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Shih, T.

Publications and source records attributed to Shih, T..

2 recordsLinked to original sources

Variations in cow milk and teat skin microbiota across the lactation cycle with intra-mammary cephalosporin use at dry-off

Cephalosporins and other broad-spectrum antibiotics are frequently administered prophylactically into the udder when dairy cows end their lactation cycle, termed dry-off, to reduce mastitis risk. However, the use of antibiotics on cows that do not have signs of infection may result in the selection of microbes resistant to antibiotics and negatively alter the udder microbiome composition. In this study, the effects of intramammary cephalosporin therapy with either Cephapirin (CB) or Ceftiofur (CH) on milk and teat skin microbiota were examined for three dairies in California. Bacterial composition was measured for cows with low somatic cell counts (SCC,<100,000 cells /mL) and high, subclinical SCC (>200,000 cells/mL). Samples were collected at dry-off (before treatment), seven days later, and 55-75 Days in Milk (DIM) in the next lactation cycle. The milk and skin microbiota were largely separated based on dairy (milk: R2 = 6.22, skin: R2 = 7.56) and day of sampling (milk: R2 = 4.74 and skin: R2 = 3.77). CB or CH use was associated with a small but significant impact on the milk microbiota beta-diversity (Bray-Curtis, p =0.003, R2= 1.4%) but no effect was observed on the skin. At one dairy (Dairy 3), milk from cows receiving CB and CH had a reduction in proportions of Staphylococcaceae at 55-75DIM compared to untreated cows. Overall, antibiotic use did not result in large significant changes to bacterial diversity in milk or on the teat skin, and instead the microbiota at those sites mainly differed between the time and location of sampling. ImportanceThe use of antibiotics in agriculture is under increasing scrutiny due to the rising spread of antimicrobial resistant bacteria. Our study showed that common preventative antibiotic intramammary treatment of cows with cephalosporins at the end their lactation (dry-off) had minimal effects on the milk and teat skin microbiota on asymptomatic cows with high somatic cell counts.

microbiology↗

Oligogenic effects of 16p11.2 copy number variation on craniofacial development

A copy number variant (CNV) of 16p11.2, which encompasses 30 genes, is associated with developmental and psychiatric disorders, head size and body mass. The genetic mechanisms that underlie these associations are not understood. To elucidate the effects of genes on development, we exploited the quantitative effects of CNV on craniofacial structure in humans and model organisms. We show that reciprocal deletion and duplication of 16p11.2 have characteristic "mirror" effects on craniofacial features that are conserved in human, rat and mouse. By testing gene dosage effects on the shape of the mandible in zebrafish, we show that the distribution of effects for all individual genes is consistent with that of the CNV, and some combinations have non-additive effects. Our results suggest that, at minimum, one third of genes within the 16p11.2 region influence craniofacial development, and the facial gestalt of each CNV represents a product of 30 dosage effects. HighlightsO_LIReciprocal CNVs of 16p11.2 have mirror effects on craniofacial structure. Copy number is associated with a positive effect on nasal and mandibular regions and a negative effect on frontal regions of the face. C_LIO_LIEffects of CNV on craniofacial development in human are well conserved in rat and mouse models of 16p11.2 deletion and duplication. C_LIO_LI7/30 genes each independently have significant effects on the shape of the mandible in zebrafish; these include SPN, C16orf54, SEZ6L2, ASPHD1, TAOK2, INO80E and FAM57B. Others (MAPK3, MVP, KCTD13) have detectable effects only in combination. C_LIO_LIOverexpression of 30 genes individually showed a distribution of effects that was skewed in the same direction as that of the full duplication, suggesting that specific facial features represent the net of all individual effects combined. C_LI

genetics↗