Ultrastructural changes in the tegument and gut of adult Fasciola hepatica following in vivo treatment with artesunate
•Artesunate caused relatively minor surface changes to triclabendazole-resistant Fasciola hepatica.•Internal changes to the tegumental system were more severe and led to loss of the apical plasma membrane.•Flooding of the tegument and internal tissues was seen.•Changes to the gut cells were more sev...
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description | •Artesunate caused relatively minor surface changes to triclabendazole-resistant Fasciola hepatica.•Internal changes to the tegumental system were more severe and led to loss of the apical plasma membrane.•Flooding of the tegument and internal tissues was seen.•Changes to the gut cells were more severe than those in the tegument and occurred more quickly.•The results suggest that artesunate enters the fluke by the oral route.
[Display omitted]
An in vivo study in the laboratory rat model has been carried out to monitor changes to the tegument and gut of adult Fasciola hepatica following treatment with artesunate. Rats infected with the triclabendazole-resistant Oberon isolate were dosed orally with artesunate at a concentration of 200 mg/kg and flukes recovered 24, 48, 72 and 96 h post-treatment (pt). The flukes were processed for scanning and transmission electron microscope examination. Changes to the external surface were limited to swelling and blebbing of the interspinal tegument. There was one exception, a specimen recovered 72 h pt, which had completely lost the syncytium over the posterior region of the fluke. Internal changes to the tegumental syncytium and cell bodies were more severe and were apparent from 48 h pt onwards. Increased numbers of secretory bodies were present in the apical region of the syncytium, the basal infolds were swollen and sloughing of the apical plasma membrane was seen at 96 h pt. In the cell bodies, there was swelling and vesiculation of the cisternae of the granular endoplasmic reticulum (ger), swelling of the mitochondria and a decrease in secretory body production. Changes to the gastrodermal cells were evident from 24 h onwards. They comprised swelling and vesiculation of the ger cisternae, swelling and lysis of the mitochondria and accumulation of autophagic vacuoles and lipid droplets. The nuclei of the cells were karyopyknotic by 96 h pt. The gut was consistently more severely affected than the tegument at all time points pt, pointing to an oral route of uptake for artesunate. This study has provided information on the primary subcellular targets for drug action in the fluke. |
doi_str_mv | 10.1016/j.exppara.2015.04.012 |
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[Display omitted]
An in vivo study in the laboratory rat model has been carried out to monitor changes to the tegument and gut of adult Fasciola hepatica following treatment with artesunate. Rats infected with the triclabendazole-resistant Oberon isolate were dosed orally with artesunate at a concentration of 200 mg/kg and flukes recovered 24, 48, 72 and 96 h post-treatment (pt). The flukes were processed for scanning and transmission electron microscope examination. Changes to the external surface were limited to swelling and blebbing of the interspinal tegument. There was one exception, a specimen recovered 72 h pt, which had completely lost the syncytium over the posterior region of the fluke. Internal changes to the tegumental syncytium and cell bodies were more severe and were apparent from 48 h pt onwards. Increased numbers of secretory bodies were present in the apical region of the syncytium, the basal infolds were swollen and sloughing of the apical plasma membrane was seen at 96 h pt. In the cell bodies, there was swelling and vesiculation of the cisternae of the granular endoplasmic reticulum (ger), swelling of the mitochondria and a decrease in secretory body production. Changes to the gastrodermal cells were evident from 24 h onwards. They comprised swelling and vesiculation of the ger cisternae, swelling and lysis of the mitochondria and accumulation of autophagic vacuoles and lipid droplets. The nuclei of the cells were karyopyknotic by 96 h pt. The gut was consistently more severely affected than the tegument at all time points pt, pointing to an oral route of uptake for artesunate. This study has provided information on the primary subcellular targets for drug action in the fluke.</description><identifier>ISSN: 0014-4894</identifier><identifier>EISSN: 1090-2449</identifier><identifier>DOI: 10.1016/j.exppara.2015.04.012</identifier><identifier>PMID: 25917645</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Administration, Oral ; Animals ; Antiplatyhelmintic Agents - administration & dosage ; Antiplatyhelmintic Agents - pharmacology ; Antiplatyhelmintic Agents - therapeutic use ; Artemisinins - administration & dosage ; Artemisinins - pharmacology ; Artemisinins - therapeutic use ; Artesunate ; Fasciola hepatica ; Fasciola hepatica - drug effects ; Fasciola hepatica - ultrastructure ; Gut ; In vivo ; Liver fluke ; Male ; Microscopy, Electron, Scanning ; Microscopy, Electron, Transmission ; Rats ; Rats, Sprague-Dawley ; Scanning electron microscopy ; Tegument ; Time Factors ; Transmission electron microscopy</subject><ispartof>Experimental parasitology, 2015-07, Vol.154, p.143-154</ispartof><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-41b0516a18d59a16c4bbedd136a889a432369a2f3de9ee66e40bc4ed9673e0c83</citedby><cites>FETCH-LOGICAL-c365t-41b0516a18d59a16c4bbedd136a889a432369a2f3de9ee66e40bc4ed9673e0c83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014489415001010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25917645$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O'Neill, J.F.</creatorcontrib><creatorcontrib>Johnston, R.C.</creatorcontrib><creatorcontrib>Halferty, L.</creatorcontrib><creatorcontrib>Brennan, G.P.</creatorcontrib><creatorcontrib>Fairweather, I.</creatorcontrib><title>Ultrastructural changes in the tegument and gut of adult Fasciola hepatica following in vivo treatment with artesunate</title><title>Experimental parasitology</title><addtitle>Exp Parasitol</addtitle><description>•Artesunate caused relatively minor surface changes to triclabendazole-resistant Fasciola hepatica.•Internal changes to the tegumental system were more severe and led to loss of the apical plasma membrane.•Flooding of the tegument and internal tissues was seen.•Changes to the gut cells were more severe than those in the tegument and occurred more quickly.•The results suggest that artesunate enters the fluke by the oral route.
[Display omitted]
An in vivo study in the laboratory rat model has been carried out to monitor changes to the tegument and gut of adult Fasciola hepatica following treatment with artesunate. Rats infected with the triclabendazole-resistant Oberon isolate were dosed orally with artesunate at a concentration of 200 mg/kg and flukes recovered 24, 48, 72 and 96 h post-treatment (pt). The flukes were processed for scanning and transmission electron microscope examination. Changes to the external surface were limited to swelling and blebbing of the interspinal tegument. There was one exception, a specimen recovered 72 h pt, which had completely lost the syncytium over the posterior region of the fluke. Internal changes to the tegumental syncytium and cell bodies were more severe and were apparent from 48 h pt onwards. Increased numbers of secretory bodies were present in the apical region of the syncytium, the basal infolds were swollen and sloughing of the apical plasma membrane was seen at 96 h pt. In the cell bodies, there was swelling and vesiculation of the cisternae of the granular endoplasmic reticulum (ger), swelling of the mitochondria and a decrease in secretory body production. Changes to the gastrodermal cells were evident from 24 h onwards. They comprised swelling and vesiculation of the ger cisternae, swelling and lysis of the mitochondria and accumulation of autophagic vacuoles and lipid droplets. The nuclei of the cells were karyopyknotic by 96 h pt. The gut was consistently more severely affected than the tegument at all time points pt, pointing to an oral route of uptake for artesunate. This study has provided information on the primary subcellular targets for drug action in the fluke.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Antiplatyhelmintic Agents - administration & dosage</subject><subject>Antiplatyhelmintic Agents - pharmacology</subject><subject>Antiplatyhelmintic Agents - therapeutic use</subject><subject>Artemisinins - administration & dosage</subject><subject>Artemisinins - pharmacology</subject><subject>Artemisinins - therapeutic use</subject><subject>Artesunate</subject><subject>Fasciola hepatica</subject><subject>Fasciola hepatica - drug effects</subject><subject>Fasciola hepatica - ultrastructure</subject><subject>Gut</subject><subject>In vivo</subject><subject>Liver fluke</subject><subject>Male</subject><subject>Microscopy, Electron, Scanning</subject><subject>Microscopy, Electron, Transmission</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Scanning electron microscopy</subject><subject>Tegument</subject><subject>Time Factors</subject><subject>Transmission electron microscopy</subject><issn>0014-4894</issn><issn>1090-2449</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE2P0zAQQC0EYsvCTwD5yCXBjh2vc0JotQtIK3Fhz9bEnrSu3Dj4owv_npQWrpzm8t6M5hHylrOWM64-7Fv8uSyQoO0Y71smW8a7Z2TD2cCaTsrhOdkwxmUj9SCvyKuc94wxzTv5klx1_cBvlOw35PgYSoJcUrWlJgjU7mDeYqZ-pmWHtOC2HnAuFGZHt7XQOFFwNRR6D9n6GIDucIHiLdAphhCf_Lw9yUd_jLQkhPJHf_JlRyEVzHWGgq_JiwlCxjeXeU0e7---335pHr59_nr76aGxQvWlkXxkPVfAtesH4MrKcUTnuFCg9QBSdEIN0E3C4YCoFEo2WoluUDcCmdXimrw_711S_FExF3Pw2WIIMGOs2XClheiF1nJF-zNqU8w54WSW5A-QfhnOzCm52ZtLcnNKbpg0a_LVe3c5UccDun_W38Yr8PEM4Pro0WMyazicLTqf0Bbjov_Pid_8eJet</recordid><startdate>201507</startdate><enddate>201507</enddate><creator>O'Neill, J.F.</creator><creator>Johnston, R.C.</creator><creator>Halferty, L.</creator><creator>Brennan, G.P.</creator><creator>Fairweather, I.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201507</creationdate><title>Ultrastructural changes in the tegument and gut of adult Fasciola hepatica following in vivo treatment with artesunate</title><author>O'Neill, J.F. ; Johnston, R.C. ; Halferty, L. ; Brennan, G.P. ; Fairweather, I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-41b0516a18d59a16c4bbedd136a889a432369a2f3de9ee66e40bc4ed9673e0c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Antiplatyhelmintic Agents - administration & dosage</topic><topic>Antiplatyhelmintic Agents - pharmacology</topic><topic>Antiplatyhelmintic Agents - therapeutic use</topic><topic>Artemisinins - administration & dosage</topic><topic>Artemisinins - pharmacology</topic><topic>Artemisinins - therapeutic use</topic><topic>Artesunate</topic><topic>Fasciola hepatica</topic><topic>Fasciola hepatica - drug effects</topic><topic>Fasciola hepatica - ultrastructure</topic><topic>Gut</topic><topic>In vivo</topic><topic>Liver fluke</topic><topic>Male</topic><topic>Microscopy, Electron, Scanning</topic><topic>Microscopy, Electron, Transmission</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Scanning electron microscopy</topic><topic>Tegument</topic><topic>Time Factors</topic><topic>Transmission electron microscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Neill, J.F.</creatorcontrib><creatorcontrib>Johnston, R.C.</creatorcontrib><creatorcontrib>Halferty, L.</creatorcontrib><creatorcontrib>Brennan, G.P.</creatorcontrib><creatorcontrib>Fairweather, I.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Neill, J.F.</au><au>Johnston, R.C.</au><au>Halferty, L.</au><au>Brennan, G.P.</au><au>Fairweather, I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrastructural changes in the tegument and gut of adult Fasciola hepatica following in vivo treatment with artesunate</atitle><jtitle>Experimental parasitology</jtitle><addtitle>Exp Parasitol</addtitle><date>2015-07</date><risdate>2015</risdate><volume>154</volume><spage>143</spage><epage>154</epage><pages>143-154</pages><issn>0014-4894</issn><eissn>1090-2449</eissn><abstract>•Artesunate caused relatively minor surface changes to triclabendazole-resistant Fasciola hepatica.•Internal changes to the tegumental system were more severe and led to loss of the apical plasma membrane.•Flooding of the tegument and internal tissues was seen.•Changes to the gut cells were more severe than those in the tegument and occurred more quickly.•The results suggest that artesunate enters the fluke by the oral route.
[Display omitted]
An in vivo study in the laboratory rat model has been carried out to monitor changes to the tegument and gut of adult Fasciola hepatica following treatment with artesunate. Rats infected with the triclabendazole-resistant Oberon isolate were dosed orally with artesunate at a concentration of 200 mg/kg and flukes recovered 24, 48, 72 and 96 h post-treatment (pt). The flukes were processed for scanning and transmission electron microscope examination. Changes to the external surface were limited to swelling and blebbing of the interspinal tegument. There was one exception, a specimen recovered 72 h pt, which had completely lost the syncytium over the posterior region of the fluke. Internal changes to the tegumental syncytium and cell bodies were more severe and were apparent from 48 h pt onwards. Increased numbers of secretory bodies were present in the apical region of the syncytium, the basal infolds were swollen and sloughing of the apical plasma membrane was seen at 96 h pt. In the cell bodies, there was swelling and vesiculation of the cisternae of the granular endoplasmic reticulum (ger), swelling of the mitochondria and a decrease in secretory body production. Changes to the gastrodermal cells were evident from 24 h onwards. They comprised swelling and vesiculation of the ger cisternae, swelling and lysis of the mitochondria and accumulation of autophagic vacuoles and lipid droplets. The nuclei of the cells were karyopyknotic by 96 h pt. The gut was consistently more severely affected than the tegument at all time points pt, pointing to an oral route of uptake for artesunate. This study has provided information on the primary subcellular targets for drug action in the fluke.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25917645</pmid><doi>10.1016/j.exppara.2015.04.012</doi><tpages>12</tpages></addata></record> |
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subjects | Administration, Oral Animals Antiplatyhelmintic Agents - administration & dosage Antiplatyhelmintic Agents - pharmacology Antiplatyhelmintic Agents - therapeutic use Artemisinins - administration & dosage Artemisinins - pharmacology Artemisinins - therapeutic use Artesunate Fasciola hepatica Fasciola hepatica - drug effects Fasciola hepatica - ultrastructure Gut In vivo Liver fluke Male Microscopy, Electron, Scanning Microscopy, Electron, Transmission Rats Rats, Sprague-Dawley Scanning electron microscopy Tegument Time Factors Transmission electron microscopy |
title | Ultrastructural changes in the tegument and gut of adult Fasciola hepatica following in vivo treatment with artesunate |
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