mechanism for regulation of ammonia excretion. , 2002, Comparative biochemistry and physiology. Toxicology & pharmacology : CBP.

[27]  H. Onken,et al.  Hyperosmoregulation in the red freshwater crab Dilocarcinus pagei (Brachyura, Trichodactylidae): structural and functional asymmetries of the posterior gills. , 2002, The Journal of experimental biology.

[28]  D. Siebers,et al.  Active osmoregulatory ion uptake across the pleopods of the isopod Idotea baltica (Pallas): electrophysiological measurements on isolated split endo- and exopodites mounted in a micro-ussing chamber. , 2000, The Journal of experimental biology.

[29]  D. Siebers,et al.  Potential of active excretion of ammonia in three different haline species of crabs , 1999, Journal of Comparative Physiology B.

[30]  D. Siebers,et al.  Active excretion of ammonia across the gills of the shore crab Carcinus maenas and its relation to osmoregulatory ion uptake , 1998, Journal of Comparative Physiology B.

[31]  D. Siebers,et al.  Inhibition of Na+/K+-ATPase and of active ion-transport functions in the gills of the shore crab Carcinus maenas induced by cadmium , 1998 .

[32]  D. Wallace,et al.  Program developed for CO{sub 2} system calculations , 1998 .

[33]  C. Mangum,et al.  Ultrastructure and Transport-Related Enzymes of the Gills and Coxal Gland of the Horseshoe Crab Limulus polyphemus. , 1996, The Biological bulletin.

[34]  P. Wright Nitrogen excretion: three end products, many physiological roles. , 1995, The Journal of experimental biology.

[35]  J. Avise,et al.  A SPECIATIONAL HISTORY OF “LIVING FOSSILS”: MOLECULAR EVOLUTIONARY PATTERNS IN HORSESHOE CRABS , 1994, Evolution; international journal of organic evolution.

[36]  S. McCormick,et al.  Methods for Nonlethal Gill Biopsy and Measurement of Na+, K+-ATPase Activity , 1993 .

[37]  E. Taylor,et al.  Transbranchial ammonia gradients and acid-base responses to high external ammonia concentration in rainbow trout (Oncorhynchus mykiss) acclimated to different salinities. , 1992, The Journal of experimental biology.

[38]  G. Marcaida,et al.  Acute ammonia toxicity is mediated by the NMDA type of glutamate receptors , 1992, FEBS letters.

[39]  W. Young-Lai,et al.  Effect of ammonia on survival and osmoregulation in different life stages of the lobsterHomarus americanus , 1991 .

[40]  A. Dickson Standard potential of the reaction: , and and the standard acidity constant of the ion HSO4− in synthetic sea water from 273.15 to 318.15 K , 1990 .

[41]  G. Somero,et al.  Pressure adaptation of Na+/K+-ATPase in gills of marine teleosts. , 1989, The Journal of experimental biology.

[42]  F. Millero,et al.  A comparison of the equilibrium constants for the dissociation of carbonic acid in seawater media , 1987 .

[43]  C. N. Shuster,et al.  A contribution to the population biology of horseshoe crabs,Limulus polyphemus (L.), in Delaware Bay , 1985 .

[44]  A. C. Taylor,et al.  Oxygen and carbon dioxide transporting properties of the blood of three sublittoral species of burrowing crab , 1985, Journal of Comparative Physiology B.

[45]  M. L. Botton The importance of predation by horseshoe crabs, Limulus polyphemus , to an intertidal sand flat community , 1984 .

[46]  N. Heisler,et al.  Studies of Ammonia in the Rainbow Trout:Physico-chemical Parameters, Acid-Base Behaviour and Respiratory Clearance , 1983 .

[47]  A. Dickson An exact definition of total alkalinity and a procedure for the estimation of alkalinity and total inorganic carbon from titration data , 1981 .

[48]  A. Rudloe The breeding behavior and patterns of movement of horseshoe crabs,Limulus polyphemus, in the vicinity of breeding beaches in Apalachee Bay, Florida , 1980 .

[49]  J. Bidwell,et al.  Ionization of Ammonia in Seawater: Effects of Temperature, pH, and Salinity , 1978 .

[50]  C. Mangum,et al.  The ionic environment of hemocyanin in Limulus polyphemus. , 1976, The Biological bulletin.

[51]  J. Truchot Carbon dioxide combining properties of the blood of the shore crab Carcinus maenas (L): carbon dioxide solubility coefficient and carbonic acid dissociation constants. , 1976, The Journal of experimental biology.

[52]  C. Culberson,et al.  MEASUREMENT OF THE APPARENT DISSOCIATION CONSTANTS OF CARBONIC ACID IN SEAWATER AT ATMOSPHERIC PRESSURE1 , 1973 .

[53]  J. Robertson OSMOTIC AND IONIC REGULATION IN THE HORSESHOE CRAB LIMULUS POLYPHEMUS (LINNAEUS) , 1970 .

[54]  D. Weihrauch,et al.  Differential acid-base regulation in various gills of the green crab Carcinus maenas: Effects of elevated environmental pCO2. , 2013, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

[55]  S. Bustin,et al.  Quantification strategies in real-time PCR , 2008 .

[56]  D. Sankar,et al.  ‘Active ammonia’ , 2005, Experientia.

[57]  M. J. Cavey,et al.  Organization of a phyllobranchiate gill from the green shore crab Carcinus maenas (Crustacea, Decapoda) , 2004, Cell and Tissue Research.

[58]  Jun Kita,et al.  Acid-base responses to lethal aquatic hypercapnia in three marine fishes , 2004 .

[59]  Ø. Hammer,et al.  PAST: PALEONTOLOGICAL STATISTICAL SOFTWARE PACKAGE FOR EDUCATION AND DATA ANALYSIS , 2001 .

[60]  O Hammer-Muntz,et al.  PAST: paleontological statistics software package for education and data analysis version 2.09 , 2001 .

[61]  P. J. Hilton,et al.  Relationship between intracellular proton buffering capacity and intracellular pH. , 1992, Kidney international.

[62]  C. Mangum,et al.  The role of the coxal gland in ionic, osmotic, and pH regulation in the horseshoe crab Limulus polyphemus. , 1982, Progress in clinical and biological research.

[63]  Shuster Cn A pictorial review of the natural history and ecology of the horseshoe crab Limulus polyphemus, with reference to other Limulidae. , 1982 .

[64]  C. N. Shuster A pictorial review of the natural history and ecology of the horseshoe crab Limulus polyphemus, with reference to other Limulidae. , 1982, Progress in clinical and biological research.

[65]  Johnson Ba,et al.  The role of the coxal gland in ionic, osmotic, and pH regulation in the horseshoe crab Limulus polyphemus. , 1982 .

[66]  Shuster Cn Distribution of the American horseshoe "crab," Limulus polyphemus (L.). , 1979 .

[67]  C. N. Shuster Distribution of the American horseshoe "crab," Limulus polyphemus (L.). , 1979, Progress in clinical and biological research.