Morphological traits are central to traditional taxonomy, yet convergent and divergent evolution can lead to inconsistencies between morphological classification and molecular phylogenetics. The distinctive "sunken head and humpback" morphology of Cromileptes altivelis and its close phylogenetic relationship with Epinephelus make it an ideal model for evaluating the weighting of morphological traits in taxonomic classification and refining the classification system. We measured and analyzed the morphological specialization process of C. altivelis, identifying key developmental stages leading to its humpback phenotype. This trait develops through cranial remodeling, involving changes in the supraoccipital, frontal, and lateral occipital bones, with structural support from predorsal bones and the first neural arch and spine. Examining the Hox gene family, we found that C. altivelis possesses 49 highly conserved Hox genes, with no significant differences in gene copy number, arrangement, or exon count among groupers. However, unique amino acid variations were identified in the Hoxa7a, Hoxa10b, and Hoxc1a proteins of C. altivelis, which are otherwise highly conserved among other teleost fishes. Functional assays confirmed that mutations in these genes enhance gene transcription activity, promoting osteoblast proliferation and differentiation. qPCR analysis showed that the expression of hoxa7a and hoxa10b was significantly upregulated during the humpback stage, implicating their contribution to the morphological specialization of C. altivelis. hoxa10b remained elevated post-humpback, suggesting a role in bone strength and homeostasis, whereas hoxc1a exhibited consistently low expression, indicating limited involvement. Our findings provide insights into resolving taxonomic discrepancies in C. altivelis and offer a framework for understanding its adaptive evolution and speciation.
{"title":"Hox Gene Variation Drives Morphological Specialization of Humpback Grouper Cromileptes altivelis.","authors":"Xiaoying Cao, Zhaowei Zhong, Lisheng Wu, Quanyin Liu, Shaoxiong Ding","doi":"10.1111/1749-4877.70016","DOIUrl":"https://doi.org/10.1111/1749-4877.70016","url":null,"abstract":"<p><p>Morphological traits are central to traditional taxonomy, yet convergent and divergent evolution can lead to inconsistencies between morphological classification and molecular phylogenetics. The distinctive \"sunken head and humpback\" morphology of Cromileptes altivelis and its close phylogenetic relationship with Epinephelus make it an ideal model for evaluating the weighting of morphological traits in taxonomic classification and refining the classification system. We measured and analyzed the morphological specialization process of C. altivelis, identifying key developmental stages leading to its humpback phenotype. This trait develops through cranial remodeling, involving changes in the supraoccipital, frontal, and lateral occipital bones, with structural support from predorsal bones and the first neural arch and spine. Examining the Hox gene family, we found that C. altivelis possesses 49 highly conserved Hox genes, with no significant differences in gene copy number, arrangement, or exon count among groupers. However, unique amino acid variations were identified in the Hoxa7a, Hoxa10b, and Hoxc1a proteins of C. altivelis, which are otherwise highly conserved among other teleost fishes. Functional assays confirmed that mutations in these genes enhance gene transcription activity, promoting osteoblast proliferation and differentiation. qPCR analysis showed that the expression of hoxa7a and hoxa10b was significantly upregulated during the humpback stage, implicating their contribution to the morphological specialization of C. altivelis. hoxa10b remained elevated post-humpback, suggesting a role in bone strength and homeostasis, whereas hoxc1a exhibited consistently low expression, indicating limited involvement. Our findings provide insights into resolving taxonomic discrepancies in C. altivelis and offer a framework for understanding its adaptive evolution and speciation.</p>","PeriodicalId":13654,"journal":{"name":"Integrative zoology","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2025-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145451853","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Avian haemosporidian infections have been associated with disease outbreaks in zoos and rehabilitation centers globally. This study aimed to determine the occurrence and genetic diversity of avian haemosporidian parasites in captive birds at the National Zoological Garden in South Africa. One hundred and eighty-three blood samples from five orders and 15 species of captive flamingos, vultures, owls, ibises and parrots were analyzed for haemosporidia by nested polymerase chain reaction assays. The samples were collected as part of the zoo's studbook and archived at South African National Biodiversity Institute's Wildlife Biobank. The overall infection rate was 36.1%, and infections by Leucocytozoon spp. (33.3%) were significantly higher than Haemoproteus spp. (14.8%) (p < 0.001). Twenty-one samples (11.5%) had mixed Haemoproteus and Leucocytozoon infections. The Spotted Eagle Owl (Bubo africanus) and Barn Owl (Tyto alba) had the highest infection rates. Twenty-six sequences, similar to published sequences of Leucocytozoon spp. (lineages lCHRKLA02, lCIAE02, and lBUVIR02) and Haemoproteus spp. (lineage hTYTAL6) were obtained. Two new lineages (lBUBCAP01 and hBOSHAG02) are described in this study. This is the first molecular survey of haemosporidian parasites in captive birds of the orders Accipitriformes, Pelecaniformes, Psittaciformes, Phoenicopteriformes, and Strigiformes in South Africa. This study provides new geographical and host records of known and novel haemosporidian lineages. It highlights the need for intensive surveys of these parasites in populations of captive and free-ranging birds in South Africa, regular monitoring of infections, updated screening methods, and insect control in the zoo's animal collection to avoid disease outbreaks.
{"title":"Prevalence and Genetic Diversity of Haemoproteus and Leucocytozoon in Raptors and Other Captive Birds at the National Zoological Garden in South Africa","authors":"Realeboga Masego Gaorekwe, Veronica Phetla, Dikeledi Petunia Malatji, Mamohale Chaisi","doi":"10.1111/1749-4877.70011","DOIUrl":"10.1111/1749-4877.70011","url":null,"abstract":"<p>Avian haemosporidian infections have been associated with disease outbreaks in zoos and rehabilitation centers globally. This study aimed to determine the occurrence and genetic diversity of avian haemosporidian parasites in captive birds at the National Zoological Garden in South Africa. One hundred and eighty-three blood samples from five orders and 15 species of captive flamingos, vultures, owls, ibises and parrots were analyzed for haemosporidia by nested polymerase chain reaction assays. The samples were collected as part of the zoo's studbook and archived at South African National Biodiversity Institute's Wildlife Biobank. The overall infection rate was 36.1%, and infections by <i>Leucocytozoon</i> spp. (33.3%) were significantly higher than <i>Haemoproteus</i> spp. (14.8%) (<i>p</i> < 0.001). Twenty-one samples (11.5%) had mixed <i>Haemoproteus</i> and <i>Leucocytozoon</i> infections. The Spotted Eagle Owl <i>(Bubo africanus</i>) and Barn Owl (<i>Tyto alba</i>) had the highest infection rates. Twenty-six sequences, similar to published sequences of <i>Leucocytozoon</i> spp. (lineages lCHRKLA02, lCIAE02, and lBUVIR02) and <i>Haemoproteus</i> spp. (lineage hTYTAL6) were obtained. Two new lineages (lBUBCAP01 and hBOSHAG02) are described in this study. This is the first molecular survey of haemosporidian parasites in captive birds of the orders Accipitriformes, Pelecaniformes, Psittaciformes, Phoenicopteriformes, and Strigiformes in South Africa. This study provides new geographical and host records of known and novel haemosporidian lineages. It highlights the need for intensive surveys of these parasites in populations of captive and free-ranging birds in South Africa, regular monitoring of infections, updated screening methods, and insect control in the zoo's animal collection to avoid disease outbreaks.</p>","PeriodicalId":13654,"journal":{"name":"Integrative zoology","volume":"21 1","pages":"203-213"},"PeriodicalIF":3.7,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12794762/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145389077","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Prenatal hypoxia poses significant risks to mammalian brain development, often leading to long-term cognitive and memory deficits. However, certain hypoxia-tolerant species, such as Brandt's vole (Lasiopodomys brandtii), have evolved unique adaptations to thrive in low-oxygen environments. This study explores the effects of prenatal environmental hypoxia on the cognitive abilities and molecular responses of Brandt's voles in adulthood. Using behavioral tests (novel object recognition and Y maze) and transcriptomic analysis, we found that Brandt's voles exposed to prenatal environmental hypoxia exhibited intact cognitive and memory functions, contrasting with the deficits observed in model organisms. Transcriptomic profiling, validated by RT-qPCR experiments, revealed adaptive changes in energy metabolism, oxygen transport, and neuroprotective mechanisms, particularly in voles exposed to hypoxia both prenatally and in adulthood. These findings suggest that moderate prenatal environmental hypoxia exposure induces developmental plasticity in Brandt's voles, enhancing their hypoxia tolerance in adulthood, which contrasts with the detrimental effects observed in model organisms under similar conditions. Our study highlights the importance of investigating non-model organisms with natural hypoxia exposure histories, providing novel insights into the mechanisms of hypoxia adaptation and potential strategies for mitigating hypoxia-related neurological damage.
{"title":"Prenatal Environmental Hypoxia Enhances Adult Hypoxia Tolerance in Brandt's Voles (Lasiopodomys brandtii): Behavioral and Transcriptomic Insights.","authors":"Mengyang Li, Congcong Qiao, Xiujuan Li, Maolin Huang, Zhenlong Wang, Luye Shi","doi":"10.1111/1749-4877.70010","DOIUrl":"https://doi.org/10.1111/1749-4877.70010","url":null,"abstract":"<p><p>Prenatal hypoxia poses significant risks to mammalian brain development, often leading to long-term cognitive and memory deficits. However, certain hypoxia-tolerant species, such as Brandt's vole (Lasiopodomys brandtii), have evolved unique adaptations to thrive in low-oxygen environments. This study explores the effects of prenatal environmental hypoxia on the cognitive abilities and molecular responses of Brandt's voles in adulthood. Using behavioral tests (novel object recognition and Y maze) and transcriptomic analysis, we found that Brandt's voles exposed to prenatal environmental hypoxia exhibited intact cognitive and memory functions, contrasting with the deficits observed in model organisms. Transcriptomic profiling, validated by RT-qPCR experiments, revealed adaptive changes in energy metabolism, oxygen transport, and neuroprotective mechanisms, particularly in voles exposed to hypoxia both prenatally and in adulthood. These findings suggest that moderate prenatal environmental hypoxia exposure induces developmental plasticity in Brandt's voles, enhancing their hypoxia tolerance in adulthood, which contrasts with the detrimental effects observed in model organisms under similar conditions. Our study highlights the importance of investigating non-model organisms with natural hypoxia exposure histories, providing novel insights into the mechanisms of hypoxia adaptation and potential strategies for mitigating hypoxia-related neurological damage.</p>","PeriodicalId":13654,"journal":{"name":"Integrative zoology","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145345079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Claudia Mediavilla, Guillermo Fandos, Sara Blázquez-Castro, Senda Reguera, Rafael Barrientos, Rodrigo Megía-Palma
We investigated the phenological variation of three genera of blood parasites of lizards (Schellackia, Karyolysus, and Lankesterella) using samples of 275 adult Psammodromus algirus and 138 Acanthodactylus erythrurus collected from April to September in 2021 and 2022. Both years experienced heatwaves, and 2022 had the warmest summer on historical record for the region. We captured lizards in two close areas that differed in vegetation quality due to differential human pressure. We found that Schellackia and Karyolysus more frequently infected P. algirus, whereas Lankesterella infected A. erythrurus. We fitted generalized additive models to explain parasite intensity, including the non-linear effect of phenology sorted by sex and the linear effects of body length, body condition, host sex, heterophil–lymphocyte ratio, distance to a road, and microclimate. We found a positive effect of body length on parasite intensity across parasite genera. The intensity of Schellackia was higher in female hosts, contradicting the dogma of higher male susceptibility to infections. The intensity of Lankesterella was lower closer to the road, indicating that parasite transmission success can vary at the microgeographic scale. We found a non-linear significant increase of Karyolysus across the activity period, suggesting a relaxation of the antiparasitic control upon this genus toward the end of the activity period. For Lankesterella, we observed a phenological increase only in female lizards, suggesting sexual differences in immunocompetence. We found higher intensity of Karyolysus and Lankesterella in 2022, conforming to the idea that heat waves may impair lizards' immunocompetence.
{"title":"Spatial, Temporal, and Host-Specificity Patterns of Three Genera of Blood Coccidian Parasites in Two Syntopic Mediterranean Lizards","authors":"Claudia Mediavilla, Guillermo Fandos, Sara Blázquez-Castro, Senda Reguera, Rafael Barrientos, Rodrigo Megía-Palma","doi":"10.1111/1749-4877.70008","DOIUrl":"10.1111/1749-4877.70008","url":null,"abstract":"<p>We investigated the phenological variation of three genera of blood parasites of lizards (<i>Schellackia</i>, <i>Karyolysus</i>, and <i>Lankesterella</i>) using samples of 275 adult <i>Psammodromus algirus</i> and 138 <i>Acanthodactylus erythrurus</i> collected from April to September in 2021 and 2022. Both years experienced heatwaves, and 2022 had the warmest summer on historical record for the region. We captured lizards in two close areas that differed in vegetation quality due to differential human pressure. We found that <i>Schellackia</i> and <i>Karyolysus</i> more frequently infected <i>P. algirus</i>, whereas <i>Lankesterella</i> infected <i>A. erythrurus</i>. We fitted generalized additive models to explain parasite intensity, including the non-linear effect of phenology sorted by sex and the linear effects of body length, body condition, host sex, heterophil–lymphocyte ratio, distance to a road, and microclimate. We found a positive effect of body length on parasite intensity across parasite genera. The intensity of <i>Schellackia</i> was higher in female hosts, contradicting the dogma of higher male susceptibility to infections. The intensity of <i>Lankesterella</i> was lower closer to the road, indicating that parasite transmission success can vary at the microgeographic scale. We found a non-linear significant increase of <i>Karyolysus</i> across the activity period, suggesting a relaxation of the antiparasitic control upon this genus toward the end of the activity period. For <i>Lankesterella</i>, we observed a phenological increase only in female lizards, suggesting sexual differences in immunocompetence. We found higher intensity of <i>Karyolysus</i> and <i>Lankesterella</i> in 2022, conforming to the idea that heat waves may impair lizards' immunocompetence.</p>","PeriodicalId":13654,"journal":{"name":"Integrative zoology","volume":"21 1","pages":"69-78"},"PeriodicalIF":3.7,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12794770/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145345084","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}