Infection of Exophiala salmonis in Atlantic Salmon (Salmo ... - BioOne

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Dec 9, 1983 - Atlantic salmon. (University of. Rhode. Island. Accession. No. M112, ..... City,. New. Jersey,. 158 pp.;. Ellis et al., 1983,. J. Fish. Dis. 6: 511-.
RESEARCH

propriate the test.

positive

MG The

and

negative

controls,

RPA is a reliable, effective presence of HI antibody

diagnostic

prerequisite,

but

cate the occurrence posure. Unfortunately,

of

would

a very

the

Control

field is not a indi-

recent

tween detectable antibody and the carrier state of mycoplasma in wild turkeys is unknown. Until more research is conducted, it can only be assumed that an MG reactor is a carrier of the disease and may be infectious

for

other

wild

and

domestic

be instituted

tion. Research Wisconsin

be-

for

similar to Wyoming,

should

ex-

relationship

programs

turkeys, Michigan,

of Exophiala and

E. J. Otis Kingston, Medicine,

R. E. Wolke,

sources, Wildlife

There

have

been

salmonis Department

three

monids

in

chael, Ajello,

1966, 1975,

fresh

Publ. 304: 126-130; Richards Fish Dis. 1: 357-368), one

llo,

pers.

comm.).

first report the United

This

of infection States.

120-123; Organ. Sci.

et al., in error

note

describes

by

E. salmonis

1978, (Ajethe in

Over a 4-mo-period (April-June 1982), three adult Atlantic salmon (University of Rhode Island Accession No. M112, M151, and M657) with similar lesions were necropsied

at

the

Comparative

Aquatic

Pa-

thology (CAP) Laboratory, University of Rhode Island. Originally obtained from hatcheries in East Orland, Maine and New Brunswick, Canada, these fish had been held at the University Aquaculture Center in a partial reuse system for up to 20 mo

publication

9 December

precau-

provided of Natural

by

the Re-

the Welder Texas, and

Agricultural and of Wisconsin,

Life SciMadison,

of Wildlife

1983.

Diseases. 21(1), © Wildlife Disease

(Salmo

1985, pp. Association

salar

and Pathology, University of of Medical Microbiology, College

to death.

City

at 12 to 18 ppt rock salt. Fish

61-64 1985

L.)

Rhode

Island,

of Veterinary

water

salinity were

was

by the fed raw

maintained addition calf’s

of liver

supplemented with vitamins. Tissues from fish were fixed in 10% neutral buffered formalin, paraffin embedded, sectioned at 6 tm and stained with hematoxylin and eosin. Special stains included periodic-acid Schiff (PAS) and Grocott’s silver of Histologic Armed Forces Washington, Accession

stain (Luna, 1968, Manual Staining Methods of the Institute of Pathology, D.C., 258 No. M112

coloration

3.0

mm

pp.). had a reddish

in diameter

dis-

on the

sur-

face of the liver which extended into the parenchyma. Postmortem examination of M151 revealed petechial hemorrhages throughout the viscera. The pyloric cecae contained approximately todes (Eubothnium capsule

parenchyma for

Wisconsin, California

USA

kidney Received

in and

Wisconsin, Sinton

Salmon

Department

prior

(Carmi5:

J.

30602,

in sal-

saltwater

Sabouraudia Pan Am. Health

Blazer,

reports

salmonis

and

in Atlantic

of Fisheries, Aquaculture

previous

of Exophiala

of infections

61

in translocated

as a necessary

Madison, Foundation,

the College of ences, University Wisconsin.

REPORTS

birds.

USA; and V. S. Athens, Georgia

Rhode Island 02881, University of Georgia,

MG those

funds were Department

Journal

Infection

NOTES/CASE

M657

was

sp.).

was

thickened

mottled cachexic.

50 adult cesThe posterior

gray. An

and Accession

ulceration

the No.

(1.0

cm

62

JOURNAL

OF WILDLIFE

1.

FIGURE

branching

Central

fungal

DISEASES,

portion

hyphae

of

VOL.

two

(arrows),

21, NO

1, JANUARY

microabscesses masses

of

1985

in the

posterior

polymorphonuclear

kidney cells,

and

of an

Atlantic

salmon.

macrophages

are

Septate,

present.

PAS

stain. x400,

diameter) was right pectoral were present

present just posterior to the fin. Petechial hemorrhages on the ventral surface be-

tween

the

pectorals.

tained

four

adult

sp.). The its capsule raised When The black

posterior opaque.

gray areas cut a white

The

hindgut

cestodes kidney The

was kidney

swollen had

1.0 cm in opaque fluid

Accession

No.

eosinophilic the submucosa.

Ml

12

had

red

to

liver. and and

inflammation lesions consisted

tubular

and a nephritis

in

necrosis,

nephrocalcinosis

diffuse granulomatous interstitial reminiscent of bacterial kidney

disease

(Wolke,

Fishes, Wisconsin

Ribeln and Migaki Press, Madison,

1975,

There

of fungal filtrated

etiology. Necrotic with polymorphonuclear

(PMN’s)

cytes

up 10.0

to

30.0

a focal

(70%),

m apart.

Grocott positive. Accession No. ic granulocytic

was

In

33-116).

and numerous septate hyphae.

microscopic

intestine, kidney and mucosa was sloughed hemorrhage, necrosis

granulocytic Kidney

and three

diameter. appeared.

surrounding parenchyma was and of a watery consistency.

changes in the The intestinal there was focal

con-

(Eubothriuni

of focal

light Hyphae wide. The M151 gastritis

Pathology

acute

Septae

had and

Univ. pp.

hepatitis

tissue

macrophages brown, were

fungus

of

(eds.), Wisconsin,

was inleuco-

(30%) branching frequently were

was an

8.0 PAS

to and

eosinophil-

enteritis,

p05-

RESEARCH

sibly

in

response

to

the

cestodiasis.

NOTES/CASE

REPORTS

63

The

posterior kidney contained masses of fungal hyphae identical to M 1 12, most often within multifocal microabscesses. The center of percentage

the

abscesses contained polymorphonuclear

of

a high leuco-

‘1

cytes (90%), while the periphery was characterized by fibroblastic proliferation and mononuclear cell infiltration. Focal congestion occurred in the liver, spleen,

and

cinosis, orrhage

abscesses, and large

kidney

of

anin were present vessels frequently and zone

in the contained

PMN’s. The of liquefactive

ments

and

this

zone

The

Nephrocal-

leucocytes were

hemmel-

1).

of

PMN’s

(70%), (10%), tubular

cells. Mononuclear at the periphery. was scant. of

M657

cells preFibroblastic was

cultured

Raised, mouse mm in diameter incubation at

C. Microscopic ined by the slide

morphology was examculture method (Riddell,

1950,

42:

Mycologia

characteristic and Stewart, Handbook, York, 436 accumulated

265-270).

pp.) in

produced balls at

For monis 25

experimental was grown

C for

sions Wolke Three gairdneni) 24.0 (IP) Two 15.5

3 wk.

Hyphal

cm) with

juvenile (total

rainbow lengths

were injected 0.2 ml of the

juvenile and 17.0

as

inoculations in the dark

were prepared (1979, J. Fish

and

to 25

(Campbell Mycology Sons, New

conidia the tips

The fungus was identified salmonis Carmichael.

on

Annellides

of Exophiala sp. 1980, The Medical John Wiley and

which (Fig. 2). Exophiala

on spore

E. salCMA at suspen-

as by Blazer and Dis. 2: 145-152). trout 13.0,

(Salmo 15.4, and

intraperitoneally hyphal suspension.

rainbow trout (total cm) were injected

lengths IP with

2.

FIGURE

Bordering

and lymphocytes interstitial and

Corn Meal Agar (CMA). dark gray colonies 7-10 appeared after 10 days

‘I

kidney. Blood histiocytes

(Fig.

masses

kidney

of

abscesses had a central necrosis, fungal ele-

histiocytes (20%) as well as necrotic epithelial dominated proliferation

M657.

focal interstitial accumulations

Eight-day-old

phiala

salmonis

nidia

accumulating

cytoplasmic

protrusion and

aqueous

phloxine,

ml

(1.6

of

x

10

Center. Twelve fish were killed, tissues fixed for

gal

elements

the

stain.

1966,

any

tissue.

infections

salmon

op. The

the

spore

sus-

of experof fun-

CMA

after inability

of

E.

to produce lesions

cit.;

Richards

lesions were

the 1.0%

x 1,000.

examination no evidence

negative C. The

been reported ic granulomatous cit.).

of

(m).

kidney

1 mo incuto experi-

mentally infect fish is consistent vious reports (Carmichael, 1966, Natural

Note

apex

cells

of

co-

annellide.

days post-inoculation the the kidneys cultured, and light microscopic exami-

in

were at 25

at

spores)

Histological fish revealed

cultures bation

an

Exo-

clavate

fish were kept in a flow in the CAP laboratory with source as the Aquaculture

pension.

nation. imental

of

KOH

of

to

moniliform

10.0%

The through system the same water

tip

(arrow)

a chain

culture

cylindrical

at the

annellide

0.2

slide

showing

acute

found and

with op.

salmonis

precit.). have

systemic chron(Carmichael, et

al.,

in

these

are

best

1978,

op.

Atlantic described

as abscesses, with the predominant cell type the polymorphonuclear leucocyte. There has been some debate as to whether fish are able to produce a purulent exudate. However, abscesses and purulent exudates have been previously reported in fish (Fijan, 1968, Bull. Wildl. Dis. Assoc. 5: 109-110; Finn and Nielson, 1971, J. Fish

JOURNAL

64

Biol.

OF WILDLIFE

3: 463-478;

op.

DISEASES,

Blazer

and

VOL

21, NO.

Wolke,

1, JANUARY

1979,

Exophiala from soil

cit.).

A review fish (Ajello,

of the 1975,

phaeohyphomycoses op. cit.; Neish

1985

cology

of and

salmonis (DeHoog, No.

15,

Schimmelcultures, The rock salt

Hughes, 1980, Fungal Diseases of Fishes, Snieszko and Axelrod (eds.), TFH Publications, Neptune City, New Jersey, 158 pp.; Ellis et al., 1983, J. Fish Dis. 6: 511-

stored

dividuals that are immunosuppressed or otherwise compromised are predisposed to these opportunistic pathogens. The Atlantic salmon in this study had not fed well in captivity, and had just undergone

Jersey, The

an unsuccessful spawning period. The cestode infections could have weakened the fish, and provided a route of entry for the fungus with subsequent hematogenous spread to the kidney.

Control

in

(Canis

latrans

Brent L. Carison and

Natural

The creasing United tional

many

Received

from

and Svend

University

coyote has frequency States and

been

wild

the

fish,

species

for

Northeastern of Connecticut, Storrs,

diseases

and

par-

to man and domestic osleri (=Filaroides osnematode reported from

of wild

canids

and

domestic

in North America, Europe, Africa, and Australia (Mills, 1967, J. Small Pract. 8: 37-43; Pence, 1978, Proc.

for

publication

28

February

with

Dr. R.

lation of the organism and A. Padhye of the for

Contribution Experiment

103-104). salinity was

0.

soil.

The

the system via in water of inwater for osCech, 1982, Ichthyology, Cliffs, New

L.

T.

Smith

Bennett

for

for

iso-

and Drs. L. Ajello Center for Disease

identification

of

No. 2173 of the Station, University

the

fungus.

Agricultural of Rhode

Island.

1879)

of Wildlife Diseases, 21(1), © Wildlife Disease

1985,

64-65 1985

pp.

Association

in Coyotes

Connecticut

observed with inin the northeastern may serve as an addi-

reservoir

pp.

contact

593 pp.). authors thank

providing

(Cobbold,

W. Nielsen,

Resources,

asites transmissible animals. Oslenus len) is a tracheal dogs Asia, Anim.

Say)

osleri

voor

(Moyle and Introduction to Inc., Englewood

Journal

of Oslerus

Baarn, to maintain

used

outdoors

moregulation Fishes: An Prentice-Hall,

isolated in My-

Centraalbureau

fungus could have entered the salt. Fish when placed creased salinity will swallow

523) shows interesting parallels to the cases herein reported. The mycoses are systemic in nature and occur only in captive or hatchery-raised fishes. It appears that in-

Prevalence

has been 1977, Studies

1984.

Research Center for Wildlife Connecticut 06268, USA

Helminthol. Morrison

and

314-316;

1979,

Dunsmore and tol. 5: 275-286; In

Worldwide

Soc. Gier,

J.

College of

Diseases,

Wash. 1978,

J.

Wildl.

Agriculture

45: 103-110; Wildl. Dis.

Dis.

14:

15: 557-559;

Spratt, Pence

1979, Vet. and Custer,

Parasi1981,

Furbearer

Conference

Pro-

ceedings, Vol. II, Chapman (eds.), Worldwide Furbearer Inc., Frostberg, Maryland, Foreyt and Foreyt, 1982,

J.

and Pursley Conference, pp. 760-845; Parasitol. 67:

284-286; Seesee et al., 1983, J. Wildl. Dis. 19: 54-55). Since there are no previous reports of 0. osleni infection in coyotes in the northeastern United States, the pres-