Microbial cardiovascular and systemic disease
Cardiovascular system and septicemia
 Blood is normally axenic, it contains no microbes
 Septicemia refers to microbial infection of the blood which can
lead to septic shock
 Depending on the type of organism, blood infections are referred
to as:
 *Bacteremia (bacterial septicemia)
 Viremia
 Fungemia
 Parasitemia
Petechiae – sign of bacteremia
 Bacteria can release toxins from a site of infection into the blood
causing toxemia
 Exotoxins: i.e., neurotoxins (botulism/tetanus)
 Endotoxins: lipid A of LPS, which can lead to shock
 Severe form of toxemia with septic shock
 Streptococcal toxic-shock-like syndrome (TSLS)
 Streptococcus pyogenes
 From infections of skin/wound
 Staphylococcal toxic shock syndrome (TSS)
 Staphylococcus aureus
 From reproductive tract infections
Cardiovascular system and septicemia
 Bacterial septicemia can be associated with
 Infections of the skin/wound
 Surgical wounds
 Urinary tract infections
 Infected teeth
 Improperly sterilized kidney dialysis machines, ….
 Caused by opportunistic or nosocomial bacteria such as
 Escherichia coli, Pseudomonas aeruginosa, Neisseria meningitidis,
Haemophilus influenzae
 Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus
pyogenes
Cardiovascular system and septicemia
 Diagnosis of septicemia involves analysis of signs/symptoms
 Culturing bacteria from the blood
 In occult septicemia the exact bacterial cause is hidden
 Treatment involves
 Use of antimicrobial drugs
 Elimination of the initial site of infection (source of
septicemia)
 Intravenous fluid replacement/Antibodies against LPS
 Toxemia caused by Gram negative bacteria
Cardiovascular system and septicemia
 Blood and lymph can carry pathogens throughout the body to
cause systemic disease
 Bacterial
 Tularemia
 Plague
 Lyme disease
 Viral
 EBV (Epstein-Barr Virus)
 Cytomegalovirus
 Protozoan
 Toxoplasmosis
 Malaria
 Chaga’s disease
 Helminths
 Schistosomiasis
Microbial systemic disease
Bacterial systemic diseases - Tularemia
 Tularemia is a zoonotic disease caused by Francisella tularensis (Gram-
negative coccobacillus)
 Virulence (endotoxin and lipid
capsule – resists phagocytosis)
 Prevalence in animals as
intracellular parasite: from mammals
(rabbit ), to birds, fish, ticks, flies,
mosquitoes, mites
 Multiple mode of transmission
 bite of a tick
 contact with infected animal/animal
slaughter
 contaminated meat or water
 aerosols produced in the laboratory
Mortality rate: ~ 5% of untreated
patients
Bacterial systemic diseases - Tularemia
 Highly virulent organism
that causes
 Skin lesion (ulcer) and
swollen pus-filled lymph
nodes near the site of
infection, lymphangitis
 General symptoms may
last for months/years
 malaise, fatigue, joint
stiffness, myalgia
 Diagnosis/treatment
 Serological testing
 Antimicrobials
 Vaccine for people at risk
 Possible use of Francisella as bioterrorism weapon – nationally
notifiable disease (CDC)
Plague – Yersinia pestis (Enterobacteriaceae)
 Bubonic plague - bite of infected flea or direct contact with infected
animal
 Pneumonic plague - bacilli spread from the blood to the lungs or are
inhaled (airborne transmission)
 Plague has caused several pandemics
Xenopsylla
cheopis
Plague – Yersinia pestis
Bubo: painfully inflamed
lymph node
Darkening of dead tissues
 Plague has been called the “Black Death”
 Bubonic plague is fatal in ~50% of
cases if untreated
 Pneumonic plague is fatal in ~100%
of cases if untreated
 Urban living, rodent and flea
control, antibacterial drugs have
almost eliminated plague
 The disease is considered endemic
in states like California, Arizona,
Nevada
 Potential bioterrorism weapon:
deadly, progresses rapidly, spread
among people
Lyme disease (zoonosis)
 Caused by the spirochete
Borrelia burgdorferi
Gram negative
 Bull’s eye rash at the site of
infection
 Untreated patients can develop
severe arthritis
Lyme disease is transmitted by a deer tick (Ixodes)
 Deer tick: a 2-years life cycle
Lyme disease
 Increase in cases of Lyme
disease
 Diagnosis: detecting
antibodies against
Borrelia
 Antimicrobial drugs can
cure the Lyme disease
(first phase)
 Treatment of later
phases involves anti-
inflammatory drugs
Viral systemic diseases – Epstein Barr virus (EBV)
 HHV-4
 Implicated with several diseases, depending on the “relative vigor”
of a host’s cellular immune response
EBV and infectious mononucleosis
 EBV is transmitted via saliva, enters the blood and infects B cells,
which become enlarged with lobed nuclei
 Cytotoxic T cells kill infected B cells
 Signs and symptoms: fever, sore throat, fatigue,
enlarged lymph nods and spleen
 Diagnosis: detecting antibody against EBV
 Recover of most patients in few weeks without
specific therapy
 EBV can become latent in the oropharynx: life
long infection which rarely cause disease
Cytomegalovirus (CMV) – Herpes virus
 Most people infected with CMV are asymptomatic
 CMV remains in a latent state in various cells
 Complications in
 Immunocompromised patients
 May develop pneumonia, blindness,
 CMV mononucleosis
 Fetuses (may be teratogenic)/newborns
 ~7.5% of neonates infected with CMV
 Bodily secretions carry CMV (saliva, mucous, milk, urine, feces,
semen, vaginal secretions) – it would require a large exchange of
secretions
Cytomegalovirus (CMV) – herpes virus
 CMV infections is one of the most common infections in humans
 Transmission usually occurs via
 Sexual intercourse
 Prenatal infection
 Vaginal birth
 Blood transfusion
 Organ transplants
 Diagnosis/Treatment involve
 Owl’s eye appearance of enlarged cells, detection of CMV and
antibodies against CMV
 Interferons, anti CMV immunoglobulins, fomivirsen against
replication of CMV in retinal cells. There is no vaccine against
CMV
Protozoan diseases – Toxoplasmosis
 Toxoplasma gondii
 Nucleated cells of wild and
domesticated mammals, birds
 Immunocompromised patients can develop the disease
 Fever, inflammation of several organs, spastic paralysis,
blindness, encephalitis, and death
 Transplacental infections – (first-trimester at higher risk) can cause
spontaneous abortion, mental retardation, blindness, or microcephaly
 Healthy individuals (mostly
asymptomatic)
 Infection normally resolves
without treatment
 Humans become infected
when ingesting undercooked
contaminated meat
 Serological detection and
microscopic identification in
tissue samples
 Treatment with a combination
of drugs in AIDS patients,
pregnant women, newborns
Wash fruits and vegetables, eat well
cooked meat!!!
Protozoan diseases – Toxoplasmosis
 Definitive host
Malaria is transmitted by
Anopheles mosquito
 Plasmodium species, including
P. falciparum (blackwater
fever)/P. vivax (chronic
malaria)
 Malarial paroxysms: cycles of
fever-chills correlate with
period of erythrocyte lysis
 Anemia and jaundice
(liver/eyes)
Protozoan diseases - Malaria
Ring-stage - trophozoites
within red blood cells
 Microscopic examination of blood smears allows diagnosis of
malaria
 Serological tests for specific diagnosis
 Treatment and supportive
measures
 Antimalarial drugs
 Anti-fever medication
 Blood transfusions
 Alternative methods involve
 Limiting contact with mosquitos
carrying Plasmodium
 Malaria vaccines (development
and testing in progress)
Protozoan diseases - Malaria
 Malaria is endemic throughout the tropics and subtropics, where
Anopheles breeds
 Mosquito eradication programs eliminated the disease in
Countries like US
 Over 500 million people
are infected
 1-3 million people die
annually
Chagas’ disease – American trypanosomiasis
 Caused by Trypanosoma cruzi
 Transmitted with the feces of the bloodsucking “kissing bug”
 Major reservoirs: opossum and armadillos though most mammals,
including humans, can carry the parasite
 ~ 1% of infected humans
develop early stages (general
symptoms)
 Intermediate asymptomatic
(chronic) stage for up to ~ 20
years
 Heart failure during final
symptomatic stage
 Clusters of parasites in the
heart muscle tissue
Trypomastigotes (infective) circulating
in the blood are ingested by the kissing
bug
Chagas’ disease – American trypanosomiasis
 The disease is endemic in Central and South America
 Affects 8-15 million people
 Thousands die each
year, including children
 Early stages can be treated
but not late stages
 No vaccine exists for
Chagas’s disease
 Prevention involves measures that protect against bugs: mud
replaced with concrete/brick, insecticides …..
Schistosomiasis is caused by blood flukes
 Genus
Schistosoma
 The larval stage
cercaria burrows
into the skin
 Feeding on blood,
matures, mates, and
releases eggs
 Eggs lodge in
tissues causing
damage to several
organs
 Treatment/control: drugs that kill the
worm in the body, sewage treatment,
and snail suppression
Egg of Schistosoma mansoni
 Diagnosis: identification of eggs -
shape of the egg and location of the
spines - in stool or urine samples
 WHO (World Health Organization) estimates that over 250 million
people are infected worldwide – Asia, Africa, South America
Schistosomiasis is caused by blood flukes
Scarlike tissue surrounds the egg

12 bio265 disease of circulatory system instructor dr di bonaventura

  • 1.
  • 2.
    Cardiovascular system andsepticemia  Blood is normally axenic, it contains no microbes  Septicemia refers to microbial infection of the blood which can lead to septic shock  Depending on the type of organism, blood infections are referred to as:  *Bacteremia (bacterial septicemia)  Viremia  Fungemia  Parasitemia Petechiae – sign of bacteremia
  • 3.
     Bacteria canrelease toxins from a site of infection into the blood causing toxemia  Exotoxins: i.e., neurotoxins (botulism/tetanus)  Endotoxins: lipid A of LPS, which can lead to shock  Severe form of toxemia with septic shock  Streptococcal toxic-shock-like syndrome (TSLS)  Streptococcus pyogenes  From infections of skin/wound  Staphylococcal toxic shock syndrome (TSS)  Staphylococcus aureus  From reproductive tract infections Cardiovascular system and septicemia
  • 4.
     Bacterial septicemiacan be associated with  Infections of the skin/wound  Surgical wounds  Urinary tract infections  Infected teeth  Improperly sterilized kidney dialysis machines, ….  Caused by opportunistic or nosocomial bacteria such as  Escherichia coli, Pseudomonas aeruginosa, Neisseria meningitidis, Haemophilus influenzae  Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes Cardiovascular system and septicemia
  • 5.
     Diagnosis ofsepticemia involves analysis of signs/symptoms  Culturing bacteria from the blood  In occult septicemia the exact bacterial cause is hidden  Treatment involves  Use of antimicrobial drugs  Elimination of the initial site of infection (source of septicemia)  Intravenous fluid replacement/Antibodies against LPS  Toxemia caused by Gram negative bacteria Cardiovascular system and septicemia
  • 6.
     Blood andlymph can carry pathogens throughout the body to cause systemic disease  Bacterial  Tularemia  Plague  Lyme disease  Viral  EBV (Epstein-Barr Virus)  Cytomegalovirus  Protozoan  Toxoplasmosis  Malaria  Chaga’s disease  Helminths  Schistosomiasis Microbial systemic disease
  • 7.
    Bacterial systemic diseases- Tularemia  Tularemia is a zoonotic disease caused by Francisella tularensis (Gram- negative coccobacillus)  Virulence (endotoxin and lipid capsule – resists phagocytosis)  Prevalence in animals as intracellular parasite: from mammals (rabbit ), to birds, fish, ticks, flies, mosquitoes, mites  Multiple mode of transmission  bite of a tick  contact with infected animal/animal slaughter  contaminated meat or water  aerosols produced in the laboratory Mortality rate: ~ 5% of untreated patients
  • 8.
    Bacterial systemic diseases- Tularemia  Highly virulent organism that causes  Skin lesion (ulcer) and swollen pus-filled lymph nodes near the site of infection, lymphangitis  General symptoms may last for months/years  malaise, fatigue, joint stiffness, myalgia  Diagnosis/treatment  Serological testing  Antimicrobials  Vaccine for people at risk  Possible use of Francisella as bioterrorism weapon – nationally notifiable disease (CDC)
  • 9.
    Plague – Yersiniapestis (Enterobacteriaceae)  Bubonic plague - bite of infected flea or direct contact with infected animal  Pneumonic plague - bacilli spread from the blood to the lungs or are inhaled (airborne transmission)  Plague has caused several pandemics Xenopsylla cheopis
  • 10.
    Plague – Yersiniapestis Bubo: painfully inflamed lymph node Darkening of dead tissues  Plague has been called the “Black Death”  Bubonic plague is fatal in ~50% of cases if untreated  Pneumonic plague is fatal in ~100% of cases if untreated  Urban living, rodent and flea control, antibacterial drugs have almost eliminated plague  The disease is considered endemic in states like California, Arizona, Nevada  Potential bioterrorism weapon: deadly, progresses rapidly, spread among people
  • 11.
    Lyme disease (zoonosis) Caused by the spirochete Borrelia burgdorferi Gram negative  Bull’s eye rash at the site of infection  Untreated patients can develop severe arthritis
  • 12.
    Lyme disease istransmitted by a deer tick (Ixodes)  Deer tick: a 2-years life cycle
  • 13.
    Lyme disease  Increasein cases of Lyme disease  Diagnosis: detecting antibodies against Borrelia  Antimicrobial drugs can cure the Lyme disease (first phase)  Treatment of later phases involves anti- inflammatory drugs
  • 14.
    Viral systemic diseases– Epstein Barr virus (EBV)  HHV-4  Implicated with several diseases, depending on the “relative vigor” of a host’s cellular immune response
  • 15.
    EBV and infectiousmononucleosis  EBV is transmitted via saliva, enters the blood and infects B cells, which become enlarged with lobed nuclei  Cytotoxic T cells kill infected B cells  Signs and symptoms: fever, sore throat, fatigue, enlarged lymph nods and spleen  Diagnosis: detecting antibody against EBV  Recover of most patients in few weeks without specific therapy  EBV can become latent in the oropharynx: life long infection which rarely cause disease
  • 16.
    Cytomegalovirus (CMV) –Herpes virus  Most people infected with CMV are asymptomatic  CMV remains in a latent state in various cells  Complications in  Immunocompromised patients  May develop pneumonia, blindness,  CMV mononucleosis  Fetuses (may be teratogenic)/newborns  ~7.5% of neonates infected with CMV  Bodily secretions carry CMV (saliva, mucous, milk, urine, feces, semen, vaginal secretions) – it would require a large exchange of secretions
  • 17.
    Cytomegalovirus (CMV) –herpes virus  CMV infections is one of the most common infections in humans  Transmission usually occurs via  Sexual intercourse  Prenatal infection  Vaginal birth  Blood transfusion  Organ transplants  Diagnosis/Treatment involve  Owl’s eye appearance of enlarged cells, detection of CMV and antibodies against CMV  Interferons, anti CMV immunoglobulins, fomivirsen against replication of CMV in retinal cells. There is no vaccine against CMV
  • 18.
    Protozoan diseases –Toxoplasmosis  Toxoplasma gondii  Nucleated cells of wild and domesticated mammals, birds  Immunocompromised patients can develop the disease  Fever, inflammation of several organs, spastic paralysis, blindness, encephalitis, and death  Transplacental infections – (first-trimester at higher risk) can cause spontaneous abortion, mental retardation, blindness, or microcephaly  Healthy individuals (mostly asymptomatic)  Infection normally resolves without treatment
  • 19.
     Humans becomeinfected when ingesting undercooked contaminated meat  Serological detection and microscopic identification in tissue samples  Treatment with a combination of drugs in AIDS patients, pregnant women, newborns Wash fruits and vegetables, eat well cooked meat!!! Protozoan diseases – Toxoplasmosis  Definitive host
  • 20.
    Malaria is transmittedby Anopheles mosquito  Plasmodium species, including P. falciparum (blackwater fever)/P. vivax (chronic malaria)  Malarial paroxysms: cycles of fever-chills correlate with period of erythrocyte lysis  Anemia and jaundice (liver/eyes)
  • 21.
    Protozoan diseases -Malaria Ring-stage - trophozoites within red blood cells  Microscopic examination of blood smears allows diagnosis of malaria  Serological tests for specific diagnosis  Treatment and supportive measures  Antimalarial drugs  Anti-fever medication  Blood transfusions  Alternative methods involve  Limiting contact with mosquitos carrying Plasmodium  Malaria vaccines (development and testing in progress)
  • 22.
    Protozoan diseases -Malaria  Malaria is endemic throughout the tropics and subtropics, where Anopheles breeds  Mosquito eradication programs eliminated the disease in Countries like US  Over 500 million people are infected  1-3 million people die annually
  • 23.
    Chagas’ disease –American trypanosomiasis  Caused by Trypanosoma cruzi  Transmitted with the feces of the bloodsucking “kissing bug”  Major reservoirs: opossum and armadillos though most mammals, including humans, can carry the parasite  ~ 1% of infected humans develop early stages (general symptoms)  Intermediate asymptomatic (chronic) stage for up to ~ 20 years  Heart failure during final symptomatic stage  Clusters of parasites in the heart muscle tissue Trypomastigotes (infective) circulating in the blood are ingested by the kissing bug
  • 24.
    Chagas’ disease –American trypanosomiasis  The disease is endemic in Central and South America  Affects 8-15 million people  Thousands die each year, including children  Early stages can be treated but not late stages  No vaccine exists for Chagas’s disease  Prevention involves measures that protect against bugs: mud replaced with concrete/brick, insecticides …..
  • 25.
    Schistosomiasis is causedby blood flukes  Genus Schistosoma  The larval stage cercaria burrows into the skin  Feeding on blood, matures, mates, and releases eggs  Eggs lodge in tissues causing damage to several organs
  • 26.
     Treatment/control: drugsthat kill the worm in the body, sewage treatment, and snail suppression Egg of Schistosoma mansoni  Diagnosis: identification of eggs - shape of the egg and location of the spines - in stool or urine samples  WHO (World Health Organization) estimates that over 250 million people are infected worldwide – Asia, Africa, South America Schistosomiasis is caused by blood flukes Scarlike tissue surrounds the egg