Phosphorescence and Potential Antibiosis Secondary to Photorhabdus Luminescens Wound Contaminations at the Battle of Shiloh, Tennessee 1862

Main Article Content

E Scott Sills

Abstract

During the American Civil War, contemporary accounts describe a peculiar luminescence phenomenon associated with untreated injuries sustained by fallen troops after the Battle of Shiloh (6-7 April 1862). While not experienced by all soldiers, field surgeons observed that the glow was somehow linked to reduced rates of wound infection and better outcomes. Given the wet springtime weather and unsheltered overnight conditions of the injured, it is plausible that some lacerations or punctures were incidentally infected with microscopic contaminants, including common soil nematodes. One endemic group likely present on riverbank groundcover is fam. Heterorhabditidae, a symbiotic host to Photorhabdus luminescens. Classified within the Morganellaceae, this Gram-negative pathogen is characterized by its unusual life cycle. With particular relevance to Shiloh, this sequence includes a blue-green phosphorescence phase accompanied by release of protein toxins having local antibiotic properties. Here, natural progression of this microbe from nematode symbiont to lethal secondary insect parasite lodged in an unclean wound is considered. Photorhabdus life-cycle is discussed as a component of the Martin-Curtis Hypothesis (2001), with new information on fluorophore isolation and recent genomic sequencing data. The Shiloh campaign is also placed within the context of the larger Western Theatre, noting that the engagement marked the heaviest Civil War casualty toll up to that point.

Article Details

How to Cite
Sills, E. S. (2023). Phosphorescence and Potential Antibiosis Secondary to Photorhabdus Luminescens Wound Contaminations at the Battle of Shiloh, Tennessee 1862. International Journal of Medical Science and Clinical Research Studies, 3(3), 302–305. https://doi.org/10.47191/ijmscrs/v3-i3-04
Section
Articles

References

I. Groom W. Why Shiloh matters. The New York Times [newspaper] April 6, 2012

doi:https://archive.nytimes.com/opinionator.blogs.nytimes.com/2012/04/06/why-shiloh-matters/

II. Durham S. Students may have answer for faster-healing Civil War wounds that glowed. U.S. Department of Agriculture Research Service; May 29, 2001 [newsletter]

doi:https://web.archive.org/web/20010617013104/http://www.ars.usda.gov/is/pr/2001/010529.htm

III. Anderson J, Peace D, Okun MS. Albert Sidney Johnston's sciatic dueling injury did not contribute to his death at the Battle of Shiloh. Neurosurgery 2008;63(6):1192-7.

doi:http://dx.doi.org/10.1227/01.NEU.0000327687.45271.45

IV. Liu J, Berry RE, Blouin MS. Identification of symbiotic bacteria (Photorhabdus and Xenorhabdus) from the entomopathogenic nematodes Heterorhabditis marelatus and Steinernema oregonense based on 16S rDNA sequence.

V. J Invertebr Pathol 2001;77(2):87-91. doi: http://dx.doi.org/10.1006/jipa.2001.5007

VI. Forst S, Dowds B, Boemare N, Stackebrandt E. Xenorhabdus and Photorhabdus spp.: Bugs that kill bugs. Annu Rev Microbiol 1997;51:47-72.

VII. doi:http://dx.doi.org/10.1146/annurev.micro.51.1.47

VIII. Chaston JM, Suen G, Tucker SL, Andersen AW, Bhasin A, Bode E, et al. The entomopathogenic bacterial endosymbionts Xenorhabdus and Photorhabdus: Convergent lifestyles from divergent genomes. PLoS One 2011;6(11):e27909.

doi:http://dx.doi.org/10.1371/journal.pone.0027909

IX. Waterfield NR, Bowen DJ, Fetherston JD, Perry RD, ffrench-Constant RH. The tc genes of Photorhabdus: A growing family. Trends Microbiol 2001;9(4):185-91.

doi:http://dx.doi.org/10.1016/s0966842x(01)01978-3

X. Daborn PJ, Waterfield N, Silva CP, Au CP, Sharma S, Ffrench-Constant RH. A single Photorhabdus gene, makes caterpillars floppy (mcf), allows Escherichia coli to persist within and kill insects. Proc Natl Acad Sci USA 2002;99(16):10742-7.

doi: http://dx.doi.org/10.1073/pnas.102068099

XI. ffrench-Constant RH, Dowling A, Waterfield NR. Insecticidal toxins from Photorhabdus bacteria and their potential use in agriculture. Toxicon 2007;49(4):436-51.

doi:http://dx.doi.org/10.1016/j.toxicon.2006.11.019

XII. Gerrard JG, McNevin S, Alfredson D, Forgan-Smith R, Fraser N. Photorhabdus species: Bioluminescent bacteria as emerging human pathogens? Emerg Infect Dis 2003;9(2):251-4.

doi: http://dx.doi.org/10.3201/eid0902.020222

XIII. Ensign JC, Bowen DJ, Petell J, Fatig R, Schoonover S, ffrench-Constant RH et al. Insecticidal protein toxin from Photorhabdus. Japan Patent Office 2005: JP3657593B2.doi:https://patents.google.com/patent/JP2004089189A/en?inventor=Jerald+C+Ensign

XIV. Muangpat P, Meesil W, Ngoenkam J, Teethaisong Y, Thummeepak R, Sitthisak S, et al. Genome analysis of secondary metabolite‑biosynthetic gene clusters of Photorhabdus akhurstii subsp. akhurstii and its antibacterial activity against antibiotic-resistant bacteria. PLoS One 2022;17(9):e0274956. doi:http://dx.doi.org/10.1371/journal.pone.0274956

XV. Wellawa DH, Lam PS, White AP, Allan B, Köster W. Characterization of colonization kinetics and virulence potential of Salmonella enteritidis in chickens by photonic detection. Front Vet Sci 2022;9:948448. doi: http://dx.doi.org/10.3389/fvets.2022.948448

XVI. Sato Y, Shimizu S, Ohtaki A, Noguchi K, Miyatake H, Dohmae N, et al. Crystal structures of the lumazine protein from Photobacterium kishitanii in complexes with the authentic chromophore, 6,7-dimethyl- 8-(1'-D-ribityl) lumazine, and its analogues, riboflavin and flavin mononucleotide at high resolution. J Bacteriol 2010;192(1):127-33.

doi: http://dx.doi.org/10.1128/JB.01015-09

XVII. Kusy D, He J, Bybee SM, Motyka M, Bi W, Podsiadlowski L, et al. Phylogenomic relationships of bioluminescent elateroids define the ‘lampyroid’ clade with clicking Sinopyrophoridae as its earliest member. Syst Entomol 2021;46:111-23.

doi:https://resjournals.onlinelibrary.wiley.com/doi/10.1111/syen.12451

XVIII. Owens ACS, Lewis SM. Artificial light impacts the mate success of female fireflies.R Soc Open Sci 2022;9(8):220468. doi: http://dx.doi.org/10.1098/rsos.220468

XIX. Yang L, Zhao Z, Luo D, Liang M, Zhang Q. Global metabolomics of fireflies (Coleoptera: Lampyridae) explore metabolic adaptation to fresh water in insects. Insects 2022;13(9):823. doi: http://dx.doi.org/10.3390/insects13090823

XX. Castaneda-Alvarez C, Machado RAR, Morales-Montero P, Boss A, Muller A, Prodan S, et al. Photorhabdus antumapuensis sp. nov., a novel symbiotic bacterial species associated with Heterorhabditis atacamensis entomopathogenic nematodes. Int J Syst Evol Microbiol 2022;72(10). doi: http://dx.doi.org/10.1099/ijsem.0.005525