Showing posts with label human-to-human. Show all posts
Showing posts with label human-to-human. Show all posts

Sunday, 22 November 2015

Updating the animal "to-do" list...

I have a couple of talks coming up, so I'm making graphics again. And I like to share those. 

This one is an update on some of the creatures that could also be considered suspects in the hunt for sources of MERS-CoV infection of humans.

Of course, camels are the ones we know to be a true risk for infection and there was that 1 bat that was positive for a very small diagnostic PCR product. Cattle contact was also recently listed, with little detail, as a significant risk factor among those acquiring MERS-CoV infection and we also know that cells from camels, horses, alpacas, cattle and goats can be infected and host genome or virus replication of MERS-CoV in the lab, or have the MERS-CoV cellular receptor, DPP4, on their surface.[1,2]

I heard that there will be more bat testing in the future, but we haven't read of any MERS-CoV targeted bat studies since 2013.

So here is the long laundry list of animal testing that needs more work - many of which have been tested in small numbers over limited time periods already - in a graphical form.

Click on image to enlarge.
You can also access this from Figshare.[3]
References...

  1. http://www.ncbi.nlm.nih.gov/pubmed/25656066
  2. http://wwwnc.cdc.gov/eid/article/22/1/15-1340_article
  3. http://figshare.com/articles/Creatures_of_interest_to_how_humans_acquire_a_MERS_CoV_infection/1609604

Monday, 13 January 2014

H5N1 case in Canada had been diagnosed with pneumonia...testing at the source would have been helpful

And now, from a fantastically detailed post onto ProMED by Fonseca and colleagues, we see that the H5N1 case was diagnosed with pneumonia.

On 28-Dec, the patient presented to a local emergency department.

"A chest X-ray and CT scan revealed a right apical infiltrate. A diagnosis of pneumonia was made; the patient was prescribed levofloxacin and discharged home."
One sad point made in the ProMED post which supports the need for constant viral vigilance the world over, coupled with the dissemination of those surveillance data, so that patient management anywhere in the world can be armed with the best possible decision-making information...
"The index of suspicion was low as travel was to an area in China where there have been no recent reports of the circulation of this virus, and coupled with no obvious exposure to poultry, the diagnostic work-up and consideration for A(H5N1) infection was very low"
As a recent J Virology article by Yu and colleagues highlights, when a sensitive testing method like the polymerase chain reaction (PCR; in this case RT-PCR because influenza viruses all have an RNA genome, not a DNA one) is applied to the search for a virus, it yields the kind of data that can:

  1. Explain from where a virus emerges
  2. Inform the search for disease aetiology - where are human cases getting infected from and if a zoonotic infection (from animals to humans), which animal(s) is the culprit?
  3. Alert the world to any risks of infection when travelling to a certain area(s)
  4. Allow the local health departments to mitigate the risk of their population acquiring infection by instigating controls (like live bird market closures). This has implications for the world since respiratory viruses have the potential (thankfully not realized for H7N9 or H5N1 to date) to spread more rapidly and efficiently that blood-borne or mosquito-borne or sexually transmitted viruses.
  5. Permit understanding of how widespread (over what geographic area is it detected) a novel or emerging virus may be and how entrenched (is the same site repeatedly positive) it is
Not doing such testing, or using less sensitive methods will not yield this information. 

In Yu's study, testing of 12 poultry markets, mostly urban, and local farms linked to 10 human infections in Hangzhou, Zhejiang province around 4th to 20th April 2013 yielded signs of H9N2, H7N9 and/or H5N1 viruses in all markets. Poultry were often positive for H7N9 and H9N2 (this finding from individual RT-PCRs was confirmed using next generation sequencing), whereas human specimens were not. These levels hadn't been turned up when 899,000 bird were tested in 2013 using (perhaps) less sensitive methods.

I think with influenza, it may be safer to presume its everywhere until that presumption can be discounted. Clearly the conditions for influenza viruses to swap gene segments and sort themselves into new subtypes and variants are commonplace and frequent; these aren't just chance occurrences of different birds passing in the night via overlapping flyways. These feathered vectors are co-infected by 2 or more viruses at a time. Luck and the constraints of viral fitness are presumably the only things keeping H7N1, H5N9, H7N2 cases from dialing up in humans? What seems to be lacking is more molecular testing at the farms supplying the markets. Not just in Zhejiang, but all over the region.

As the authors noted, 100,000s of people visit these live bird markets each day and very few influenza cases seem to be due to them. Long may that last. But it's a tinderbox for which matches are already being struck; if the viruses should bud of that one-in-a-million variant that is enabled to readily spread from person-to-person, whooshka

More testing guys, keep testing.

Wednesday, 7 August 2013

A detailed report of a Jiangsu H7N9 infection family cluster and the probable involvement of human-to-human transmission

Qi and colleagues describe in the British Medical Journal (BMJ), their detailed analysis of a likely human-to-human (h2h) transmission event by influenza A(H7N9) virus. The infection is likely to have traveled a 60-year old father to his 32-year old daughter, but not to any close contacts-1 "passage" of transmission. 

This event was previously defined as a family cluster, but the new BMJ report adds to the information published in the NEJM article by Li et al in April (see "Jiangsu Family Cluster", Figure 3).


The conclusion is that H7N9 likely spread to one other person but no further, in this instance, using these tests to define infection. As the accompanying editorial by Rudge and Coker notes, it's not surprising to see this happen. The media have become somewhat carried away in suggesting this is the first case of h2h transmission. That "honour" probably goes to the family of the first announced case, the 87-year old male from Shanghai and his family cluster

To be pedantic, this new BMJ analysis does not actually prove h2h transmission (hence the word "probable" in the title I suspect) highlighting just how hard it is to do that in the "wild" and after the transmission event has occurred. It is probable though. However, we know for certain that H7N9 can be transmitted between the 4-legged furry kind of animal (see related posts here, here and here).

Some key take home messages...

  • 2 patients (60M and his daughter 32F) 13 samples of the environment were tested by PCR
  • 60M, who had hypertension, developed respiratory disease March 8th and was hospitalized March 11th. He died of multi-organ failure and disseminated coagulation May 4th.
    • An endotracheal aspirate (ETA) was H7N9 POS, but a throat swab was NEG
    • No diarrhoea was linked to infection 
  • 32F was an otherwise healthy developed symptoms March 21st and was hospitalized March 24th. She died of multi-organ and heart attack on April 24th
    • Throat swab and ETA were H7N9 POS
  • 3 viral isolates were able to be grown in culture and 2 complete genomes (8 segments each) were deposited onto, but not yet released from, GenBank
    • The sequences from eh two human cases reportedly differ a little, mostly in the NS and NA segments whereas the environmental isolate's M segment showed the most divergence from the 2 human cases. The genome details are...
      • KF034916-KF034923 - 60M (A/Wuxi/2/2013)
      • KF034908-KF034915  - 32F (A/Wuxi/1/2013)
      • KF150605-KF150612 - (A/Environment/Wuxi/1/2013)
  • All samples were negative for other respiratory viruses
  • The study did not include interviews with the 2 cases as they were too ill so some avenues of infection could not be excluded
  • Both cases were treated with oseltamivir 3-10 days after symptom onset-the US CDC recommends commencement within 48-hours of symptoms, which can be difficult to achieve as patients may present some time after disease is well underway
  • Of 43 close contacts, none were RNA positive for H7N9 nor were any positive for antibodies to H7N9 suggesting they had not hosted an infection that was missed by PCR
  • The in-house ("home made") antibody test was considered, by the authors, to be insufficiently sensitive and may have missed evidence of exposure in contacts. Prospective screening of contacts was not done.