Molecular detection of Yersinia pestis in dental pulp

ثبت نشده
چکیده

Gilbert et al. (2004) report on the lack of Yersinia pestis DNA detection in 108 teeth collected in five northern Europe suspected plague sites, thus challenging our discoveries in three southern Europe sites (Drancourt et al., 1998; Raoult et al., 2000). The interpretation of these negative results is either the absence of Y. pestis in tested specimens or a failure to detect it. Particularities in the epidemiology of Black Death in medieval northern Europe including the absence of the suitable rat species in some countries led to a controversy regarding the aetiology of Black Death in these countries. It is possible that different microbes were responsible for epidemics during the Middle Ages but present work does not help to resolve this issue. We detected specific Y. pestis sequences in three different sites in southern Europe, thus clearly demonstrating that Y. pestis was involved in historical plague epidemics in southern countries (Drancourt et al., 1998; Raoult et al., 2000). Basically, our strategy was based on the use of dental pulp as the sample and specific Y. pestis primers for detection. The reason why we choose dental pulp is that it is a well vascularized soft tissue in contrast to bone or dentine (Drancourt et al., 1998). It is sterile in patients without bacteraemia (Potsch et al., 1992). It may be equivalent to a small blood sample. We were able to recover viable Coxiella burnetii after apparent cure from the dental pulp of experimentally infected animals (Aboudharam, 2001). That dental pulp is a suitable tissue on which to base molecular detection of microbial nucleic acid was demonstrated not only by our work on ancient plague (Drancourt et al., 1998; Raoult et al., 2000) but also in an experimental animal model (Aboudharam et al., 2000) and detection of specific RNA sequences in HIV-infected patients (Glick et al., 1989, 1991). In contrast, dentine has never been tested experimentally for this purpose. We doubt that it may be superior to bone as it is not a soft, well vascularized tissue. To use dentine and not the dental pulp makes the use of teeth a nonsense.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Coxiella burnetii in Ticks, Argentina

6. Janse I, Hamidjaja RA, Bok JM, van Rotterdam BJ. Reliable detection of Bacillus anthracis, Francisella tularensis and Yersinia pestis by using multiplex qPCR including internal controls for nucleic acid extraction and amplification. BMC Microbiol. 2010;10:314. 7. Adjemian JZ, Adjemian MK, Foley P, Chomel BB, Kasten RW, Foley JE. Evidence of multiple zoonotic agents in a wild rodent community...

متن کامل

Simple and Rapid Detection of Yersinia Pestis and Francisella Tularensis using Multiplex-PCR

Background: Yersinia pestis and Francisella tularensis cause plague and tularemia, which are known as diseases of the newborn and elderly, respectively. Immunological and culture-based detection methods of these bacteria are time-consuming, costly, complicated and require advanced equipment. We aimed to design and synthesize a gene structure as positive control for molecular detection of these ...

متن کامل

Genotyping, Orientalis-like Yersinia pestis, and Plague Pandemics

Three pandemics have been attributed to plague in the last 1,500 years. Yersinia pestis caused the third, and its DNA was found in human remains from the second. The Antiqua biovar of Y. pestis may have caused the first pandemic; the other two biovars, Medievalis and Orientalis, may have caused the second and third pandemics, respectively. To test this hypothesis, we designed an original genoty...

متن کامل

Immuno-PCR - A New Tool for Paleomicrobiology: The Plague Paradigm

BACKGROUND The cause of past plague pandemics was controversial but several research teams used PCR techniques and dental pulp as the primary material to reveal that they were caused by Yersinia pestis. However, the degradation of DNA limits the ability to detect ancient infections. METHODS We used for the first time immuno-PCR to detect Yersinia pestis antigens; it can detect protein concent...

متن کامل

The molecular detection of the causative agent of plague on the basis of the pla gene

Yersinia pestis, a gram-negative rod belonging to the Enterobacteriaceae family, is the causative agent of plague. Classical methods of detecting the organisms are time-consuming, expensive and dangerous. The aim of the study was to design a Real-time PCR assay on the basis of the pla gene of Yersinia pestis. In this research the Real- time PCR test was optimized by using special primers for ta...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2004