Association of single nucleotide polymorphism in NLRC3, NLRC5, HIP1, and LRP8 genes with fecal egg counts in goats naturally infected with Haemonchus contortus

Haemonchus contortus is a common, intractably pathogenic and economically important gastrointestinal nematode for goat producers worldwide, especially in tropical and subtropical regions. The objective of this study is to identify single nucleotide polymorphisms (SNPs) of 12 candidate goat genes mai...

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Veröffentlicht in:Tropical animal health and production 2020-07, Vol.52 (4), p.1583-1598
Hauptverfasser: Omar, Abdullah Ibne, Alam, Mahmuda Bilkis Bintee, Notter, David Russell, Zhao, Shuhong, Faruque, Md.Omar, Thi, Thuy Nhien Tran, Yin, Lilin, Li, Jingjin, Azmal, Syed Ali, Du, Xiaoyong
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container_end_page 1598
container_issue 4
container_start_page 1583
container_title Tropical animal health and production
container_volume 52
creator Omar, Abdullah Ibne
Alam, Mahmuda Bilkis Bintee
Notter, David Russell
Zhao, Shuhong
Faruque, Md.Omar
Thi, Thuy Nhien Tran
Yin, Lilin
Li, Jingjin
Azmal, Syed Ali
Du, Xiaoyong
description Haemonchus contortus is a common, intractably pathogenic and economically important gastrointestinal nematode for goat producers worldwide, especially in tropical and subtropical regions. The objective of this study is to identify single nucleotide polymorphisms (SNPs) of 12 candidate goat genes mainly related to the innate immune response associated with fecal egg counts (FECs) of Haemonchus contortus in goat as an indicator of the level of parasite infection. Phenotypic data including FEC and blood traits were recorded in 189 native goats from China and 191 ones from Bangladesh, respectively. Bangladeshi goats had significantly ( P < 0.01) lower FEC compared to that of Chinese goats, suggesting higher susceptible and infection rates in Chinese goat populations. FEC was significantly positive correlated with body weight ( r = 0.64, P < 0.01) and hemoglobin ( r = 0.49, P < 0.01) value, but negative with pack cell volume ( r = − 0.63, P < 0.05) in goats. Genotyping of SNPs was performed using a matrix-assisted laser desorption ionization time of flight mass spectrometry assay and a generalized linear model was used to evaluate the association between each SNP and goat FEC trait. Eleven novel SNPs in the NLRC3 , NLRC5 , HIP1 , and LRP8 , out of 46 variants from these 12 genes, were significantly associated with FEC of goats with a nominal significance level of P < 0.05. Of these 11 SNPs, linkage disequilibrium were revealed among SNPs in LRP8 ( r 2 = 0.87 to 1), between SNPs in NLRC3 , NLRC5 , and HIP1 ( r 2 = 0.96 to 0.99), respectively. Further, haplotypes within NLRC3 , NLRC5 , and HIP1 were significantly associated ( P < 0.001) with FEC. In artificial challenge trail, quantitative real-time PCR exposed that the relative expression of mRNA was higher in the resistant group for NLRC3 ( P < 0.01), LRP8 and HIP1 ( P < 0.001) but lower in the resistant group for NLRC5 ( P < 0.0001), compared to the susceptible group. The possible SNP markers and genes identified in this study could be potentially used in marker-assisted selection for breeding local goats breeds resistant to gastrointestinal nematode parasite particularly for Haemonchus contortus , and then for improving health and productivity of goat.
doi_str_mv 10.1007/s11250-019-02154-z
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The objective of this study is to identify single nucleotide polymorphisms (SNPs) of 12 candidate goat genes mainly related to the innate immune response associated with fecal egg counts (FECs) of Haemonchus contortus in goat as an indicator of the level of parasite infection. Phenotypic data including FEC and blood traits were recorded in 189 native goats from China and 191 ones from Bangladesh, respectively. Bangladeshi goats had significantly ( P < 0.01) lower FEC compared to that of Chinese goats, suggesting higher susceptible and infection rates in Chinese goat populations. FEC was significantly positive correlated with body weight ( r = 0.64, P < 0.01) and hemoglobin ( r = 0.49, P < 0.01) value, but negative with pack cell volume ( r = − 0.63, P < 0.05) in goats. Genotyping of SNPs was performed using a matrix-assisted laser desorption ionization time of flight mass spectrometry assay and a generalized linear model was used to evaluate the association between each SNP and goat FEC trait. Eleven novel SNPs in the NLRC3 , NLRC5 , HIP1 , and LRP8 , out of 46 variants from these 12 genes, were significantly associated with FEC of goats with a nominal significance level of P < 0.05. Of these 11 SNPs, linkage disequilibrium were revealed among SNPs in LRP8 ( r 2 = 0.87 to 1), between SNPs in NLRC3 , NLRC5 , and HIP1 ( r 2 = 0.96 to 0.99), respectively. Further, haplotypes within NLRC3 , NLRC5 , and HIP1 were significantly associated ( P < 0.001) with FEC. In artificial challenge trail, quantitative real-time PCR exposed that the relative expression of mRNA was higher in the resistant group for NLRC3 ( P < 0.01), LRP8 and HIP1 ( P < 0.001) but lower in the resistant group for NLRC5 ( P < 0.0001), compared to the susceptible group. The possible SNP markers and genes identified in this study could be potentially used in marker-assisted selection for breeding local goats breeds resistant to gastrointestinal nematode parasite particularly for Haemonchus contortus , and then for improving health and productivity of goat.]]></description><identifier>ISSN: 0049-4747</identifier><identifier>EISSN: 1573-7438</identifier><identifier>DOI: 10.1007/s11250-019-02154-z</identifier><identifier>PMID: 31828571</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal husbandry ; Animal populations ; Animals ; Biomarkers ; Biomedical and Life Sciences ; Body weight ; Body Weight - genetics ; Breeding ; Cell size ; Economic importance ; Feces - parasitology ; Female ; Gene expression ; Gene polymorphism ; Generalized linear models ; Genes ; Genetic Predisposition to Disease ; Genotyping ; Goat Diseases - genetics ; Goat Diseases - parasitology ; Goats ; Goats - genetics ; Haemonchiasis - veterinary ; Haemonchus ; Haemonchus contortus ; Haplotypes ; Hemoglobin ; Immune response ; Immunity, Innate ; Innate immunity ; Intestinal Diseases, Parasitic - genetics ; Intestinal Diseases, Parasitic - parasitology ; Intestinal Diseases, Parasitic - veterinary ; Intestinal parasites ; Ionization ; Ions ; Life Sciences ; Linkage disequilibrium ; Marker-assisted selection ; Mass spectrometry ; Mass spectroscopy ; mRNA ; Nematodes ; Nucleotides ; Parasite Egg Count - veterinary ; Parasites ; Pest resistance ; Polymorphism ; Polymorphism, Single Nucleotide ; Regular Articles ; Single-nucleotide polymorphism ; Statistical models ; Veterinary Medicine/Veterinary Science ; Zoology</subject><ispartof>Tropical animal health and production, 2020-07, Vol.52 (4), p.1583-1598</ispartof><rights>Springer Nature B.V. 2019</rights><rights>Springer Nature B.V. 2019.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-38dc7ecb8185f9cd35f111e7dcf18be3b17513369b80123e02c97ab2157c3aaa3</citedby><cites>FETCH-LOGICAL-c375t-38dc7ecb8185f9cd35f111e7dcf18be3b17513369b80123e02c97ab2157c3aaa3</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/s11250-019-02154-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11250-019-02154-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31828571$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Omar, Abdullah Ibne</creatorcontrib><creatorcontrib>Alam, Mahmuda Bilkis Bintee</creatorcontrib><creatorcontrib>Notter, David Russell</creatorcontrib><creatorcontrib>Zhao, Shuhong</creatorcontrib><creatorcontrib>Faruque, Md.Omar</creatorcontrib><creatorcontrib>Thi, Thuy Nhien Tran</creatorcontrib><creatorcontrib>Yin, Lilin</creatorcontrib><creatorcontrib>Li, Jingjin</creatorcontrib><creatorcontrib>Azmal, Syed Ali</creatorcontrib><creatorcontrib>Du, Xiaoyong</creatorcontrib><title>Association of single nucleotide polymorphism in NLRC3, NLRC5, HIP1, and LRP8 genes with fecal egg counts in goats naturally infected with Haemonchus contortus</title><title>Tropical animal health and production</title><addtitle>Trop Anim Health Prod</addtitle><addtitle>Trop Anim Health Prod</addtitle><description><![CDATA[Haemonchus contortus is a common, intractably pathogenic and economically important gastrointestinal nematode for goat producers worldwide, especially in tropical and subtropical regions. The objective of this study is to identify single nucleotide polymorphisms (SNPs) of 12 candidate goat genes mainly related to the innate immune response associated with fecal egg counts (FECs) of Haemonchus contortus in goat as an indicator of the level of parasite infection. Phenotypic data including FEC and blood traits were recorded in 189 native goats from China and 191 ones from Bangladesh, respectively. Bangladeshi goats had significantly ( P < 0.01) lower FEC compared to that of Chinese goats, suggesting higher susceptible and infection rates in Chinese goat populations. FEC was significantly positive correlated with body weight ( r = 0.64, P < 0.01) and hemoglobin ( r = 0.49, P < 0.01) value, but negative with pack cell volume ( r = − 0.63, P < 0.05) in goats. Genotyping of SNPs was performed using a matrix-assisted laser desorption ionization time of flight mass spectrometry assay and a generalized linear model was used to evaluate the association between each SNP and goat FEC trait. Eleven novel SNPs in the NLRC3 , NLRC5 , HIP1 , and LRP8 , out of 46 variants from these 12 genes, were significantly associated with FEC of goats with a nominal significance level of P < 0.05. Of these 11 SNPs, linkage disequilibrium were revealed among SNPs in LRP8 ( r 2 = 0.87 to 1), between SNPs in NLRC3 , NLRC5 , and HIP1 ( r 2 = 0.96 to 0.99), respectively. Further, haplotypes within NLRC3 , NLRC5 , and HIP1 were significantly associated ( P < 0.001) with FEC. In artificial challenge trail, quantitative real-time PCR exposed that the relative expression of mRNA was higher in the resistant group for NLRC3 ( P < 0.01), LRP8 and HIP1 ( P < 0.001) but lower in the resistant group for NLRC5 ( P < 0.0001), compared to the susceptible group. The possible SNP markers and genes identified in this study could be potentially used in marker-assisted selection for breeding local goats breeds resistant to gastrointestinal nematode parasite particularly for Haemonchus contortus , and then for improving health and productivity of goat.]]></description><subject>Animal husbandry</subject><subject>Animal populations</subject><subject>Animals</subject><subject>Biomarkers</subject><subject>Biomedical and Life Sciences</subject><subject>Body weight</subject><subject>Body Weight - genetics</subject><subject>Breeding</subject><subject>Cell size</subject><subject>Economic importance</subject><subject>Feces - parasitology</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene polymorphism</subject><subject>Generalized linear models</subject><subject>Genes</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotyping</subject><subject>Goat Diseases - genetics</subject><subject>Goat Diseases - parasitology</subject><subject>Goats</subject><subject>Goats - genetics</subject><subject>Haemonchiasis - veterinary</subject><subject>Haemonchus</subject><subject>Haemonchus contortus</subject><subject>Haplotypes</subject><subject>Hemoglobin</subject><subject>Immune response</subject><subject>Immunity, Innate</subject><subject>Innate immunity</subject><subject>Intestinal Diseases, Parasitic - genetics</subject><subject>Intestinal Diseases, Parasitic - parasitology</subject><subject>Intestinal Diseases, Parasitic - veterinary</subject><subject>Intestinal parasites</subject><subject>Ionization</subject><subject>Ions</subject><subject>Life Sciences</subject><subject>Linkage disequilibrium</subject><subject>Marker-assisted selection</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>mRNA</subject><subject>Nematodes</subject><subject>Nucleotides</subject><subject>Parasite Egg Count - veterinary</subject><subject>Parasites</subject><subject>Pest resistance</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Regular Articles</subject><subject>Single-nucleotide polymorphism</subject><subject>Statistical models</subject><subject>Veterinary Medicine/Veterinary Science</subject><subject>Zoology</subject><issn>0049-4747</issn><issn>1573-7438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kcFu1DAURSMEokPhB1ggS2xYTMDPjsfOshoBU2kEVQVry3FeMqkSe7AdVdOf4VdxmwISC1bPss-5tnyL4jXQ90Cp_BABmKAlhbqkDERV3j0pViAkL2XF1dNiRWlVl5Ws5FnxIsYbSrOmNs-LMw6KKSFhVfy8iNHbwaTBO-I7EgfXj0jcbEf0aWiRHP14mnw4HoY4kcGRL_vrLV8_DLEmu8srWBPjWrK_vlKkR4eR3A7pQDq0ZiTY98T62aV47_be5IUzaQ5mHE95K1MJ28XYGZy8s4c5ZsUlH9IcXxbPOjNGfPU4z4vvnz5-2-7K_dfPl9uLfWm5FKnkqrUSbaNAia62LRcdAKBsbQeqQd6AFMD5pm4UBcaRMltL0-Rfk5YbY_h58W7JPQb_Y8aY9DREi-NoHPo5asaZ4BQ2Fc3o23_QGz8Hl1-nWQUbVstaVJliC2WDjzFgp49hmEw4aaD6vj691KdzffqhPn2XpTeP0XMzYftH-d1XBvgCxHzkegx_7_5P7C-Tt6Y3</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Omar, Abdullah Ibne</creator><creator>Alam, Mahmuda Bilkis Bintee</creator><creator>Notter, David Russell</creator><creator>Zhao, Shuhong</creator><creator>Faruque, Md.Omar</creator><creator>Thi, Thuy Nhien Tran</creator><creator>Yin, Lilin</creator><creator>Li, Jingjin</creator><creator>Azmal, Syed Ali</creator><creator>Du, Xiaoyong</creator><general>Springer Netherlands</general><general>Springer Nature B.V</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>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20200701</creationdate><title>Association of single nucleotide polymorphism in NLRC3, NLRC5, HIP1, and LRP8 genes with fecal egg counts in goats naturally infected with Haemonchus contortus</title><author>Omar, Abdullah Ibne ; Alam, Mahmuda Bilkis Bintee ; Notter, David Russell ; Zhao, Shuhong ; Faruque, Md.Omar ; Thi, Thuy Nhien Tran ; Yin, Lilin ; Li, Jingjin ; Azmal, Syed Ali ; Du, Xiaoyong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-38dc7ecb8185f9cd35f111e7dcf18be3b17513369b80123e02c97ab2157c3aaa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal husbandry</topic><topic>Animal populations</topic><topic>Animals</topic><topic>Biomarkers</topic><topic>Biomedical and Life Sciences</topic><topic>Body weight</topic><topic>Body Weight - genetics</topic><topic>Breeding</topic><topic>Cell size</topic><topic>Economic importance</topic><topic>Feces - parasitology</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene polymorphism</topic><topic>Generalized linear models</topic><topic>Genes</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotyping</topic><topic>Goat Diseases - genetics</topic><topic>Goat Diseases - parasitology</topic><topic>Goats</topic><topic>Goats - genetics</topic><topic>Haemonchiasis - veterinary</topic><topic>Haemonchus</topic><topic>Haemonchus contortus</topic><topic>Haplotypes</topic><topic>Hemoglobin</topic><topic>Immune response</topic><topic>Immunity, Innate</topic><topic>Innate immunity</topic><topic>Intestinal Diseases, Parasitic - genetics</topic><topic>Intestinal Diseases, Parasitic - parasitology</topic><topic>Intestinal Diseases, Parasitic - veterinary</topic><topic>Intestinal parasites</topic><topic>Ionization</topic><topic>Ions</topic><topic>Life Sciences</topic><topic>Linkage disequilibrium</topic><topic>Marker-assisted selection</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>mRNA</topic><topic>Nematodes</topic><topic>Nucleotides</topic><topic>Parasite Egg Count - veterinary</topic><topic>Parasites</topic><topic>Pest resistance</topic><topic>Polymorphism</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Regular Articles</topic><topic>Single-nucleotide polymorphism</topic><topic>Statistical models</topic><topic>Veterinary Medicine/Veterinary Science</topic><topic>Zoology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Omar, Abdullah Ibne</creatorcontrib><creatorcontrib>Alam, Mahmuda Bilkis Bintee</creatorcontrib><creatorcontrib>Notter, David Russell</creatorcontrib><creatorcontrib>Zhao, Shuhong</creatorcontrib><creatorcontrib>Faruque, Md.Omar</creatorcontrib><creatorcontrib>Thi, Thuy Nhien Tran</creatorcontrib><creatorcontrib>Yin, Lilin</creatorcontrib><creatorcontrib>Li, Jingjin</creatorcontrib><creatorcontrib>Azmal, Syed Ali</creatorcontrib><creatorcontrib>Du, Xiaoyong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; 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The objective of this study is to identify single nucleotide polymorphisms (SNPs) of 12 candidate goat genes mainly related to the innate immune response associated with fecal egg counts (FECs) of Haemonchus contortus in goat as an indicator of the level of parasite infection. Phenotypic data including FEC and blood traits were recorded in 189 native goats from China and 191 ones from Bangladesh, respectively. Bangladeshi goats had significantly ( P < 0.01) lower FEC compared to that of Chinese goats, suggesting higher susceptible and infection rates in Chinese goat populations. FEC was significantly positive correlated with body weight ( r = 0.64, P < 0.01) and hemoglobin ( r = 0.49, P < 0.01) value, but negative with pack cell volume ( r = − 0.63, P < 0.05) in goats. Genotyping of SNPs was performed using a matrix-assisted laser desorption ionization time of flight mass spectrometry assay and a generalized linear model was used to evaluate the association between each SNP and goat FEC trait. Eleven novel SNPs in the NLRC3 , NLRC5 , HIP1 , and LRP8 , out of 46 variants from these 12 genes, were significantly associated with FEC of goats with a nominal significance level of P < 0.05. Of these 11 SNPs, linkage disequilibrium were revealed among SNPs in LRP8 ( r 2 = 0.87 to 1), between SNPs in NLRC3 , NLRC5 , and HIP1 ( r 2 = 0.96 to 0.99), respectively. Further, haplotypes within NLRC3 , NLRC5 , and HIP1 were significantly associated ( P < 0.001) with FEC. In artificial challenge trail, quantitative real-time PCR exposed that the relative expression of mRNA was higher in the resistant group for NLRC3 ( P < 0.01), LRP8 and HIP1 ( P < 0.001) but lower in the resistant group for NLRC5 ( P < 0.0001), compared to the susceptible group. The possible SNP markers and genes identified in this study could be potentially used in marker-assisted selection for breeding local goats breeds resistant to gastrointestinal nematode parasite particularly for Haemonchus contortus , and then for improving health and productivity of goat.]]></abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>31828571</pmid><doi>10.1007/s11250-019-02154-z</doi><tpages>16</tpages></addata></record>
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source MEDLINE; Springer Nature - Complete Springer Journals
subjects Animal husbandry
Animal populations
Animals
Biomarkers
Biomedical and Life Sciences
Body weight
Body Weight - genetics
Breeding
Cell size
Economic importance
Feces - parasitology
Female
Gene expression
Gene polymorphism
Generalized linear models
Genes
Genetic Predisposition to Disease
Genotyping
Goat Diseases - genetics
Goat Diseases - parasitology
Goats
Goats - genetics
Haemonchiasis - veterinary
Haemonchus
Haemonchus contortus
Haplotypes
Hemoglobin
Immune response
Immunity, Innate
Innate immunity
Intestinal Diseases, Parasitic - genetics
Intestinal Diseases, Parasitic - parasitology
Intestinal Diseases, Parasitic - veterinary
Intestinal parasites
Ionization
Ions
Life Sciences
Linkage disequilibrium
Marker-assisted selection
Mass spectrometry
Mass spectroscopy
mRNA
Nematodes
Nucleotides
Parasite Egg Count - veterinary
Parasites
Pest resistance
Polymorphism
Polymorphism, Single Nucleotide
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Single-nucleotide polymorphism
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Veterinary Medicine/Veterinary Science
Zoology
title Association of single nucleotide polymorphism in NLRC3, NLRC5, HIP1, and LRP8 genes with fecal egg counts in goats naturally infected with Haemonchus contortus
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