Emma Rabino Massa

Technical Note : A Rapid Diagnostic Test Detects Plague in Ancient Human Remains: An Example of the Interaction Between Archeological and Biological Approaches (Southeastern France, 16th-18th Centuries)

A rapid diagnostic test (RDT) that detects Yersinia pestis F1 antigen was applied to 28 putative plague victims exhumed from seven burial sites in southeastern France dating to the 16th-18th centuries. Yersinia pestis F1 antigen was detected in 19 of the 28 (67.9%) samples. The 27 samples used as negative controls yielded negative results. Soil samples taken from archeological sites related to both positive and negative samples tested negative for F1 antigen. The detection threshold of the RDT for plague (0.5 ng/ml) is sufficient for a preliminary retrospective diagnosis of Y. pestis infection in human remains. The high specificity and sensitivity of the assay were confirmed. For two sites positive to F1 antigen (Lambesc and Marseille), Y. pestis-specific DNA (pla gene) had been identified previously by PCR-sequence based analyses. Specifically, the positive results for two samples, from the Lambesc cemetery and the Marseille pit burial, matched those previously reported using PCR. Independent analyses in Italy and France of different samples taken from the same burial sites (Draguignan and Martigues) led to the identification of both Y. pestis F1 antigen and Y. pestis pla and gplD genes. These data are clear evidence of the presence of Y. pestis in the ancient human remains examined in this study.

Gm and Km immunoglobulin allotypes in Sicily.

The aim of this study was to evaluate the intra- and inter-population variability of the Gm/Km system in the Madonie Mountains, one of the main geographical barriers in north-central Sicily. We analysed 392 samples: 145 from Alia, 128 from Valledolmo, 25 from Cerda and 94 from Palermo. Serum samples were tested for G1m (1,2,3,17), G2m (23), G3m (5,6,10,11,13,14,15,16,21,24,28) and Km (1) allotypes by the standard agglutination-inhibition method. We found the typical genetic patterns of populations in peripheral areas of the Mediterranean basin, with a high frequency of haplotypes Gm5*;3;23 and Gm5*;3;... The frequency of Gm21,28;1,17;... (about 16%) is rather high compared with other southern areas. Of great importance is the presence of the common African haplotype Gm 5*;1,17;..., ranging in frequency from 1.56% at Valledolmo to 5.5% at Alia. The presence of this haplotype suggests past contacts with peoples from North Africa. The introduction of African markers could be due to the Phoenician colonization at the end of the 2nd millennium b.c. or to the more recent Arab conquest (8th–9th centuries a.d.).

Neural tube defect in a 4000-year-old Egyptian infant mummy: A case of meningocele from the museum of anthropology and ethnography of Turin (Italy)

This paper reports a paleopathological study of a severe neural tube defect in an ancient mummy, more specifically, a meningocele in an Egyptian infant from the XI dynasty (2100-1955B.C.). This is one of the most ancient cases of meningocele in mummified human remains described in paleopathological literature. Prehistoric and early historic examples of severe congenital defects of the vertebral column and neural tube are rare, because of the precarious preservation conditions of ancient human remains. Further, since the majority are only the skeletal remains, paleopathological and paleoepidemiological analysis based on the observation of bones is even more difficult. Hence, it is not easy to investigate this disease in the past in all its complexities and true diffusion. The case presented here is peculiar, since it concerns a mummy with almost all soft tissues preserved, thus allowing us to describe the defect in an infant. Only targeted, minimally invasive examinations were performed. An anthropological investigation with helical CT scan and histological analysis was used to diagnose the defect and identify post-mortem transformation processes. The analyses confirmed the diagnosis of meningocele in an approximately six-month-old infant.

Preliminary note on the ultrastructure of the hair from an Egyptian mummy using the Scanning Electron Microscope

Abstract Preliminary data on the ultrastructure of hairs from an Egyptian mummy using the Scanning Electron Microscope are presented here. The study under the S.E.M. of breakage surfaces of human hair of different chronological age could provide indications on the change which these structures underwent during time.

Multidetector CT of an Antillean Zemi Idol

Volumetric multidetector computed tomography (CT) was performed on an anthropomorphic cotton zemi idol from the Taino culture, which flourished in the Antilles between the 13th and 15th centuries ad. The zemi belongs to the permanent collection of the Museum of Anthropology and Ethnography at the University of Torino in Italy. According to some researchers of Taino culture, this is the only known cotton figure functioning as a reliquary that contains a partially preserved human skull. Postprocessing consisted of multiplanar and three-dimensional reformation of the axial CT scans. The built-in capacity of CT to measure the density of materials allowed detailed characterization of the structure of the zemi, which includes vegetable fibers, wood, stone, shells, and bone-in particular, the anterior part of a human skull. The results of this multidisciplinary study involving radiologists and physical anthropologists confirm the importance of multidetector CT in the noninvasive study of delicate museum objects and have awakened anthropologic interest in the form of multidisciplinary studies that are currently underway to better identify the social meaning of the object. These studies will undoubtedly provide new information about Taino culture.