Release of Angiostrongylus cantonensis larvae from live intermediate hosts under stress
The metastrongyloid nematode Angiostrongylus cantonensis causes eosinophilic meningitis in a variety of homeothermic hosts including humans. Third-stage infectious larvae develop in gastropods as intermediate hosts. Humans are usually infected by intentional or incidental ingestion of an infected mo...
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creator | Šipková, Anna Anettová, Lucia Izquierdo-Rodriguez, Elena Velič, Vivienne Modrý, David |
description | The metastrongyloid nematode
Angiostrongylus cantonensis
causes eosinophilic meningitis in a variety of homeothermic hosts including humans. Third-stage infectious larvae develop in gastropods as intermediate hosts. Humans are usually infected by intentional or incidental ingestion of an infected mollusk or paratenic host (poikilothermic vertebrates and invertebrates). The infection may also hypothetically occur through ingestion of food or water contaminated by third-stage larvae spontaneously released from gastropods. Larvae are thought to be released in greater numbers from the intermediate host exposed to stress. This study aimed to compare larval release from stressed with unstressed gastropods. Experimentally infected
Limax maximus
and
Lissachatina fulica
were exposed to a stress stimulus (shaking on an orbital shaker). The mucus was collected before and after the stress and examined microscopically and by qPCR for the presence of
A. cantonensis
larvae and their DNA. In the case of
L. maximus
, no larvae were detected microscopically in the mucus, but qPCR analysis confirmed the presence of
A. cantonensis
DNA in all experimental replicates, without clear differences between stressed and non-stressed individuals. In contrast, individual larvae of
A. cantonensis
were found in mucus from
Li. fulica
after stress exposure, which also reflects an increased number of DNA-positive mucus samples after stress. Stress stimuli of intensity similar to the transport or handling of mollusks can stimulate the release of larvae from highly infected intermediate hosts. However, these larvae are released in small numbers. The exact number of larvae required to trigger neuroangiostrongyliasis is unknown. Therefore, caution is essential when interacting with potential intermediate hosts in regions where
A. cantonensis
is endemic. |
doi_str_mv | 10.1007/s00436-024-08232-y |
format | Article |
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Angiostrongylus cantonensis
causes eosinophilic meningitis in a variety of homeothermic hosts including humans. Third-stage infectious larvae develop in gastropods as intermediate hosts. Humans are usually infected by intentional or incidental ingestion of an infected mollusk or paratenic host (poikilothermic vertebrates and invertebrates). The infection may also hypothetically occur through ingestion of food or water contaminated by third-stage larvae spontaneously released from gastropods. Larvae are thought to be released in greater numbers from the intermediate host exposed to stress. This study aimed to compare larval release from stressed with unstressed gastropods. Experimentally infected
Limax maximus
and
Lissachatina fulica
were exposed to a stress stimulus (shaking on an orbital shaker). The mucus was collected before and after the stress and examined microscopically and by qPCR for the presence of
A. cantonensis
larvae and their DNA. In the case of
L. maximus
, no larvae were detected microscopically in the mucus, but qPCR analysis confirmed the presence of
A. cantonensis
DNA in all experimental replicates, without clear differences between stressed and non-stressed individuals. In contrast, individual larvae of
A. cantonensis
were found in mucus from
Li. fulica
after stress exposure, which also reflects an increased number of DNA-positive mucus samples after stress. Stress stimuli of intensity similar to the transport or handling of mollusks can stimulate the release of larvae from highly infected intermediate hosts. However, these larvae are released in small numbers. The exact number of larvae required to trigger neuroangiostrongyliasis is unknown. Therefore, caution is essential when interacting with potential intermediate hosts in regions where
A. cantonensis
is endemic.</description><identifier>ISSN: 0932-0113</identifier><identifier>EISSN: 1432-1955</identifier><identifier>DOI: 10.1007/s00436-024-08232-y</identifier><identifier>PMID: 38755287</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Angiostrongylus cantonensis ; Angiostrongylus cantonensis - physiology ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Deoxyribonucleic acid ; DNA ; Food contamination ; Gastropoda ; Gastropoda - parasitology ; Immunology ; Larva - physiology ; Larvae ; Leukocytes (eosinophilic) ; Medical Microbiology ; Meningitis ; Microbiology ; Mucus ; Real-Time Polymerase Chain Reaction ; Stress, Physiological ; Strongylida Infections - parasitology</subject><ispartof>Parasitology research (1987), 2024-05, Vol.123 (5), p.212-212, Article 212</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c426t-90673ef2a8f8b62a5445057578b2104ffc0bbb2c0e8b1e699ee74d0e1ce21ed43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00436-024-08232-y$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00436-024-08232-y$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38755287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Šipková, Anna</creatorcontrib><creatorcontrib>Anettová, Lucia</creatorcontrib><creatorcontrib>Izquierdo-Rodriguez, Elena</creatorcontrib><creatorcontrib>Velič, Vivienne</creatorcontrib><creatorcontrib>Modrý, David</creatorcontrib><title>Release of Angiostrongylus cantonensis larvae from live intermediate hosts under stress</title><title>Parasitology research (1987)</title><addtitle>Parasitol Res</addtitle><addtitle>Parasitol Res</addtitle><description>The metastrongyloid nematode
Angiostrongylus cantonensis
causes eosinophilic meningitis in a variety of homeothermic hosts including humans. Third-stage infectious larvae develop in gastropods as intermediate hosts. Humans are usually infected by intentional or incidental ingestion of an infected mollusk or paratenic host (poikilothermic vertebrates and invertebrates). The infection may also hypothetically occur through ingestion of food or water contaminated by third-stage larvae spontaneously released from gastropods. Larvae are thought to be released in greater numbers from the intermediate host exposed to stress. This study aimed to compare larval release from stressed with unstressed gastropods. Experimentally infected
Limax maximus
and
Lissachatina fulica
were exposed to a stress stimulus (shaking on an orbital shaker). The mucus was collected before and after the stress and examined microscopically and by qPCR for the presence of
A. cantonensis
larvae and their DNA. In the case of
L. maximus
, no larvae were detected microscopically in the mucus, but qPCR analysis confirmed the presence of
A. cantonensis
DNA in all experimental replicates, without clear differences between stressed and non-stressed individuals. In contrast, individual larvae of
A. cantonensis
were found in mucus from
Li. fulica
after stress exposure, which also reflects an increased number of DNA-positive mucus samples after stress. Stress stimuli of intensity similar to the transport or handling of mollusks can stimulate the release of larvae from highly infected intermediate hosts. However, these larvae are released in small numbers. The exact number of larvae required to trigger neuroangiostrongyliasis is unknown. Therefore, caution is essential when interacting with potential intermediate hosts in regions where
A. cantonensis
is endemic.</description><subject>Angiostrongylus cantonensis</subject><subject>Angiostrongylus cantonensis - physiology</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Food contamination</subject><subject>Gastropoda</subject><subject>Gastropoda - parasitology</subject><subject>Immunology</subject><subject>Larva - physiology</subject><subject>Larvae</subject><subject>Leukocytes (eosinophilic)</subject><subject>Medical Microbiology</subject><subject>Meningitis</subject><subject>Microbiology</subject><subject>Mucus</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Stress, Physiological</subject><subject>Strongylida Infections - parasitology</subject><issn>0932-0113</issn><issn>1432-1955</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU1rFEEQhhtRzCb6BzxIgxcvo9XfPScJIRohIIjisemZrdlMmO2OXTML--_tdWP8OHjqgnrq6Spexl4IeCMA3FsC0Mo2IHUDXirZ7B-xldC1EK0xj9kK2lqDEOqEnRLdAghntX7KTpR3xkjvVuzbZ5wwEvI88PO0GTPNJafNflqI9zHNOWGikfgUyy4iH0re8mncIR_TjGWL6zHOyG_qGPElrbHwKkCiZ-zJECfC5_fvGfv6_vLLxVVz_enDx4vz66bX0s5NC9YpHGT0g--sjEZrA8YZ5zspQA9DD13XyR7QdwJt2yI6vQYUPUqBa63O2Luj927p6jY9prnEKdyVcRvLPuQ4hr87abwJm7wLQkDrvRXV8PreUPL3BWkO25F6nKaYMC8UFBhrrbDOVvTVP-htXkqq9x0o00oL6iCUR6ovmajg8LCNgHAILhyDCzW48DO4sK9DL_-842HkV1IVUEeAaittsPz--z_aH5Q1pkc</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Šipková, Anna</creator><creator>Anettová, Lucia</creator><creator>Izquierdo-Rodriguez, Elena</creator><creator>Velič, Vivienne</creator><creator>Modrý, David</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><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><scope>5PM</scope></search><sort><creationdate>20240501</creationdate><title>Release of Angiostrongylus cantonensis larvae from live intermediate hosts under stress</title><author>Šipková, Anna ; Anettová, Lucia ; Izquierdo-Rodriguez, Elena ; Velič, Vivienne ; Modrý, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-90673ef2a8f8b62a5445057578b2104ffc0bbb2c0e8b1e699ee74d0e1ce21ed43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Angiostrongylus cantonensis</topic><topic>Angiostrongylus cantonensis - physiology</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Food contamination</topic><topic>Gastropoda</topic><topic>Gastropoda - parasitology</topic><topic>Immunology</topic><topic>Larva - physiology</topic><topic>Larvae</topic><topic>Leukocytes (eosinophilic)</topic><topic>Medical Microbiology</topic><topic>Meningitis</topic><topic>Microbiology</topic><topic>Mucus</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Stress, Physiological</topic><topic>Strongylida Infections - parasitology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Šipková, Anna</creatorcontrib><creatorcontrib>Anettová, Lucia</creatorcontrib><creatorcontrib>Izquierdo-Rodriguez, Elena</creatorcontrib><creatorcontrib>Velič, Vivienne</creatorcontrib><creatorcontrib>Modrý, David</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Parasitology research (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Šipková, Anna</au><au>Anettová, Lucia</au><au>Izquierdo-Rodriguez, Elena</au><au>Velič, Vivienne</au><au>Modrý, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Release of Angiostrongylus cantonensis larvae from live intermediate hosts under stress</atitle><jtitle>Parasitology research (1987)</jtitle><stitle>Parasitol Res</stitle><addtitle>Parasitol Res</addtitle><date>2024-05-01</date><risdate>2024</risdate><volume>123</volume><issue>5</issue><spage>212</spage><epage>212</epage><pages>212-212</pages><artnum>212</artnum><issn>0932-0113</issn><eissn>1432-1955</eissn><abstract>The metastrongyloid nematode
Angiostrongylus cantonensis
causes eosinophilic meningitis in a variety of homeothermic hosts including humans. Third-stage infectious larvae develop in gastropods as intermediate hosts. Humans are usually infected by intentional or incidental ingestion of an infected mollusk or paratenic host (poikilothermic vertebrates and invertebrates). The infection may also hypothetically occur through ingestion of food or water contaminated by third-stage larvae spontaneously released from gastropods. Larvae are thought to be released in greater numbers from the intermediate host exposed to stress. This study aimed to compare larval release from stressed with unstressed gastropods. Experimentally infected
Limax maximus
and
Lissachatina fulica
were exposed to a stress stimulus (shaking on an orbital shaker). The mucus was collected before and after the stress and examined microscopically and by qPCR for the presence of
A. cantonensis
larvae and their DNA. In the case of
L. maximus
, no larvae were detected microscopically in the mucus, but qPCR analysis confirmed the presence of
A. cantonensis
DNA in all experimental replicates, without clear differences between stressed and non-stressed individuals. In contrast, individual larvae of
A. cantonensis
were found in mucus from
Li. fulica
after stress exposure, which also reflects an increased number of DNA-positive mucus samples after stress. Stress stimuli of intensity similar to the transport or handling of mollusks can stimulate the release of larvae from highly infected intermediate hosts. However, these larvae are released in small numbers. The exact number of larvae required to trigger neuroangiostrongyliasis is unknown. Therefore, caution is essential when interacting with potential intermediate hosts in regions where
A. cantonensis
is endemic.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38755287</pmid><doi>10.1007/s00436-024-08232-y</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | Parasitology research (1987), 2024-05, Vol.123 (5), p.212-212, Article 212 |
issn | 0932-0113 1432-1955 |
language | eng |
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source | MEDLINE; SpringerNature Journals |
subjects | Angiostrongylus cantonensis Angiostrongylus cantonensis - physiology Animals Biomedical and Life Sciences Biomedicine Deoxyribonucleic acid DNA Food contamination Gastropoda Gastropoda - parasitology Immunology Larva - physiology Larvae Leukocytes (eosinophilic) Medical Microbiology Meningitis Microbiology Mucus Real-Time Polymerase Chain Reaction Stress, Physiological Strongylida Infections - parasitology |
title | Release of Angiostrongylus cantonensis larvae from live intermediate hosts under stress |
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