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Background: Retraction is a mechanism for correcting the literature and a warning for readers in relation to publications that contain serious flaws or erroneous data. As a result of growth and development of Iranian publications in the last two decades, that brings unethical behavior of researchers led to retraction of their publications. We aimed to investigate Iranian retracted publications indexed in PubMed database. Methods: All Iranian retracted publications published in PubMed up to Dec 2017 have been retrieved. Bibliographic information of retracted publications, retraction notice, time lag between article publication date and the date of retraction notice, reasons of retraction, Issuer of retraction and acknowledge information of retracted publication were recorded. Additionally, citation data of retracted publications before 2013 were analyzed. Results: Overall, 164 Iranian retracted publications were identified. Meantime lag was 20.8 months. "Islamic Azad University" and "Tehran University of Medical Sciences (TUMS)" were two affiliations that have received highest number of retracted publications. The most issuer of retraction publications was editor-in-chief and the most mentioned reasons for retractions were authorship issues, plagiarism, and redundant publication. Thirty-three (20.12%) publications have received funds from various agencies. Citation study of retracted publications indicates that these publications have received 789 citations (Citation per publication=11.6). Conclusion: Although Iranian retracted publications represent small portion of all Iranian publications, but the number of retracted publications has increased. More than half of retracted publications have had authorship issues and plagiarism that requires more attention to research ethics authorities.

Background: Salmonella enterica serovar Typhi, as causative agent of typhoid fever, is one of the most important endemic pathogens. Non-typhoidal Salmonella serovars, including Typhimurium, Infantis, and Enteritidis are amongst the most prevalent serotypes worldwide and in developing areas such as Iran. The aim of this study was to apply a uniplex PCR for rapid detection of Salmonella spp., and a multiplex PCR for the simultaneous detection of the four most common Salmonella serovars in Iran. Methods: Current research was done in 2010 at Molecular Biology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran. For detection of Salmonella spp a pair of primers was used to replicate a chromosomal sequence. Four other sets of primers were also designed to amplify the target genes of four Salmonella species including S. typhi, and three non-typhoidal Salmonella spp (S. enteritidis, S. infantis, and S. typhimurium). The assay specificity was investigated by testing 15 different Salmonella serovars and 8 other additional non-Salmonella species. Results: The Salmonella genus-specific PCR yielded the expected DNA band of 404 bp in all Salmonella spp., strains tested. The uniplex and multiplex PCR assays produced also the expected fragments of 489 bp, 304 bp, 224 bp, and 104 bp for serovars Typhi, Enteritidis, Typhimurium, and Infantis, respectively. Each species-specific primer pair set did not show any cross-reactivity when tested on other Salmonella serovars or other non- but related- Salmonella strains. Conclusion: Both uniplex and multiplex PCR protocols had a good specificity. They can provide an important tool for the rapid and simultaneous detection and differentiation of the four most prevalent Salmonella serovars in Iran.

Shigella species are among the common causes of bacterial diarrhoeal diseases. Traditional detection methods are time-consuming resulting in delay in treatment and control of Shigella infections thus there is a need to develop molecular methods for rapid and simultaneous detection of Shigella spp. In this study a rapid multiplex PCR were developed for simultaneous detection of three pathogenic Shigella species.For detection of Shigella spp., a pair of primers was used to replicate a chromosomal sequence. Three other sets of primers were also designed to amplify the target genes of three most common species of Shigella in Iran including S. sonnei, S. flexneri and S. boydii. The multiplex PCR assay was optimized for simultaneous detection and differentiation of three pathogenic Shigella species. The assay specificity was investigated by testing different strains of Shigella and other additional strains belonging to non Shigella species, but responsible for foodborne diseases.The Shigella genus specific PCR yielded the expected DNA band of 159 bp in all tested strains belonging to four Shigella species. The standard and multiplex PCR assays also produced the expected fragments of 248 bp, 503 bp, and 314 bp, for S. boydii, S. sonnei and S. flexneri, respectively. Each species-specific primer pair did not show any cross-reactivity.Both standard and multiplex PCR protocols had a good specificity. They can provide a valuable tool for the rapid and simultaneous detection and differentiation of three most prevalent Shigella species in Iran.