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1.
J Exp Zool A Ecol Integr Physiol ; 341(5): 563-577, 2024 06.
Artigo em Inglês | MEDLINE | ID: mdl-38470019

RESUMO

Future climate change scenarios project that the increase in surface temperatures will affect ocean temperatures, inducing shifts in marine biodiversity. Sea turtles are species that are particularly vulnerable to the effects of climate change because temperature is a factor that influences embryonic development. We collected clutches of olive ridley turtles from a mass-nesting beach in the Mexican Pacific, which were incubated in ex situ conditions. When the hatchlings emerged, we measured the body condition index-which evaluates the weight-length relationship-and swim thrust, both were considered traits associated with fitness, termed "fitness proxies," and evaluated the effects of incubation temperature, maternal effects, and paternity on these fitness proxies. The body condition index was correlated positively and significantly with the arribada month and temperature during the last third of the incubation period but showed an inverse relationship with the maternal effect. While swim thrust was positively correlated with the maternal effect and the arribada month, there was an inverse relationship with incubation temperature during the first third of the period. Paternity, whether single or multiple, did not have a significant effect on either fitness proxies; however, it may have effects on the average fitness of a population of hatchlings. These results underscore the need to expand research on the sublethal effects of high incubation temperatures on the adaptation and survival of sea turtles, particularly in scenarios of rapid climate change.


Assuntos
Temperatura , Tartarugas , Animais , Tartarugas/fisiologia , Feminino , México , Masculino , Mudança Climática , Oceano Pacífico , Comportamento de Nidação/fisiologia
2.
Front Microbiol ; 12: 671480, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34322099

RESUMO

The discovery of ammonia-oxidizing archaea (AOA) and complete ammonia-oxidizing (comammox) bacteria widespread in terrestrial ecosystems indicates an important role of these organisms in terrestrial nitrification. Recent evidence indicated a higher ammonia affinity of comammox bacteria than of terrestrial AOA and ammonia-oxidizing bacteria (AOB), suggesting that comammox bacteria could potentially represent the most low-nutrient adapted nitrifiers in terrestrial systems. We hypothesized that a nutrient-limited enrichment strategy could exploit the differences in cellular kinetic properties and yield enrichments dominated by high affinity and high yield comammox bacteria. Using soil with a mixed community of AOA, AOB, and comammox Nitrospira, we compared performance of nutrient-limited chemostat enrichment with or without batch culture pre-enrichment in two different growth media without inhibitors or antibiotics. Monitoring of microbial community composition via 16S rRNA and amoA gene sequencing showed that batch enrichments were dominated by AOB, accompanied by low numbers of AOA and comammox Nitrospira. In contrast, nutrient-limited enrichment directly from soil, and nutrient-limited sub-cultivation of batch enrichments consistently yielded high enrichments of Nitrosocosmicus-affiliated AOA associated with multiple canonical nitrite-oxidizing Nitrospira strains, whereas AOB numbers dropped below 0.1% and comammox Nitrospira were lost completely. Our results reveal competitiveness of Nitrosocosmicus sp. under nutrient limitation, and a likely more complex or demanding ecological niche of soil comammox Nitrospira than simulated in our nutrient-limited chemostat experiments.

4.
Mol Genet Genomic Med ; 8(11): e1387, 2020 11.
Artigo em Inglês | MEDLINE | ID: mdl-32936536

RESUMO

BACKGROUND: Congenital muscular dystrophy type 1A (MDC1A), also termed merosin-deficient congenital muscular dystrophy (CMD), is a severe form of CMD caused by mutations in the laminin α2 gene (LAMA2). Of the more than 300 likely pathogenic variants found in the Leiden Open Variant Database, the majority are truncating mutations leading to complete LAMA2 loss of function, but multiple copy number variants (CNVs) have also been reported with variable frequency. METHODS: We collected a cohort of individuals diagnosed with likely MDC1A and sought to identify both single nucleotide variants and small and larger CNVs via exome sequencing by extending the analysis of sequencing data to detect splicing changes and CNVs. RESULTS: Standard exome analysis identified multiple novel LAMA2 variants in our cohort, but only four cases carried biallelic variants. Since likely truncating LAMA2 variants are often found in heterozygosity without a second allele, we performed additional splicing and CNV analysis on exome data and identified one splice change outside of the canonical sequences and three CNVs, in the remaining four cases. CONCLUSIONS: Our findings support the expectation that a portion of MDC1A cases may be caused by at least one CNV allele and show how these changes can be effectively identified by additional analysis of existing exome data.


Assuntos
Variações do Número de Cópias de DNA , Laminina/genética , Distrofia Muscular do Cíngulo dos Membros/genética , Mutação , Frequência do Gene , Testes Genéticos/estatística & dados numéricos , Heterozigoto , Humanos , Lactente , Distrofia Muscular do Cíngulo dos Membros/diagnóstico , Polimorfismo de Nucleotídeo Único , Sequenciamento do Exoma/estatística & dados numéricos
5.
Child Adolesc Ment Health ; 25(3): 150-156, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32542953

RESUMO

BACKGROUND: Improving child and adolescent mental health requires states and jurisdictions to invest in school mental health efforts. In recent years, there has been notable expansion and improvement in school mental health services in the state of South Carolina related to a number of investments that are cumulatively promoting capacity building. METHODS: This narrative overview examines the history of the school mental health movement in one southern state and details efforts by multiple key stakeholders that have coalesced to form a strong system for advancing school mental health. RESULTS: Resting on a strong university-community partnership, five separate initiatives are described that together provide enhanced workforce training and support and expansion of school mental health services. Themes of this work are identified with a goal of supporting and advancing the development of school mental health systems in the United States. CONCLUSION: Strong collaborations and communication efforts both within the university setting and between partners in education and community settings, along with engaged funders keen to enhance well-being of children, youth, and families statewide have set the stage for the growth and expansion of school mental health services.


Assuntos
Serviços de Saúde Mental , Saúde Mental , Serviços de Saúde Escolar , Adolescente , Experiências Adversas da Infância , Fortalecimento Institucional , Criança , Humanos , Resiliência Psicológica , South Carolina
6.
J Autism Dev Disord ; 50(5): 1497-1508, 2020 May.
Artigo em Inglês | MEDLINE | ID: mdl-30062397

RESUMO

Here we report the results of the subgroup analyses of an observational cohort of children whose parents completed the Autism Treatment Evaluation Checklist (ATEC) over the period of several years. A linear mixed effects model was used to evaluate longitudinal changes in ATEC scores within different patient subgroups. All groups decreased their mean ATEC score over time indicating improvement of symptoms, however there were significant differences between the groups. Younger children improved more than the older children. Children with milder ASD improved more than children with more severe ASD in the Communication subscale. There was no difference in improvement between females vs. males. One surprising finding was that children from developed English-speaking countries improved less than children from non-English-speaking countries.


Assuntos
Transtorno Autístico/terapia , Lista de Checagem/estatística & dados numéricos , Avaliação da Deficiência , Fatores de Tempo , Transtorno Autístico/psicologia , Criança , Desenvolvimento Infantil , Pré-Escolar , Feminino , Humanos , Modelos Lineares , Estudos Longitudinais , Masculino , Avaliação de Resultados em Cuidados de Saúde , Pais , Resultado do Tratamento
7.
Neurogenetics ; 20(2): 91-98, 2019 05.
Artigo em Inglês | MEDLINE | ID: mdl-30982090

RESUMO

Genetic mutations associated with brain malformations can lead to a spectrum of severity and it is often difficult to determine whether there are additional pathogenic variants contributing to the phenotype. Here, we present a family affected by a severe brain malformation including bilateral polymicrogyria, hydrocephalus, patchy white matter signal changes, and cerebellar and pontine hypoplasia with elongated cerebellar peduncles leading to the molar tooth sign. While the malformation is reminiscent of bilateral frontoparietal polymicrogyria (BFPP), the phenotype is more severe than previously reported and also includes features of Joubert syndrome (JBTS). Via exome sequencing, we identified homozygous truncating mutations in both ADGRG1/GPR56 and KIAA0556, which are known to cause BFPP and mild brain-specific JBTS, respectively. This study shows how two independent mutations can interact leading to complex brain malformations.


Assuntos
Anormalidades Múltiplas/genética , Cerebelo/anormalidades , Anormalidades do Olho/genética , Hidrocefalia/genética , Doenças Renais Císticas/genética , Proteínas Associadas aos Microtúbulos/genética , Polimicrogiria/genética , Receptores Acoplados a Proteínas G/genética , Retina/anormalidades , Criança , Exoma , Saúde da Família , Feminino , Homozigoto , Humanos , Imageamento por Ressonância Magnética , Masculino , Mesencéfalo/patologia , Mutação , Linhagem , Fenótipo , Prosencéfalo/patologia , Análise de Sequência de DNA , Sudão , Substância Branca/patologia , Sequenciamento do Exoma , Adulto Jovem
8.
Children (Basel) ; 5(2)2018 Feb 16.
Artigo em Inglês | MEDLINE | ID: mdl-29462954

RESUMO

Most early-intervention Autism Spectrum Disorder (ASD) clinical trials are limited by the availability of psychometric technicians who assess each child's abilities before and after therapeutic intervention. If parents could administer regular psychometric evaluations of their children, then the cost of clinical trials will be reduced, enabling longer clinical trials with the larger number of participants. The Autism Treatment Evaluation Checklist (ATEC) was designed nearly two decades ago to provide such a tool, but the norms on the longitudinal changes in ATEC in the "treatment as usual" population were lacking. Here we report the norms of the observational cohort who voluntarily completed ATEC evaluations over the period of four years from 2013 to 2017.

9.
Rev Med Inst Mex Seguro Soc ; 48(4): 443-6, 2010.
Artigo em Espanhol | MEDLINE | ID: mdl-21194516

RESUMO

BACKGROUND: To preserve the umbilical cord blood (UCB), the volume containing the cells must be reduced before freezing, but the quality, quantity and functionality of the cells has to be preserved during this procedure. The aim is to compare the performance of two different techniques for volume reduction. METHODS: A semiautomatic system and an automatic system were compared as two different UCB volume reduction techniques. Total nucleated cell (TNC) counts and viability were measured before and after volume reduction. The CD34+ cell counts also were measured. RESULTS: Seventy units of cord blood cells (UCB) were collected. Thirty-three volume reduction procedures were performed by semiautomatic system and thirty-seven by automatic system. The volume recovered and the CD34+ count in both techniques was similar, although the viability differed slightly (1% higher by Optipress II). CONCLUSIONS: The semiautomatic and automatic techniques are suitable to reduce volumes of UCB units.


Assuntos
Preservação de Sangue/métodos , Sangue Fetal , Células Sanguíneas , Humanos
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