Vibrios – A
Survey of the Marine Microbes
©1998
Jonathan Lowrie
Introduction
Just mentioning the word “Vibrio” around veteran aquarists
can cause quite a stir. These small
comma shaped bacteria, when discussed as a genus, refer to gram-negative, motile, facultatively anaerobic
curved rods. They can also spell
disaster for marine aquarists, as Vibrios are pathogeneic to many marine
organisms. There are tentatively over
175 species of Vibrios, and possibly many more when sub-strains are taken into account. Some Vibrios release enterotoxins that affect
intestinal tissue, while others release exotoxins that are so fast acting that mortality
can result within hours after exposure. As such, certain species pose a risk not only
to various marine animals, but also to humans who are in contact with
them. The following is an overview of
some of the more well known Vibrios in the marine environment, their
identification, effect, and treatment for both marine animals and humans.
General Description
Vibrios belong to the family Vibronacae, a group composed of curved gram-negative, catalase and
oxidase producing bacteria that include three genera: Vibrio, Aeromonas, and
Plesiomonas. Gram-negative rods, as a
group, are considered important because of the public health risks typically associated
with them. The gram negative rods can be further divided into: aerobic rods and
cocci, facultative anaerobic rods, and anaerobic straight, curved, and helical
rods - typically motile with polar flagella.
The term "vibrioid" is used to describe the typical curvature
in their shape. Vibrio belong to the facultative aerobe group, as they can grow
under both aerobic and anaerobic conditions. They are fermentative to a variety
of substrates, can reduce nitrate to nitrite, and many are capable of digesting
chitin and cellulose
The following chart lists common facultative anaerobic gram-negative
rods that are pathogenic to man (and many higher animals), exclusive of Vibrio
Escherichia
coli
|
Opportunistic
and occasionally lethal infections
|
Shigella
dysenteriae
|
dysentery
|
Salmonella
typhi
|
Typhoid
fever
|
Salmonella
sp.
|
Food
poisoning
|
Klebsiella
pneumoniae
|
Pneumonia
|
Yersinia
pestis
|
Bubonic
plague
|
Pasteurella
multocida
|
Animal
bite infections
|
Haemophilus
influenzae
|
Meningitis,
pediatric disease
|
Location
Vibrios are found worldwide, primarily in water, and are
often found in marine and brackish environments such as coastal waters and estuaries.
They are found most often in nutrient rich, warm, polluted and relatively
unflushed areas. Vibrios also prefer
alkaline environments with a pH of 8.5-9.0. Most also grow best in salinites
that range from 5-20 ppt. Both pathogenic and non-pathogenic strains are
commonly isolated from bays, river outlets, and sewage treatment sites, as well
as some species occurring in oceanic waters.
As such, many are halophilic,
meaning “loving salt . Most marine Vibrios can grow in sea water with ammonium
and glycerol alone as nutrients. This environment is also ideal for the
shellfish so commonly associated with
Vibrio infections. Those species
common to open ocean and low nutrient water tend to be smaller and coccoid in
shape.
Much work needs to be done is isolating various sources for
Vibrios in the environment, as they are periodically found associated with
various micorenvironments such as sediments, zooplankton, shellfish, worms,
plants, and the intestinal tracts of marine vertebrates. Vibrios are also found normally in the
intestinal tract of animals feeding on zooplankton, and in sediments enriched
with the feces of animals who have fed on zooplankton. Many other Vibrios exist
in the marine environment, some completely unknown and/or unspeciated, and may
be more or less pathogenic to fish and humans.
Occurrence of Some Common Vibrios
|
Open ocean
|
Estuaries
|
Mollusks
|
sediment
|
Fish
|
Crust
aceans
|
Corals
|
Fresh
water
|
aesturaianus
|
|
X
|
|
|
|
|
|
|
alginolyticus
|
X
|
X
|
X
|
X
|
X
|
X
|
X
|
X
|
anguillarum
|
X
|
X
|
X
|
|
X
|
X
|
|
X
|
campbelli
|
|
|
X
|
|
|
|
|
|
carchariae
|
X
|
|
X
|
|
X
|
X
|
|
X
|
Charcharia
|
|
|
|
|
|
|
X
|
|
cholerae
|
X
|
X
|
|
|
X
|
|
|
X
|
cincinnatiensis
|
|
|
|
|
|
|
|
|
damsela
|
X
|
|
X
|
|
X
|
|
|
|
diazotrophicus
|
|
X
|
|
|
|
|
|
|
fischeri
|
X
|
X
|
|
|
X
|
X
|
|
|
fluvialis
|
|
X
|
|
|
|
|
|
|
furnissii
|
|
|
|
|
|
|
|
|
harevyi
|
|
|
X
|
|
X
|
|
|
|
hollisae
|
|
|
|
|
|
|
|
|
marinus
|
X
|
X
|
X
|
|
|
X
|
|
X
|
Mediterranei
|
|
|
|
|
|
|
X
|
|
metschinikovii
|
X
|
X
|
X
|
|
|
X
|
|
X
|
mimicus
|
|
|
|
|
|
|
|
|
ordalli
|
X
|
X
|
X
|
|
X
|
X
|
|
|
orientalis
|
|
|
X
|
|
|
|
|
|
parahaemolyticus
|
|
X
|
X
|
X
|
X
|
X
|
X
|
|
pelagia
|
X
|
|
X
|
|
|
|
|
|
splendidis
|
|
|
X
|
|
|
X
|
|
|
vulnificus
|
|
X
|
X
|
X
|
X
|
X
|
X
|
|
Biology
Vibrios have a fermentative and respiratory metabolism. They are typically flagellated, contributing
to their nature as highly pathogenic. Generally, Vibrios are of high tissue
virulence, although not all have high epidemic virulence. In other words, they
are generally not highly contagious. Hemolysins, exotoxins, and enterotoxins
are commonly produced by Vibrios as part of their pathogenic response in
affected animals. At least some species
also produce their own antimicrobial agents effective against other bacteria. These
compounds are vibriocin and microcin. Interestingly, V. cholerae and other Vibrio
spp. from estuarine and other marine environments also produce
tetradotoxin, a potent neuromuscular toxin previously associated only with
pufferfish.
Some Vibrios are called "swarers," and have
lateral, rather than polar, flagella that aide in their attachment to
substrates.
Commercial Hazards
Vibrio is not only a human public health hazard, but it’s an
economic hazard since it can infect shellfish and become a common economic
problem when harvests are contaminated with Vibrios. Many of the recent "seafood scares"
in public media have been based on oysters contaminated with V. vulnificus. Also, many commercially
important food fish and eels are susceptible to Vibrio infections, thus
depleting the numbers available for fishermen.
Caught fish typically have a normal intestinal flora of slightly less
than 50% Vibrio spp., with bottom
dwelling, sediment-associated and commercially available flatfish (flounder,
halibut, sole) having up to 100% of the normal
intestinal flora composed of Vibrio
spp.. V. marinus is but one such
common component of fish gut flora. V.
fischeri, also a gut flora species, is
now considered to be part of a newer taxa of luminescent bacteria, Photobacterium spp .
Animal Hazards
Vibrio spp. affect
other terrestrial animals than humans, as well. V. parahaemolyticus , most
commonly associated with muddy sediments and zooplankton, can cause acute
enteritis in avian species like mynahs, canaries, parakeets, and finches. Water
fowl and game are also at risk, as V. metchinokovii
can produce a subacute disease characterized by hemorrhagic enteritis. The same symptoms can be caused by a Vibrio sp. in masupials and
monotremes. Swine and other peccaries
can contract a severe intestinal malady
from V. coli. Vi. chloerae can affect primates, and has been isolated in
frogs and birds. One of the common factors in many cases of Vibrio disease is the source. Contaminated water seems to be a prevalent
source for Vibrio infection. Most of the
terrestrial animals that succumb to the numerous Vibrio infections have
encountered, drank from, or bathed in water ripe with Vibrios. Most of the birds and land mammals that
contract Vibrio do so via a common
watering hole. It is possible that
original freshwater contamination of many of these sites was from the bird
droppings of an infected avian.
Human Hazards
As a human public health hazard, Vibrio ranks very high,
causing a number of primarily enteric (intestinal) infections. Vibrios affect
humans primarily through the ingestion or contact with infected shellfish (raw
oysters, clams, and crustaceans). Vibrio
cholerae, the agent that causes cholera in humans, is common in third-world
nations with less than ideal sanitary conditions and poor sewage management
practices. The disease is caused by drinking water contaminated with the V. cholerae bacterium, and it can cause
severe dehydration from diarrhea. Vibrio
parahaemolyticus is a bacteria which causes an infection of the intestinal
system. The disease is characterized by
watery diarrhea and abdominal cramps.
The main transmission of this Vibrio to humans is through eating raw
oysters. Vibrio vulnificus is another deadly Vibrio to humans. It is also one associated with shell fish
poisoning, and the ingestion of this bacteria by healthy individuals can lead
to gastroenteritis and death. Death by
diarrhea is not a pleasant thought, and it is no wonder that so much media
attention has been focused on this species in recent years.
Eleven Vibrio species
are known to be pathogenic to humans and are found in the marine environment.
There are likely to be other human pathogenic species yet to be identified, as
well as unreported cases of either misidentified Vbrio species, or of known but
unnamed species. The Centers for Disease Control and Prevention also have
evidence of disease being caused by those working with fish and marine mammals.
Workes are reported as getting Vibrio associated skin lesions just from handling fish, shellfish or
pinnepeds. Humans are at risk of
Vibrio caused zoonosis from animal sources, as well.
Vibrios Pathogenic to Humans
|
Disease caused
|
V. alginolyticus
|
Septicemia
Enterocolitis
Conjunctivitis
Stump/skin ulcers
|
V. carchariae
|
Gastroenteritis
|
V. cholerae
|
Cholera
|
V. damsela
|
Skin lesions
|
V. fluvialis
|
Gastroenteritis
|
V. furnissi
|
Gastroenteritis
|
V. hollisae
|
Gastroenteritis
|
V. marinus
|
Skin lesions
|
V. metschinikovii
|
Gastroenteritis (?)
|
V. mimicus
|
Gastroenteritis
|
V. parahaemolyticus
|
Gastroenteritis,
Septicemia,
Wound infection
|
V. vulnificus
|
Gastroenteritis,
Septicemia,
Wound infection,
Meningitis,
Pneumonia,
Keratitis
|
Marine Animal Hazards
There are also a number of Vibrios that are pathogenic to
fish species. These include V. fischeri, V. anguillarum, V. damsela, V. ordelli, V.alginolyticus,
V. vulnificus and V. carcharriae,
among others. In fish, the term vibriosis
describes a number of symptoms and synonyms, including “red pest,” "red
sore," "red spot," "red disease," saltwater
furunculosis, boil disease, Hitra disease, and ulcer disease caused by V anguillarum. Vibriois, a type of
septicemia can cause skin discoloration, lesions, mouth and fin infections,
gastric infections, exopthalmia, gut and organ distention and swelling,
hemorrhagic lesions, and local necrosis. Poor water conditions, overcrowding in
aquaculture facilities, heavy nutrient loading of coastal waters, and high
temperature can all lead to increased outbreaks and infection. The treatment
for Vibrio infections in fish populations is generally acoomplished with the
use of sulfa antibiotics.
Vibrio angulliformes and V.
damsela are a hazard for American eels.
At various stages, these infections reach epidemic proportions within
the eel population. The infected eels
cannot be used for human consumption, and this is an economic hardship. Other commercial fishes are also
affected. Common skin lesions show up on
fish in the infections resulting from
Vibrio parahaemolyticus.
Interestingly, the shellfish infected with Vibrios do not
usually show signs of infection, as Vibrio are typically non-pathogenic to
them. For example, it is not easy to
tell if a contaminated oyster has active disease, as it will show no signs of
illness without histological examination.
Most invertebrates, especially those adapted for filter feeding and
bacterial capture, seem largely immune to Vibrio virulence except in
opportunistic infections resulting from stressful conditions.. However,
V. anguillarum, V. alginolyticus, V. parahaemolyticus, V. pelagia, and V splendidus can cause Vibriosis in
oysters and shellfish with an exotoxin that inhibits larval swimming. In adult
shellfish, the effects of Vibrio pathogenicty are typically a loss of digestive
function , loss of motility, and velum abnormalities. Mass mortalites are more
frequent during the warmer summer months. Cytolysis and/or hemolysis may occur
in advanced stages. Even so, it has been repeatedly mentioned in such reports
that these cases are ones in which
Vibrio pathogens in shellfish are regarded as opportunistic since such occurrences typically occur in
highly stressed hatcheries.
V. anguillarum
plays a very clear role in fish and eel disease, but the problem with
determinations of many ubiquitously associated Vibrios is that they are common
to both healthy and diseased fish and marine life. Thus, their role in
pathogenicity, if any, is often quite loosely fit. Furthermore, there are two
Vibrios now classified as Photobacterium spp., that are associated with
bioluminescent organs. A mutualistic relationship existss between sea urchins
and V. diazotrophicus, as well as between other Vibrio spp. and shellfish.
Vibrios Pathogenic to Marine Life
|
Fish
|
Mollusks
|
Crustaceans
|
Cnidarians
|
Type AK-1
|
|
|
|
X
|
V. alginolyticus
|
X
ulcer disease
|
X
|
X
|
|
V. anguillarum
|
X
vibriosis
|
|
|
|
V. campbelli
|
|
X
|
|
|
V. carchariae
|
X
vasculitis
|
|
|
|
V. cholerae
|
X
Petechial
hemorrahage
|
|
|
|
V. damsela
|
X
Skin lesions
|
X
|
|
|
V. fischeri
|
X
|
|
|
|
V. harveyi
|
X
|
X
|
|
Briareum sp.?
|
V. metschnikovii
|
|
X
|
|
|
V. ordalli
|
X
vibriosis
|
|
|
|
V. orientalis
|
|
X
|
|
|
V. parahaemolyticus
|
X
Ulcer disease
|
|
|
|
V. splendidis
|
|
X
|
|
|
V. vulnificus
|
X
Skin lesions
|
|
|
|
Susceptibility and
Determination.
The three basic tests used to isolate the genus from other
bacteria are growth: on TCBS nutrient medium, anaerobic growth, and
susceptibility to the 0/129 compound. Agent 0/129 (2,4 diamin, -6, 7
diisopropyl pteridine) is a compound used in determinative assays of Vibrio,
and is a vibriostatic agent to which many Vibrios are susceptible. Approximately 50% of species are susceptible
to the antibiotics chloramphenicol and polymyxin-B. Tetracycline is also
commonly used along with terramycin is sensitivity assays. Many Vibrios are susceptible to one or more
these agents. Most are resistant to heavy metals. Various substrates and agars
can be used, along with fermentation tests, etc. in the speciation of Vibrios
in basic determinative bacterial plating assays.
General Determination of Vibrios
Exclusive of Strains
Algino
lyticus
|
Anguil
larum
|
Car
chariae
|
Cholerae
|
Damsela
|
Fluvialis
|
Metsch
nikovii
|
Ordalli
|
Para
haemo
lyticus
|
Vulni
ficus
|
|
R
S
|
S
S
|
R
S
|
S
S
|
S
S
|
|
|
S
S
|
R
S
|
S
S
|
0/129
10µg
150µg
|
+
|
-
|
+
|
-
|
-
|
|
|
-
|
V
|
-
|
Swarming
|
-
+
+/V
|
+
-
-
|
-
+
+
|
-
+
+
|
+
-
-
|
+
-
-
|
V
V
-
|
-
-
-
|
-
+
+
|
-
+
+/-/V
|
Amino acids
Arg
Lys
Orn
|
A
-
a
-
a/+
|
A
-
a
-
a
|
A
-
a
a
a
|
A
-/+
a
-
a/+
-
|
Ag
-
ag
-
-
|
-
+
+
|
V
-
+
-
|
A
-
-
-
a
|
A
-
a
-
-
V
|
A
A
A
A
-
|
Fermentation
Glu
Lac
Man
Sal
Suc
Ara
|
-
|
-
|
+
|
-
|
+
|
|
|
-
|
V
|
V/-
|
urease
|
+
|
+
|
+
|
+
|
-
|
-
|
V
|
-
|
-/+
|
-/+
|
Indole
|
-
+
+
+
+
|
V
+
+
v
-
|
-
+
+
+
-
|
V/-
+
v
-
-
|
-
+
v
-
-
|
V
-
|
-
V
-
|
-
+
+
-
-
|
-
+
+
+
-
|
-
+
+/-
-
-
|
%NaCl growth
0
3
6
8
10
|
+
|
-
|
-
|
+
|
-
|
|
|
-
|
+
|
+/-
|
42oC
|
+
|
|
|
+
|
|
+
|
-
|
|
+
|
+
|
NO3>NO2
|
+
|
|
|
+
|
|
+
|
-
|
|
+
|
+
|
oxidase
|
The, synergistic combination on sulfonamides and
trimethoprim is a commonly used antibiotic treatment of Vibrio infections. Polymyxin B is another antibiotic commonly
used for its effect on many species of
Vibrio. Increased oxygen tension can also be used for a bacteriostatic effect.
Some are also effected by hydrostatic pressure - in other words, they are less
likely to grow at deep depths, as has been shown for V. alginolyticus and V.
marinus.
General Antibiotic Susceptibility for Vibrios
|
Dosage
|
Route
|
Target
|
Species affected
|
Aminoglycosides
|
|
|
|
V. vulnificus
|
Ampicillin
|
|
|
|
V. vulnificus
|
Chlorampenicol
|
|
|
|
Vibrios.
V. vulnificus,
parahaemolyticus
|
Cotrimoxazole
|
|
|
|
V. vulnificus
|
Erythromycin
|
|
|
|
V. parahaemolyticus
|
Furanace
|
2 mg/l
|
Bath
|
Trout
|
Vibrios
|
Gentamycin
|
|
|
|
V. parahaemolyticus
|
Halquinol
|
25 mg/l
|
Bath
|
Turbot
|
Vibrios
|
Kanamycin
|
|
|
|
V. parahaemolyticus
|
Piromidic acid
|
10-40 mg/kg
|
Oral
|
Salmon, eels
|
Vibrios
|
Polymyxin B
|
|
|
|
Vibrios
|
Sulfadoxine - TMP
|
30 mg.kg
|
Oral
|
Ayu
|
Vibrios
|
Sulfamethoxazole -
TMP
|
25 mg/l
|
Bath
|
Turbot
|
Vibrios
|
Teracycline
|
|
|
|
Vibrios,
V. vulnificus,
parahaemolyticus, cholerae
|
Vibrios on the Reef and in Aquaria
As mentioned, Vibrios are ubiquitous and important
components of marine environments. Their occurrence in oceanic and reef
environments is much less common, but they still exist. Vibrios are found in all types of sediments
and on substrates, especially those
enriched with organic material. Soft
lagoonal sediments will find higher numbers of
Vibrio spp than coarse reef sediments.
Vibrios play a role in denitrification and nutrient regeneration, as
they are capable of fermentation and reduction.
Vibrios are also extremely common
components of coral mucus. Their pathogenicity to invertebrates is unreported
except as opportunistic species capable of potential pathogenicity. One species has found to induce coral bleaching in
extenuating circumstances Some, like V.
vulnificus, may be nutrient limited; in the case of V. vulnificus, iron appears to be essential for the cytolysin
activity. Under nutrient limitation, Vibrio readjust their metabolism toward
long term stasis, adhering tightly to substrates until conditions are more
suitable for their growth and reproduction.
Thus, it is unlikely that one can “get rid” of Vibrios in a marine
environment.
Corals are known to both culture and utilize both bacteria
and bacterial byproducts that are grown on and near their mucus. Most Vibrios
associated with coral mucus are swarmers, and seem especially suited to their
carbohydrate rich medium. Several species are part of the normal bacterial
flora of coral mucus and can comprise well in excess of 50% of total microbial
populations in both soft and stony corals.
The two Vibrio species persistently found associated with coral mucus
are V. parahaemolyticus and V. alginolyticus. At least V. parahaemolyticus shows the potential
to be pathogenic to coral tissue, especially under stress, although their
presence seems to indicate that both are non-pathogenic and normal flora
associated with corals. V. campbelli and V. haloplanktis have been found as normal non-pathogenic strains on
healthy colonies of Briareum abestinum.
Decomposing coral tissue (and any decomposing organic matter) seems to be
quickly settled by Vibrios, and various unidentified strains, along with V. fluvialis, V. furnissi, and V haloplanktis have been identified in
such cases.
To further illustarte the innateness of reef invertebrates
and Vibrios, the toxin of V. cholerae
peptides from V. alginolyticus, and
small molecules of V. cholerae present
in bacterial film, induce the settlement of various invertebrate larvae. Corals, especially, seem likely to settle on
bacterial films dominated by those species common to their normal microbial
flora, specifically V. alginolyticus..
Gorgonians and other soft corals produce a number of antimicrobial compounds
that show a wide range of effects on various bacteria, with specificty leant
towards those bacteria which are potentially non-native and pathogenic to their
area and surface composition. Perhaps
not coincidentally, they have been found to have a very low activity against
Vibrios. Similarly, scleractinian corals
also produce a wide range of antimicrobial substances that help reduce surface
fouling that can lead to pathogenicity and stress. V.
parahaemolyticus and V. algnolyticus
are often initial colonizers in such cases, as might be expected by their
abundance and regular presence on coral and substrate surfaces. As with
gorgonian studies, stony corals show little activity towards V. parahaemolyticus, despite most corals
showing significant and often specific activity towards various other bacterial
species. Only Tubastraea sp. shows any significant activity, and this is against
against V. alginolyticus. Given their
propensity to have these bacteria dwelling on their surface, if pathogenicity
was a significant threat, it is likely that substances would be produced to
show antibacterial action towards them; yet, this does not occur in species
studied thus far over the past 40 years to the very recent studies The discovery several years ago of an unnamed
Vibrio (type AK-1) as an agent of coral bleaching was the first record of Vibrio
pathogenicity in corals. Brown
(1997) has confirmed that the
circumstances of its occurrence were unusual.
Conclusion
Vibrios are a unique bacterial constituent of marine and
estuarine environments. They have become
quite infamous because of their tendency towards virulence and pathogenicity in
humans and ornamental fish. Certainly,
they can be quite dangerous, and care should be excercised when working with
aquariums, specifically corals and substrates where these microbes tend to
exist prolifically. Cuts and openings in
the skin should be protected, with hand washing using a true antibacterial soap
performed after handling or working in aquarium water. Any cuts or abrasions that occur from working
in an aquarium should be immediately attended to with antibiotic
applications. Not only are Vibrios a
potential danger in aquaria, but there are many other genera which have equally
dangerous potentials for infection and disease.
Nonetheless, it should be apparent that the thought of Vibrios in the
aquarium should not be met with trepidation, but understanding. These bacteria play a number of important
roles in marine habitats, from denitrification to providing settlement cues and
acting as trophical resources for many organisms. Their presence is normal to the environment,
and, hopefully, understanding these bacteria will allow them to be met with
less fear and a greater appreciation of their role and presence both in the
wild and in marine aquaria.
References
Austin,
B. 1988. Marine Microbiology. Cambridge University Press, Cambridge: 122-7.
Baross,
John A., Joe Hanus, and Richard Y. Morita. 1976. Effects of hydrostatic
pressure on uracil uptake, ribonucleic
acid synthesis, and growth of three obligately psychrophilic
marine Vibrios, Vibrio alginolyticus,
and Escherichia coli. In: Marine Microbiology (Carole D. Litchfield,
ed.). Dowden, Hutchinson & Ross, Inc., Stroudsberg,
Pennsylvania: 180-201.
Carpenter,
C.C.J. 1979. More pathogenic vibrios. N. Engl. J. Med. 300: 39-41.
Coffroth,
M.A. 1990. Mucous sheet formation on poritid corals: an evaluation of coral mucus as a nutrient source on reefs.
Marine Biology. 105: 39-49.
Colwell, Rita R., ed. 1984. Vibrios in the Environment. John
Wiley & Sons, New York. 512+ pp.
Colwell, R.R., and D,J. Grimes. 1984. Vibrio diseases of
marine fish populations. Helgolaender
Meeresuntersuchungen 37: 265-87.
Colwell, Rita R. 1982. Genetically engineered organisms in
the ocean environment – risks and
benefits. In: Microbes in the Sea (M.A. Sleigh, ed.). Halsted Press, New York: 182-90.
Colwell, R.R. 1977. Vibrios. Science 198: 344-96.
Colwell, R.R., and R.Y. Morita. 1974. Effect of the Ocean
Environment on Microbial Activities.
Proceedings of the 2nd United States-Japan Conference on Marine Microbiology. University Park Press,
Baltimore.
Colwell, R. R., and J. Liston. 1961. Taxonomic relationships
among the Psuedomonads. J. Bacteriol.
82: 1-14.
Ducklow,
Hugh W., and Ralph Mitchell. 1979.
Composition of mucus released by coral reef
coelenterates. Limnol. Oceanogr. 24: 706-14.
Ducklow,
Hugh W., and Ralph Mitchell. 1979.
Bacterial populations and adaptations in the
mucus layers on living corals. Limnol. Oceanogr. 24: 715-25.
Fernandez,
C.R., and G.A. Pankey. 1975. Tissue invasion by unnamed marine vibrios. J. Am. Med. Assoc. 233:
1173-6.
Ford,
Timothy Edgcumbe, ed.1993. Aquatic
Microbiology: An Ecological Approach. Blackwell
Scientific Publications., Boston.
Gratzek, John B., and Janice R. Matthews. 1992. Aquariology:
The Science of Fish health Management.
Tetra Press, N.J. 330 pp.
Gray, Larry D., and Arnold S. Kreger. 1985. Purification and
characterization of an extracellular
cytolysin produced by Vibrio vulnificus.
Infection & Immunity 48: 62- 72.
Grimes, D.J., et. al. 1984. Vibrio species as agents of elasmobranch disease. Helgolander Meersuntersuchungen 37: 309-15.
Ivanova, E.P., et. al. 1998. Impact of conditions of
cultivation and adsorption on antimicrobial
activity of marine bacteria. Marine
Biology 130: 545-51.
Jensen, P.R., et. al. 1996. Antimicrobial activity of
extracts of Caribbean gorgonian corals.
Mar. Biol. 125: 411-19.
Johnson, Craig R., et. al. 1997. Bacterial induction of
settlement and metamorphosis in marine
invertebrates. 2: 1219-24.
Joklik, Wolfgang K., et. al., eds. 1988. Zinsser
Microbiology. Appleton & Lange, Norwalk,
Connecticut. 1053 pp.
Kjelleberg, S., M. Hermansson, and P. Marden. 1987. The
transient phase between growth and
nongrowth of heterotrophic bacteria, with emphasis on the marine environment. Ann. Rev. Microbiol.
41: 25-49.
Koh, Esther G.L. 1997. Do scleractinian corals in engage in
chemical warfare against microbes.
J. Chem. Ecol. 23: 379-98.
Kreger, Arnold, and Donald Lockwood. 1981. Detection of
extracellular toxins produced by Vibrio vulnificus. Infection &
Immunity 33: 583-90.
Krupp, David A. 1984. Mucus production by corals exposed
during and extreme low tide. Pacific
Science 38: 1-11.
Kushmaro,
A., Y. Loya, M. Fine, and L Rosenberg.
1996. Bacterial infection and coral bleaching. Nature 380: 396.
Litchfield, Carol D., ed. 1976. Marine Microbiology. Dowden,
Hutchinson & Ross, Inc., Strousberg,
Pennsylvania.
Meikle,
P., G.N. Richards, and D. Yellowlees. 1988. Structural investigations on the mucus from six species of coral.
Marine Biology. 99: 187-93.
Pascal,
Helene, and Eveline Vacelet. 1981. Bacterial utilization of mucus on the coral
reef of Aqaba (Red Sea). Proc. Fourth
Int'l. Coral Reef Symp. 1: 669-77.
Paul, John H., Mary DeFlaun and Wade H. Jeffrey. 1986.
Elevated levels of microbial
activity in the coral surface microlayer. Mar. Ecol. - Prog. Ser.
Ritchie, Kim B., and Garriet W. Smith 1995. Preferential
carbon utilizaton by surface bacterial
communities from water mass, normal, and white-band diseased Acropora cervicornis.
Mol. Mar. Biol Biotech. 4: 345-52.
Ritchie, K.B., and G.W. Smith. 1997. Physiological
comparison of bacterial communities from
various species of scleractinian corals. Proc 8th Int Coral Reef
Sym. 1: 521-6.
Schiller,
Christian, and Gerhard J. Herndi. 1989. Evidence of enhanced microbial activity
in the interstitial space of branched
corals: possible implications for coral metabolism. Coral Reefs 7: 179-84.
Sera,
Hirsohi, Yuzaburo Ishida, and Hajime Kadota. 1976. Bacterial flora in the
digestive tracts of marine fish. .
In: Marine Microbiology (Carole D. Litchfield, ed.). Dowden, Hutchinson & Ross, Inc., Stroudsberg,
Pennsylvania: 467-90.
Shewan,
J.M., G. Hobbs, and W. Hodgkiss. 1960. A determinative scheme for the identification of certain genera of
gram-negative bacteria, with special reference to the Psuedomonadacae. J. Appl. Bacteriol. 23: 379-90.
Sieburth,
John McNeil. 1979. Fermentative rods and
coccoids. Sea Microbes. Oxford Univeristy
Press, New York: 259-64.
Stanley,
Howard Hada. 1981. A survey of the incidence and function of plasmids in marine Vibrio spp. PhD thesis, University of Houston, Houston, TX.
Sutton,
D.C., and R. Garrick. 1993. Bacterial disease of cultured giant clam Tridacna gigas larvae. Dis. Aquat. Org. 16: 47=53.
Unemoto,
Tsutomu, at. al. 1976. Localizations and salt modifications of phosphohydrolases in slightly halophilic Vibrio alginolyticus. In: Marine Microbiology (Carole D. Litchfield,
ed.). Dowden, Hutchinson & Ross, Inc., Stroudsberg,
Pennsylvania: 46-71.
Wahbeh,
M.I., and A.M. Mahasneh. 1988. Composition and bacterial utilization of mucus of corals from Aqaba (Red Sea), Jordan. Proc.
6th Int Coral Reef Sym. 2: 53-7.
ZoBell,
Claude E., and Harvey C. Upham. 1944. A list of marine bacteia including descriptions of sixty new species. From;
Bull. Scripps Inst. Oceanogr. Univ. Calif. 5:
239-92.
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