The CUPID (Cultural and Psychosocial Influences on Disability) study: methods of data collection and characteristics of study sample

Background

The CUPID (Cultural and Psychosocial Influences on Disability) study was established to explore the hypothesis that common musculoskeletal disorders (MSDs) and associated disability are importantly influenced by culturally determined health beliefs and expectations. This paper describes the methods of data collection and various characteristics of the study sample.

Methods/Principal Findings

A standardised questionnaire covering musculoskeletal symptoms, disability and potential risk factors, was used to collect information from 47 samples of nurses, office workers, and other (mostly manual) workers in 18 countries from six continents. In addition, local investigators provided data on economic aspects of employment for each occupational group. Participation exceeded 80% in 33 of the 47 occupational groups, and after pre-specified exclusions, analysis was based on 12,426 subjects (92 to 1018 per occupational group). As expected, there was high usage of computer keyboards by office workers, while nurses had the highest prevalence of heavy manual lifting in all but one country. There was substantial heterogeneity between occupational groups in economic and psychosocial aspects of work; three- to five-fold variation in awareness of someone outside work with musculoskeletal pain; and more than ten-fold variation in the prevalence of adverse health beliefs about back and arm pain, and in awareness of terms such as “repetitive strain injury” (RSI).

Conclusions/Significance

The large differences in psychosocial risk factors (including knowledge and beliefs about MSDs) between occupational groups should allow the study hypothesis to be addressed effectively.     

HrpM is involved in glucan biosynthesis,biofilm formation and pathogenicity in Xanthomonas citri ssp. citri

Xanthomonas citri ssp. citri (Xcc) is the causal agent of citrus canker. This bacterium develops a characteristic biofilm on both biotic and abiotic surfaces. A biofilm‐deficient mutant was identified in a screening of a transposon mutagenesis library of the Xcc 306 strain constructed using the commercial Tn5 transposon EZ‐Tn5 <KAN‐2> Tnp Transposome (Epicentre). Sequence analysis of a mutant obtained in the screening revealed that a single copy of the EZ‐Tn5 was inserted at position 446 of hrpM, a gene encoding a putative enzyme involved in glucan synthesis. We demonstrate for the first time that the product encoded by the hrpM gene is involved in β‐1,2‐glucan synthesis in Xcc. A mutation in hrpM resulted in no disease symptoms after 4 weeks of inoculation in lemon and grapefruit plants. The mutant also showed reduced ability to swim in soft agar and decreased resistance to H ₂ O ₂ in comparison with the wild‐type strain. All defective phenotypes were restored to wild‐type levels by complementation with the plasmid pBBR1‐MCS containing an intact copy of the hrpM gene and its promoter. These results indicate that the hrpM gene contributes to Xcc growth and adaptation in its host plant.     

Differential expression of PDZ domain-containing proteins in human diseases - challenging topics and novel issues

The general features of the PDZ domain structure and functions have been extensively studied during the last decade. PDZ domains are generally present in proteins that are involved in multiple interactions to assemble functional protein complexes that control key cellular processes. One of the best characterized functions of PDZ domain-containing proteins is control of epithelial cell polarity and cell-cell contacts. In the present review, we summarize the current knowledge on regulation of expression of certain PDZ polarity proteins localized at the intercellular junctions. In addition, we provide a critical overview of recent findings regarding the role of these proteins during development of human diseases. Complete understanding of these issues is valuable for the design of novel therapeutic intervention for common pathologies, such as cancer.     

The development of <Emphasis Type="Italic">Gymnophallus australis</Emphasis> Szidat, 1962 (Digenea: Gymnophallidae) from the Patagonian coast (Argentina) from metacercaria to adult,with an amended diagnosis of <Emphasis Type="Italic">Gymnophallus</Emphasis> Odhner, 1905

Parvatrema australis (Szidat, 1962) Szidat, 1965 was described based on larval stages found in specimens of the mussel Mytilus edulis from the Buenos Aires Province, Argentina. Although Szidat later examined hundreds of mussels, this parasite has never been found again until now. In the present study, larval stages, including germinal sacs, found in mytilids from the Patagonian coast were identified as P. australis. Metacercariae were incubated in vitro at 39 degrees C in physiological solution for 18-20 hours, by which time 80% of the specimens had eggs. P. australis is redescribed, on the basis of infective metacercariae and adults obtained in the laboratory, and is reassigned to Gymnophallus Odhner, 1900, the genus in which it was originally described. The generic diagnosis of Gymnophallus is here amended to include as diagnostic characters the presence or absence of the lateral lips, the form and position of the vitellarium (compact or follicular) and the presence of a pars prostatica (i.e. prostatic cells open into proximal part of the ejaculatory duct). The validity of some characters (i.e. the presence of lateral lips of the oral sucker, the form of the vitellarium and excretory vesicle, the extent of the uterus) as diagnostic at the generic level within the family Gymnophallidae is discussed. It is proposed that the least unambiguous characters that can be used to distinguish gymnophallid genera include the position of the ovary, the presence of a ventral pit and a pars prostatica, and caecal diverticula.     

Zooming in on Cadherin-23: Structural Diversity and Potential Mechanisms of Inherited Deafness

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