Protein undernutrition reduces the efficacy of praziquantel in a murine model of Schistosoma mansoni infection
Background Undernutrition and schistosomiasis are public health problems and often occur in low and middle-income countries. Protein undernutrition can alter the host-parasite environment system and aggravate the course of schistosomiasis. This study aimed to assess the impact of a low-protein diet...
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Veröffentlicht in: | PLoS neglected tropical diseases 2022-07, Vol.16 (7), p.e0010249-e0010249 |
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creator | Kadji Fassi, Joseph Bertin Boukeng Jatsa, Hermine Membe Femoe, Ulrich Greigert, Valentin Brunet, Julie Cannet, Catherine Kenfack, Christian Mérimé Gipwe Feussom, Nestor Tienga Nkondo, Emilienne Abou-Bacar, Ahmed Pfaff, Alexander Wilhelm Kamgang, René Kamtchouing, Pierre Tchuem Tchuenté, Louis-Albert |
description | Background Undernutrition and schistosomiasis are public health problems and often occur in low and middle-income countries. Protein undernutrition can alter the host-parasite environment system and aggravate the course of schistosomiasis. This study aimed to assess the impact of a low-protein diet on the efficacy of praziquantel. Methodology/Principal findings Thirty-day-old mice were fed with a low-protein diet, and 40 days later, they were individually infected with fifty Schistosoma mansoni cercariae. A 28-day-treatment with praziquantel at 100 mg/kg for five consecutive days followed by distilled water begins on the 36.sup.th day post-infection. Mice were sacrificed on the 64.sup.th day post-infection. We determined the parasitological burden, liver and intestine histomorphometry, liver injury, and immunomodulation parameters. Praziquantel treatment of infected mice fed with a standard diet (IN-PZQ) resulted in a significant reduction of worm and egg burdens and a normalization of iron and calcium levels. The therapy also improved schistosomiasis-induced hepatopathy and oxidative stress. The anti-inflammatory and immunomodulatory activities of praziquantel were also significant in these mice. When infected mice receiving the low-protein diet were treated with praziquantel (ILP-PZQ), the body weight loss and hepatomegaly were not alleviated, and the worm and liver egg burdens were significantly higher than those of IN-PZQ mice (P < 0.001). The treatment did not reduce the increased activities of ALT and [gamma]-GGT, the high malondialdehyde concentration, and the liver granuloma volume. The iron and calcium levels were not ameliorated and differed from those of IN-PZQ mice (P < 0.001 and P < 0.05). Moreover, in these mice, praziquantel treatment did not reverse the high level of IL-5 and the low mRNA expression of CCL3/MIP-1[alpha] and CXCL-10/IP-10 induced by S. mansoni infection. Conclusion/Significance These results demonstrated that a low-protein diet reduced the schistosomicidal, antioxidant, anti-inflammatory, and immunomodulatory activities of praziquantel. |
doi_str_mv | 10.1371/journal.pntd.0010249 |
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Protein undernutrition can alter the host-parasite environment system and aggravate the course of schistosomiasis. This study aimed to assess the impact of a low-protein diet on the efficacy of praziquantel. Methodology/Principal findings Thirty-day-old mice were fed with a low-protein diet, and 40 days later, they were individually infected with fifty Schistosoma mansoni cercariae. A 28-day-treatment with praziquantel at 100 mg/kg for five consecutive days followed by distilled water begins on the 36.sup.th day post-infection. Mice were sacrificed on the 64.sup.th day post-infection. We determined the parasitological burden, liver and intestine histomorphometry, liver injury, and immunomodulation parameters. Praziquantel treatment of infected mice fed with a standard diet (IN-PZQ) resulted in a significant reduction of worm and egg burdens and a normalization of iron and calcium levels. The therapy also improved schistosomiasis-induced hepatopathy and oxidative stress. The anti-inflammatory and immunomodulatory activities of praziquantel were also significant in these mice. When infected mice receiving the low-protein diet were treated with praziquantel (ILP-PZQ), the body weight loss and hepatomegaly were not alleviated, and the worm and liver egg burdens were significantly higher than those of IN-PZQ mice (P < 0.001). The treatment did not reduce the increased activities of ALT and [gamma]-GGT, the high malondialdehyde concentration, and the liver granuloma volume. The iron and calcium levels were not ameliorated and differed from those of IN-PZQ mice (P < 0.001 and P < 0.05). Moreover, in these mice, praziquantel treatment did not reverse the high level of IL-5 and the low mRNA expression of CCL3/MIP-1[alpha] and CXCL-10/IP-10 induced by S. mansoni infection. Conclusion/Significance These results demonstrated that a low-protein diet reduced the schistosomicidal, antioxidant, anti-inflammatory, and immunomodulatory activities of praziquantel.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0010249</identifier><identifier>PMID: 35839247</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Animal models ; Biology and Life Sciences ; Biomarkers ; Body weight ; Body weight loss ; Calcium ; CCL3 protein ; Cholesterol ; Cytokines ; Diet ; Distilled water ; Dosage and administration ; Effectiveness ; Eggs ; Feces ; Gene expression ; Granuloma ; Granulomas ; Health aspects ; Health problems ; High density lipoprotein ; Histomorphometry ; Immunomodulation ; Infections ; Inflammation ; Interleukin 5 ; Intestine ; Intestines ; IP-10 protein ; Iron ; Laboratory animals ; Liver ; Low density lipoprotein ; Low protein diet ; Malnutrition ; Medicine and Health Sciences ; Nutrient deficiency ; Nutritional status ; Oxidative stress ; Parasites ; Praziquantel ; Proteins ; Public health ; Schistosoma mansoni ; Schistosomiasis ; Testing ; Therapy ; Triglycerides ; Tropical diseases ; Undernutrition ; Weight loss ; Worms</subject><ispartof>PLoS neglected tropical diseases, 2022-07, Vol.16 (7), p.e0010249-e0010249</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Kadji Fassi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 Kadji Fassi et al 2022 Kadji Fassi et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c601t-10b9eb9c410ecf1c120cc6968503c6dc3fb2549619f3d906e442aaf3d78190803</citedby><cites>FETCH-LOGICAL-c601t-10b9eb9c410ecf1c120cc6968503c6dc3fb2549619f3d906e442aaf3d78190803</cites><orcidid>0000-0002-9838-8570</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328564/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328564/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2104,2930,23873,27931,27932,53798,53800</link.rule.ids></links><search><contributor>Mitre, Edward</contributor><creatorcontrib>Kadji Fassi, Joseph Bertin</creatorcontrib><creatorcontrib>Boukeng Jatsa, Hermine</creatorcontrib><creatorcontrib>Membe Femoe, Ulrich</creatorcontrib><creatorcontrib>Greigert, Valentin</creatorcontrib><creatorcontrib>Brunet, Julie</creatorcontrib><creatorcontrib>Cannet, Catherine</creatorcontrib><creatorcontrib>Kenfack, Christian Mérimé</creatorcontrib><creatorcontrib>Gipwe Feussom, Nestor</creatorcontrib><creatorcontrib>Tienga Nkondo, Emilienne</creatorcontrib><creatorcontrib>Abou-Bacar, Ahmed</creatorcontrib><creatorcontrib>Pfaff, Alexander Wilhelm</creatorcontrib><creatorcontrib>Kamgang, René</creatorcontrib><creatorcontrib>Kamtchouing, Pierre</creatorcontrib><creatorcontrib>Tchuem Tchuenté, Louis-Albert</creatorcontrib><title>Protein undernutrition reduces the efficacy of praziquantel in a murine model of Schistosoma mansoni infection</title><title>PLoS neglected tropical diseases</title><description>Background Undernutrition and schistosomiasis are public health problems and often occur in low and middle-income countries. Protein undernutrition can alter the host-parasite environment system and aggravate the course of schistosomiasis. This study aimed to assess the impact of a low-protein diet on the efficacy of praziquantel. Methodology/Principal findings Thirty-day-old mice were fed with a low-protein diet, and 40 days later, they were individually infected with fifty Schistosoma mansoni cercariae. A 28-day-treatment with praziquantel at 100 mg/kg for five consecutive days followed by distilled water begins on the 36.sup.th day post-infection. Mice were sacrificed on the 64.sup.th day post-infection. We determined the parasitological burden, liver and intestine histomorphometry, liver injury, and immunomodulation parameters. Praziquantel treatment of infected mice fed with a standard diet (IN-PZQ) resulted in a significant reduction of worm and egg burdens and a normalization of iron and calcium levels. The therapy also improved schistosomiasis-induced hepatopathy and oxidative stress. The anti-inflammatory and immunomodulatory activities of praziquantel were also significant in these mice. When infected mice receiving the low-protein diet were treated with praziquantel (ILP-PZQ), the body weight loss and hepatomegaly were not alleviated, and the worm and liver egg burdens were significantly higher than those of IN-PZQ mice (P < 0.001). The treatment did not reduce the increased activities of ALT and [gamma]-GGT, the high malondialdehyde concentration, and the liver granuloma volume. The iron and calcium levels were not ameliorated and differed from those of IN-PZQ mice (P < 0.001 and P < 0.05). Moreover, in these mice, praziquantel treatment did not reverse the high level of IL-5 and the low mRNA expression of CCL3/MIP-1[alpha] and CXCL-10/IP-10 induced by S. mansoni infection. Conclusion/Significance These results demonstrated that a low-protein diet reduced the schistosomicidal, antioxidant, anti-inflammatory, and immunomodulatory activities of praziquantel.</description><subject>Animal models</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers</subject><subject>Body weight</subject><subject>Body weight loss</subject><subject>Calcium</subject><subject>CCL3 protein</subject><subject>Cholesterol</subject><subject>Cytokines</subject><subject>Diet</subject><subject>Distilled water</subject><subject>Dosage and administration</subject><subject>Effectiveness</subject><subject>Eggs</subject><subject>Feces</subject><subject>Gene expression</subject><subject>Granuloma</subject><subject>Granulomas</subject><subject>Health aspects</subject><subject>Health problems</subject><subject>High density lipoprotein</subject><subject>Histomorphometry</subject><subject>Immunomodulation</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Interleukin 5</subject><subject>Intestine</subject><subject>Intestines</subject><subject>IP-10 protein</subject><subject>Iron</subject><subject>Laboratory animals</subject><subject>Liver</subject><subject>Low density lipoprotein</subject><subject>Low protein diet</subject><subject>Malnutrition</subject><subject>Medicine and Health Sciences</subject><subject>Nutrient deficiency</subject><subject>Nutritional status</subject><subject>Oxidative stress</subject><subject>Parasites</subject><subject>Praziquantel</subject><subject>Proteins</subject><subject>Public health</subject><subject>Schistosoma mansoni</subject><subject>Schistosomiasis</subject><subject>Testing</subject><subject>Therapy</subject><subject>Triglycerides</subject><subject>Tropical diseases</subject><subject>Undernutrition</subject><subject>Weight loss</subject><subject>Worms</subject><issn>1935-2735</issn><issn>1935-2727</issn><issn>1935-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>DOA</sourceid><recordid>eNptkl2L1DAUhoso7rr6DwQLgngzY9J8tLkRlsWPhQUF9Tqkyck0Q5vMJqmw_npTp8qOLLlIOHnOe07enKp6idEWkxa_24c5ejVuDz6bLUIYNVQ8qs6xIGzTtIQ9vnc-q56ltEeICdbhp9UZYR0RDW3PK_81hgzO17M3EP2co8su-DqCmTWkOg9Qg7VOK31XB1sfovrlbmflM4x1SVP1NEfnoZ6CKZFCfNODSzmkMJU75VPwroAW9KL7vHpi1ZjgxbpfVD8-fvh-9Xlz8-XT9dXlzUZzhPMGo15ALzTFCLTFGjdIay54xxDR3Ghi-4ZRwbGwxAjEgdJGqXJuOyxQh8hF9eqoexhDkqtVSTYtIrhFLeOFuD4SJqi9PEQ3qXgng3LyTyDEnVQxOz2CJJgKw4oLnemoLt5ZbUWxm_aYKNubovV-rTb3ExgNPkc1noie3ng3yF34KQVpOsZpEXi7CsRwO0PKcnJJwzgqD2EufXOBEeWM4YK-_g99-HUrtVPlAcX-UOrqRVRetrjhtKFoKbt9gCrLwOR08GBdiZ8kvLmXMIAa85DCOC9fm05BegR1DClFsP_MwEgu4_u3a7mMr1zHl_wGrfPjpQ</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Kadji 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of praziquantel in a murine model of Schistosoma mansoni infection</title><author>Kadji Fassi, Joseph Bertin ; Boukeng Jatsa, Hermine ; Membe Femoe, Ulrich ; Greigert, Valentin ; Brunet, Julie ; Cannet, Catherine ; Kenfack, Christian Mérimé ; Gipwe Feussom, Nestor ; Tienga Nkondo, Emilienne ; Abou-Bacar, Ahmed ; Pfaff, Alexander Wilhelm ; Kamgang, René ; Kamtchouing, Pierre ; Tchuem Tchuenté, Louis-Albert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c601t-10b9eb9c410ecf1c120cc6968503c6dc3fb2549619f3d906e442aaf3d78190803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animal models</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers</topic><topic>Body weight</topic><topic>Body weight loss</topic><topic>Calcium</topic><topic>CCL3 protein</topic><topic>Cholesterol</topic><topic>Cytokines</topic><topic>Diet</topic><topic>Distilled water</topic><topic>Dosage and administration</topic><topic>Effectiveness</topic><topic>Eggs</topic><topic>Feces</topic><topic>Gene expression</topic><topic>Granuloma</topic><topic>Granulomas</topic><topic>Health aspects</topic><topic>Health problems</topic><topic>High density lipoprotein</topic><topic>Histomorphometry</topic><topic>Immunomodulation</topic><topic>Infections</topic><topic>Inflammation</topic><topic>Interleukin 5</topic><topic>Intestine</topic><topic>Intestines</topic><topic>IP-10 protein</topic><topic>Iron</topic><topic>Laboratory animals</topic><topic>Liver</topic><topic>Low density lipoprotein</topic><topic>Low protein diet</topic><topic>Malnutrition</topic><topic>Medicine and Health Sciences</topic><topic>Nutrient deficiency</topic><topic>Nutritional status</topic><topic>Oxidative stress</topic><topic>Parasites</topic><topic>Praziquantel</topic><topic>Proteins</topic><topic>Public health</topic><topic>Schistosoma mansoni</topic><topic>Schistosomiasis</topic><topic>Testing</topic><topic>Therapy</topic><topic>Triglycerides</topic><topic>Tropical diseases</topic><topic>Undernutrition</topic><topic>Weight loss</topic><topic>Worms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kadji Fassi, Joseph Bertin</creatorcontrib><creatorcontrib>Boukeng Jatsa, Hermine</creatorcontrib><creatorcontrib>Membe Femoe, Ulrich</creatorcontrib><creatorcontrib>Greigert, Valentin</creatorcontrib><creatorcontrib>Brunet, Julie</creatorcontrib><creatorcontrib>Cannet, Catherine</creatorcontrib><creatorcontrib>Kenfack, Christian Mérimé</creatorcontrib><creatorcontrib>Gipwe Feussom, Nestor</creatorcontrib><creatorcontrib>Tienga Nkondo, Emilienne</creatorcontrib><creatorcontrib>Abou-Bacar, Ahmed</creatorcontrib><creatorcontrib>Pfaff, Alexander Wilhelm</creatorcontrib><creatorcontrib>Kamgang, René</creatorcontrib><creatorcontrib>Kamtchouing, Pierre</creatorcontrib><creatorcontrib>Tchuem Tchuenté, Louis-Albert</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 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Fassi, Joseph Bertin</au><au>Boukeng Jatsa, Hermine</au><au>Membe Femoe, Ulrich</au><au>Greigert, Valentin</au><au>Brunet, Julie</au><au>Cannet, Catherine</au><au>Kenfack, Christian Mérimé</au><au>Gipwe Feussom, Nestor</au><au>Tienga Nkondo, Emilienne</au><au>Abou-Bacar, Ahmed</au><au>Pfaff, Alexander Wilhelm</au><au>Kamgang, René</au><au>Kamtchouing, Pierre</au><au>Tchuem Tchuenté, Louis-Albert</au><au>Mitre, Edward</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protein undernutrition reduces the efficacy of praziquantel in a murine model of Schistosoma mansoni infection</atitle><jtitle>PLoS neglected tropical diseases</jtitle><date>2022-07-01</date><risdate>2022</risdate><volume>16</volume><issue>7</issue><spage>e0010249</spage><epage>e0010249</epage><pages>e0010249-e0010249</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Background Undernutrition and schistosomiasis are public health problems and often occur in low and middle-income countries. Protein undernutrition can alter the host-parasite environment system and aggravate the course of schistosomiasis. This study aimed to assess the impact of a low-protein diet on the efficacy of praziquantel. Methodology/Principal findings Thirty-day-old mice were fed with a low-protein diet, and 40 days later, they were individually infected with fifty Schistosoma mansoni cercariae. A 28-day-treatment with praziquantel at 100 mg/kg for five consecutive days followed by distilled water begins on the 36.sup.th day post-infection. Mice were sacrificed on the 64.sup.th day post-infection. We determined the parasitological burden, liver and intestine histomorphometry, liver injury, and immunomodulation parameters. Praziquantel treatment of infected mice fed with a standard diet (IN-PZQ) resulted in a significant reduction of worm and egg burdens and a normalization of iron and calcium levels. The therapy also improved schistosomiasis-induced hepatopathy and oxidative stress. The anti-inflammatory and immunomodulatory activities of praziquantel were also significant in these mice. When infected mice receiving the low-protein diet were treated with praziquantel (ILP-PZQ), the body weight loss and hepatomegaly were not alleviated, and the worm and liver egg burdens were significantly higher than those of IN-PZQ mice (P < 0.001). The treatment did not reduce the increased activities of ALT and [gamma]-GGT, the high malondialdehyde concentration, and the liver granuloma volume. The iron and calcium levels were not ameliorated and differed from those of IN-PZQ mice (P < 0.001 and P < 0.05). Moreover, in these mice, praziquantel treatment did not reverse the high level of IL-5 and the low mRNA expression of CCL3/MIP-1[alpha] and CXCL-10/IP-10 induced by S. mansoni infection. Conclusion/Significance These results demonstrated that a low-protein diet reduced the schistosomicidal, antioxidant, anti-inflammatory, and immunomodulatory activities of praziquantel.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>35839247</pmid><doi>10.1371/journal.pntd.0010249</doi><orcidid>https://orcid.org/0000-0002-9838-8570</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1935-2735 |
ispartof | PLoS neglected tropical diseases, 2022-07, Vol.16 (7), p.e0010249-e0010249 |
issn | 1935-2735 1935-2727 1935-2735 |
language | eng |
recordid | cdi_plos_journals_2703170756 |
source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Public Library of Science (PLoS) Journals Open Access; PubMed Central |
subjects | Animal models Biology and Life Sciences Biomarkers Body weight Body weight loss Calcium CCL3 protein Cholesterol Cytokines Diet Distilled water Dosage and administration Effectiveness Eggs Feces Gene expression Granuloma Granulomas Health aspects Health problems High density lipoprotein Histomorphometry Immunomodulation Infections Inflammation Interleukin 5 Intestine Intestines IP-10 protein Iron Laboratory animals Liver Low density lipoprotein Low protein diet Malnutrition Medicine and Health Sciences Nutrient deficiency Nutritional status Oxidative stress Parasites Praziquantel Proteins Public health Schistosoma mansoni Schistosomiasis Testing Therapy Triglycerides Tropical diseases Undernutrition Weight loss Worms |
title | Protein undernutrition reduces the efficacy of praziquantel in a murine model of Schistosoma mansoni infection |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-04T07%3A27%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Protein%20undernutrition%20reduces%20the%20efficacy%20of%20praziquantel%20in%20a%20murine%20model%20of%20Schistosoma%20mansoni%20infection&rft.jtitle=PLoS%20neglected%20tropical%20diseases&rft.au=Kadji%20Fassi,%20Joseph%20Bertin&rft.date=2022-07-01&rft.volume=16&rft.issue=7&rft.spage=e0010249&rft.epage=e0010249&rft.pages=e0010249-e0010249&rft.issn=1935-2735&rft.eissn=1935-2735&rft_id=info:doi/10.1371/journal.pntd.0010249&rft_dat=%3Cgale_plos_%3EA712642404%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2703170756&rft_id=info:pmid/35839247&rft_galeid=A712642404&rft_doaj_id=oai_doaj_org_article_3149d5eff8d84c358fcf90244b13afbd&rfr_iscdi=true |