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Possible bite-induced abscess and osteomyelitis in Lufengosaurus (Dinosauria: sauropodomorph) from the Lower Jurassic of the Yimen Basin, China

Scientific Reportsvolume 8, Article number: 5045 (2018) | Download Citation

Abstract

We report an osseous abnormality on a specimen of the sauropod dinosaur Lufengosaurus huenei from the Fengjiahe Formation in Yuxi Basin, China. A gross pathological defect occurs on the right third rib, which was subjected to micro-computed tomographic imaging as an aid in diagnosis. The analysis of pathological characteristics and the shape of the abnormality is incompatible with impact or healed trauma, such as a common rib fracture, and instead suggests focal penetration of the rib, possibly due to a failed predator attack. The identification of characteristics based on gross morphology and internal micro-morphology presented by the specimen, suggests an abscess with osteomyelitis as the most parsimonious explanation. Osteomyelitis is a severe infection originating in the bone marrow, usually resulting from the introduction of pyogenic (pus-producing) bacteria into the bone. Micro-tomographic imaging of the lesion suggests a degree of healing and bone remodelling following post-traumatic wound infection with evidence of sclerotic bone formation at the site of pathological focus, indicating that L. huenei survived the initial trauma. However, as osteomyelitis can express through widespread systemic effects, including a lowering of immune response and overall condition, this disease may have been a contributing factor to the eventual death of the individual.

Introduction

We report evidence for pathological lesions in a partial skeleton of Lufengosaurus huenei from the Fengjiahe Formation in Yuxi Basin, Yunnan Province, China, which may be attributed to a failed predator attack on this sauropod. The analysis of osseous abnormalities can provide critical insight into palaeo-immunology, behavioural and life history information for dinosaurs, as well as environmental insights into ancient ecosystems1,2,3. A modern understanding of forensic trauma analysis and pathology, as well as pathologies in modern birds, reptiles and mammals provides a platform for identification of similar palaeopathologies in the fossil record. The fundamental principle underlying the inference of palaeopathological conditions from modern comparative analysis is that of uniformitarianism4, and this approach has yielded significant data regarding the expression and response to disease and trauma in the dinosauria. In particular, the fossil record of China has yielded a range of reports of palaeo-bone pathologies including healed bite marks in Sinraptor5, bacterial infection in the fibula of the basal ceratopsian Psittacosaurus6, a healed fracture in the theropod Yangchuanosaurus7, osteoarthritis in the theropods Caudipteryx, Confuciusornis and Microraptor8, tooth loss and alveolar remodeling in Sinosaurus triassicus9, and vertebral fusions in sauropodomorph dinosaurs1. The specimen reported here adds evidence of both bone-pathology, as well as inferred behaviour, to this growing hypodigm of skeletal pathologies.

Geological setting

The Fengjiahe Formation is the oldest Lower Jurassic red bed unit in the region and varies in thickness throughout10. The formation is stratigraphically positioned between the Upper Middle Jurassic Zhanghe Formation, and the Lower Triassic Shezi Formation. The Fengjiahe Formation is 1500 m thick in some regions, and its upper contact with the Shezi formation is conformable10. The formation is characterised by purple-red mudstone and argillaceous siltstone interbedded with gray-green and yellow-green quartz sandstone and feldspathic quartz sandstone. The formation is also associated with a rich track-bearing horizon.

The Fengjiahe Formation has yielded a diversity of vertebrate fossils and is renowned for the Lufengosaurus fauna, consisting mostly of the basal sauropodomorphs, Lufengosaurus and Yunnanosaurus11. The fauna recovered from this formation is comparable with fauna from the Lufeng Formation12. The Lufeng Formation is the most famous and prolific unit of the Mesozoic strata of Yunnan Province in China. This formation contains a rich vertebrate fauna, including dinosaurs (sauropodomorph, theropod and ornithischian), early mammals and non-mammalian eucynodonts, basal crocodylomorphs, and sphenodontians13,14,15,16,17.

Materials and Methods

The specimen analysed during the course of this study was recovered from the Yuxi Basin, Yunnan Province, China (Fig. 1) and is housed at Yuxi Museum, Yunnan, under accession number YX V0003. The specimen was referred to Lufengosaurus huenei based on the manus being longer than the ulna and the pubis-illium length ratio of 1.118,19,20,21. YX V003 comprises a partial articulated skeleton which includes 9 cervical vertebrae, 10 dorsal vertebrae, 3 sacral vertebrae, 7 caudal vertebrae, scapulas, humeri, hip bones, and limb bones. The specimen was recovered from the No.3 bonebed, Jiaojiedian Village, Shijie Township, Yimen County, Yunnan Provence, China. The entire specimen was inspected morphoscopically for any evidence of paleopathological lesions.

Figure 1
Figure 1

Map showing the position of the Lufengosaurus huenei dinosaur fossil locality in Yunnan Province, China. Line drawing modified from Xing and colleagues1.

Only a single skeletal element showed clear evidence of skeletal pathology. The osseous abnormality is located on the third right rib of YX V003 (Fig. 2); no other osseous lesions or pathological traces were identified elsewhere on the partial skeleton. The rib is complete and has a chord length between the dorsal and ventral ends of 394 mm, with an overall circumferential (curve) length of 452 mm (Fig. 3).

Figure 2
Figure 2

Museum reconstruction of the Lufengosaurus huenei YX V0003 sauropod. Arrow shows the anatomical location of the affected rib. Photograph by L.X.

Figure 3
Figure 3

External morphology of the YX V0003 third rib. (A) lateral view; (B) medial view; (C) anterior (cranial) view; (D) posterior (caudal) view; (E) dorsal view. Scale bar is 10 cm. Photographs by L.X.

In order to investigate the pathology affecting the specimen, the fossil was subjected to high-resolution imaging using micro-computed tomography (micro-CT). This non-invasive imaging technique has been demonstrated to provide a significant diagnostic advantage over conventional whole-bone morphoscopic or microscopic methods of imaging in cases of fossilised pathology22,23. Micro-CT imaging of the YX V003 rib was carried out using a Nikon Metrology XTH 225/320 LC dual source industrial micro-computed tomographic scanner, housed in the China University of Geosciences, Beijing (CUGB), China. Due to the size of the specimen in relation to the detector size and gantry size of the scanner, the lesion was imaged in two focussed portions split into a dorsal half (volume identifier [VI] XLD02) and a ventral half (VI XLD03) with a small zone of overlap between the two volumes of interest (VOI). Both VOI were scanned using a potential difference of 135 kV and a current of 67 µA, at an effective resolution of 37 µm; a TIFF-format image stack was generated in VG Studio Max following volume reconstruction. Further reconstruction by PSR-Q was undertaken using Avizo Amira 5.4 to generate both 2D orthoslice and 3D surface rendered views based on the volume data; multi-planar mode was used in Amira to allow the recovery of homologous orthoslices through the specimen for comparative purposes. Differential diagnosis based on established pathological and palaeopathological criteria was subsequently undertaken24,25,26,27.

Description

The defect presents as a well-defined aperture which affects the lateral, medial and anterior surfaces of the rib (see Fig. 3A–C), and is located some 108 mm ventrally in the coronal plane (146 mm circumferentially) from the costovertebral junction. Viewed from the lateral and medial aspects, the defect presents as a semi-circular (concave) removal of bone, the loss of which extends almost half-way through the antero-posterior thickness of the shaft of the rib, to an approximate depth of 15.4 mm on the lateral surface. The defect is teardrop-shaped when viewed from the anterior aspect (Fig. 3C). The defect has a total external length of 54 mm, with the widest point some 20 mm from the blunted (dorsal end), reducing in width inferiorly to form a sharp tail at the ventral end of the aperture. The margin of the defect is largely intact and undamaged, although a comminuted block of cortical bone (15 mm long and 8.4 mm wide) has been lost on the opposing (medial/pleural) side of the rib (Fig. 3C,D), the margins of which clearly follow lines of post-fossilisation cracking – the loss of this area of bone is thus unrelated to the formation of the pathological defect. None of the fractures observed across the wider specimen are consistent with peri-mortem trauma or in-vivo failure, and instead present as transverse or right-angled breaks, showing block-comminution between major fracture blocks, and are thus ‘dry bone’ fractures and post-mortem/fossilisation in nature28,29. Many of these fracture boundaries have subsequently been infilled with calcite, particularly those following longitudinal split lines along the grain of the rib shaft.

Externally, the margin of the defect is rounded, with clear softening and remodelling of the bone around the aperture (Fig. 4) – this creates a ridge which extends some 3 mm above the original bone surface. Where remaining cortical surface of the fossil survives intact, the surface is observed as irregular and slightly puffy, suggesting remnants of systematic sub-periosteal reaction or cortical remodelling, indicative of reactive new bone formation. No evidence of bone tumors, exostoses or spurs was observed.

Figure 4
Figure 4

External morphology of the pathological Lufengosaurus huenei sauropod rib reconstructed from surface render of micro-computed tomographic (MCT) image volume. Schematic overlay of the photograph highlights the regions of interest (ROI) based on the respective MCT volumes ROIA and ROIB. Each ROI shows (1) lateral view; (2) medial view; (3) anterior (cranial) view; (4) posterior (caudal) view. Note, the section lines labelled A to F indicate the anatomical locations of MCT orthoslices presented in Fig. 5. Photograph by Lida Xing. Volume renders produced by P.S.R.-Q.

Internally, the defect comprises two distinct zones, separated by a convex bulge or island of bone (see Fig. 4A3,B3) coincidental with an external change of curvature of the rib shaft; there is clear evidence of remodelling and reactive bone formation surrounding the defect which extends into the medulla of the shaft. In cross-section, the defect and surrounding cortical bone present clearly defined zones of active surface and internal remodelling, with both exosteal and endosteal surfaces displaying areas of radiolucency indicative of reactive bone formation (Fig. 5A–F), which is present both as sequestra of necrotic bone and as involcrum formation. This contrasts with the presence of normal un-modified trabecular bone within the structure of the residual (normal) body of the shaft. Well-defined sclerotic zones are noted in cross-section, occurring extensively around the expanded margins of the defect and within the medula (Fig. 5A,D,E), and along the body of the shaft (where they are observed underlying zones of remodelling), indicating a quiescent condition with healing of the lesion.

Figure 5
Figure 5

Transverse orthoslices produced from micro-computed tomography of the YX V0003 rib. Each slice represents an aligned transverse x-ray slice taken perpendicular to the cortical surface of the bone at the locations marked A to F in Fig. 4. Abbreviations: cbe = cortical bone expansion; inv = involcrum; itrb = internal trabeculae; pnvc = primary neurovascular canal; sbr = sequestered bone region; snvc = secondary neurovascular canal; zsb = zone of sclerotized bone. Photograph by Lida Xing. Orthoslices produced by P.S.R.-Q.

Differential diagnosis

Diagnosis was undertaken using both palaeopathological and clinical diagnostic criteria24,25,26,27 with clinical character recognition adapted for use in cases of micro-tomographic volume imaging22,23,30. The accumulated evidence for both osteolytic and osteosclerotic processes indicates that the disease process was both chronic (long-term) and clinically active at the time of death of the animal. The damage was associated with reactive new bone formation, and thus can be attributed to a phenomenon which occurred during the animal’s life2,26,31. Clear evidence of bone remodelling suggests that the dinosaur lived past the initial event that caused the damage to the osseous tissue. The limited distribution of the pathology rules out systemic diseases1,26. The position of the pathology (unassociated with a joint) also rules out consideration of gout, arthritis, or pseudarthrosis25,26. No other bioerosional bone damage was identified on the specimen, with any fractures or breaks post-mortem/fossilisation in nature.

A lytic lesion produced as a result of a bone infection is the most likely explanation due to the associated cortical bone loss and subsequent remodelling of the rib2,31,32, with osteomyelitis being suggested as the most parsimonious explanation. Osteomyelitis is a severe infection originating in the bone marrow, usually resulting from the introduction of pyogenic (pus-producing) bacteria into the bone; most commonly today this is staphylococcus, although streptococcus, salmonella, enterococcus and other organisms have been implicated as pathogenic vectors33. These pathogens can enter either via the bloodstream, or through wounds and open fractures which will introduce bacteria into the periosteum, cortex, marrow, and cancellous tissue. A distinctive feature of osteomyelitis in the skeleton is extensive new bone formation. This may totally encase the cortex of infected bone (sequestrum) as a shell of new bone, which is termed an involucrum. Sequestrated bone varies in size ranging from one or more small areas within an element to the entire diaphysis. Involucrum is the product of periosteal reaction to tissue necrosis, and although cortical bone may be dead as a consequence of infection, the periosteum may be viable and forms new bone to ensure continued normal function. Involucrum tends to be formed quickly and typically has an irregular surface. Present on the surface of the involucrum are often found large, circular openings or cloacae, which are channels of drainage for pus produced by the bacteria33. Such general features are evidenced in the YX V0003 specimen, supporting a diagnosis of osteomyelitis.

Discussion

Osteomyelitis is a bacterial infection frequently distinguished by progressive inflammatory destruction of bone, in which the primary skeletal focus is in the bone marrow, and which thus occurs endosteally within the medulla. This is in contrast with osteitis, which primarily occurs within compact bone, and periostitis, which affects the outer layer of bone and its associated periosteal sheath. It is common for all three areas of bone to be involved in an infectious disorder, and determining the primary skeletal site of pathology may be difficult. In the case of YX V0003 the defect is localised and connects through to the medulla, providing both a focal site and a clear diagnosis. There are two primary categories of acute osteomyelitis: hematogenous osteomyelitis, caused by the seeding of the bacteria from a remote source, and direct or contiguous inoculation osteomyelitis, caused by direct contact of the tissue and bacteria during trauma34. In the case of YX V003, the loss of bone marrow with exposure of the medulla supports the hypothesis that direct osteomyelitis is the most likely process to have caused this bone pathology2,31. Reactive new bone in the form of periosteal reaction35,36 is a significant characteristic of bird or reptile osteomyelitis27. Other studies have also suggested that in modern mammals bone deformation can also be produced by osteomyelitis37. Long-term clinical symptoms include abrupt onset of high fever, local oedema, erythema, non-healing ulcers, sinus tract drainage, sepsis and tissue necrosis33,38,39.

Osteomyelitis has previously been observed in non-avian dinosaurs2,8,26,40 and attributed to, fractures and/or other injuries2. Reports of bone marrow infection (e.g., osteomyelitis) is rare in dinosaurs, especially Sauropodomorpha dinosaurs2,32. Our identification of osteomyelitis in a sauropodomorph is second only to that of García and colleagues2 who reported the pathology in a Baurutitan britoi from Argentina. The pathology reported here from Lufengosaurus huenei is the first recognition of an abscess in sauropods, and the third example of surviving osseous abnormalities or pathologies from the Yunnan area1,9. This discovery enriches the record of infections in dinosaurs, and extends our understanding of the frequency of paleopathology in Sauropodomorpha dinosaurs.

Given the physical location of the lesion within the thorax, and the relatively exposed nature of the costal margin to external insult, we suggest that the infection may have been initiated by a physical injury, such as a puncture or bite26,33. This suggests that the observed pathological processes arose as the result of a subsequently transferred (acquired) infective agent32,41. If so, the infective process would have been present for an extended period. If the infection extended in different directions with a similar speed42,43, the shape of the bone puncture would reflect the shape of the wound, in this instance a wide blunt opening with a sharpened end. The morphology of the damage suggests that the damage was produced as a result of a tooth or claw incision44. Whilst the large defect may be representative of a remodelled cloaca following localised necrosis (rather than a bite or puncture) we suggest that the size of the defect would preclude this. Such a large cloaca would likely produce a much greater degree of involucrum formation than is expressed here, and we consider it more likely that the primary area of bone loss represents a bite or tooth puncture as a consequence; the general tear-drop shape and overall pattern of the defect is in keeping with the morphology of bite-induced trauma and predatory behaviours recorded elsewhere in the dinosaur fossil record5,45,46,47,48.

No theropod skeletons have yet been recovered from the Fengjiahe Formation. However, the faunally-similar Lufeng formation has yielded four theropod genera Sinosaurus9,49,50, Eshanosaurus51, Panguraptor52. Eshanosaurus belongs to therizinosaur, which is considered to be herbivore51,53. Panguraptor are small coelophysids and may have not have the ability to attack Lufengosaurus. However, Sinosaurus is a famous and larger bodied predator, and would be able to attack Lufengosaurus9,50, and thus is a possible suspect for producing the injuries which resulted in the abscess and osteomyelitis. Whilst the exact identity of the proposed attacker is not critical, it is clear is that the attack was unsuccessful, and that the associated symptoms of the infection likely influenced the future life-history of the Lufengosaurus. Osteomyelitis is known to produce the fever, fatigue, nausea, loss of range of motion, tenderness, and discomfort, although necrotizing tracts of pasteurella bacteria extending to the brain have been reported in clinical cases in reptiles54, which are associated with elevated morbidity. Any or all of these symptoms would have negatively impacted the survival potential of the injured Lufengosaurus in the dynamic and complex ecosystems during the Jurassic.

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References

  1. 1.

    Xing, L. D. et al. Vertebral fusion in two Early Jurassic sauropodomorph dinosaurs from the Lufeng Formation of Yunnan, China. Acta Palaeontol. Pol. 60, 643–649 (2015).

  2. 2.

    García, R. A., Cerda, I. A., Heller, M., Rothschild, B. M. & Zurriaguz, V. The first evidence of osteomyelitis in a sauropod dinosaur. Lethaia 50, 227–236 (2016).

  3. 3.

    Anné, J., Hedrick, B. P. & Schein, J. P. First diagnosis of septic arthritis in a dinosaur. Roy. Soc. Open Sci. 3, 160222 (2016).

  4. 4.

    Rothschild, B. M. & Martin, L. D. Skeletal Impact of Disease. (New Mexico Museum of Natural History Press, 2006).

  5. 5.

    Tanke, D. H. & Currie, P. J. Head-biting behaviour in theropod dinosaurs: paleopathological evidence. Gaia 15, 167–184 (1998).

  6. 6.

    Lü, J. C., Kobayashi, Y., Lee, Y. N. & Ji, Q. A new Psittacosaurus (Dinosauria: Ceratopsia) specimen from the Yixian Formation of western Liaoning, China: The first pathological psittacosaurid. Cretaceous Res. 28, 272–276 (2007).

  7. 7.

    Xing, L. D. et al. A scapular fracture in Yangchuanosaurus hepingensis (Dinosauria: Theropoda). Geol. Bull. China 28, 1390–1395 (2009).

  8. 8.

    Rothschild, B. M., Zheng, X. T. & Martin, L. Osteoarthritis in the early avian radiation: Earliest recognition of the disease in birds. Cretaceous Res. 35, 178–180 (2012).

  9. 9.

    Xing, L. D. et al. Novel insect traces on a dinosaur skeleton from the Lower Jurassic Lufeng Formation of China. Paleogeogr. Palaeoclimatol. Palaeoecol. 388, 58–68 (2013).

  10. 10.

    Zhang, Z. Y. Stratigraphy (Lithostratic) of Yunnan Province. (China University of Geosciences Press, 1996).

  11. 11.

    Fang, X. S. & Li, P. X. Jurassic red bed in the central Yunnan of China. (Geological Publishing House, 2008).

  12. 12.

    Xing, L. D., Lockley, M. G., Hu, S. J., Li, Q. F. & Persons, W. S. I. Early Jurassic Anomoepus track from the Fengjiahe Formation of Northern Central Yunnan, China. New Mex. Mus. Nat. Hist. Sci. Bull. 74, 327–330 (2016).

  13. 13.

    Sun, A. L., Cui, G. H., Li, Y. H. & Wu, X. C. A verified list of Lufeng saurischian fauna. Vertebrat. PalAsiatic. 23, 1–12 (1985).

  14. 14.

    Xing, L. D. Tooth loss and alveolar remodeling in Sinosaurus triassicus (Dinosauria: Theropoda) from the Lower Jurassic strata of the Lufeng Basin, China. Chin. Sci. Bull. 58, 1931–1935 (2013).

  15. 15.

    Xing, L. D. et al. First Early Jurassic small ornithischian tracks from Yunnan Province, southwestern China. PALAIOS 31, 516–524 (2016).

  16. 16.

    Xing, L. D. et al. First Early Jurassic Ornithischian and theropod footprint assemblage and a New Ichnotaxon Shenmuichnus wangi ichnosp. nov. from Yunnan Province, southwestern China. Hist. Biol. 28, 721–733 (2016).

  17. 17.

    Xing, L. D., Lockley, M. G., Klein, H., Zhang, J. P. & Persons, W. S. I. A new ornithischian-dominated and theropod footprint assemblage from the Lower Jurassic Lufeng Formation of China. New Mex. Mus. Nat. Hist. Sci. Bull. 74, 331–338 (2016).

  18. 18.

    Young, C. C. A complete osteology of Lufengosaurus huenei Young (gen, et sp. nov.) from Lufeng, Yunnan, China. Palaeontol. Sinica (Series C) 7, 1–53 (1941).

  19. 19.

    Young, C. C. The Lufeng saurischian fauna. Palaeontol. Sinica (Series C) 13, 1–96 (1951).

  20. 20.

    Galton, P. M. & Upchurch, P. In The Dinosauria (eds D. B. Weishampel, P. Dodson, & H. Osmólska) 232–258 (University of California Press, 2004).

  21. 21.

    Barrett, P. M., Upchurch, P. & Wang, X. L. Cranial osteology of Lufengosaurus huenei Young (Dinosauria: Prosauropoda) from the Lower Jurassic of Yunnan, People’s Republic of China. J. Vert. Paleontol. 25, 806–822 (2005).

  22. 22.

    Odes, E. J. et al. Osteopathology and insect traces in the Australopithecus africanus skeleton StW 431. S. Afr. J. Sci. 113, a#2016-0143 (2017).

  23. 23.

    Odes, E. J. et al. Earliest hominin cancer: 1.7 million year old osteosarcoma from Swartkrans Cave, South Africa. S. Afr. J. Sci. 112, a#2015–0471 (2016).

  24. 24.

    Bahk, Y.-W. Combined Scintigraphic and Radiographic Diagnosis of Bone and Joint Diseases. (Springer, 2007).

  25. 25.

    Resnick, D. Radiology of Bone and Joint Disorders. (Saunders, 2002).

  26. 26.

    Rothschild, B. M. In The Complete Dinosaur (eds J. O. Farlow & M. K. Brett-Surman) 426–448 (Indiana University Press, 1997).

  27. 27.

    Rothschild, B. M., Schultze, H.-P. & Pelligrini, R. Herpetologic Osteopathology. (Springer, 2012).

  28. 28.

    L’Abbe, E. et al. Evidence of fatal skeletal injuries on Malapa hominins 1 and 2. Scientific Reports 5, e15120 (2015).

  29. 29.

    Symes, S., L’Abbe, E., Stull, K., La Croix, M. & Pokines, J. In Manual of Forensic Taphonomy (eds J. Pokines & S. Symes) 341–365 (CRC Press, 2014).

  30. 30.

    Randolph-Quinney, P. S. et al. Osteogenic spinal tumor in Australopithecus sediba: Earliest evidence for neoplasia in the human lineage. S. Afr. J. Sci. 112, a#2015–0470 (2016).

  31. 31.

    Reisz, R. R., Scott, D. M. & Pynn, B. R. Osteomyelitis in a Paleozoic reptile: ancient evidence for bacterial infection and its evolutionary significance. Naturwissenschaften 98, 551–555 (2011).

  32. 32.

    Lew, P. A. & Waldvogel, F. A. Osteomyelitis. Lancet 364, 369–379 (2004).

  33. 33.

    Jacobson, E. R. In Infectious Diseases and Pathology of Reptiles (ed. E. R. Jacobson) 461–526 (CRC Press, 2007).

  34. 34.

    Ehara, S. Complications of skeletal trauma. Radiol. Clin. N. Am. 35, 767–771 (1997).

  35. 35.

    Dwek, J. R. The periosteum: what is it, where is it, and what mimics it in its absence? Skel. Radiol. 39, 319–323 (2010).

  36. 36.

    Shapiro, F. Bone development and its relation to fracture repair. The role of mesenchymal osteoblasts and surface osteoblasts. Europ. Cell. Mat. 15, 53–76 (2008).

  37. 37.

    Kumari, P., Devi, S. & Singh, G. Osteomyelitis: Identification and Management. MOJ Orthop. Rheumat. 5, 00195 (2016).

  38. 38.

    Miller, B. R. & Schiller, W. R. Pyogenic vertebral osteomyelitis after transcolonic gunshot wound. Milit. Med. 154, 64–66 (1989).

  39. 39.

    Schluter, B., Bergmann, U., Josten, C., Walz, M. & Konig, W. Impairment of specific host defense-mechanisms in patients with chronic posttraumatic osteomyelitis. J. Trauma 31, 68–73 (1991).

  40. 40.

    Barbosa, F. H. S., Pereira, P. V. L. G., Bergqvist, L. P. & Rothschild, B. M. Multiple neoplasms in a single dinosaur from the Upper Cretaceous of Brazil. Cretaceous Res. 62, 13–17 (2016).

  41. 41.

    Chen, J. S. et al. Establishment of rabbit models of chronic femoral osteomyelitis. Chin. J. Tiss. Eng. Res. 19, 7885–7889 (2015).

  42. 42.

    Edwards, R. & Harding, K. G. Bacteria and wound healing. Curr. Op. Infect. Dis. 17, 91–96 (2004).

  43. 43.

    Healy, B. & Freedman, A. ABC of wound healing: infections. Brit. Med. J. 332, 838–841 (2006).

  44. 44.

    Phillips, L. L., Semple, J., & Lanteri, C. A. In Auerbach’s Wilderness Medicine (eds P. S. Auerbach, T. A. Cushing, & N. S. Harris) 618–869 (Elsevier, 2016).

  45. 45.

    Bell, P. R. & Currie, P. J. A tyrannosaur jaw bitten by a confamilial: scavenging or fatal agonism? Lethaia 43, 278–281 (2010).

  46. 46.

    DePalma, R. A., Burnham, D. A., Martin, L. D., Rothschild, B. M. & Larson, P. L. Physical final evidence of predatory behavior in Tyrannosaurus rex. P. Natl. Acad. Sci. USA 110, 12560–12564 (2013).

  47. 47.

    Rothschild, B. M., Martin, L. D. & Schulp, A. S. Sharks eating mosasaurs, dead or alive. Neth. J. Geosci. 84, 335–340 (2005).

  48. 48.

    Xing, L. D. et al. A sauropod rib with an embedded theropod tooth: direct evidence for feeding behaviour in the Jehol group, China. Lethaia 45, 500–506 (2012).

  49. 49.

    Hu, S. J. A new Theropoda (Dilophosaurus sinensis sp. nov.) from Yunnan, China. Vertebrat. PalAsiatic. 31, 65–69 (1993).

  50. 50.

    Xing, L. D. Sinosaurus from Southwestern China. MSc thesis (University of Alberta, 2012).

  51. 51.

    Xu, X., Zhao, X. & Clark, J. M. A new therizinosaur from the Lower Jurassic lower Lufeng Formation of Yunnan, China. J. Vert. Pal. 21, 477–483 (2001).

  52. 52.

    You, H. L., Azuma, Y., Wang, T., Wang, Y. M. & Dong, Z. M. The first well-preserved coelophysoid theropod dinosaur from Asia. Zootaxa 3873, 233–249 (2014).

  53. 53.

    Pu, H. Y. et al. An unusual basal Therizinosaur with an ornithischian dental arrangement from northeastern China. PLoS One 8, e63423 (2013).

  54. 54.

    Snipes, K. P. In Diseases of Amphibians and Reptiles (eds G. L. Hoff, F. L. Frye, & E. R. Jacobson) 25–36 (Plenum Press, 1984).

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Acknowledgements

We would like to acknowledge the assistance and help of the following people in the production of this research: Qinfang Fang from the China University of Geosciences (Beijing) for undertaking the micro-computed tomographic scanning; First Affiliated Hospital of Kunming Medical University, Sichuan Province for providing initial advice on x-radiography of the fossil. This research was funded by the National Natural Science Foundation of China (No. 41790455, 41772008), the Fundamental Research Funds for the Central Universities (No. 2652017215), the State Key Laboratory of Palaeobiology and Stratigraphy (Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences) (No. 173127). Direct research support for P.S.R-Q. was provided by the School of Forensic and Applied Sciences, University of Central Lancashire.

Author information

Affiliations

  1. State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing, 100083, China

    • Lida Xing
  2. School of the Earth Sciences and Resources, China University of Geosciences, Beijing, 100083, China

    • Lida Xing
  3. Division of Vertebrate Paleontology, Carnegie Museum of Natural History, 4400 Forbes Avenue, Pittsburgh, PA, 15271, USA

    • Bruce M. Rothschild
  4. West Virginia University School of Medicine, Morgantown, WV, 26506, USA

    • Bruce M. Rothschild
  5. School of Forensic and Applied Sciences, University of Central Lancashire, Preston, PR1 2HE, UK

    • Patrick S. Randolph-Quinney
  6. Evolutionary Studies Institute, University of the Witwatersrand, Wits, 2050, Johannesburg, South Africa

    • Patrick S. Randolph-Quinney
  7. School of Anatomical Sciences, University of the Witwatersrand Medical School, Johannesburg, South Africa

    • Patrick S. Randolph-Quinney
    •  & Alexander H. Parkinson
  8. Yuxi Museum, Yunnan, 653100, China

    • Yi Wang
  9. School of Geosciences, University of the Witwatersrand, Wits, 2050, Johannesburg, South Africa

    • Alexander H. Parkinson
  10. State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650223, China

    • Hao Ran
  11. Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection, Ministry of Education, Guilin, 541004, China

    • Hao Ran

Authors

  1. Search for Lida Xing in:

  2. Search for Bruce M. Rothschild in:

  3. Search for Patrick S. Randolph-Quinney in:

  4. Search for Yi Wang in:

  5. Search for Alexander H. Parkinson in:

  6. Search for Hao Ran in:

Contributions

L.X., Y.W., H.R. and B.M.R. undertook the primary analysis and wrote the original draft of the manuscript. P.S.R.-Q. undertook the micro-tomographic reconstruction and subsequent analysis in conjunction with A.H.P., and edited the original manuscript. A.H.P. produced the composite plates from photographic and orthoslice and three-dimensional volume data; all authors contributed equally to analysis and editing.

Competing Interests

The authors declare no competing interests.

Corresponding authors

Correspondence to Patrick S. Randolph-Quinney or Hao Ran.

About this article

Publication history

Received

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Published

DOI

https://doi.org/10.1038/s41598-018-23451-x

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