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Nasopulmonary mites (Acari: Halarachnidae) as potential vectors of bacterial pathogens, including Streptococcus phocae, in marine mammals

Risa Pesapane, Andrea Chaves, Janet Foley, Nadia Javeed, Samantha Barnum, Katherine Greenwald, Erin Dodd, Christine Fontaine, Padraig Duignan, Michael Murray, Melissa Miller

PLoS One. 2022; 17(6): e0270009. Published online 2022 Jun 16. doi: 10.1371/journal.pone.0270009

PMCID:: PMC9202935

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STREPTOCOCCUS PHOCAE ISOLATED FROM A SPOTTED SEAL (PHOCA LARGHA) WITH PYOMETRA IN ALASKA

Karsten Hueffer, Camilla L. Lieske, Lisa M. McGilvary, Rebekah F. Hare, Debra L. Miller, Todd M. O’Hara

J Zoo Wildl Med. Author manuscript; available in PMC 2013 Feb 20.

Published in final edited form as: J Zoo Wildl Med. 2011 Mar; 42(1): 108–112. doi: 10.1638/2010-0064.1

PMCID:: PMC3576814

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Genome Sequence of Streptococcus phocae subsp. salmonis Strain C-4^T, Isolated from Atlantic Salmon (Salmo salar)

Ruben Avendaño-Herrera, Rudy Suarez, Eduardo Lazo, Diego Bravo, Katerina O. Llegues, Jesús L. Romalde, Marcos G. Godoy

Genome Announc. 2014 Nov-Dec; 2(6): e01269-14. Published online 2014 Dec 11. doi: 10.1128/genomeA.01269-14

PMCID:: PMC4263830

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Genome Sequence of Streptococcus phocae subsp. phocae Strain ATCC 51973^T Isolated from a Harbor Seal (Phoca vitulina)

Ruben Avendaño-Herrera, Matías Poblete-Morales

Genome Announc. 2015 Nov-Dec; 3(6): e01307-15. Published online 2015 Nov 19. doi: 10.1128/genomeA.01307-15

PMCID:: PMC4653777

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Optimization of media components for enhanced production of streptococcus phocae pi80 and its bacteriocin using response surface methodology

P. Kanmani, R. Satish kumar, N. Yuvaraj, K. A. Paari, V. Pattukumar, V. Arul

Braz J Microbiol. 2011 Apr-Jun; 42(2): 716–720. Published online 2011 Jun 1. doi: 10.1590/S1517-838220110002000038

PMCID:: PMC3769839

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Streptococcal Infections in Marine Mammals

Daniela Numberger, Ursula Siebert, Marcus Fulde, Peter Valentin-Weigand

Microorganisms. 2021 Feb; 9(2): 350. Published online 2021 Feb 10. doi: 10.3390/microorganisms9020350

PMCID:: PMC7916692

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First Identification of Streptococcus phocae Isolated from Atlantic Salmon (Salmo salar)

A. Gibello, A. I. Mata, M. M. Blanco, A. Casamayor, L. Domínguez, José F. Fernández-Garayzabal

J Clin Microbiol. 2005 Jan; 43(1): 526–527. doi: 10.1128/JCM.43.1.526-527.2005

PMCID:: PMC540139

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Identification and Molecular Characterization of Beta-Hemolytic Streptococci Isolated from Harbor Seals (Phoca vitulina) and Grey Seals (Halichoerus grypus) of the German North and Baltic Seas

A. Vossen, A. Abdulmawjood, C. Lämmler, R. Weiß, U. Siebert

J Clin Microbiol. 2004 Jan; 42(1): 469–473. doi: 10.1128/JCM.42.1.469-473.2004

PMCID:: PMC321648

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Pup mortality in New Zealand sea lions (Phocarctos hookeri) at Enderby Island, Auckland Islands, 2013-18

Sarah A. Michael, David T. S. Hayman, Rachael Gray, Ji Zhang, Lynn Rogers, Wendi D. Roe

PLoS One. 2019; 14(11): e0225461. Published online 2019 Nov 21. doi: 10.1371/journal.pone.0225461

PMCID:: PMC6874089

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After the bite: bacterial transmission from grey seals (Halichoerus grypus) to harbour porpoises (Phocoena phocoena)

Maarten J. Gilbert, Lonneke L. IJsseldijk, Ana Rubio-García, Andrea Gröne, Birgitta Duim, John Rossen, Aldert L. Zomer, Jaap A. Wagenaar

R Soc Open Sci. 2020 May; 7(5): 192079. Published online 2020 May 13. doi: 10.1098/rsos.192079

PMCID:: PMC7277243

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A Review of Circumpolar Arctic Marine Mammal Health—A Call to Action in a Time of Rapid Environmental Change

Ashley Barratclough, Steven H. Ferguson, Christian Lydersen, Peter O. Thomas, Kit M. Kovacs

Pathogens. 2023 Jul; 12(7): 937. Published online 2023 Jul 14. doi: 10.3390/pathogens12070937

PMCID:: PMC10385039

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Bacterial Pathogenesis in Various Fish Diseases: Recent Advances and Specific Challenges in Vaccine Development

Aadil Ahmed Irshath, Anand Prem Rajan, Sugumar Vimal, Vasantha-Srinivasan Prabhakaran, Raja Ganesan

Vaccines (Basel) 2023 Feb; 11(2): 470. Published online 2023 Feb 17. doi: 10.3390/vaccines11020470

PMCID:: PMC9968037

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Current Status of the Use of Antibiotics and the Antimicrobial Resistance in the Chilean Salmon Farms

Claudio D. Miranda, Felix A. Godoy, Matthew R. Lee

Front Microbiol. 2018; 9: 1284. Published online 2018 Jun 18. doi: 10.3389/fmicb.2018.01284

PMCID:: PMC6016283

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Probiotics as Means of Diseases Control in Aquaculture, a Review of Current Knowledge and Future Perspectives

Seyed Hossein Hoseinifar, Yun-Zhang Sun, Anran Wang, Zhigang Zhou

Front Microbiol. 2018; 9: 2429. Published online 2018 Oct 12. doi: 10.3389/fmicb.2018.02429

PMCID:: PMC6194580

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Mustelids

Bruce H. Williams, Kathy Burek Huntington, Melissa Miller

Pathology of Wildlife and Zoo Animals. 2018 : 287–304. Published online 2018 Oct 26. doi: 10.1016/B978-0-12-805306-5.00011-0

PMCID:: PMC7149534

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Streptococcus iniae outbreaks in Brazilian Nile tilapia (Oreochromis niloticus L:) farms

H. C. P. Figueiredo, L. Nobrega Netto, C. A. G. Leal, Ulisses P. Pereira, Glaúcia F. Mian

Braz J Microbiol. 2012 Apr-Jun; 43(2): 576–580. Published online 2012 Jun 1. doi: 10.1590/S1517-83822012000200019

PMCID:: PMC3768829

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What Happened to the Streptococci: Overview of Taxonomic and Nomenclature Changes

Richard Facklam

Clin Microbiol Rev. 2002 Oct; 15(4): 613–630. doi: 10.1128/CMR.15.4.613-630.2002

PMCID:: PMC126867

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Streptococcosis a Re-Emerging Disease in Aquaculture: Significance and Phytotherapy

Hien Van Doan, Mehdi Soltani, Alexandra Leitão, Shafigh Shafiei, Sepideh Asadi, Alan J. Lymbery, Einar Ringø

Animals (Basel) 2022 Sep; 12(18): 2443. Published online 2022 Sep 16. doi: 10.3390/ani12182443

PMCID:: PMC9495100

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Host–Pathogen Interactions of Marine Gram-Positive Bacteria

Hajarooba Gnanagobal, Javier Santander

Biology (Basel) 2022 Sep; 11(9): 1316. Published online 2022 Sep 5. doi: 10.3390/biology11091316

PMCID:: PMC9495620

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Vibriosis Outbreaks in Aquaculture: Addressing Environmental and Public Health Concerns and Preventive Therapies Using Gilthead Seabream Farming as a Model System

Gracinda M. M. Sanches-Fernandes, Isabel Sá-Correia, Rodrigo Costa

Front Microbiol. 2022; 13: 904815. Published online 2022 Jul 11. doi: 10.3389/fmicb.2022.904815

PMCID:: PMC9309886

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PMC Images search for Streptococcus phocae

Fig 2Histopathological findings in infected mink.

(A) A section from the inoculation site in the left hind leg in mink inoculated with A. phocae and novel Streptococcus sp. s.c./i.d. shows acute, severe superficial and deep, diffuse neutrophilic inflammation. (B) Severe haemorrhage and diffuse neutrophilic inflammation is seen in the inoculation site in mink inoculated solely with A. phocae s.c./i.d. (C/D) A skin section from the mink inoculated with A. phocae and novel Streptococcus sp. shows sub corneal pustular inflammation with haemorrhages. (E) More deep diffuse neutrophilic inflammation is demonstrated in picture E from skin section from the mink inoculated with A. phocae s.c./i.d. (F) Severe necropurulent inflammation is seen in mink inoculated s.c./i.d. with tissue extract of FENP affected mink. (G) Similar inflammation is seen in mink inoculated with A. phocae. (H/I) Skin section from the control mink injected s.c./i.d. with NaCl solution showed no histopathological lesions.

Experimental Infection of Mink Enforces the Role of Arcanobacterium phocae as Causative Agent of Fur Animal Epidemic Necrotic Pyoderma (FENP)

PLoS One. 2016;11(12):e0168129.
Figure 2

Phylogenetic trees based on genomic sequences from isolated bacteria obtained from the uterus of a spotted seal in Alaska. A. 16S ribosomal RNA gene. Streptococcus phocae sequences as well as the most closely related Streptococcus type strain sequences with at least 800 base pairs aligning with our isolates were downloaded from the 16S rRNA database project and a tree constructed using the most likelihood method and the program PAUP*. Individual S. phocae sequences are indicated by their GenBank accession numbers. The grouping of the isolate with S. phocae sequences has a bootstrap support of 100. B. Phylogenetic tree using partial sequences of the cpn60 gene also yielded bootstrap support of 100 for the grouping of the isolate with S. phocae. C. Phylogenetic tree based on partial sequence of the sodA gene also yielded a bootstrap support of 100 for the grouping of the isolate with S. phocae.

STREPTOCOCCUS PHOCAE ISOLATED FROM A SPOTTED SEAL (PHOCA LARGHA) WITH PYOMETRA IN ALASKA

J Zoo Wildl Med. ;42(1):108-112.
Fig 1Gross pathological changes in infected mink.

(A) Crust formation was detected in i.d./s.c. inoculation site with A. phocae. (B) A incision made in the inoculation site of i.d./s.c. inoculation with A. phocae and novel Streptococcus sp. revealed oedema, necrosis and haemorrhages and pus formation in the skin and in the subcutaneous tissues. (C) Enlarged spleen with mottled surface was detected in mink inoculated with both A. phocae and novel Streptococcus sp. Splenomegaly is a typical change in clinical cases of FENP.

Experimental Infection of Mink Enforces the Role of Arcanobacterium phocae as Causative Agent of Fur Animal Epidemic Necrotic Pyoderma (FENP)

PLoS One. 2016;11(12):e0168129.
Figure 1

Plantar hyperkeratotic and suppurative pododermatitis on the hind (left) and front feet (right) representative of lesions submitted by Canadian mink farmers for A. phocae PCR testing.

Staphylococcus spp., Streptococcus canis, and Arcanobacterium phocae of healthy Canadian farmed mink and mink with pododermatitis

Can J Vet Res. 2015 Apr;79(2):129-135.